AU2013202011B2 - In vivo temporal control of activatable matrix-degrading enzymes - Google Patents

Abstract

Methods and combinations are provided for controlling the duration of action, in vivo, of matrix-degrading enzymes. The methods and combinations permit temporary in-vivo activation of matrix-degrading enzymes upon administration to the extra cellular matrix (or "ECM"). Matrix-degrading enzymes having a controlled duration of action can be used to treat ECM-mediated diseases or disorders characterized by increased deposition or accumulation of one or more ECM components.

Description

AUSTRALIA Regulation 3.2 Patents Act 1990 Complete Specification Standard Patent APPLICANT: Halozyme, Inc. Invention Title: IN VIVO TEMPORAL CONTROL OF ACTIVATABLE MATRIX DEGRADING ENZYMES The following statement is a full description of this invention, including the best method of performing it known to me: WO 2009/111083 PCT/US2009/001486

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IN VIVO TEMPORAL CONTROL OF ACTIVATABLE MATRIX DEGRADING ENZYMES RELATED APPLICATIONS Benefit of priority is claimed to U.S. Provisional Application Serial No. 5 61/068,667, to Gilbert Keller and Gregory Frost, entitled "In Vivo Temporal Control of Activatable Matrix-Degrading Enzymes," filed March 06, 2008, and to U.S. Provisional Application Serial No. 61/127,725, to Gilbert Keller and Gregory Frost, entitled "In Vivo Temporal Control of Activatable Matrix-Degrading Enzyme," filed May 14, 2008. Where permitted, the subject matter of the above-noted applications 10 are incorporated by reference in its entirety. This application also is related to U.S. Patent Application Serial No. (Attorney Dkt. No. 119374-00082/ 3056), entitled "In Vivo Temporal Control of Activatable Matrix-Degrading Enzymes," which claims priority to U.S. Provisional Application Serial No. 61/068,667 and to U.S. Provisional Application Serial No. 61/127,725. 15 This application also is related to U.S. Provisional Patent Application Serial No. (Attorney Dkt. No. I 19374-00103/p3O77), entitled "'TemperatureSensitive Mutants of Matrix Metalloproteases and Uses Thereof." Where permitted, the subject matter of the above-noted related applications is incorporated by reference in its entirety. 20 Incorporation by reference of Sequence Listing provided on compact discs An electronic version on compact disc (CD-R) of the Sequence Listing is filed herewith in four copies (labeled COPY 1, COPY 2, COPY 3, and CRF), the contents of which are incorporated by reference in their entirety. The computer-readable file on each of the aforementioned compact discs, created on March 6, 2009, is identical, 25 1.96 megabytes in size, and titled 3056SEQ.PCI.txt. FIELD OF THE INVENTION Methods and combinations are provided for controlling the duration of action, in vivo, of matrix-degrading enzymes. The methods and combinations permit temporary in vivo activation of matrix-degrading enzymes upon administration to the 30 extra cellular matrix (or "ECM"). Matrix-degrading enzymes having a controlled duration of action can be used to treat ECM-mediated diseases or disorders characterized by increased deposition or accumulation of one or more ECM components. RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 -2 BACKGROUND The extracellular matrix (ECM) provides a critical structural support for cells and tissues. Defects or changes in the extracellular matrix as a result of excessive deposition or accumulation of ECM components can lead to ECM-mediated diseases 5 or conditions. Among these are collagen-mediated diseases or conditions characterized by the presence of abundant fibrous septae of collagen. Often the only approved treatment for such diseases or conditions is surgery, which can be highly invasive. Other treatments, such as needle aponeurotomy for the treatment of Dupuytren's syndrome (also called Dupuytren's contracture) or liposuction for 10 cellulite, also are highly invasive. Collagenase, an enzyme active at neutral pH that degrades collagen, has been used to treat ECM-mediated conditions such as cellulite (see e.g., published U.S. application serial No. US20070224184); Dupuytren's syndrome (see e.g. U.S. Patent No. USRE39941; 5589171; 6086872); and Peyronie's disease (see e.g., U.S. Patent 15 6022539). Collagenase, however, is capable of irreversibly cleaving collagens of type I, II and III. The prolonged activity of collagenase limits the dosages that can be administered and also risks side effects associated with prolonged activation. Hence, there is a need for alternative treatments of ECM-mediated diseases and conditions. Accordingly, it is among the objects herein to provide methods and combinations of 20 activatable matrix-degrading enzymes for the treatment of ECM-mediated diseases and conditions. SUMMARY Provided are methods for treating diseases or conditions of the extracellular matrix (ECM) by administering an activatable matrix-degrading enzyme (AMDE) and 25 an activator. Generally a therapeutically effective amount of the AMDE is administered. The amount is a function of the disease or condition treated and can be empirically determined. The AMDE that is selected is one that is inactive in the in vivo locus of administration, such as the ECM. AMDEs include naturally-occurring matrix-degrading (MD) enzymes, species and allelic and other variants thereof, such 30 as enzymes modified to alter an activity, such as substrate specificity or property, such as stability. The AMDEs can be modified by processes and methods to have properties, such as increased specificity for a cleaving a particular type of collagen or to have an altered pH curve or optimum for the methods herein. Administration in WO 2009/111083 PCT/US2009/001486 -3 conjunction with an activator or combination of activators, not present in the locus of administration results in an AMDE that is active for a limited period of time as the activator dissipates or is otherwise removed from the locus. The AMDE and activator can be administered sequentially, simultaneously in the same or separate composition, 5 or intermittently. Conditions can be selected so that the period of time of activity is predetermined. An AMDE can require more than one activator for activity or full activity. The AMDE can be administered as a zymogen, as a full-length mature polypeptide, such as a single-chain or two-chain polypeptide, or as precursor polypeptide. The AMDE can be provided in a composition, such as a solution or 10 suspension, or in crystallized or lyophilized form. Exemplary AMDEs include, but are not limited to, cathepsins, calpains and heparanases. Generally, the AMDE is administered sub-epidermally. When administered to other loci, including topically, the AMDE is selected so that the AMDE is substantially active (typically at least about or 10%, 11%, 12%, 13% or 15% of the 15 activity compared to at its pH maximum remains) at pH 5.5. In addition, for such administration, the AMDE typically is inactive (less than about or 10%, 11%, 12%, 13% or 15% of the activity remains) at neutral pH. Diseases and conditions of the ECM, include for example, collagen-mediated diseases and conditions. Such diseases and conditions include, but are not limited to: cellulite; Dupuytren's disease surgical 20 adhesions, keloids, hypertrophic scars and depressed scars; Peyronie's disease; Ledderhose fibrosis; stiff joints; including a frozen shoulder; existing scars, including surgical adhesions, keloids, hypertrophic scars and depressed scars; scleroderma; lymphedema and collagenous colitis. Sub-epidermal administration includes, but is not limited to subcutaneous administration, intramuscular administration, intralesional 25 administration and intradermal administration. Thus, provided are methods for treating a disease or condition of the extracellular matrix (ECM) by sub-epidermally administering to the ECM an activatable matrix-degrading enzyme (AMDE) and an activator. The AMDE is inactive or partially inactive in the ECM in the absence of the activator; the activator, 30 when administered to the ECM, provides an activating condition for the enzyme whereby the AMDE is active, and the activating condition is generally not present in the ECM prior to administration of the activator. In some embodiments the AMDE is selected to be an enzyme that is substantially inactive at neutral pH.

WO 2009/111083 PCT/US2009/001486 -4 Also provided are methods of treating a disease or condition of the extracellular matrix (ECM) by administering an activatable matrix-degrading enzyme (AMDE) and an activator, wherein the AMDE is inactive at neutral pH, the activator provides an acidic pH activating condition for the enzyme such that the AMDE is 5 active upon or after administration, and the activating condition is not present at the site of administration prior to administration of the activator; and the AMDE is substantially active at pH 5.5. The AMDE and activator can be administered by any suitable route, including, but not limited to, subcutaneous, intramuscular, intralesional, intradermal, topical, transdermal, intravenous, oral and rectal 10 administration. For example, administration can be sub-epidermal administration. Also provided are methods for treating a disease or condition of the extracellular matrix (ECM) by administering an activatable matrix-degrading enzyme (AMDE) and an activator, where the AMDE is inactive in the ECM in the absence of the activator such that the activator, when administered, provides an activating 15 condition for the enzyme such that the AMDE is active, the activating condition is not present in the ECM prior to administration of the activator, and the activator is selected from among a metal ion, temperature and ionic strength of excipient, or a reducing or oxidizing agent. The AMDE and activator or combination of activators can be administered by any suitable route, including, but not limited to, subcutaneous, 20 intramuscular, intralesional, intradermal, topical, transdermal, intravenous, oral and rectal administration. For example, administration can be sub-epidermal administration. In an exemplary embodiment, provided are methods for treating a disease or condition of the extracellular matrix (ECM) by administering to the ECM an 25 activatable matrix-degrading enzyme (AMDE) and an activator, where the AMDE is inactive in the ECM in the absence of the activator such that the activator, when administered to the ECM, provides an activating condition for the enzyme such that the AMDE is active, the activating condition is not present in the ECM prior to administration of the activator; and the activator is selected from among metal ions, 30 temperature and ionic strength. The AMDE and activator can be administered by any suitable route, including, but are not limited to, subcutaneous, intramuscular, intralesional, intradermal, topical, transdermal, intravenous, oral and rectal administration. For example, administration can be sub-epidermal administration.

WO 2009/111083 PCT/US2009/001486 -5 In other exemplary embodiments provided are methods for treating a collagen mediated disease or condition by sub-epidermally administering to the ECM a therapeutically effective amount of an activatable cathepsin L and an activator, where the activatable cathepsin L is inactive in the ECM in the absence of the activator, the 5 activator, when administered to the ECM, provides an activating condition for the enzyme such that the activatable cathepsin L is active, the activating condition is not present in the ECM prior to administration of the activator; and the activating condition is acidic pH. Exemplary cathepsin L polypeptides are those that include a sequence of amino acids set forth in SEQ ID NO: 1 or allelic, species or other variant 10 thereof, where such variants are modified to have altered properties or activities and, typically have at least or have 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity compared to a sequence of amino acids set forth in any of SEQ ID NO: 1. In general over time in the methods herein, the activator will be removed or 15 dissipated or neutralized by the local environment so that the AMDE is no longer active. Activating conditions and/or activators can be selected or prepared so that the AMDE is active for a limited or predetermined time. The activator can be provided or administered in the same composition as the AMDE or in a separate composition, and they can be administered sequentially, simultaneously or intermittently. For example, 20 the AMDE is exposed to the activator prior to administration or upon administration, whereby the enzyme is active upon administration. Activating conditions include, but are not limited to, pH, ionic strength, temperature and metal ions. Among the activating conditions is pH, such as acidic pH, for example at or about in a range of 3 to 6.5, or 3.5 to 6, or 3 to 5.5, or 3 to 4.5, or 4 to 6, or 4 to 5.5, or 4.5 to 5, or 5 to 6, 25 such as 3, 3.5, 4, 4.5, 5, 5.5, 6 or 6.5. pH can be obtained by contacting the AMDE with a buffered solution at the desired pH. Buffers can include those that contain an acid selected from among 2-(N-morpholino)ethanesulfonic acid (MES), acetic acid, citric acid, maleate, succinate, lactate, glycinate, citric phosphate and histidine. Other exemplary activity conditions include, but are not limited to, metal ions and 30 temperature. For example, the activating condition can be a metal ion, such as Ca2+ Zn2+ or Mg 2 +. Temperature can be low or high temperature, where the enzyme is substantially inactive at the temperature of the locus of administration, typically 37"C. Thus, the activating condition is temperature and the temperature is or is about 20 *C, RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 -6 21 *C, 22 *C, 23 *C, 24 *C, 25 00, 26 0C, 27 0C, 28 0C, 29 00, 30 0 or above 37 *C, such as 40 *C, 41 *C, 42 0C, 43 0C, 44 *C, 45 0C, 46 0C, 47 *C, 48 *C, 49 0C, 50 *C, 55 0C, 60 *C, 65 *C, 70 *C, 80 0C and higher up to any temperature tolerated that does not damage in vivo tissues or cells. 5 Temporal control of the activity can be achieved, for example, by selection of the buffering capacity of the buffer and/or ionic strength thereof. A predetermined time for activity can be effected by selection of such conditions, which can be determined empirically or by any method known to one of skill in the art. Predetermined times can range from less than or about a minute to hours, such as 10 about or 1 minute, 2 minutes, 3 minutes, 4 minutes, 5 minutes, 6 minutes, 7 minutes, 8 minutes, 9 minutes, 10 minutes, 20 minutes, 30 minutes, 40 minutes, 50 minutes, I hour, 2 hours, 3 hours and 4 hours. As noted an AMDE can be any matrix degrading enzyme that is activatable or that is modified so that it is activatable by a particular activator or activation 15 condition. Among the AMDEs for use in the methods herein are lysosomal enzymes. AMDEs include, for example, cathepsins, such as cathepsins that are cysteine or aspartic proteases. These include, for example, cathepsin S, cathepsin K, cathepsin L, cathepsin B, cathepsin C, cathepsin H, cathepsin F, cathepsin 0, cathepsin R, cathepsin V, cathepsin W, cathepsin D and cathepsin E. Exemplary of such 20 cathepsins are any selected from a cathepsin that has a sequence of amino acids set forth in any of SEQ ID NOS: 57, 60, 1, 65, 180, 68, 71, 74, 77, 183, 186, 189, 80, 195, 90, 93 and 96, or an allelic, or species variant or other variant of any of SEQ ID NOS: 57, 60, 1, 65, 180, 68, 71, 74, 77, 183, 186, 189, 80, 195, 90, 93 and 96. Other variants, include, for example, enzymes modified to have an altered property, such as 25 stability, or activity, such as substrate specificity. Variants can have, for example, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% more sequence identity with any of the polypeptides whose sequence of amino acids is set forth in any of SEQ ID NOS: 57, 60, 1, 65, 180, 68, 71, 74, 77, 183, 186, 189, 80, 195, 90, 93 and 96. 30 In the methods herein, the AMDE, upon administration, can cleave any one or more extracellular matrix (ECM) components. Such cleavage occurs for a limited time, which can be predetermined. ECM components that are cleaved, include, but are not limited to, for example, collagens, elastins, fibronectins and proteoglycans, RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 -7 such as a type I, type II, type III or type IV collagen. The AMDEs can be modified, such as by directed evolution methods or other methods, to have altered properties or activities, such as increased substrate specificity for type I collagen over type IV collagen. 5 Other agents can be administered with the activator and enzymes. Administration can be in the same composition as the activator and/or enzyme or as separate compositions. Administration can be performed simultaneously, separately or intermittently. Exemplary agents, include, but are not limited to, for example, pharmacologic agents selected from among other biologics, small molecule 10 compounds, dispersing agents, anesthetics and vasoconstrictors and/or combinations thereof. Exemplary of a dispersing agent is a hyaluronan degrading enzyme, for example a hyaluronidase, such as PH20, such as a soluble form thereof, particularly rHuPH20. Such a hyaluronidase typically is administered prior to administration of the enzyme and activator. Exemplary of a soluble hyaluronidase is the product 15 designated rHuPH20, which is encoded by nucleic acid the encodes a polypeptide that has a sequence of amino acids set forth in SEQ ID NO:226, or is an allelic or species variant or other variant thereof or a variant of such polypeptide that has at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or more sequence identity to the sequence of amino acids set forth in SEQ ID NO:226. 20 Other agents include anesthetics, such as lidocaine, and vasoconstrictors, such as alpha adrenergic receptor agonists, including, for example, levonordefrin, epinephrine and norepinephrine. Typically such agents are administered with or before the AMDE and activator. Thus, provided are methods of treating a disease or condition of the extracellular matrix (ECM) by sub-epidermally administering an 25 activatable matrix-degrading enzyme (AMDE), as described above, an activator, a hyaluronidase, lidocaine and epinephrine. The AMDE is inactive in the ECM in the absence of the activator. The enzyme, hyaluronidase, lidocaine and epinephrine can be administered simultaneously, sequentially or intermittently, provided that the lidocaine is administered prior to the enzyme. For example, the hyaluronidase, 30 lidocaine and epinephrine are administered prior to administration of the enzyme or the hyaluronidase, lidocaine and epinephrine are administered simultaneously or the hyaluronidase, lidocaine and epinephrine can be administered in a single composition. The AMDE and activator and other agents can be administered by any suitable route, WO 2009/111083 PCT/US2009/001486 -8 including, but not limited to, subcutaneous, intramuscular, intralesional, intradermal, topical, transdermal, intravenous, oral and rectal administration. For example, administration can be sub-epidermal administration. Also provided are products, including compositions, containers, combinations 5 and kits that can be used to effect the methods. For example, provided are containers that contain two compartments. A first compartment contains a therapeutically effective amount of an activatable matrix-degrading enzyme (AMDE), where the amount is for single dosage or a plurality of dosages and a single dosage is effective for treatment of a disease or condition of the ECM ; and a second compartment 10 contains an activator, where the activator is one that activates the enzyme. AMDEs include, for example lysosomal enzymes, such as cathepsins, calpains and heparanases, including those described above for use in the methods. The AMDEs in the containers are those as described above, including, for example, an AMDE that is substantially active at pH 5.5, and, optionally is substantially inactive at neutral pH. 15 The activators provide for activating conditions such as those described above. Hence the second compartment can contain a composition that effects a change or maintains a pH, such as a buffer, or ionic strength or provides a metal ion, such as Ca2+, Zn2+ Mg2+. Exemplary buffers include those that contain acids from among 2-(N morpholino)ethanesulfonic acid (MES), acetic acid, citric acid, maleate, succinate, 20 lactate, glycinate, citric phosphate and histidine. The diseases and conditions, include those described above. The containers can also include a mixing compartment to effect mixing of the components in the first and second compartments. Exemplary containers, include tubes and bottles, sterile contains, such a syringe, with or without a needle for injection. 25 The AMDE and activator are provided in an amount for single or multiple dosage administration. The AMDE in the container can be provided in an amount that is or is about 10 pg to 100 mg, 50 pg to 75 mg, 100 pg to 50 mg, 250 pg to 25 mg, 500 pg to 10 mg, I mg to 5 mg, or 2 mg to 4 mg. It can be provided as a solid, such as in crystallized form or lyophilized form, or in liquid form, such as solution or 30 suspension, a gel or other suitable form. The total volume of liquid in the container, for example, can be or is about 1 -100 ml, 1 -50 ml, 10- 50 ml, 10-30 ml, 1-20 ml, and 1-10 ml. RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 -9 In an exemplary embodiment provided are containers that have at least two compartments, where a first compartment contains a therapeutically effective amount of an activatable cathepsin L and the amount is effective for treatment of a disease or condition of the extracellular matrix (ECM); and a second compartment contains an 5 acidic buffer that is one that activates the cathepsin L. The diseases and conditions are those described above for the method of treatment. The activator can be pH that is provided by a buffer, particularly an acidic buffer has a range that is or is about pH 4.0-5.0, particularly 4.5 to 6, more particularly, 4.0, 4.5, 5, 5.5 or 6. Exemplary buffers are among acidic buffers that contain an acid,,such as, 2-(N 10 morpholino)ethanesulfonic acid (MES), acetic acid, citric acid, succinic acid, lactic acid, maleic acid, glycine-hydrochloric acid, citric phosphate and histidine. Exemplary cathepsin L polypeptides are those that include a sequence of amino acids set forth in SEQ ID NO: I or allelic, species or other variant thereof, where such variants are modified to have altered properties or activities and, typically have at 15 least or have 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity compared to a sequence of amino acids set forth in any of SEQ ID NO: 1. The activatable cathepsin L can be provided as a lyophilized powder, particularly of an activated mature form that is two-chain or single-chain form. The amount of activatable cathepsin L in the container is 20 therapeutically effective for the particular disease or condition, and can range, for example, from about or: 10 jig to or 100 mg, 50 pg to 75 mg, 100 jig to 50 mg, 250 pgto25mg,500 pgto 10mg, 1 mgto5mgand2mgto4mg. Theparticular amount can depend on the particular disease or condition, and, if necessary, can be empirically determined. The cathepsin L can be provided as a solid, such as a 25 lyophilized powder, a paste or liquid, such as a suspension, dispersion, or solution. The volume in the container is suitable for the amount of cathepsin L and the intended route and/or locus of administration. For example, a typical volume in the container is or is about 1 -100 ml, 1 -50 ml, 10- 50 ml, 10-30 ml, 1-20 ml, or 1-10 ml. Also provided are combinations that include the above-described container(s) 30 and one or more additional containers containing another pharmacologically effective agent. Such agents can be selected from among biologics, small molecule compounds, dispersing agents, anesthetics and vasoconstrictors and combinations thereof. These agents include the agents and amounts as described above with RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 -10 reference to the methods. For example, an additional container can contain a hyaluronidase, such as rHuPH20. The amount can be for example from about/or: 10 Units to 500,000 Units, 100 Units to 100,000 Units, 500 Units to 50,000 Units, 1000 Units to 10,000 Units, 5000 Units to 7500 Units, 5000 Units to 50,000 Units, or 1,000 5 Units to 10,000 Units. Other containers can contain anesthetics, such as lidocaine, in an amount, for example of at or about 10 mg to 1000 mg, 100 mg to 500 mg, 200 mg to 400 mg, 20 mg to 60 mg, or 30 mg to 50 mg, and/or a vasoconstrictor, such as an alpha adrenergic receptor agonist, including levonordefrin, epinephrine or norepinephrine in an amount to effect vasoconstriction at the locus and region of 10 administration. The amount, for example, can be at or about 10 ptg to 5 mg, 50 jig to 1 mg, 50 ptg to 500 pig, 50 pg to 250 ptg, 100 jig to 500 pg, 200 pig to 400 pg, I mg to 5 mg or 2 mg to 4 mg of, for example, epinephrine or other vasoconstrictor. Each of the additional pharmacologically effective agents can be mixed in any combination in one container or can be provided in single containers. They can be provided as 15 liquids or solids as exemplified and described above for cathepsin L. In exemplary embodiments, the combinations, can contain the AMDE and activator, and the container can contain at least two pharmacologically effect agents, where the pharmacologic agents are provided as separate compositions separated from each other or are provided in the same container in the same composition. For 20 example, the additional container can contain one or more of a hyaluronidase, lidocaine and epinephrine. The additional container can be in the form of a syringe with or without a needle. The total volume in the additional container(s) is or is about 1 -100 ml, 1 -50 ml, 10- 50 ml, 10-30 ml, 1-20 ml, or 1-10 ml. In exemplary embodiments, the combination includes cathepsin L and the 25 hyaluronidase, such as rHuPH20. They can be provided as separate compositions or are in a single composition in one container. The combination can include an acidic buffer that activates the cathepsin L. The buffer can be provided in a separate container or mixed with one or both of the cathepsin L and hyaluronidase. Also provided are pharmaceutical compositions that contain an amount of cathepsin L 30 effective for treatment of an ECM-mediated disease or condition upon administration simultaneously or sequentially with an acidic buffer, where the composition is formulated for single dosage administration; and the buffer has a pH that activates cathepsin L. The amount of cathepsin L is effective for the particular disease or WO 2009/111083 PCT/US2009/001486 condition, and for example, is or is about 10 pg to 100 mg, 50 tg to 75 mg, 100 pg to 50 mg, 250 ptg to 25 mg, 500 pg to 10 mg, 1 mg to 5 mg, or 2 mg to 4 mg. The composition can further contain one or more of lidocaine, epinephrine and a hyaluronidase. 5 The containers and/or combinations and compositions can be packaged as kits. The kits contain the containers and/or combinations and optionally additional reagents for use in the methods provided herein, devices for administration, such as vials, tubes, syringes and needles, provided herein and/or instructions for such use. BRIEF DESCRIPTION OF THE FIGURES 10 Figure 1: Figure 1 is an alignment of zymogen MMPs, indicating the propeptide, the catalytic domain, linker region, hemopexin domains 1-4, fibronectin type II repeats, the basic region, the cysteine switch, the calcium (Ca) binding sites I and II, and the zinc binding site. The alignment includes zymogen MMPs, including MMP-1 (SEQ ID NO:327), MMP-8 (amino acids 21-467 of SEQ ID NO:101), MMP-13 (amino 15 acids 20-471 of SEQ ID NO:104), MMP-18 (amino acids 18-467 of SEQ ID NO:107), MMP-2 (amino acids 30-660 of SEQ ID NO:1 10), MMP-9 (amino acids 20-707 of SEQ ID NO: 113), MMP-3 (amino acids 18-477 of SEQ ID NO: 116), MMP-10 (amino acids 18-476 of SEQ ID NO: 119), MMP-1 1 (amino acids 32-488 of SEQ ID NO:122), MMP-7 (amino acids 18-267 of SEQ ID NO:125), MMP-26 20 (amino acids 18-261 of SEQ ID NO:128), MMP-12 (amino acids 17-470 of SEQ ID NO:131), and MMP-19 (amino acids 19-508 of SEQ ID NO:146). A "*" means that the residues or nucleotides in that column are identical in all sequences in the alignment, a ":" means that conserved substitutions have been observed, and a means that semi-conserved substitutions are observed. 25 Figure 2: Figure 2 is an alignment of the catalytic domains of exemplary MMPs, indicating exemplary conserved and conservative amino acid residues. It is understood that other conserved and conservative amino acid residues exist between and among MMPs. Thus, this figure and identification of residues is not intended to limit corresponding residues between and among MMPs. The exemplary MMPs 30 include: MMP-1 (amino acids 81-242 of SEQ ID NO:327), MMP-8 (amino acids 101 242 of SEQ ID NO:101), MMP-13 (amino acids 104-248 of SEQ ID NO:104), MMP 18 (amino acids 100-246 of SEQ ID NO:107), MMP-2 (amino acids 110-417 of SEQ ID NO:1 10), MMP-9 (amino acids 94-425 of SEQ ID NO: 113), MMP-3 (amino acids WO 2009/111083 PCT/US2009/001486 - 12 100-247 of SEQ ID NO: 116), MMP-10 (amino acids 99-246 of SEQ ID NO: 119), MMP-1 1 (amino acids 98-228 of SEQ ID NO:122), MMP-7 (amino acids 95-242 of SEQ ID NO:125), MMP-26 (amino acids 90-236 of SEQ ID NO:128), MMP-12 (amino acids 106-247 of SEQ ID NO:13 1), and MMP-19 (amino acids 98-239 of SEQ 5 ID NO: 146). Exemplary conserved and conservative substitutions are highlighted. DETAILED DESCRIPTION Outline A. Definitions B. The Extracellular Matrix 10 1. Components of the ECM a. Collagens b. Elastin c. Fibronectin d. Glycosaminoglycans (GAGs) 15 i. Proteoglycans ii. Hyaluronic Acid 2. Histology of the Skin a. The Epidermis b. The Dermis 20 c. The Hypodermis 3. Diseases of the ECM C. Matrix-Degrading Enzymes 1. Enzyme Activation a. Serine Proteases 25 b. Cysteine Proteases i. Cathepsins Cathepsin L ii. Calpain c. Aspartic Proteases 30 d. Metalloproteases e. Heparanase D. Activatable Matrix-Degrading Enzymes (AMDE) 1. Activating Conditions and Methods for Activation of Activatable Matrix-Degrading Enzymes 35 a. Activating Condition - Acidic pH b. Activating Condition - Metal Cation Concentration c. Activating Condition - Reducing Agent d. Activating Condition - Temperature i. Temperature-Sensitive Matrix Metalloprotease 40 Mutants 1) Exemplary tsMMP-1 Modifications 2) Combinations 3) Additional Modifications 4) Other MMPs 45 2. Combinations of Matrix-Degrading Enzymes and Activator WO 2009/111083 PCT/US2009/001486 - 13 E. Methods of Producing Nucleic Acids Encoding Matrix-Degrading Enzymes, and Polypeptides Thereof 1. Vectors and Cells 2. Expression 5 a. Prokaryotic Cells b. Yeast Cells c. Insect Cells d. Mammalian Cells e. Plants 10 3. Purification Techniques F. Preparation, Formulation and Administration of Activatable Matrix-Degrading Enzymes 1. Injectables, solutions and emulsions Lyophilized Powders 15 2. Topical Administration 3. Compositions for other routes of administration 4. Combination Therapies a. Hyaluronan Degrading Enzymes i. Hyaluronidases 20 1) Mammalian-type hyaluronidases 2) Bacterial Hyaluronidases 3) Hyaluronidases from leeches, other parasites and crustaceans ii. Other hyaluronan degrading enzymes 25 iii. Soluble hyaluronan degrading enzymes 1) Soluble Human PH20 2) rHuPH20 iv. Modifications of hyaluronan degrading enzymes to improve their pharmacokinetic properties 30 G. Packaging and Articles of Manufacture of Activatable Matrix Degrading Enzymes 1. Single Chamber Apparatus 2. Dual Chamber Apparatus 3. Kits 35 H. Methods of Assessing Activity of Matrix-Degrading Enzymes 1. Methods of Assessing Enzymatic Activity 2. Methods of Assessing ECM Degradation a. In vitro assays b. In vivo assays 40 c. Non-human animal models I. Exemplary Methods of Treating Diseases or Defects of ECM Collagen-Mediated Diseases or Conditions a. Cellulite b. Dupuytren's Disease 45 c. Peyronie's Disease d. Ledderhose Fibrosis e. Stiff Joints f. Existing Scars i. Surgical Adhesions WO 2009/111083 PCT/US2009/001486 -14 ii. Keloids ii. Hypertrophic scars iv. Depressed Scars g. Scleroderma 5 h. Lymphedema i. Collagenous colitis J. Examples A. DEFINITIONS Unless defined otherwise, all technical and scientific terms used herein have 10 the same meaning as is commonly understood by one of skill in the art to which the invention(s) belong. All patents, patent applications, published applications and publications, Genbank sequences, databases, websites and other published materials referred to throughout the entire disclosure herein, unless noted otherwise, are incorporated by reference in their entirety. In the event that there are a plurality of 15 definitions for terms herein, those in this section prevail. Where reference is made to a URL or other such identifier or address, it understood that such identifiers can change and particular information on the internet can come and go, but equivalent information can be found by searching the internet. Reference thereto evidences the availability and public dissemination of such information. 20 As used herein, the extracellular matrix (ECM) refers to a complex meshwork structure that surrounds and provides structural support to cells of specialized tissues and organs. The ECM is made up of structural proteins such as collagen and elastin; specialized proteins such as fibronectin; and proteoglycans. The exact biochemical composition varies from tissue to tissue. In the skin, for example, it is the dermal 25 layer that contains the ECM. Reference to the "interstitium" is used interchangeably herein to refer to the ECM. As used herein, components of the ECM refers to any material produced by cells of connective tissue and secreted into the interstitium. For purposes herein, references to ECM components refers to proteins and glycoproteins, and not to other 30 cellular components or other components of the ECM. Exemplary ECM components include, but are not limited to, collagen, fibronectin, elastin and proteoglycans. As used herein, -a matrix degrading enzyme refers to any enzyme that degrades one or more components of the ECM. Matrix-degrading enzymes include protease, which are enzymes that catalyze the hydrolysis of covalent peptidic bonds. Matrix 35 degrading enzymes include any known to one of skill in the art, such as any WO 2009/111083 PCT/US2009/001486 - 15 described herein (see, e.g., Table 3), allelic or species variants or other variants thereof As used herein, a matrix metalloprotease (MMP) refers to a type of matrix degrading enzyme that are zinc-dependent endopeptidases that contain an active site 5 Zn 2 required for activity. MMPs include enzymes that degrade components of the ECM including, but not limited to, collagen, fibronectin, elastin and proteoglycans. MMPs generally contain a propeptide, a catalytic domain, a proline linker and a hemopexin (also called haemopexin-like C-terminal) domain. Some MMPs contain additional domains. Exemplary MMPs are set forth in Table 5. Reference to an 10 MMP includes all forms, for example, the precursor form (containing the signal sequence), the proenzyme form (containing the propeptide), the processed active form, and forms thereof lacking one or more domains. For example, reference to an MMP refers to MMPs containing only the catalytically active domain. Domains of exemplary MMPs are identified in Figure 1. MMPs also include allelic or species 15 variants or other variants thereof. As used herein, a modified matrix-degrading enzyme (or variant of a matrix degrading enzyme) refers to an enzyme that has one or more modifications in primary sequence compared to a wild-type enzyme. The one or more mutations can be one or more amino acid replacements (substitutions), insertions, deletions and any 20 combination thereof A modified enzyme includes those with 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 or more modified positions. A modified enzyme retains the activity of a wild-type enzyme, but may have altered substrate specificity or stability. A modified enzyme typically has 60%, 70%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to a 25 corresponding sequence of amino acids of a wildtype enzyme. As used herein, a lysosomal enzyme refers to enzymes whose degradative function is optimal at acidic pH. By virtue of the requirement of low pH, such enzymes generally are present in the lysosomes of cells. Lysosomal enzymes include, but are not limited to, cathepsin S, K, L B, C, H, F, 0, R, V, D and E. 30 Exemplary of lysosomal enzymes include precursor forms set forth in any of SEQ ID NOS:56, 59, 62, 64, 179, 67, 70, 73, 76, 182, 185, 188, 79, 194, 89, 92 and 95 and mature forms thereof set forth in SEQ ID NOS:57, 60, 1, 65, 180, 68, 71, 74, 77, 183, 186, 189, 80, 195, 90, 93 and 96 or allelic variants or species variants or other WO 2009/111083 PCT/US2009/001486 -16 variants thereof. Other lysosomal enzymes include, but are not limited to, lysosomal acid lipase, gastric lipase, lysosomal phospholipase and bile salt-activated lipase (nucleic acid sequences encoding amino acids sequences, including mature forms thereof, are set forth in any of SEQ ID NOS: 196-207). 5 As used herein, a temperature sensitive (ts) mutant or mutation or variant or modification conferring temperature sensitivity refers to a polypeptide that is modified to exhibit higher enzymatic activity at some temperatures called permissive temperatures compared to other temperatures called nonpermissive temperatures. Generally, a temperature-sensitive mutant exhibits higher enzymatic activity at lower 10 temperatures then at higher temperatures. As used herein, permissive temperature is the temperature at which a polypeptide exhibits a higher enzymatic activity then at a second temperature called the nonpermissive temperature. Hence, the modified enzymes provided herein exhibit different activities at different temperatures that is higher at one temperature then at 15 another temperature. The temperature at which it exhibits more activity is the permissive temperature. As used herein, a nonpermissive temperature is the temperature where a polypeptide exhibits lower enzymatic activity then at the permissive temperature and exhibits reduced activity compared to the enzyme that is not modified. Temperature 20 sensitive mutants provided herein exhibit enzymatic activity at the nonpermissive temperature that is at or about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80% or 90% up to less then 100% the activity at the permissive temperature. The temperature sensitive mutants provided herein also exhibit 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 20%, 30%, 40%, 50%, 60%, 25 70%, 80% or 90% up to less then 100% of the activity at the nonpermissive temperature compared to the enzyme that is not modified (e.g. wildtype enzyme) at the nonpermissive temperature. As used herein, the ratio of enzymatic activity at the permissive temperature compared to the nonpermissive temperature refers to the relation of enzymatic activity 30 at the permissive and nonpermissive temperatures. It is expressed by the quotient of the division of the activity at the permissive temperature by the activity at the nonpermissive temperature. RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 -17 As used herein, physiological temperature refers to temperature conditions maintained in the body, which is approximately 37*C, for example, at or about 34"C, 35"C, 36"C, 37*, 38"C or 39"C. It is understood that the normal range of a human body temperature varies depending on factors such as the rate of metabolism, the 5 particular organ and other factors. For purposes herein, physiological temperature is the temperature that exists for a non-fasting, comfortably dressed subject that is indoors in a room that is kept at a normal room temperature (e.g. 22.7 to 24.4*C). As used herein, reversible refers to a modified enzyme whose activity at the permissive temperature is capable of being recovered or partially recovered upon 10 exposure to the nonpermissive temperature and reexposure to the permissive temperature. Hence, the activity of a reversible enzyme once it is exposed to the nonpermissive temperature is the same or substantially retained compared to the activity of the enzyme exposed only to the permissive conditions and is greater then the activity of the enzyme exposed only to the nonpermissive temperature. For 15 example,-upon return to permissive conditions from nonpermissive conditions, reversible enzymes exhibit at or about 120%, 125%, 130%, 140%, 150%, 160%, 170%, 180%, 200% or more the activity of the enzyme exposed only to the nonpermissive temperatures and retain the activity of the enzyme exposed only to the permissive temperature. 20 As used herein, irreversible or nonreversible refers to a modified enzyme whose enzymatic activity at the permissive temperature is not recovered upon exposure to the nonpermissive temperature and reexposure to the permissive temperature. Hence, the activity of an irreversible enzyme once it is exposed to the nonpermissive temperature is less then the activity of the enzyme exposed only to the 25 permissive temperature and also is less then or the same or substantially the same as the activity of the enzyme exposed only to the nonpermissive conditions. For example, upon return to permissive conditions, irreversible enzymes exhibit at or about 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, 105%, 110%, 115%, or 120% the activity at nonpermissive temperatures and less then 100% of the activity at 30 the activity of the enzyme exposed only to the permissive temperature. As used herein, a domain refers to a portion (a sequence of three or more, generally 5 or 7 or more amino acids) of a polypeptide that is a structurally and/or functionally distinguishable or definable. For example, a domain includes those that RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 -18 can form an independently folded structure within a protein made up of one or more structural motifs (e.g. combinations of alpha helices and/or beta strands connected by loop regions) and/or that is recognized by virtue of a functional activity, such as kinase activity. A protein can have one, or more than one, distinct domain. For 5 example, a domain can be identified, defined or distinguished by homology of the sequence therein to related family members, such as homology and motifs that define an extracellular domain. In another example, a domain can be distinguished by its function, such as by enzymatic activity, e.g. kinase activity, or an ability to interact with a biomolecule, such as DNA binding, ligand binding, and dimerization. A 10 domain independently can exhibit a function or activity such that the domain independently or fused to another molecule. can perform an activity, such as, for example proteolytic activity or ligand binding. A domain can be a linear sequence of amino acids or a non-linear sequence of amino acids from the polypeptide. Many polypeptides contain a plurality of domains. For example, the domain structure of 15 MMPs is set forth in Figure 1. Those of skill in the art are familiar with domains and can identify them by virtue of structural and/or functional homology with other such domains. As used herein, a catalytic domain refers to any part of a polypeptide that exhibits a catalytic or enzymatic function. Such domains or regions typically interact 20 with a substrate to result in catalysis thereof. For MMPs, the catalytic domain contains a zinc binding motif, which contains the Zn 2 ion bound by three histidine residues and is represented by the conserved sequence HExxHxxGxxH. As used herein, a proline rich linker (also called the hinge region) refers to a flexible hinge or linker region that has no determinable function. Such a region is 25 typically is found between domains or regions and contributes to the flexibility of a polypeptide. As used herein, a hemopexin binding domain or haemopexin-like C-terminal domain refers to the C-terminal region of MMP. It is a four bladed 9- propeller structure, which is involved in protein-protein interactions. For example, the 30 hemopexin binding domain of MMPs interact with various substrates and also interact with inhibitors, for example, tissue inhibitor of metalloproteases (TIMPs). As used herein, consisting essentially of or recitation that a polypeptide consists essentially of a particular domain, for example the catalytic domain RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 -19 means that the only MMP portion of the polypeptide is the domain or a catalytically active portion thereof. The polypeptide optionally can include additional non-MMP derived sequences of amino acids, typically at least 3, 4, 5, 6 or more, such as by insertion into another polypeptide or linkage thereto. 5 As used herein, a "zymogen" refers to an enzyme that is an inactive precursor and requires some change, such as proteolysis of the polypeptide, to become active. Some zymogens also require the addition of cofactors such as, but not limited to, pH, ionic strength, metal ions or temperature for activation. Zymogens include the proenzyme form of enzymes. Hence, zymogens, generally, are inactive and can be 10 converted to a mature polypeptide by catalytic or autocatalytic cleavage of the proregion from the zymogen in the presence or absence of additional cofactors. As used herein, a prosegment or proregion refers to a region or a segment that is cleaved to produce a mature protein. This can include segments that function to suppress the enzymatic activity by masking the catalytic machinery. A proregion is a 15 sequence of amino acids positioned at the amino terminus of a mature polypeptide and can be as little as a few amino acids or can be a multidomain structure. As used herein, an activation sequence refers to a sequence of amino acids in a zymogen that are the site required for activation cleavage or maturation cleavage to form an active protease. Cleavage of an activation sequence can be catalyzed 20 autocatalytically or by activating partners. Activation cleavage is a type of maturation cleavage in which a conformational change required for activity occurs. Activation can result in production of multi-chain forms of the proteases, for example, two-chain forms. In some instances, single chain forms of the protease can exhibit proteolytic activity as a 25 single chain. As used herein, a cofactor refers to a condition or factor that is required for activity of an enzyme. Cofactors includes anything required for enzymatic activity. Examples of cofactors include, but are not limited to, pH, ionic strength, metal ions or temperature. With reference to in vivo administration of an enzyme, cofactors include 30 endogenously present factors and exogenously provided factors. As used herein, an activating condition refers to any physical condition or combination of conditions that is required for an enzyme's activity. For purposes herein, an activating condition for an activatable matrix-degrading enzyme (AMDE) RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 - 20 includes those that are not present at the site of administration, for example, not present in the extracellular matrix, in amounts (i.e. quantity, degree, level or other physical measure) required for activation of the enzyme. Exemplary of activating conditions include, but are not limited to, pH, metal ions, reducing or oxidizing 5 agents, temperature and ionic strength. For example, in the case of lysosomal matrix degrading-enzymes that are active at conditions of low pH but inactive at neutral pH, exposure of the inactive enzyme to an activating condition that is acidic pH results in activation of the enzyme. By virtue of the fact that the activating condition is not present at the site of administration of the enzyme, but must be added exogenously, 10 the activating condition will dissipate and/or be neutralized over time, such that the activating condition is no longer present to activate the enzyme. Hence, the enzyme will be active for a limited or predetermined time upon administration. As used herein, an activator refers to any composition that provides an activating condition for an activatable matrix-degrading enzyme. Examples of 15 activators include, but are not limited to an acidic pH buffer, a cold buffer, or a calcium buffer. As used herein, an "activatable matrix-degrading enzyme (AMDE)" refers to a matrix degrading enzyme that requires an activating condition in order to be active. For purposes herein, for example, an AMDE is substantially inactive in the ECM 20 unless exposed to activators before, with or subsequent to administration of the AMDE, thereby providing an activating condition for the enzyme. Hence, activation of activatable enzymes is controlled by exogenous conditions so that the period of time at an in vivo locus or site during which the enzyme is active can be predetermined and/or controlled as a result of the dissipation and/or neutralization of 25 the activation condition (i.e. temporally controllable or time-controlled). Thus, by virtue of exposure to an activating condition, the enzymes are active for a limited time and/or to a limited extent in the ECM (i.e. are conditionally active). The extent and time of activation can be controlled by selection of activator or activating conditions, and can be for a predetermined time. For example, a lysosomal enzyme, such as a 30 cathepsin L, is activatable in that it can be activated by exposure to the activating condition of pH, such as provided by an acidic buffered solution. Upon administration of the activated enzyme to the neutral pH environment of the ECM, the pH environment will return to neutrality in a time period that can be predetermined WO 2009/111083 PCT/US2009/001486 -21 based upon the buffering capacity of the acidic buffer, such that the enzyme will become inactive. As used herein, "amount of an activator" refers to the quantity, degree or level of an activator. The amount of an activator can be a concentration or absolute 5 amount, or a particular temperature or pH. For purposes herein, the amount of an activator is typically an amount that is sufficient to result in the conditional activation of an enzyme. The amount can be adjusted to alter the duration of activation so that activation can be for a limited or predetermined time. As used herein, a "therapeutically effective amount" or a "therapeutically 10 effective dose" refers to an agent, compound, material, or composition containing a compound that is at least sufficient to produce a therapeutic effect. As used herein, an enzyme that is active for a limited time or for limited duration refers to an active enzyme having activity that dissipates and/or is neutralized over time. Thus, by virtue of the absence of an activation condition, the enzyme is 15 rendered inactive. As used herein, predetermined time means a limited that that is known before and can be controlled. The dissipation and/or neutralization of an activation condition required for an enzyme's activity can be titrated so that the time required for an active enzyme to become inactive is known. For example, an acid activated enzyme that is 20 administered in acid medium and exposed to an in vivo environment having a neutral pH (i.e. the ECM) will, over time, be exposed to a gradually increased pH such that the enzyme will remain active for only a limited time. The rate of pH increase can be controlled, for example, by varying buffering capacity of the acidic buffer such that the period of time required for an active enzyme to become inactive can be pre 25 determined. For purposes herein, an enzyme can be active for a predetermined time that is or is about 1 minute, 2 minutes, 3 minutes, 4 minutes, 5 minutes, 6 minutes, 7 minutes, 8 minutes, 9 minutes, 10 minutes, 15 minutes, 20 minutes, 30 minutes, I hour, 2 hours, 3 hours, or 4 hours. As used herein, substantially inactive at neutral pH means that the enzyme, 30 when at neutral pH, exhibits less than 10% of the activity of the enzyme at its pH optima under similar conditions (except for the pH differences), i.e. assay, buffer, ionic strength.

WO 2009/111083 PCT/US2009/001486 - 22 As used herein, substantially active at pH 5.5 means that the enzyme, when at pH 5.5, exhibits greater than 10%, for example, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 96%, 97%, 98%, 99% or 100% of the activity of the enzyme at its pH optima under similar conditions (except for the pH differences), i.e. assay, buffer, 5 ionic strength. As used herein, sub-epidermal administration refers to any administration that results in delivery of the enzyme under the outer-most layer of the skin. Sub epidermal administration does not include topical application onto the outer layer of the skin. Examples of sub-epidermal administrations include, but are not limited to, 10 subcutaneous, intramuscular, intralesional and intradermal routes of administration. As used herein, substrate refers to a molecule that is cleaved by an enzyme. Minimally, a target substrate includes a peptide containing the cleavage sequence recognized by the protease, and therefore can be two, three, four, five, six or more residues in length. A substrate also includes a full-length protein, allelic variant, 15 isoform or any portion thereof that is cleaved by an enzyme. Additionally, a substrate includes a peptide or protein containing an additional moiety that does not affect cleavage of the substrate by the enzyme. For example, a substrate can include a four amino acid peptide, or a full-length protein chemically linked to a fluorogenic moiety. As used herein, cleavage refers to the breaking of peptide bonds or other 20 bonds by an enzyme that results in one or more degradation products. As used herein, activity refers to a functional activity or activities of a polypeptide or portion thereof associated with a full-length (complete) protein. Functional activities include, but are not limited to, biological activity, catalytic or enzymatic activity, antigenicity (ability to bind or compete with a polypeptide for 25 binding to an anti-polypeptide antibody), immunogenicity, ability to form multimers, and the ability to specifically bind to a receptor or ligand for the polypeptide. As used herein, enzymatic activity or catalytic activity or cleavage activity refers to the activity of a protease as assessed in in vitro proteolytic assays that detect proteolysis of a selected substrate. 30 As used herein, an active enzyme refers to an enzyme that exhibits enzymatic activity. For purposes herein, active enzymes are those that cleave any one or more components of the ECM, such as collagen. Active enzymes include those in single chain or two-chain form.

WO 2009/111083 PCT/US2009/001486 -23 As used herein, an inactive enzyme refers to an enzyme that exhibits substantially no activity (i.e. catalytic activity or cleavage activity), such as less than 10% of the maximum activity of the enzyme. The enzyme can be inactive by virtue of its conformation, the absence of an activating conditions required for its activity, or 5 the presence of an inhibitor or any other condition or factor or form that renders the enzyme substantially inactive. As used herein, a human protein is one encoded by a nucleic acid molecule, such as DNA, present in the genome of a human, including all allelic variants and conservative variations thereof. A variant or modification of a protein is a human 10 protein if the modification is based on the wildtype or prominent sequence of a human protein. As used herein, a hyaluronan degrading enzyme refers to an enzyme that catalyzes the cleavage of a hyaluronan polymer (also referred to as hyaluronic acid or HA) into smaller molecular weight fragments. Exemplary of hyaluronan degrading 15 enzymes are hyaluronidases, and particular chondroitinases and lyases that have the ability to depolymerize hyaluronan. Exemplary chondroitinases that are hyaluronan degrading enzymes include, but are not limited to, chondroitin ABC lyase (also known as chondroitinase ABC), chondroitin AC lyase (also known as chondroitin sulfate lyase or chondroitin sulfate eliminase) and chondroitin C lyase. Chondroitin 20 ABC lyase comprises two enzymes, chondroitin-sulfate-ABC endolyase (EC 4.2.2.20) and chondroitin-sulfate-ABC exolyase (EC 4.2.2.21). Exemplary chondroitin-sulfate ABC endolyases and chondroitin-sulfate-ABC exolyases include, but are not limited to, those from Proteus vulgaris and Flavobacterium heparinum (the Proteus vulgaris chondroitin-sulfate-ABC endolyase is set forth in SEQ ID NO:305; Sato et al. (1994) 25 Appl. Microbiol. Biotechnol. 41(1):39-46). Exemplary chondroitinase AC enzymes from the bacteria include, but are not limited to, those from Flavobacterium heparinum Victivallis vadensis, set forth in SEQ ID NO:3 08, and Arthrobacter aurescens (Tkalec et al. (2000) Applied and Environmental Microbiology 66(1 ):29 35; Ernst et al. (1995) Critical Reviews in Biochemistry and Molecular Biology 30 30(5):387-444). Exemplary chondroitinase C enzymes from the bacteria include, but are not limited to, those from Streptococcus and Flavobacterium (Hibi et al. (1989) FEMS-Microbiol-Lett. 48(2):121-4; Michelacci et al. (1976) J. Biol. Chem. 251:1154 8; Tsuda et al. (1999) Eur. J. Biochem. 262:127-133).

WO 2009/111083 PCT/US2009/001486 -24 As used herein, hyaluronidase refers to an enzyme that degrades hyaluronic acid. Hyaluronidases include bacterial hyaluronidases (EC 4.2.99.1), hyaluronidases from leeches, other parasites, and crustaceans (EC 3.2.1.36), and mammalian-type hyaluronidases (EC 3.2.1.35). Hyaluronidases also include any of non-human origin 5 including, but not limited to, murine, canine, feline, leporine, avian, bovine, ovine, porcine, equine, piscine, ranine, bacterial, and any from leeches, other parasites, and crustaceans. Exemplary non-human hyaluronidases include any set forth in any of SEQ ID NOS: 237- 260. Exemplary human hyaluronidases include HYALI (SEQ ID NO:262), HYAL2 (SEQ ID NO:263), HYAL3 (SEQ ID NO:264), HYAL4 (SEQ ID 10 NO:265), and PH20 (SEQ ID NO:232). Also included amongst hyaluronidases are soluble human PH20 and soluble rHuPH20. Reference to hyaluronidases includes precursor hyaluronidase polypeptides and mature hyaluronidase polypeptides (such as those in which a signal sequence has been removed), truncated forms thereof that have activity, and includes allelic 15 variants and species variants, variants encoded by splice variants, and other variants, including polypeptides that have at least 40%, 45%, 50%, 55%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or more sequence identity to the precursor polypeptide set forth any of SEQ ID NO:232 or the mature form thereof. Hyaluronidases also include those that contain chemical or posttranslational 20 modifications and those that do not contain chemical or posttranslational modifications. Such modifications include, but are not limited to, pegylation, albumination, glycosylation, farnesylation,l carboxylation, hydroxylation, phosphorylation, and other polypeptide modifications known in the art. As used herein, soluble human PH20 or sHuPH20 include mature 25 polypeptides lacking all or a portion of the glycosylphospatidylinositol (GPI) attachment site at the C-terminus such that upon expression, the polypeptides are soluble. Exemplary sHuPH20 polypeptides include mature polypeptides having an amino acid sequence set forth in any one of SEQ ID NOS:226-23 1. The precursor polypeptides for such exemplary sHuPH20 polypeptides include an amino acid signal 30 sequence. Exemplary of a precursor is set forth in SEQ ID NOS:225, which contains a 35 amino acid signal sequence at amino acid positions 1-35. Soluble HuPH20 polypeptides can be degraded during or after the production and purification methods described herein. RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 -25 As used herein, soluble rHuPH20 refers to a soluble form of human PH20 that is recombinantly expressed in Chinese Hamster Ovary (CHO) cells. Soluble rHuPH20 is encoded by nucleic acid encoding amino acids 1-482 set forth in SEQ ID NO:225. Also included are DNA molecules that are allelic variants thereof and other soluble 5 variants. The nucleic acid encoding soluble rHuPH20 is expressed in CHO cells which secrete the mature polypeptide. As produced in the culture medium there is heterogeneity at the C-terminus so that the product includes a mixture of species of SEQ ID NOS:226-231. Corresponding allelic variants and other variants also are included. Other variants can have 60%, 70%, 80%, 85%, 90%, 91%, 92%, 93%, 10 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity with any of SEQ ID NOS:226-231 as long they retain a hyaluronidase activity and are soluble. As used herein, hyaluronidase activity refers to any activity exhibited by a hyaluronidase polypeptide. Such activities can be tested in vitro and/or in vivo and include, but are not limited to, enzymatic activity, such as to effect cleavage of 15 hyaluronic acid, ability to act as a dispersing or spreading agent and antigenicity. Exemplary assays include the microturbidity assay (see e.g. Example 16) that measures cleavage of hyaluronic acid by hyaluronidase indirectly by detecting the insoluble precipitate formed when the uncleaved hyaluronic acid binds with serum albumin. 20 As used herein, the residues of naturally occurring a-amino acids are the residues of those 20 o-amino acids found in nature which are incorporated into protein by the specific recognition of the charged tRNA molecule with its cognate mRNA codon in humans. As used herein, nucleic acids include DNA, RNA and analogs thereof, 25 including peptide nucleic acids (PNA) and mixtures thereof. Nucleic acids can be single or double-stranded. When referring to probes or primers, which are optionally labeled, such as with a detectable label, such as a fluorescent or radiolabel, single stranded molecules are contemplated. Such molecules are typically of a length such that their target is statistically unique or of low copy number (typically less than 5, 30 generally less than 3) for probing or priming a library. Generally a probe or primer contains at least 14, 16 or 30 contiguous nucleotides of sequence complementary to or identical to a gene of interest. Probes and primers can be 10, 20, 30, 50, 100 or more nucleic acids long.

WO 2009/111083 PCT/US2009/001486 - 26 As used herein, a peptide refers to a polypeptide that is from 2 to 40 amino acids in length. As used herein, the amino acids which occur in the various sequences of amino acids provided herein are identified according to their known, three-letter or 5 one-letter abbreviations (Table 1). The nucleotides which occur in the various nucleic acid fragments are designated with the standard single-letter designations used routinely in the art. As used herein, an "amino acid" is an organic compound containing an amino group and a carboxylic acid group. A polypeptide contains two or more amino acids. 10 For purposes herein, amino acids include the twenty naturally-occurring amino acids, non-natural amino acids and amino acid analogs (i.e., amino acids wherein the a carbon has a side chain). As used herein, "amino acid residue" refers to an amino acid formed upon chemical digestion (hydrolysis) of a polypeptide at its peptide linkages. The amino 15 acid residues described herein are presumed to be in the "L" isomeric form. Residues in the "D" isomeric form, which are so designated, can be substituted for any L-amino acid residue as long as the desired functional property is retained by the polypeptide.

NH

2 refers to the free amino group present at the amino terminus of a polypeptide. COOH refers to the free carboxy group present at the carboxyl terminus of a 20 polypeptide. In keeping with standard polypeptide nomenclature described in J. Biol. Chem., 243:3552-3559 (1969), and adopted 37 C.F.R.. §§ 1.821-1.822, abbreviations for amino acid residues are shown in Table 1: Table 1 - Table of Correspondence SYMBOL 1-Letter 3-Letter AMINO ACID Y Tyr Tyrosine G Gly Glycine F Phe Phenylalanine M Met Methionine A Ala Alanine S Ser Serine I Ile Isoleucine L Leu Leucine T Thr Threonine V Val Valine P Pro Proline K Lys Lysine WO 2009/111083 PCT/US2009/001486 - 27 SYMBOL 1-Letter 3-Letter AMINO ACID H His Histidine Q Gln Glutamine E Glu Glutamic Acid Z Glx Glu and/or Gln W Trp Tryptophan R Arg Arginine D Asp Aspartic Acid N Asn Asparagine B Asx Asn and/or Asp C Cys Cysteine X Xaa Unknown or other It should be noted that all amino acid residue sequences represented herein by formulae have a left to right orientation in the conventional direction of amino terminus to carboxyl-terminus. In addition, the phrase "amino acid residue" is 5 broadly defined to include the amino acids listed in the Table of Correspondence (Table 1) and modified and unusual amino acids, such as those referred to in 37 C.F.R. §§ 1.821-1.822, and incorporated herein by reference. Furthermore, it should be noted that a dash at the beginning or end of an amino acid residue sequence indicates a peptide bond to a further sequence of one or more amino acid residues, to 10 an amino-terminal group such as NH 2 or to a carboxyl-terminal group such as COOH. As used herein, "naturally occurring amino acids" refer to the 20 L-amino acids that occur in polypeptides. As used herein, "non-natural amino acid" refers to an organic compound that has a structure similar to a natural amino acid but has been modified structurally to 15 mimic the structure and reactivity of a natural amino acid. Non-naturally occurring amino acids thus include, for example, amino acids or analogs of amino acids other than the 20 naturally-occurring amino acids and include, but are not limited to, the D isostereomers of amino acids. Exemplary non-natural amino acids are described herein and are known to those of skill in the art. 20 As used herein, a DNA construct is a single or double stranded, linear or circular DNA molecule that contains segments of DNA combined and juxtaposed in a manner not found in nature. DNA constructs exist as a result of human manipulation, and include clones and other copies of manipulated molecules.

WO 2009/111083 PCT/US2009/001486 -28 As used herein, a DNA segment is a portion of a larger DNA molecule having specified attributes. For example, a DNA segment encoding a specified polypeptide is a portion of a longer DNA molecule, such as a plasmid or plasmid fragment, which, when read from the 5' to 3' direction, encodes the sequence of amino acids of the 5 specified polypeptide. As used herein, the term polynucleotide means a single- or double-stranded polymer of deoxyribonucleotides or ribonucleotide bases read from the 5' to the 3' end. Polynucleotides include RNA and DNA, and can be isolated from natural sources, synthesized in vitro, or prepared from a combination of natural and synthetic 10 molecules. The length of a polynucleotide molecule is given herein in terms of nucleotides (abbreviated "nt") or base pairs (abbreviated "bp"). The term nucleotides is used for single- and double-stranded molecules where the context permits. When the term is applied to double-stranded molecules it is used to denote overall length and will be understood to be equivalent to the term base pairs. It will be recognized 15 by those skilled in the art that the two strands of a double-stranded polynucleotide can differ slightly in length and that the ends thereof can be staggered; thus all nucleotides within a double-stranded polynucleotide molecule can not be paired. Such unpaired ends will, in general, not exceed 20 nucleotides in length. As used herein, "similarity" between two proteins or nucleic acids refers to the 20 relatedness between the sequence of amino acids of the proteins or the nucleotide sequences of the nucleic acids. Similarity can be based on the degree of identity and/or homology of sequences of residues and the residues contained therein. Methods for assessing the degree of similarity between proteins or nucleic acids are known to those of skill in the art. For example, in one method of assessing sequence 25 similarity, two amino acid or nucleotide sequences are aligned in a manner that yields a maximal level of identity between the sequences. "Identity" refers to the extent to which the amino acid or nucleotide sequences are invariant. Alignment of amino acid sequences, and to some extent nucleotide sequences, also can take into account conservative differences and/or frequent substitutions in amino acids (or nucleotides). 30 Conservative differences are those that preserve the physico-chemical properties of the residues involved. Alignments can be global (alignment of the compared sequences over the entire length of the sequences and including all residues) or local WO 2009/111083 PCT/US2009/001486 - 29 (the alignment of a portion of the sequences that includes only the most similar region or regions). "Identity" per se has an art-recognized meaning and can be calculated using published techniques. (See, e.g.: Computational Molecular Biology, Lesk, A.M., ed., 5 Oxford University Press, New York, 1988; Biocomputing: Informatics and Genome Projects, Smith, D.W., ed., Academic Press, New York, 1993; Computer Analysis of Sequence Data, Part I, Griffin, A.M., and Griffin, H.G., eds., Humana Press, New Jersey, 1994; Sequence Analysis in Molecular Biology, von Heinje, G., Academic Press, 1987; and Sequence Analysis Primer, Gribskov, M. and Devereux, J., eds., M 10 Stockton Press, New York, 1991). While there exists a number of methods to measure identity between two polynucleotide or polypeptides, the term "identity" is well known to skilled artisans (Carillo, H. & Lipton, D., SIAM JApplied Math 48:1073 (1988)). As used herein, homologous (with respect to nucleic acid and/or amino acid 15 sequences) means about greater than or equal to 25% sequence homology, typically greater than or equal to 25%, 40%, 50%, 60%, 70%, 80%, 85%, 90% or 95% sequence homology; the precise percentage can be specified if necessary. For purposes herein the terms "homology" and "identity" are often used interchangeably, unless otherwise indicated. In general, for determination of the percentage homology 20 or identity, sequences are aligned so that the highest order match is obtained (see, e.g.: Computational Molecular Biology, Lesk, A.M., ed., Oxford University Press, New York, 1988; Biocomputing: Informatics and Genome Projects, Smith, D.W., ed., Academic Press, New York, 1993; Computer Analysis of Sequence Data, Part I, Griffin, A.M., and Griffin, H.G., eds., Humana Press, New Jersey, 1994; Sequence 25 Analysis in Molecular Biology, von Heinje, G., Academic Press, 1987; and Sequence Analysis Primer, Gribskov, M. and Devereux, J., eds., M Stockton Press, New York, 1991; Carillo et al. (1988) SIAM JApplied Math 48:1073). By sequence homology, the number of conserved amino acids is determined by standard alignment algorithms programs, and can be used with default gap penalties established by each supplier. 30 Substantially homologous nucleic acid molecules would hybridize typically at moderate stringency or at high stringency all along the length of the nucleic acid of interest. Also contemplated are nucleic acid molecules that contain degenerate codons in place of codons in the hybridizing nucleic acid molecule.

WO 2009/111083 PCT/US2009/001486 - 30 Whether any two molecules have nucleotide sequences or amino acid sequences that are at least 60%, 70%, 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% "identical" or "homologous" can be determined using known computer algorithms such as the "FASTA" program, using for example, the default parameters as in 5 Pearson et al. (1988) Proc. Natl. Acad. Sci. USA 85:2444 (other programs include the GCG program package (Devereux, J., et al., Nucleic Acids Research 12():387 (1984)), BLASTP, BLASTN, FASTA (Atschul, S.F., et al., JMolec Biol 215:403 (1990)); Guide to Huge Computers, Martin J. Bishop, ed., Academic Press, San Diego, 1994, and Carillo et al. (1988) SIAM JApplied Math 48:1073). For example, 10 the BLAST function of the National Center for Biotechnology Information database can be used to determine identity. Other commercially or publicly available programs include, DNAStar "MegAlign" program (Madison, WI) and the University of Wisconsin Genetics Computer Group (UWG) "Gap" program (Madison WI). Percent homology or identity of proteins and/or nucleic acid molecules can be 15 determined, for example, by comparing sequence information using a GAP computer program (e.g., Needleman et al. (1970) J. Mol. Biol. 48:443, as revised by Smith and Waterman (1981) Adv. Apple. Math. 2:482). Briefly, the GAP program defines simi larity as the number of aligned symbols (i.e., nucleotides or amino acids), which are similar, divided by the total number of symbols in the shorter of the two sequences. 20 Default parameters for the GAP program can include: (1) a unary comparison matrix (containing a value of I for identities and 0 for non-identities) and the weighted com parison matrix of Gribskov et al. (1986) Nucl. Acids Res. 14:6745, as described by Schwartz and Dayhoff, eds., ATLAS OF PROTEIN SEQUENCE AND STRUCTURE, National Biomedical Research Foundation, pp. 353-358 (1979); (2) a penalty of 3.0 25 for each gap and an additional 0.10 penalty for each symbol in each gap; and (3) no penalty for end gaps. Therefore, as used herein, the term "identity" or "homology" represents a comparison between a test and a reference polypeptide or polynucleotide. As used herein, the term at least "90% identical to" refers to percent identities from 90 to 99.99 30 relative to the reference nucleic acid or amino acid sequence of the polypeptide. Identity at a level of 90% or more is indicative of the fact that, assuming for exemplification purposes a test and reference polypeptide length of 100 amino acids are compared, no more than 10% (i.e., 10 out of 100) of the amino acids in the test RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 -31 polypeptide differs from that of the reference polypeptide. Similar comparisons can be made between test and reference polynucleotides. Such differences can be represented as point mutations randomly distributed over the entire length of a polypeptide or they can be clustered in one or more locations of varying length up to 5 the maximum allowable, e.g. 10/100 amino acid difference (approximately 90% identity). Differences are defined as nucleic acid or amino acid substitutions, insertions or deletions. At the level of homologies or identities above about 85-90%, the result should be independent of the program and gap parameters set; such high levels of identity can be assessed readily, often by manual alignment without relying 10 on software. As used herein, an aligned sequence refers to the use of homology (similarity and/or identity) to align corresponding positions in a sequence of nucleotides or amino acids. Typically, two or more sequences that are related by 50% or more identity are aligned. An aligned set of sequences refers to 2 or more sequences that 15 are aligned at corresponding positions and can include aligning sequences derived from RNAs, such as ESTs and other cDNAs, aligned with genomic DNA sequence. As used herein, "primer" refers to a nucleic acid molecule that can act as a point of initiation of template-directed DNA synthesis under appropriate conditions (e.g., in the presence of four different nucleoside triphosphates and a polymerization 20 agent, such as DNA polymerase, RNA polymerase or reverse transcriptase) in an appropriate buffer and at a suitable temperature. It will be appreciated that a certain nucleic acid molecules can serve as a "probe" and as a "primer." A primer, however, has a 3' hydroxyl group for extension. A primer can be used in a variety of methods, including, for example, polymerase chain reaction (PCR), reverse-transcriptase (RT) 25 PCR, RNA PCR, LCR, multiplex PCR, panhandle PCR, capture PCR, expression PCR, 3' and 5' RACE, in situ PCR, ligation-mediated PCR and other amplification protocols. As used herein, "primer pair" refers to a set of primers that includes a 5' (upstream) primer that hybridizes with the 5' end of a sequence to be amplified (e.g. 30 by PCR) and a 3' (downstream) primer that hybridizes with the complement of the 3' end of the sequence to be amplified. As used herein, "specifically hybridizes" refers to annealing, by complementary base-pairing, of a nucleic acid molecule (e.g. an oligonucleotide) to a WO 2009/111083 PCT/US2009/001486 - 32 target nucleic acid molecule. Those of skill in the art are familiar with in vitro and in vivo parameters that affect specific hybridization, such as length and composition of the particular molecule. Parameters particularly relevant to in vitro hybridization further include annealing and washing temperature, buffer composition and salt 5 concentration. Exemplary washing conditions for removing non-specifically bound nucleic acid molecules at high stringency are 0.1 x SSPE, 0.1% SDS, 65*C, and at medium stringency are 0.2 x SSPE, 0.1% SDS, 50*C. Equivalent stringency conditions are known in the art. The skilled person can readily adjust these parameters to achieve specific hybridization of a nucleic acid molecule to a target 10 nucleic acid molecule appropriate for a particular application. Complementary, when referring to two nucleotide sequences, means that the two sequences of nucleotides are capable of hybridizing, typically with less than 25%, 15% or 5% mismatches between opposed nucleotides. If necessary, the percentage of complementarity will be specified. Typically the two molecules are selected such that they will hybridize 15 under conditions of high stringency. As used herein, substantially identical to a product means sufficiently similar so that the property of interest is sufficiently unchanged so that the substantially identical product can be used in place of the product. As used herein, it also is understood that the terms "substantially identical" or 20 "similar" varies with the context as understood by those skilled in the relevant art. As used herein, an allelic variant or allelic variation references any of two or more alternative forms of a gene occupying the same chromosomal locus. Allelic variation arises naturally through mutation, and can result in phenotypic polymorphism within populations. Gene mutations can be silent (no change in the 25 encoded polypeptide) or can encode polypeptides having altered amino acid sequence. The term "allelic variant" also is used herein to denote a protein encoded by an allelic variant of a gene. Typically the reference form of the gene encodes a wildtype form and/or predominant form of a polypeptide from a population or single reference member of a species. Typically, allelic variants, which include variants between and 30 among species typically have at least 80%, 90% or greater amino acid identity with a wildtype and/or predominant form from the same species; the degree of identity depends upon the gene and whether comparison is interspecies or intraspecies. Generally, intraspecies allelic variants have at least about 80%, 85%, 90% or 95% WO 2009/111083 PCT/US2009/001486 - 33 identity or greater with a wildtype and/or predominant form, including 96%, 97%, 98%, 99% or greater identity with a wildtype and/or predominant form of a polypeptide. Reference to an allelic variant herein generally refers to variations n proteins among members of the same species. 5 As used herein, "allele," which is used interchangeably herein with "allelic variant" refers to alternative forms of a gene or portions thereof. Alleles occupy the same locus or position on homologous chromosomes. When a subject has two identical alleles of a gene, the subject is said to be homozygous for that gene or allele. When a subject has two different alleles of a gene, the subject is said to be 10 heterozygous for the gene. Alleles of a specific gene can differ from each other in a single nucleotide or several nucleotides, and can include substitutions, deletions and insertions of nucleotides. An allele of a gene also can be a form of a gene containing a mutation. As used herein, species variants refer to variants in polypeptides among 15 different species, including different mammalian species, such as mouse and human. As used herein, a splice variant refers to a variant produced by differential processing of a primary transcript of genomic DNA that results in more than one type of mRNA. As used herein, modification is in reference to modification of a sequence of 20 amino acids of a polypeptide or a sequence of nucleotides in a nucleic acid molecule and includes deletions, insertions, and replacements of amino acids and nucleotides, respectively. Methods of modifying a polypeptide are routine to those of skill in the art, such as by using recombinant DNA methodologies. As used herein, the term promoter means a portion of a gene containing DNA 25 sequences that provide for the binding of RNA polymerase and initiation of transcription. Promoter sequences are commonly, but not always, found in the 5' non-coding region of genes. As used herein, isolated or purified polypeptide or protein or biologically active portion thereof is substantially free of cellular material or other contaminating 30 proteins from the cell or tissue from which the protein is derived, or substantially free from chemical precursors or other chemicals when chemically synthesized. Preparations can be determined to be substantially free if they appear free of readily detectable impurities as determined by standard methods of analysis, such as thin WO 2009/111083 PCT/US2009/001486 - 34 layer chromatography (TLC), gel electrophoresis and high performance liquid chromatography (HPLC), used by those of skill in the art to assess such purity, or sufficiently pure such that further purification would not detectably alter the physical and chemical properties, such as enzymatic and biological activities, of the substance. 5 Methods for purification of the compounds to produce substantially chemically pure compounds are known to those of skill in the art. A substantially chemically pure compound, however, can be a mixture of stereoisomers. In such instances, further purification might increase the specific activity of the compound. The term substantially free of cellular material includes preparations of 10 proteins in which the protein is separated from cellular components of the cells from which it is isolated or recombinantly produced. In one embodiment, the term substantially free of cellular material includes preparations of enzyme proteins having less that about 30% (by dry weight) of non-enzyme proteins (also referred to herein as a contaminating protein), generally less than about 20% of non-enzyme proteins or 15 10% of non-enzyme proteins or less that about 5% of non-enzyme proteins. When the enzyme protein is recombinantly produced, it also is substantially free of culture medium, i.e., culture medium represents less than about or at 20%, 10% or 5% of the volume of the enzyme protein preparation. As used herein, the term substantially free of chemical precursors or other 20 chemicals includes preparations of enzyme proteins in which the protein is separated from chemical precursors or other chemicals that are involved in the synthesis of the protein. The term includes preparations of enzyme proteins having less than about 30% (by dry weight), 20%, 10%, 5% or less of chemical precursors or non-enzyme chemicals or components. 25 As used herein, synthetic, with reference to, for example, a synthetic nucleic acid molecule or a synthetic gene or a synthetic peptide refers to a nucleic acid molecule or polypeptide molecule that is produced by recombinant methods and/or by chemical synthesis methods. As used herein, production by recombinant means by using recombinant DNA 30 methods means the use of the well known methods of molecular biology for expressing proteins encoded by cloned DNA. As used herein, vector (or plasmid) refers to discrete elements that are used to introduce a heterologous nucleic acid into cells for either expression or replication WO 2009/111083 PCT/US2009/001486 - 35 thereof. The vectors typically remain episomal, but can be designed to effect integration of a gene or portion thereof into a chromosome of the genome. Also contemplated are vectors that are artificial chromosomes, such as yeast artificial chromosomes and mammalian artificial chromosomes. Selection and use of such 5 vehicles are well known to those of skill in the art. As used herein, an expression vector includes vectors capable of expressing DNA that is operatively linked with regulatory sequences, such as promoter regions, that are capable of effecting expression of such DNA fragments. Such additional segments can include promoter and terminator sequences, and optionally can include 10 one or more origins of replication, one or more selectable markers, an enhancer, a polyadenylation signal, and the like. Expression vectors are generally derived from plasmid or viral DNA, or can contain elements of both. Thus, an expression vector refers to a recombinant DNA or RNA construct, such as a plasmid, a phage, recombinant virus or other vector that, upon introduction into an appropriate host cell, 15 results in expression of the cloned DNA. Appropriate expression vectors are well known to those of skill in the art and include those that are replicable in eukaryotic cells and/or prokaryotic cells and those that remain episomal or those which integrate into the host cell genome. As used herein, vector also includes "virus vectors" or "viral vectors." Viral 20 vectors are engineered viruses that are operatively linked to exogenous genes to transfer (as vehicles or shuttles) the exogenous genes into cells. As used herein, operably or operatively linked when referring to DNA segments means that the segments are arranged so that they function in concert for their intended purposes, e.g., transcription initiates in the promoter and proceeds 25 through the coding segment to the terminator. As used herein the term assessing is intended to include quantitative and qualitative determination in the sense of obtaining an absolute value for the activity of a protease, or a domain thereof, present in the sample, and also of obtaining an index, ratio, percentage, visual or other value indicative of the level of the activity. 30 Assessment can be direct or indirect and the chemical species actually detected need not of course be the proteolysis product itself but can for example be a derivative thereof or some further substance. For example, detection of a cleavage product of a complement protein, such as by SDS-PAGE and protein staining with Coomasie blue.

WO 2009/111083 PCT/US2009/001486 - 36 As used herein, biological activity refers to the in vivo activities of a compound or physiological responses that result upon in vivo administration of a compound, composition or other mixture. Biological activity, thus, encompasses therapeutic effects and pharmaceutical activity of such compounds, compositions and 5 mixtures. Biological activities can be observed in in vitro systems designed to test or use such activities. Thus, for purposes herein a biological activity of a protease is its catalytic activity in which a polypeptide is hydrolyzed. As used herein equivalent, when referring to two sequences of nucleic acids, means that the two sequences in question encode the same sequence of amino acids or 10 equivalent proteins. When equivalent is used in referring to two proteins or peptides, it means that the two proteins or peptides have substantially the same amino acid sequence with only amino acid substitutions that do not substantially alter the activity or function of the protein or peptide. When equivalent refers to a property, the property does not need to be present to the same extent (e.g., two peptides can exhibit 15 different rates of the same type of enzymatic activity), but the activities are usually substantially the same. As used herein, "modulate" and "modulation" or "alter" refer to a change of an activity of a molecule, such as a protein. Exemplary activities include, but are not limited to, biological activities, such as signal transduction. Modulation can include 20 an increase in the activity (i.e., up-regulation or agonist activity) a decrease in activity (i.e., down-regulation or inhibition) or any other alteration in an activity (such as a change in periodicity, frequency, duration, kinetics or other parameter). Modulation can be context dependent and typically modulation is compared to a designated state, for example, the wildtype protein, the protein in a constitutive state, or the protein as 25 expressed in a designated cell type or condition. As used herein, a composition refers to any mixture. It can be a solution, suspension, liquid, powder, paste, aqueous, non-aqueous or any combination thereof. As used herein, a combination refers to any association between or among two or more items. The combination can be two or more separate items, such as two 30 compositions or two collections, can be a mixture thereof, such as a single mixture of the two or more items, or any variation thereof. The elements of a combination are generally functionally associated or related.

WO 2009/111083 PCT/US2009/001486 - 37 As used herein, a kit is a packaged combination that optionally includes other elements, such as additional reagents and instructions for use of the combination or elements thereof In particular, for purposes herein, a "kit" refers to a combination of an activatable matrix-degrading enzyme provided herein and another item for a 5 purpose including, but not limited to, activation, administration, diagnosis, and assessment of a biological activity or property. Kits optionally include instructions for use. As used herein, "disease or disorder" refers to a pathological condition in an organism resulting from cause or condition including, but not limited to, infections, 10 acquired conditions, genetic conditions, and characterized by identifiable symptoms. Diseases and disorders of interest herein are those involving components of the ECM. As used herein, an ECM-mediated disease or condition is one where any one or more ECM components is involved in the pathology or etiology. For purposes herein, an ECM-mediated disease or conditions includes those that are caused by an 15 increased deposition or accumulation of one or more ECM component. Such conditions include, but are not limited to, cellulite, Duputyren's syndrome, Peyronie's disease, frozen shoulders, existing scars such as keloids, scleroderma and lymphedema. As used herein, "treating" a subject with a disease or condition means that the 20 subject's symptoms are partially or totally alleviated, or remain static following treatment. Hence treatment encompasses prophylaxis, therapy and/or cure. Prophylaxis refers to prevention of a potential disease and/or a prevention of worsening of symptoms or progression of a disease. Treatment also encompasses any pharmaceutical use of a modified interferon and compositions provided herein. 25 As used herein, a pharmaceutically effective agent, includes any therapeutic agent or bioactive agents, including, but not limited to, for example, anesthetics, vasoconstrictors, dispersing agents, conventional therapeutic drugs, including small molecule drugs and therapeutic proteins. As used herein, treatment means any manner in which the symptoms of a 30 condition, disorder or disease or other indication, are ameliorated or otherwise beneficially altered. As used herein therapeutic effect means an effect resulting from treatment of a subject that alters., typically improves or ameliorates the symptoms of a disease or WO 2009/111083 PCT/US2009/001486 - 38 condition or that cures a disease or condition. A therapeutically effective amount refers to the amount of a composition, molecule or compound which results in a therapeutic effect following administration to a subject. As used herein, the term "subject" refers to an animal, including a mammal, 5 such as a human being. As used herein, a patient refers to a human subject. As used herein, amelioration of the symptoms of a particular disease or disorder by a treatment, such as by administration of a pharmaceutical composition or other therapeutic, refers to any lessening, whether permanent or temporary, lasting or 10 transient, of the symptoms that can be attributed to or associated with administration of the composition or therapeutic. As used herein, prevention or prophylaxis refers to methods in which the risk of developing disease or condition is reduced. As used herein, an effective amount is the quantity of a therapeutic agent 15 necessary for preventing, curing, ameliorating, arresting or partially arresting a symptom of a disease or disorder. As used herein, unit dose form refers to physically discrete units suitable for human and animal subjects and packaged individually as is known in the art. As used herein, a single dosage formulation refers to a formulation for direct 20 administration. As used herein, an "article of manufacture" is a product that is made and sold. As used throughout this application, the term is intended to encompass activatable matrix degrading enzymes contained in articles of packaging. As used herein, fluid refers to any composition that can flow. Fluids thus 25 encompass compositions that are in the form of semi-solids, pastes, solutions, aqueous mixtures, gels, lotions, creams and other such compositions. As used herein, a cellular extract or lysate refers to a preparation or fraction which is made from a lysed or disrupted cell. As used herein, animal includes any animal, such as, but are not limited to 30 primates including humans, gorillas and monkeys; rodents, such as mice and rats; fowl, such as chickens; ruminants, such as goats, cows, deer, sheep; ovine, such as pigs and other animals. Non-human animals exclude humans as the contemplated WO 2009/111083 PCT/US2009/001486 -39 animal. The enzymes provided herein are from any source, animal, plant, prokaryotic and fungal. Most enzymes are of animal origin, including mammalian origin. As used herein, a control refers to a sample that is substantially identical to the test sample, except that it is not treated with a test parameter, or, if it is a plasma 5 sample, it can be from a normal volunteer not affected with the condition of interest. A control also can be an internal control. As used herein, the singular forms "a," "an" and "the" include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to a compound, comprising "an extracellular domain" includes compounds with one or a 10 plurality of extracellular domains. As used herein, ranges and amounts can be expressed as "about" a particular value or range. About also includes the exact amount. Hence "about 5 bases" means "about 5 bases" and also "5 bases." As used herein, "optional" or "optionally" means that the subsequently 15 described event or circumstance does or does not occur, and that the description includes instances where said event or circumstance occurs and instances where it does not. For example, an optionally substituted group means that the group is unsubstituted or is substituted. As used herein, the abbreviations for any protective groups, amino acids and 20 other compounds, are, unless indicated otherwise, in accord with their common usage, recognized abbreviations, or the IUPAC-IUB Commission on Biochemical Nomenclature (see, (1972) Biochem. 11:1726). B. THE EXTRACELLULAR MATRIX Provided herein are activatable matrix-degrading enzymes (AMDE) that 25 degrade one or more protein components of the extracellular matrix (ECM) in a time controlled manner. By virtue of such targeting and the temporal in vivo activation, diseases and/or conditions of the ECM can be treated. The activatable matrix degrading enzyme can degrade any component of the ECM; enzyme selection can depend upon the targeted component and/or the particular disease or condition to be 30 treated. The ECM makes up the connective tissue or interstitium that surrounds the spaces outside cells and the vascular and lymphatic system, thereby providing mechanical and structural support with and between different tissues. The complex WO 2009/111083 PCT/US2009/001486 - 40 and dynamic microenvironment of the ECM represents a structural and signaling system within connective tissues, such as the skin. Due to the complex nature of the ECM, it can serve diverse functions such as providing support and anchorage for cells, segregating tissues, regulating intercellular communication, and sequestering 5 cellular growth factors. Defects or changes in the organization, or make-up, of the ECM can contribute to a number of diseases or conditions. For example, changes in the synthesis, degradation and organization of collagen fibers contribute to lipodystrophy (e.g., cellulite) and lymphedema. The ECM is composed of fibrous structural proteins, such as collagens, 10 polysaccharides, such as proteoglycans and hyaluronic acid, and adhesion proteins that link components of the matrix to each other and to cells. Some connective tissues, such as tendon and cartilage, are principally made up of ECM. The ECM making up the connective tissue of the skin, however, also is distributed with fibroblasts, blood vessels and other components. The ECM also serves as the space 15 where water and its dissolved constituents move from the blood plasma to the lymphatics. The interstitial fluid is nearly isosmotic with the cytoplasm and is bicarbonate buffered providing an extracellular environment that is at neutral pH. 1. Components of the ECM The ECM (also called the interstitial matrix) is a complex three-dimensional 20 dynamic structure that contains numerous structural macromolecules including fibrous proteins such as collagens, elastin and fibronection, in which glycosyaminoglycans (GAGs) form a hydrated gel-like substance. The components of the ECM are produced by resident cells, typically fibroblasts or cells of the fibroblast family, and are secreted via exocytosis where they interact with other 25 components of the ECM. It is the variation in the relative amount and the way in which the components organize and form together that give rise to diverse connective tissues such as bone, skin or cornea (Albert et al., "Cell Junctions, Cell Adhesions and the Extracellular Matrix." Molecular Biology of the Cell. New York: Garland Publishers, 1994. Page 972.) 30 a. Collagens Collagen is the major structural constituent of connective tissues, such as the skin, and plays a role in the development and maintenance of tissue architecture, tissue strength and cell-cell interactions. Collagens include a family of structurally- WO 2009/111083 PCT/US2009/001486 -41 related proteins of the ECM that contain one or more domains having the conformation of a collagen triple helix (Van der Rest et al. (1991) FASEB J., 5:2814 2823). Collagens contain a Gly-X-Y repeating structure, which allows collagen chains to twist into a helical structure. Each collagen molecule contains three chains 5 twisted around each other to form a triple helix, designated al-a3. The triple helix structure provides a high mechanical strength to a collagen molecule. There are at least 27 different types of collagens, which differ in amino acid sequence and chain composition. For example, depending on the type of collagen, the three chains forming the triple helix can be the same or different. Collagens can be homotrimeric 10 (i.e. all three polypeptide chains of the triple helix are made up of the same collagen) or can be heterotypic (i.e. fibrils made of more than one collagen type). Collagens can be divided into several families depending on the structure they form. These include fibrillar collagens (also called interstitial collagens; e.g., Type I, II, III, V and XI) and non-fibrillar collagens such as facit (e.g., Type IX, XII, XIV), short chain 15 (e.g., Type VIII, X), basement membrane (e.g., Type IV), and other collagens (e.g., Type VI, VII, and XIII). Table 2 below sets forth common collagen types and their representative location (Van der Rest et al. (1991) FASEB J., 5:2814-2823); www.collagenlife.com/page_ 167323108078.html; www.indstate.edu/thcme/mwking/extracellularmatrix.html). 20 Among the interstitial collagens, collagen molecules associate to form large fibrils, which have a distinctive banding pattern. The banding pattern results from overlap between adjacent molecules. The strength of collagen fibers is based on a multiplicity of intra- and intermolecular linkages of the collagen fibers that form the dense collagen fiber network of connective tissues. The most common of fibrillar 25 collagens include type I, II and III collagens. Type I collagen is found in most connective tissues such as skin, bone, tendon and cornea, and is a made up of two l(I) chains and one oQ2(I) chain ([al(I)1 2 o2(I)). Type II collagen is homotrimeric ([al (II)]3) and is predominantly found in the cartilage. Type III collagen also is homotrimeric ([al(I)13) and is predominantly found in the skin and vessels. 30 Not all collagens form fibril networks. For example, the basement membrane type IV collagen is non-fibrous and has non-helical interruptions in the helix, which acts as a hinge giving the molecule greater flexibility. Thus, type IV collagen forms a sheet made by a meshwork of filaments rather than by linear fibrils. RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 - 42 The most abundant protein of the skin is collagen, which is primarily made up of type 1 (80-85%) and type III (8-11%) of the total collagen of the skin. Type I collagen associates with type III collagen to form the major collagen fibers of the dermis. The tensile strength of skin is due predominantly to these fibrillar collagen 5 molecules, which assemble into microfibrils in a head-to-tail and staggered side-to side lateral arrangement. Collagen molecules become cross-linked to adjacent collagen molecules, creating additional strength and stability in collagen fibers. For example, type V collagen also associates with type 1/111 collagen fibers, and regulates the fibril diameter. Other collagen types in the skin include, for example, type IV, 10 type VI, type VII, type XII, type XIV and type XVII. Table 2: Types of Collagens Type Molecule Composition Representative tissue Fibrillar Collagens I [al(I)] 2 [02(I)] Skin, bone, tendon, dentin, ligaments, interstitial tissues II [al (II)]3 Cartilage, vitreous humor III [al (111)]3 Skin, muscle, blood vessels; frequently associated with type I V [al(V)][o2(v)][a3(V)] Similar to Type I, also cell cultures, fetal tissues; associates with Type I XI [al (XI)][o2(XI)][a3(XI)] Cartilage, intervertebral cartilage and bone enamel Non-fibrillar collagens IV [adl(IV)] 2 [02 (IV)] Basement membrane VI [al(VI)][o2(VI)][a3(VI)] Most interstitial tissues; associates with type I VII [al(VII)] 3 epithelia VIII [al(VIII)] 3 Unknown, some endothelial cells IX [al(IX)][co2(IX)][a3(IX)] Cartilage; associates with Type II X [ad(X)] 3 Heterotrophic and mineralizing cartilage XII [al (XII)] 3 Ligaments, tendons and tooth WO 2009/111083 PCT/US2009/001486 - 43 enamel; interacts with types I and III b. Elastin A network of elastic fibers in the ECM provides flexibility to tissues that require resilience to recoil after stretching, such as the skin, arteries and lungs. The 5 main component of elastic fibers is the elastin molecule, which creates cross-links to adjacent elastin molecules. These molecules form a core of elastic fibers and are covered by fibrillin, a large glycoprotein that binds to elastin and is important for the integrity of elastic fibers. c. Fibronectin 10 Fibronectin is a glycoprotein that exists as a pair of two large subunits joined by a pair of disulfide bonds near the carboxyl termini. Each subunit contains functionally distinct domains specific for other matrix macromolecules and receptors on the surface of cells. For example, distinct domains on fibronectin bind collagen (separate domains for types I, II and III), heparin, fibrin and cell surface receptors 15 such as integrins. Fibronectin is present in both plasma and tissue. In tissue, fibronectin functions to link together different types of ECM molecules and cells. It also contains an important cell-binding domain made up of the three amino acids, Arg-Gly-Asp (RGD), which is recognized by integrin receptors in the plasma membranes of cells. The binding of fibronectin molecules to integrin receptors on 20 cells leads to the stimulation of signaling pathways that promote cell attachment, migration and differentiation. These characteristics allow fibronection to play an important role in cell adhesion and to communicate signals between cells and components of the ECM. d. Glycosaminoglycans (GAGs) 25 GAGs are unbranched polysaccharide chains made of repeating disaccharide units that are strongly hydrophilic. GAGs are highly negatively charged and therefore attract osmotically active Na+, causing large amounts of water to be drawn into their structure to keep the ECM hydrated. GAGs, such as dermatan sulfate, typically contain multiple glycosaminoglycan chains of 70-200 sugars long (formed from 30 repeating disaccharide units) that branch from a linear protein core. This results in GAGs occupying a huge volume relative to their mass and forming gels at very low WO 2009/111083 PCT/US2009/001486 - 44 concentrations. The hydrophilic nature of GAGs causes a swelling pressure, or turgor, which allows the ECM to withstand compression forces. In the ECM, GAGs are attached to ECM proteins to form proteoglycans or, in the case of hyaluronic acid (also called hyaluronan), exist as a non-proteoglycan 5 matrix component. Extracellular proteoglycans are large, highly hydrated molecules that help cushion cells in the ECM. Glycosaminoglycans such as hyaluronan contribute to the "ground substance" by creating a barrier to bulk fluid flow through the interstitial collagenous matrix by way of their viscosity and water of hydration. Proteoglycans and non-proteoglycan GAGs associate to form large polymeric 10 complexes in the ECM. They associate with each other, and also with fibrous proteins such as collagen. i. Proteoglycans There are three main types of GAGs that form proteoglycans of the ECM, including dermatan sulfate and chondroitin sulfate, heparin and heparan sulfate, and 15 keratan sulfate. Generally, a proteoglycan is 95% carbohydrate by weight, typically in the form of long unbranched GAG chains. Besides providing hydrated space around cells, proteoglycans also regulate traffic of molecules and cells, bind signaling molecules thereby playing a role in cell activation, and bind other secreted proteins such as proteases and protease inhibitors to regulate the activities of secreted proteins 20 (Albert et al., "Cell Junctions, Cell Adhesions and the Extracellular Matrix." Molecular Biology of the Cell. New York: Garland Publishers, 1994. pp. 972-978.) For example, the heparin sulfate chains of proteoglycans bind to several different growth factors, including fibroblast growth factors (FGFs), helping them to bind to their specific cell surface receptors. 25 Aggrecan is a proteoglycan, which principally contains chondroitin sulfate and heparan sulfate GAGs, and is typically found in cartilage forming large aggregates with hyaluronan to provide mechanical support. Decorin is another exemplary GAG of connective tissues made up primarily of chondroitin sulfate and dermatan sulfate GAGs. It binds to type I collagen fibrils. Perlecan and betaglycan are other 30 exemplary proteoglycans of the ECM. Not all proteoglycans are associated with the ECM: for example, serglycin is associated with secretory vesicles where it helps to package and store secretory molecules, and syndecans are found on the cell surface and act as co-receptors (Albert et al., "Cell Junctions, Cell Adhesions and the WO 2009/111083 PCT/US2009/001486 - 45 Extracellular Matrix." Molecular Biology of the Cell. New York: Garland Publishers, 1994. pp. 972-978.) Heparan sulfate proteoglycans (HSPGs) are ubiquitous macromolecules associated with the cell surface and extracellular matrix (ECM) of a wide range of 5 cells of vertebrate and invertebrate tissues (Wight, T. N., Kinsella, M. G., and Qwarnstromn, E. E. (1992) Curr. Opin. Cell Biol., 4,793-801; Jackson, R. L., Busch, S. J., and Cardin, A. L. (1991) Physiol. Rev., 71,481-539; Wight, T. N. (1989) Arteriosclerosis, 9,1-20; Kjellen, L., and Lindahl, U. (1991) Annu. Rev. Biochem., 60,443-475; and Ruoslahti, E., and Yamaguchi, Y. (1991) Cell, 64,867-869). The 10 basic HSPG structure consists of a protein core to which several linear heparan sulfate chains are covalently attached. The polysaccharide chains are typically composed of repeating hexuronic and D-glucosamine disaccharide units that are substituted to a varying extent with N- and O-linked sulfate moieties and N-linked acetyl groups. Studies on the involvement of ECM molecules in cell attachment, growth and 15 differentiation revealed a central role of HSPGs in embryonic morphogenesis, angiogenesis, metastasis, neurite outgrowth and tissue repair. The heparan sulfate (HS) chains, which are unique in their ability to bind a multitude of proteins, ensure that a wide variety of effector molecules cling to the cell surface. HSPGs are also prominent components of blood vessels. In large vessels they are concentrated mostly 20 in the intima and inner media, whereas in capillaries they are found mainly in the subendothelial basement membrane where they support proliferating and migrating endothelial cells and stabilize the structure of the capillary wall. The ability of HSPGs to interact with ECM macromolecules such as collagen, laminin and fibronectin, and with different attachment sites on plasma membranes suggests a key role for this 25 proteoglycan in the self-assembly and insolubility of ECM components, as well as in cell adhesion and locomotion. ii. Hyaluronic acid Hyaluronic acid (HA; also called hyaluronan) is a large GAG that attracts water, and when bound to water exists in a viscous, gel-like form. Thus, HA serves as 30 a lubricant, holding together gel-like connective tissues. HA is a polymer of disaccharides (sometimes as many as 25,000 repeats in length) and is composed of repeating units of two modified simple sugars: glucuronic acid and N-acetyl glucosamine. HA is part of the ECM of many connective tissues. HA is found in the WO 2009/111083 PCT/US2009/001486 - 46 greatest amount in the skin with almost 50% of the body's HA found in the skin. The HA provides continuous moisture to the skin by binding up water. Decreased production of HA, such as by age, results in wrinkled and unhealthy skin. HA, principally through its receptor CD44, also functions to regulate cell 5 behavior during embryonic development and morphogenesis, wound healing, repair and regeneration, inflammation and tumor progression and invasion (Harada et al. (2006) J. Biol. Chem., 8:5597-5607). HA is degraded by hyaluronidases. The degradation products of HA can be found in increased amounts in damaged or growing tissues, and in a variety of inflammatory conditions. HA fragments promote 10 angiogenesis and can stimulate cytokine production by macrophages and dendritic cells in tissue injury and skin transplant. 2. Histology of the Skin The skin is composed of several distinct layers, principally the epidermis and dermis. The epidermis is a specialized epithelium derived from the ecotoderm, and 15 beneath this is the dermis, which is a derivative of the mesoderm and is a vascular dense connective tissue. These two layers are firmly adherent to one another and form a region which varies in overall thickness form approximately 0.5 to 4 mm in different areas of the body. Beneath the dermis is a layer of loose connective tissue, which varies from areolar to adipose in character. This is referred to as the 20 hypodermis, but is typically considered not to be part of the skin. The dermis is connected to the hypodermis by connect tissue fibers that pass from one layer to the other. a. The Epidermis The epidermis is the skin layer directly above the dermis, and is the surface 25 layer of the skin. The principle function of the epidermis is to act as a protective barrier against water loss, chemical injury and invading pathogens. The epidermis is a thin layer of approximately fifteen cell layers that is about 0.1 to 1.5 millimeters thick composed primarily of keratinocytes (Inlander, Skin, New York, N.Y.: People's Medical Society, 1-7 (1998)). The epidermis is itself divided into several layers (e.g., 30 stratum basale, stratum spinosum, stratum granulosum, stratum lucidum, stratum corneum) based on the state of differentiation of the keratinocytes. Keratinocytes originate in the basal layer from keratinocyte stem cells. As the keratinocytes grow and divide, they undergo gradual differentiation eventually reaching the stratum WO 2009/111083 PCT/US2009/001486 - 47 corneum where they form a layer of enucleated, flattened, highly keratinized cells called squamous cells (also called corneocytes). Besides being made up of corneocytes, the stratum corneum also contains sebum. The sebum is secreted by sebaceous glands, which are usually found in hair-covered areas connected to hair 5 follicles. Sebum is a slightly acid layer that helps to hold the corneocytes together and holds moisture in. This acidity is due to the presence of amphoteric amino acids, lactic acid and fatty acids that make up sebum. Thus, the pH of the skin surface is normally between 5 and 6, typically about 5.5. Sebum acts to waterproof hair and skin, and keep them from becoming dry, brittle and cracked, and it also inhibits the 10 growth of microorganisms on skin. The term "acid mantle" refers to the presence of the water-soluble substances on most regions of the skin. b. The Dermis The connective tissue of the skin is called the dermis. The dermis is 1.5 to 4 milliliters thick. In the skin, the dermis contains ECM components; the main protein 15 components are collagen and elastin. The dermis also is home to most of the skin's structures, including sweat and oil glands that secrete substances through openings in the skill called pores, or comedos, hair follicles, nerve endings, and blood and lymph vessels (Inlander, Skin, New York, N.Y.: People's Medical Society, 1-7 (1998)). c. The Hypodermis 20 Below the dermis is the hypodermis, which is a fatty layer and is the deepest layer of the skin. It acts both as an insulator for body heat conservation and as a shock absorber for organ protection -(Inlander, Skin, New York, N.Y.: People's Medical Society, 1-7 (1998)). In addition, the hypodermis also stores fat for energy reserves. 25 3. Diseases of the ECM Certain diseases and conditions result from defects or changes in the architecture of the extracellular matrix due to aberrant expression or production of ECM components. For example, in some inflammatory conditions such as occur upon wound healing, cytokines are secreted, which stimulate fibroblasts to secrete 30 ECM components such as collagen. The ECM components accumulate and become locally deposited, resulting in a wide range of fibrotic conditions. Matrix deposition is a frequent feature in many chronic inflammatory diseases and in other diseases and conditions. Included among these are collagen-mediated disease conditions such as, WO 2009/111083 PCT/US2009/001486 - 48 but not limited to, scars such as keloid and hypertrophic scars, Duputyren's syndrome, Peyronie's disease and lymphedema. Cellulite also is a prominent disease of the ECM that, in addition to increased adipogenicity, is characterized by alterations in the connective tissue matrix resulting in an abnormal fibrous septae network of collagen 5 (Rawlings et al. (2006) Int. J Cos. Science, 28:175-190). Diseases and conditions of the ECM that are characterized by aberrant expression or overproduction of matrix components, resulting in their accumulation and unwanted deposition, can be treated by the activatable matrix-degrading enzymes provided herein. By virtue of the temporal activation of such enzymes upon in vivo 10 administration, the treatment of such diseases and conditions is regulated to limit the enzymatic degradation of the matrix components. For example, by limiting the duration of action of matrix degradation, unwanted side effects associated with uncontrolled protein degradation is minimized. C. Matrix-Degrading Enzymes 15 Provided herein are compositions, combinations and containers containing activatable matrix-degrading enzymes, and methods of using activatable matrix degrading enzymes to treat ECM-mediated diseases or conditions. Matrix-degrading enzymes degrade protein components or glycoproteins of the ECM, including, but not limited to, collagen, elastin, fibronectin and proteoglycans. By virtue of their ability 20 to cleave one or more ECM components, activatable matrix-degrading enzymes provided herein can be used to modify the matrix of tissues, particularly those exhibiting structural defects or changes due to excess of one or more ECM protein or unwanted accumulation of fibrous tissue rich in one or more ECM proteins, such as collagen. Thus, such enzymes are useful in treating diseases or conditions in which 25 ECM proteins are involved. Among matrix-degrading enzymes are proteases and glycosyl hydrolases. Hence, matrix-degrading enzymes include proteins that are protein-degrading enzymes that recognize sequences of amino acids or a polypeptide substrate within a target protein and also hydrolases that recognize non-peptide bonds such as ester 30 bonds or glycosyl groups. Among proteases are exoproteases of the seine, cysteine, aspartic and metallo-protease families. Upon recognition of the substrate sequence, proteases catalyze the hydrolysis or cleavage of a target protein. Such hydrolysis of a target protein, depending on the location of the peptide bond within the context of the WO 2009/111083 PCT/US2009/001486 - 49 full-length sequence of the target sequence, can inactivate, or in some instances activate, a target. Several distinct types of catalytic mechanisms are used by proteases ( Barret et al. (1994) Meth. Enzymol. 244:18-61; Barret et al. (1994) Meth. Enzymol 244:461 5 486; Barret et al. (1994) Meth. Enzymol. 248:105-120; Barret et al. (1994) Meth. Enzymol. 248:183-228). Based on their catalytic mechanism, the proteases that cleave peptide bonds are subdivided into serine-, cysteine-, aspartic-, threonine- and metallo proteases. Serine-type peptidases have a serine residue involved in the active center, aspartic-type peptidases have two aspartic acids in the catalytic center, cysteine-type 10 peptidases have a cysteine residue, threonine-type peptidases have a threonine residue, and metallo-peptidases use a metal ion in the catalytic mechanism. The catalytic activity of the proteases is required to cleave a target substrate. Serine and metalloproteinases are most active at neutral pH, while cysteine and aspartic proteases, found predominantly in lysosomes, have acidic pH optima. Thus, 15 lysosomal proteases include proteases of the cysteine and aspartic protease families. Other families of enzymes include the hydrolases such as esterases that act on ester bonds and glycolases that hydrolyze 0- or S-glycosyl compounds or N-glycosyl compounds. Exemplary of a glycosyl hydrolase is heparanase. Exemplary matrix-degrading enzymes are set forth in TABLE 3 (see e.g., 20 Chapman et al., Am J. Physiol Heart Circ. Physiol. (2004) 286:1-10; lozzo RV, Proteoglycans: Structure, biology, and Molecular Interactions, CRC Press (2000), pp. 94-96; Owen et al. (1999) J. Leuk. Biol., 65:137-150; Buhling et al. (2004) Eur. Respir. J., 23:620-628; Thomas Kreis and Ronald Cale, Extracellular Matrix, Anchor and Adhesion Proteins, Oxford University Press (1999) pp. 515-523; Ian M. Clark 25 and Gillian Murphy. "Matrix Proteinases," in Dynamics of Bone and Cartilage Metabolism, Academic Press (2006), pp. 181-198; Buck et al. (1992) Biochem J., 282:273-278). The sequence identifiers (SEQ ID NO) for the nucleotide sequence (mRNA) and encoded amino acid sequence of the precursor polypeptide for each of the exemplary proteases are depicted in the Table. The sequence identifiers (SEQ ID 30 NO) for the amino acid sequence of the proprotein for each of the exemplary proteases also are depicted in the Table, as well as the amino acid positions within the proprotein that correspond to the propeptide. Variations also exist among allelic and species variants and other variants known in the art, and such variants also are WO 2009/111083 PCT/US2009/001486 - 50 contemplated for use as activatable enzymes. The Table also sets forth exemplary ECM target substrates for each enzyme. Reference to such substrates is for reference and exemplification, and are not intended to represent an exhaustive list of all target substrates. One of skill in the art knows or can empirically determine ECM target 5 substrates for a desired enzyme using routine assays, just as any described herein. Matrix-degrading enzymes can be produced or isolated by any method known in the art including isolation from natural sources, isolation of recombinantly produced proteins in cells, tissues and organisms and by recombinant methods and by methods including in silicon steps, synthetic methods and any methods known to those 10 of skill in the art. Typically, enzymes are produced or isolated in an inactive form. Conditional activation can be achieved as described below. TABLE 3: Matrix-Degrading Enzymes Protease Substrate Enzyme GenBank SEQ ID NO databank No. access Precursor mature code nt aa aa (EC) (aa of signal www.exp sequence(ss); asy.ch/sp aa of pro rot/enzy peptide (pp) me.html Serine Protease Pancreatic elastin 3.4.21.36 Q9UNI1; 19 20 21 elastase NM_00197 (ss aa 1-8; (PEl; pp aa 9-18) Elastase-1) Elastase-2A elastin 3.4.21.71 P08217; 22 23 24 NM_03344 (ss aa 1-16; 0 pp aa 17-28) Elastase-2B elastin 3.4.21.71 P08218; 25 26 27 NM_01584 (aa aa 1-16; 9 pp aa 17-28) Neutrophil Elastin, 3.4.21.37 P08246 28 29 30 elastase (NE; fibronectin, NM_00197 (ss aa 1-17; leukocyte laminin, 2 pp aa 28-29) elastase; collagen type elastase-2) II, IV, VI, proteoglycans Proteinase-3 elastin, 3.4.21.76 P24158 31 32 33 (PR-3; fibronectin, NM_00277 (ss aa 1-25; myeloblastin) laminin, 7 pp aa 26-27, vitronectin, 249-256) collagen type WO 2009/111083 PCT/US2009/001486 - 51 TABLE 3: Matrix-Degrading Enzymes Protease Substrate Enzyme GenBank SEQ ID NO databank No. access Precursor mature code nt aa aa (EC) (aa of signal www.exp sequence(ss); asy.ch/sp aa of pro rot/enzy peptide (pp) me.html IV Endogenous elastin 3.4.21.46 S73894 34 35 36 vascular (Rattus sp.) (ss aa 1-20; elastase pp aa 21-25) (EVE; tissue elastase; complement factor D) Cathepsin G collagen type EC P08311 37 38 39 IV, laminin, 3.4.21.20 NM_00191 (ss aa 1-18; fibronectin, 1 pp aa 19-20) proteoglycan, elastin Mast cell collagen type 3.4.21.39 P23946 40 41 42 chymase IV, laminin, NM_00183 (ss aa 1-19; fibronectin, 6 pp aa 20-21) proteoglycan Mast cell fibronectin, 3.4.21.59 Q9BZJ3 43 44 45 tryptase fibrinogen, NM_01221 (ss aa 1-18; collagen type 7 pp aa 19-30) IV, proteoglycan Plasmin Proteoglycan, 3.4.21.7 P00747 46 47 48 fibronectin, NM_00030 (ss aa 1-19; laminin 1 pp aa 20-97) Thrombin proteoglycan 3.4.21.5 P00734 49 50 51 NM_00050 (ss aa 1-24; 6 pp aa 25-43) Granzyme B proteoglycan 3.4.21.79 P10144 52 53 54 NM_00413 (ss aa 1-18; pp aa 19-20) Cysteine Protease Cathepsin S Elastin, EC P25774 55 56 57 collagen 3.4.22.27 NM_00407 (ss 1-16; pp 9 17-114) Cathepsin K elastin, EC P43235 58 59 60 collagen I and 3.4.22.38 NM_ 00039 (ss aa 1-15; III 6 pp aa 16-114) Cathepsin L elastin, EC P07711 61 62 collagen I and 3.4.22.15 (ss aa 17; pp WO 2009/111083 PCT/US2009/001486 -52 TABLE 3: Matrix-Degrading Enzymes Protease Substrate Enzyme GenBank SEQ ID NO databank No. access Precursor mature code nt aa aa (EC) (aa of signal www.exp sequence(ss); asy.ch/sp aa of pro rot/enzy peptide (pp) me.html IV aa 18-113) Cathepsin B Collagen IV, EC P07858 63 64 65 laminin, 3.4.22.1 NM_00190 (ss aa 1-17; fibronectin 8 pp aa 18-79) Cathepsin C Proteoglycans EC P53634 178 179 180 (decorin) 3.4.14.1 NM_00181 (ss aa 1-24; 4 ppaa135 230) Cathepsin H fibronectin EC P09668 66 67 68 3.4.22.16 X16832 (ss aa 1-22; pp aa 23-97) Cathepsin F Collagen EC Q9R013 69 70 71 fragments 3.4.22.41 NM_01986 (ss aa 1-19; 1 (Mus pp aa 20-248) musculus) Cathepsin F Collagen EC Q9UBX1 181 182 183 fragments 3.4.22.41 NM 00379 (ss aa 1-19; 3 pp 20-270) Cathepsin 0 fibrinogen EC Q8BM88 72 73 74 3.4.22.42 NM_17766 (aa aal-23; 2 (mus pp aa 24-98) musculus) Cathepsin O fibrinogen EC P43234 184 185 186 3.4.22.42 NM 00133 (ss aa 1-23; 4 pp aa 24-107) Cathepsin R EC3.4.22. Q9JIA9 75 76 77 NM_02028 (ss aa 1-17; 4 (mus pp aa 18-114) musculus) Cathepsin V collagen EC 060911 187 188 189 (Cathepsin 3.4.22.43 NM_00133 (ss aa 1-17; L2) 3 pp aa 18-113) Cathepsin W EC P56202 78 79 80 3.4.22.- NM_00133 (ss aa 1-21; 5 pp aa 22-127) Calpain 1 fibronectin, EC Calpain 1 81 82 vitronectin, 3.4.22.52 large proteoglycans subunit: P07384 NM_00518 6 WO 2009/111083 PCT/US2009/001486 - 53 TABLE 3: Matrix-Degrading Enzymes Protease Substrate Enzyme GenBank SEQ ID NO databank No. access Precursor mature code nt aa aa (EC) (aa of signal www.exp sequence(ss); asy.ch/sp . aa of pro rot/euzy peptide (pp) me.html Calpain 2 fibronectin, EC3.4.22. Calpain 2 83 84 85 vitronectin, 53 large (aa 1 proteoglycans subunit: initiating P17655 methionine) NM_00174 18 Calpain small subunit 1 86 87 (associates with Calpain 1 and 2 large subunits) P04632 NM 001749 Legumain EC Q99538 190 191 192 3.4.22.34 NM_00560 (ss aa 1-17; 6 pp aa 324 433) Cathepsin Z EC Q9UBR2 193 194 195 (cathepsin X) 3.4.22.- NM_00133 (ss aa 1-23; 6 pp aa 24-61) Aspartic Protease Cathepsin D proteoglycan EC P07339 88 89 90 3.4.23.5 NM_00190 (ss aa 1-18; 9 pp aa 19-64) Cathepsin E proteoglycan EC P14091 3.4.23.34 Isoform a 91 92 93 NM_00191 (ss aa 1-17; 0 pp aa 18-53) Isoform b 94 95 96 NM 14896 (ss aa 1-17; 4 pp aa 18-53) Metallo-Protease MMP-1 collagen I, II, 3.4.24.7 P03956, 97 98 99 (collagenase III, VII, VIII, NM_00242 (ss aa 1-19; -1) X, XI, gelatin, 1 pp aa 20-99) proteoglycan, fibronectin, glycoprotein MMP-8 collagen I, II, 3.4.24.34 P22894 100 101 102 (collagenase- III, aggrecan NM_00242 (ss aa 1-20; 2) 4 pp aa 21-100) WO 2009/111083 PCT/US2009/001486 - 54 TABLE 3: Matrix-Degrading Enzymes Protease Substrate Enzyme GenBank SEQ ID NO databank No. access Precursor mature code nt aa aa (EC) (aa of signal www.exp sequence(ss); asy.ch/sp aa of pro rot/ezy peptide (pp) me.html MMP-13 collagen 1, 11, 3.4.24.- P45452 103 104 105 (collagenase III, IV, VI, NM_00242 (ss aa 1-19; -3) IX, X, XIV, 7 pp aa 20-103) gelatin, proteoglycan, fibronectin, glycoprotein MMP-18 collagen I 3.4.24.- Xenopus 106 107 108 (collagenase- laevis (ss aa 1-17; 4) 013065 pp aa 18-99) MMP-2 gelatins, 3.4.24.24 P08253 109 110 111 (gelatinase collagen 1, 11, NM_00453 (ss aa 1-29; A) III, IV, V, 0 pp 30-109) VII, X, XI, elastin, fibronectin, laminin, proteoglycan, glycoprotein MMP-9 gelatin, 3.4.24.35 P14780 112 113 114 (gelatinase collagen IV, NM_00499 (ss aa 1-19; B) V, VI, XIV, 4 pp aa 20-93) elastin, laminin, proteoglycan, glycoprotein MMP-3 fibronectin, 3.4.24.17 P08254 115 116 117 (stromelysin- elastin, NM_00242 (ss aa 1-17; 1) laminin, 2 pp aa 18-99) gelatin, proteoglycan, glycoprotein, collagen III, IV, V, VII, IX, X, XI MMP-10 collagen III, 3.4.24.22 P09238 118 119 120 (stromelysin- IV, V, elastin, NM_00242 (ss aa 1-17; 2) gelatin, 5 pp aa 18-98) fibronectin, aggrecan MMP-I1 Gelatin, 3.4.24.- P24347 121 122 123 (stromelysin- fibronectin, X57766 (ss aa 1-31; WO 2009/111083 PCT/US2009/001486 - 55 TABLE 3: Matrix-Degrading Enzymes Protease Substrate Enzyme GenBank SEQ ID NO databank No. access Precursor mature code nt aa aa (EC) (aa of signal www.exp sequence(ss); asy.ch/sp aa of pro rot/enzy peptide (pp) me.html 3) laminin, pp aa 32-97) collagen IV MMP-7 fibronectin, 3.4.24.23 P09237 124 125 126 (matrilysin) laminin, NM_00242 (ss aa 1-17; elastin, 3 pp aa 18-94) gelatin, collagen I, IV, proteoglycan, glycoprotein MMP-26 collagen IV, 3.4.24.- Q9NREl 127 128 129 (matrilysin-2) fibronectin, NM_02180 (ss aa 1-17; gelatin, 1 pp aa 18-89) proteoglycan MMP-12 elastin, 3.4.24.65 P39900 130 131 132 (metalloelast fibronectin, NM_00242 (ss aa 1-16; ase) laminin, 6 pp aa 17-105) collagen I, IV, V, gelatin, proteoglycan, glycoprotein MMP-14 Collagen I, II, 3.4.24.80 P50281 133 134 135 (MTI-MMP) III, gelatin, NM_00499 (ss aa 1-20; aggregcan, 5 pp aa 21-111) fibronectin, laminin, proteoglycan, glycoprotein MMP-15 aggregan, EC P51511 136 137 138 (MT2-MMP) fibronectin, 3.4.24.- NM_00242 (ss aa 1-41; laminin, 8 pp aa 42-131) glycoprotein MMP-16 Collagen III, EC P51512 139 140 141 (MT3-MMP) fibronectin, 3.4.24.- NM_00594 (ss aa 1-31; laminin, pp aa 32-119) gelatin, proteoglycan MMP-17 gelatin EC Q9ULZ9 142 143 144 (MT4-MMP) 3.4.24.- AB021225 (ss aa 1-38; pp aa 39-128) MMP-24 fibronectin, EC Q9Y5R2 309 310 311 (MT5-MMP) gelatin, 3.4.24.- NM_00669 (ss aa 1-52; Transmembra proteoglycan 0 pp aa 53-155) WO 2009/111083 PCT/US2009/001486 - 56 TABLE 3: Matrix-Degrading Enzymes Protease Substrate Enzyme GenBank SEQ ID NO databank No. access Precursor mature code nt aa aa (EC) (aa of signal www.exp sequence(ss); asy.ch/sp aa of pro rot/enzy peptide (pp) me.html ne MMP-25 collagen IV, EC Q9NPA2 312 313 314 (MT6-MMP) gelatin, 3.4.24.- NM_0224 (ss aa 1-21; GPI anchor fibronectin, 68 pp aa 22-107) proteoglycan MMP-19 collagen IV, EC Q99542 145 146 147 gelatin, 3.4.24.- NM_00242 (ss aa 1-18; laminin, 9 pp aa 19-97) aggregan, fibronectin, glycoprotein MMP-20 aggrecan EC 060882 148 149 150 (enamelysin) 3.4.24.- Y12779 (ss aa 1-22; pp aa 23-107) MMP-x No substrates EC 093470 151 152 153 (MMP-21) defined 3.4.24.- NM_00108 (ss aa 1-22; (XMMP) 5816 pp aa 23-180) (Xenopus) MMP-21 gelatin EC Q8N119 315 316 317 3.4.24.- NM_14719 (ss aa 1-24; 1 pp aa 25-144) MMP-23 gelatin EC 075900 318 319 320 CA-MMP 3.4.24.- AJ005256 MMP-27 gelatin EC Q9H306 321 322 323 CMMP 3.4.24.- NM_02212 (ss aa 1-17; 2 pp aa 18-98) MMP-28 EC Q9H239 324 325 326 (epilysin) 3.4.24.- NM_02430 (ss aa 1-22; 2 pp aa 23-122) ADAMTS-1 aggrecan EC Q9UHI18 157 158 159 3.4.24. NM_00698 (ss aa 1-49; 8 pp aa 50-252) ADAMTS-2 Procollagen I, EC 095450 160 161 162 procollagen II 3.4.24. AJO03125 (ss aa 1-29; pp aa 30-253) ADAMTS-3 Procollagen II EC 015072 163 164 165 3.4.24.14 NM_01424 (aa 1-229) 3 ADAMTS-4 aggrecan EC 075173 166 167 168 (aggrecanase- 3.4.24.82 NM_00509 (ss aa 1-51; 1) , , 9 pp aa 52-212) WO 2009/111083 PCT/US2009/001486 - 57 TABLE 3: Matrix-Degrading Enzymes Protease Substrate Enzyme GenBank SEQ ID NO databank No. access Precursor mature code nt aa aa (EC) (aa of signal www.exp sequence(ss); asy.ch/sp aa of pro rot/enzy peptide (pp) me.html ADAMTS-5 aggrecan EC Q9UNAO 169 170 171 (aggrecanase- 3.4.24. NM_00703 (ss aa 1-16; 2) 8 pp aa 17-261) ADAMTS-14 Procollagen I EC Q8WXS8 172 173 174 3.4.24. Isoform a (ss aa 1-22; NM_13915 pp aa 23-252) 5 Isoform a 175 176 177 NM_08072 (ss aa 1-22; 2 pp aa 23-252) Other Heparanase Proteoglycan EC 3.2.-.- Q9Y251 154 155 156 AF152376 (ss aa 1-35; pp aa 110 157) 1. Enzyme Activation Most proteases are synthesized and secreted as inactive forms and require 5 further processing to become active. Activation is typically achieved by conformational, steric or other changes that reveal the enzymes active site. With the exception of calpains, all protease enzymes are typically synthesized as zymogens. Zymogen activation prevents unwanted protein degradation that could occur if proteases were always present in an active form. Generally, zymogens contain N 10 terminal portions (or prosegments or proregions) that sterically block the active site of the protease and prevent access of substrates to the active site of the protease. The prosegments of the zymogens range in size from two residues to 150 residues. Upon secretion from a preproenzyme form, the proenzyme (containing the prosegment) is inactive. 15 Upon proteolytic removal of the prosegment of the zymogen, either autocatalytically or by other proteases, the active site of the enzyme is exposed WO 2009/111083 PCT/US2009/001486 - 58 resulting in a mature protease, and typically, activation. In some cases, however, additional cofactors also are required for complete activation. For example, pH change triggers the activation of enzymes of the cysteine, aspartic and metalloprotease families. Low pH acts to increase the susceptibility of the prosegment as a substrate 5 during zymogen conversion or causes a conformational change in the prosegment or enzyme (Jerala et al. (1998) J Biol. Chem., 273:11498-11504). Lysosomal enzymes, such as cathepsins of the cysteine and aspartic protease families, require acidic conditions before complete activation is achieved. Besides pH, other cofactors include, but are not limited to, salt concentration, reducing agents such as cysteine, 10 DTT and TCEP, metal ions such as calcium, heat or temperature. Thus, various mechanisms of zymogen conversion exist and vary between protease families (see e.g., Khan et al. (1998) Protein Science, 7:815-836; Khan et al. (1999) PNAS, 96: 10968-10975). For example, zymogen conversion to the active enzyme often occurs as a result of proteolysis by autocatalysis or actions of other proteases, changes in pH, 15 or the involvement of accessory molecules or ions, or a combination or one or more of the above conditions. Further control over the time and location of action often is achieved by protein inhibitors (Stroud et al. (1977) Ann. Rev. Biophys. Bioeng., 6:177-93) a. Serine Proteases 20 Serine proteases (SPs), which include secreted enzymes and enzymes sequestered in cytoplasmic storage organelles, have a variety of physiological roles, including blood coagulation, wound healing, digestion, immune responses and tumor invasion and metastasis. Many seine proteases degrade components of the extracellular matrix (see Table 2 above). For example, proteases involved in the 25 degradation and remodeling of extracellular matrix (ECM) contribute to tissue remodeling, and are necessary for cancer invasion and metastasis. The activity of proteases in the seine protease family is dependent on a set of amino acid residues that form their active site. One of the residues is always a seine; hence their designation as seine proteases. The mechanism of cleavage of a target 30 protein by a serine protease is based on nucleophilic attack of the targeted peptidic bond by a seine. The catalytic seine forms a covalently-attached tetrahedral intermediate with the carbonyl atom of the scissile peptide bond of substrates. In many cases the nucleophilic property of the group is improved by the presence of a WO 2009/111083 PCT/US2009/001486 - 59 histidine, held in a "proton acceptor state" by an aspartate. Aligned side chains of serine, histidine and aspartate build the catalytic triad common to most serine proteases. Most serine proteases exist as zymogens in the precursor form, and thus are 5 inactive. In the zymogen form of the protease active site for catalysis is distorted compared to the active enzyme. In fact, serine proteases are the only family of proteases who have conformational differences in the active site between the zymogen and active form of the protease. Thus, the catalytic triad exists in the zymogen, but a distorted loop from the proenzyme partially obstructs the substrate 10 binding cleft. As a result, the substrate polypeptide cannot bind effectively, and proteolysis does not occur. Only after activation, during which the conformation and structure of the zymogen change and the active site is opened, can proteolysis occur. Serine proteases are active at neutral pH. Zymogen conversion occurs following limited proteolysis, such as by highly specific catalytic cleavage by another 15 protease or by auto-activation. For example, the conversion of the inactive prothrombin to the active form of the enzyme (thrombin) is achieved by a highly specific catalytic cleavage of the prosegment by another of the clotting enzymes (factor Xa). Other seine proteases use similar mechanisms, but the activation cleavage sites differ and thus seine proteases typically are activated by different 20 convertases. Granule-associated seine proteases, including but not limited to, granzymes A and B, cathepsin G, neutrophil elastase, proteinase 3, and mast cell tryptase and chymase require a dual proteolytic event for activation. These enzymes are synthesized as preproenzymes; cleavage of the signal peptide results in a proenzyme 25 zymogen form that is inactive. Granule-associated seine proteases contain a prodipeptide at the N-terminus of the enzyme, and also contain a carboxyl-terminal extension which also must be removed for activation. The prodipeptide prevents folding of the mature enzyme into a catalytically active formation. Activation of the granule-associated seine proteases is achieved by cleavage of both the carboxy 30 terminal extension and the prodipeptide. Cathepsin C has been implicated in cleavage of the prodipeptide in at least some granule-associated seine proteases (Kummer et al. (1996) J Biol. Chem., 271:9281-9286). b. Cysteine Proteases WO 2009/111083 PCT/US2009/001486 -60 Cysteine proteases contain a Cys-His pair in their active site, and their catalytic activation involves a cysteine sulfhydryl group. Deprotonation of the cysteine sulfhydryl by an adjacent histidine residue is followed by nucleophilic attack of the cysteine on the peptide carbonyl carbon. A thioester linking the new carboxy 5 terminus to the cysteine thiol is an intermediate of the reaction (comparable to the acyl-enzyme intermediate of a serine protease). Cysteine proteases include papain, cathepsin, caspases, and calpains. The mechanisms of activation of these different families of cysteine proteases differ. i. Cathepsins 10 Papain-like cysteine proteases, including cathepsin, are a family of thiol dependent endo-peptidases related by structural similarity to papain. They form a two-domain protein with the domains labeled R and L (for right and left) and loops from both domains form a substrate recognition cleft. The cathepsins are synthesized as zymogens containing a prosegment; the prosegment acts as an N-terminal 15 inhibitory prosegment. Although there is about 25% sequence identify among the mature enzymes, the prosegments exhibit little sequence similarity. The prosegment functions as a potent inhibitor of the mature enzyme. The prosegment also serves other functions such as playing a role in the folding and stability of the enzyme during synthesis and transport at neutral pH. 20 Cathepsins of the cysteine protease family are lysosomal enzymes and thus are optimally active below pH 7 and become inactive above pH 7. Cathepsins are synthesized as inactive precursors (i.e. zymogens), and are activated by proteolytic removal of the prosegment. This results in the generation of single-chain enzymes. Generally, the single chain enzymes can be processed into two chain forms containing 25 a heavy chain and a light chain. Typically, the two chains are held together via noncovalent interactions or via disulfide bridges. Hence, mature cathepsins exist in single-chain or in two-chain form. The removal of the prosegment can be facilitated either by activation by other proteases or by autocatalytic activation at acidic pH (Turk et al. (2001) The EMBO 30 Journal, 20:4629-4633). The pH dependence of the zymogen conversion process is regulated by conserved salt bridges in the prosegment (e.g., Asp 2p and Arg38p and Glu87p and Arg48p in procathepsin L set forth in SEQ ID NO:62). Disruption of the salt bridges by protonation of the carboxylate groups at the lower pH disrupts the WO 2009/111083 PCT/US2009/001486 -61 hydrophobic core of the prosegment resulting in dissociation of the prosegment from the active site (Khan et al. (1998) Protein Science, 7:815-836). The residues conferring formation of salt bridges can differ between cathepsins. For example, pro cathepsin B uses alternative salt-bridge interactions for its pH-dependent zymogen 5 conversion (Coulombe et al. (1996) EMBO J., 15:5492-5503). Acidic pH conditions are required for the activity of mature cathepsins; zymogen conversion itself is not sufficient for enzyme activity. In addition to its requirement for activity, the acidic pH also stabilizes the enzyme. Inactivation and destabilization of cathepsins at higher pH conditions is caused by deprotonation of the 10 imidazole moiety of the active site -S-/H~im- ion pair, and "unzipping" of the structure along the active site groove (Dehrmann et al. (1995) Arch. Biochem. Biophys., 324:93-98). Hence, most cathepsins have optimal activity and stability at an acidic pH. For example, cathepsins B, F, H, K, L and V are optimally active in acidic environments and are only weakly active or not active at neutral pH (Lutgens et 15 al. (2007) The FASEB J., 21: 3029-3041). Some cathepsins, e.g. cathepsin L, lose their activity quickly after incubation at a neutral pH. Some cathepsins maintain their enzymatic activity even after incubation at neutral pH, and thus can degrade matrix proteins under physiological conditions. Cathepsins C and S have been found to have the highest pH stability, while cathepsins K and V display intermediate pH stability. In 20 vitro investigations have shown that cathepsin K can degrade fibril proteins at neutral pH. (Buhling et al. (2004) Eur. Respir. J., 23:620-628). Cathepsin L Cathepsin L (CatL) is a lysosomal acid cysteine protease that belongs to the papain family. The human cathepsin L gene encodes a 333 amino acid cysteine 25 protease that contains a 17 amino acid signal peptide, a 96-amino acid propeptide and a 220 amino acid mature region (see SEQ ID NOS:61 and 62 and GenBank Accession No. P07711). Cathepsin L also includes allelic and species variants, and other variants. Exemplary of such variants are any set forth in SEQ ID NOS:208 to 223 and 234. Cathepsin L is synthesized as an inactive proenzyme, and like other proteases, 30 contains a propeptide corresponding to amino acids 18-113 of the sequence of amino acids set forth in SEQ ID NO:62. The propeptide inhibits the proteolytic activity of the enzyme. The propeptide segment also functions to stabilize the proenzyme from the denaturing effects of neutral to alkaline pH (Coulombe et al. (1996) The EMBO J., RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 - 62 15:5492-5503). Cleavage of the propeptide occurs by autoprocessing under acidic conditions resulting in a mature enzyme that is active and has catalytic activity under acidic conditions. The mature cathepsin L (set forth in SEQ ID NO:1) can exist as a single chain form of about 28 kDa and/or as a two-chain form of about 24 and 4 kDa 5 (heavy and light chain, respectively). Allelic and species variants of cathepsin L are known. Exemplary species variants are any set forth in SEQ ID NOS:208-223, including nucleic acids and encoded polypeptide and mature forms thereof lacking the signal sequence and propeptide. Exemplary allelic variants are any set forth in SEQ ID NO:234. 10 Cathepsin L is primarily localized to endosomes and lysosomes. The optimal proteolytic capacity of mature cathepsin L is achieved at an acidic pH of about 5.5, and it is inactive at neutral pH (Bohley P et al., "Intracellular Protein Turnover." in S. Holzer and H. Tschcsche (eds.). Biological Functions ofProteinases, pp. 17-34, Berlin: Springer-Verlag. 1979). The pH optima of cathepsin L can be influenced by 15 ionic strength, and therefore the pH optima differs between buffers (Dehrmann et al. (1995) Arch. Biochem. Biophys., 324: 93-98). Procathepsin L is stable under neutral and slightly alkaline pH, conditions where mature cathepsin L is inactivated (Jerala et al. (1998) J Biol. Chem., 273:11498-11 504). For example, at acidic pH the enzyme is more stable, acts less on itself, but actively catalyzes hydrolysis of protein 20 substrates. At pH closer to neutral or physiologic pH and in the presence of elevated temperature such as 37*C, the enzyme is highly unstable because it prefers itself as a substrate (autocatalysis) versus other protein substrates. A reducing agent, if added to an active cathepsin L, can enchance these activities both at acidic and physiologic pH. The activated form of cathepsin L has seven half cysteine residues, which 25 include three disulfinde cysteins and I free cysteine (the active site Cys 25 that is conserved in the cysteine protease family). The presence of a reduced sulfhydryl group (-SH) of the Cys25 is required for activity. Hence, the presence of a reducing agent such as Cysteine or a reduced form of glutathioe can help keep the active site sulfhydryl in the reduced state. Alternately, or in addition, the reducing agent can 30 reduce the disulfides and help attain a more favorable protein conformation (secondary and tertiary) that induces better binding and catalysis of in vivo substrates. Cathepsin L degrades proteins substrates, including, but not limited to, collagen, IL-8 precursor, neurotransmitter precursor, pro-enkephalin, and RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 - 63 immunoglobulin light chain-associated (AL) amyloid deposits and azocasein (Barret & Kirschke (1981) Methods Enzymol., 80:535-561; Mason et al., (1985) Biochem. J., 226:233-241). CatL is rapidly inhibited by Z-Phe-Ala-CHN2. ii. Calpain 5 Calpain is a Ca 2 +-dependent cytoplasmic cysteine protease that exists in two predominant forms, p-calpain (calpain 1) and m-calpain (calpain 2). Calpain substrates include cytoskeletal proteins, signal-transducing enzymes, transcriptional regulatory factors and integral membrane proteins. Among ECM components, calpains degrade fibronectin, vitronectin and proteoglycans (Ian M. Clark and Gillian 10 Murphy. "Matrix Proteinases," in Dynamics of Bone and Cartilage Metabolism, Academic Press (2006), pp. 181-198). Calpains exist as inactive heterodimers (and -80 kDa and -30 kDa subunits), and require Ca2+ for autocatalysis. p-calpain and m-calpain differ in their sensitivity to Ca2+ required for activation; p-calpain is half-maximally activated at low 15 micromolar calcium concentrations, which is about an order of magnitude lower than those concentrations required to activate m-calpain (Meyer et al. (1996) Biochem. J, 314:511-519). Upon activation, both subunits of calpain undergo limited autolysis that removes the N-terminal prosegment and increases calcium sensitivity. Autolysis itself is not sufficient to activate calpain because the autolyzed protease still requires 20 calcium to cleave substrate (Meyer et al. (1996) Biochem. J., 314:511-519). Thus, sustained activation of calpain requires the presence of calcium. The calcium requirements are considerably higher than physiological Ca2+ concentrations, which is generally 1 pM. For example, in vitro i-calpain requires a calcium concentration of 10-50 ptM and m-calpain requires a calcium concentration of 300-500 piM (Hosfield 25 et al. (1999) The EMBO J., 18:6880-6889). Due to the calcium requirement, calpain is regulated by regional calcium fluxes and/or membrane binding (Molinari and Carafoli (1997) JMembr. Bio., 43:543-5.) Calcium likely induces a conformation change to expose the active site of the protease. Calpastatin is a specific cellular inhibitor of calpains. 30 c. Aspartic Proteases Aspartate proteases include some proteases found in lysosomes that have been shown to degrade ECM components. Included among these are cathepsins D and E. For activity, two aspartate residues participate in acid/base catalysis at the active site.

WO 2009/111083 PCT/US2009/001486 - 64 In the initial reaction, one aspartate accepts a proton from an active site H 2 0, which attacks the carbonyl carbon of the peptide linkage. Simultaneously, the other aspartate donates a proton to the oxygen of the peptide carbonyl group. The zymogen form of aspartate proteases contain a positively charged N 5 terminal prosegment that interacts with the central portion of the enzyme forming salt bridges with the negatively charged segment. Due to the positioning of the prosegment and the formation of the salt bridges, substrates are prevented from accessing the active site. Zymogen conversion to an active enzyme occurs by disruption of the salt bridges at low pH. Exposure to low pH results in protonation of 10 the carboxylate side chains of Asp and Glu residues, resulting in destabilization of salt bridges between the prosegment and mature enzyme. Once removed, the prosegment is autocatalytically degraded by the active enzyme. Subsequent hydrolysis of the prosegment ensures that activation is irreversible, and that the released prosegment will not act as a competitive inhibitor of the active enzyme. Further, no other 15 accessory molecules are required for conversion (Khan et al. (1998) Protein Science, 7:815-836). Like cathepsins of the cysteine protease family, however, acidic pH conditions are required for activity and stability of the mature enzymes. d. Metalloproteases Metalloproteases (also called Zinc proteases) include the digestive enzymes 20 carboxypeptidases, various matrix metalloproteases (MMPs) that are secreted by cells, ADAMs (a disintegrin and metalloprotease domain), ADAMTS (a disintegrin and a metalloproteinase domain with thrombospondin motifs) and lysosomal proteases. These enzymes, including ADAMs and MMPs, have roles in embryonic development, cell growth and proliferation, inflammatory responses, wound repair, 25 multiple sclerosis, arthritis, and cancer progression and metastasis (Manzetti et al., (2003) J of Computer-Aided Mol. Design, 17: 551). Most MMPs (e.g., collagenase) are involved in degradation of the extracellular matrix, for example, during tissue remodeling. For example, many of these enzymes can cleave components of the basement membrane and extracellular matrix. 30 Metalloproteases contain a Zn" ion at the active center of the enzyme required for catalytic activity. A zinc binding motif at the active site of a metalloprotease includes two histidine residues whose imidazole side-chains are ligands to the Zn". During catalysis, the Zn" promotes nucleophilic attack on the WO 2009/111083 PCT/US2009/001486 -65 carbonyl carbon by the oxygen atom of a water molecule at the active site. An active site base (a glutamate residue in carboxypeptidase) facilitates this reaction by extracting a proton from the attacking water molecule. Generally, these enzymes have a common zinc binding motif (HExxHxxGxxH) in their active site, and a 5 conserved methionine turn following the active site. Mutation of any one of the histidines ablates catalytic activity. The zymogen form of metalloproteases contains a prosegment of about 80-100 residues in length. In the zymogen form, the residues within the substrate binding site of the mature enzyme and the catalytic Zn** ions are in the same conformational 10 position as in the active form, and do not change upon zymogen conversion. The enzyme is inactive because the prosegment is positioned to block the site, thus preventing access to substrates. Conversion of the zymogen to the active enzyme results from cleavage of the prosegment from the mature enzyme. Multiple mechanisms are capable of initiating cleavage events, including actions by other 15 proteases, heat, mercurial agents (e.g., 4-amino-phenylmercuric acetate), SH-reactive agents, reactive oxygen and detergents (see e.g., Khan et al. (1998) Protein Science, 7:815-836; Okada et al. (1988) Biochem J., 254:731-741; Okada & Nakanashi (1989) FEBS Lett., 249:353-356; Nagase et al. (1990) Biochemistry, 29:5783-5789; Koklitis et al. (1991) Biochem J., 276:217-221; Springman et al. (1990) PNAS, 87:364-8; 20 Murphy et al. (1997) Matrix Biol., 15:511-8). e. Heparanase Heparanase is a glycosylated enzyme that is involved in the catabolism of certain glycosaminoglycans. It is an endo-B-glucuronidase that cleaves heparan sulfate at specific intrachain sites. Heparanase is a member of the glycosyl hydrolase clan A 25 (GH-A), which share a common catalytic mechanism that involves two conserved acidic residues, a putative proton donor at Glu 225 and a nucleophile at Glu"' (Hulett et al. (2000) Biochemistry, 39:15659-15667). Interaction of T and B lymphocytes, platelets, granulocytes, macrophages and mast cells with the subendothelial extracellular matrix (ECM) is associated with degradation of heparan sulfate by 30 heparanase activity. Human heparanase cDNA encodes a protein that is initially synthesized as a pre-pro-protein with a signal peptide sequence that is removed by signal peptidase upon translocation into the endoplasmic reticulum (ER). The resulting 65 kDa pro- WO 2009/111083 PCT/US2009/001486 - 66 enzyme form is further processed by proteolytic cleavage resulting in excision of an intervening 6 kDa fragment generating an 8 kDa polypeptide and a 50 kDa polypeptide, forming a heterodimer. The sequence of amino acids of the mature heparanase is set forth in SEQ ID NO:156. Heparanase activity and localization is 5 tightly regulated. For example, the enzyme is highly sensitive to changes in local pH, exerting a high enzymatic activity under acidic conditions that exists in the vicinity of tumors and in inflammatory sites with little or no activity at physiological pH. Thus, heparanase-mediated cleavage of the HS scaffold is a pH-dependent process; maximal enzymatic activity is achieved at pH values ranging from 4 to 6.8 (Gilat et al. (1995) J 10 Exp. Med., 181:1929-1934; Goldshmidt et al. (2003) The FASEB J., 17:1015-1025). At physiological pH, heparanase exhibits little activity. The pH-dependence ensures that the structural breakdown of the ECM is confined to more acidic conditions, such as occurs in endosome and at sites of injury or inflammation (McKenzie et al. (2003) Biochem. J, 373:423-435). 15 D. Activatable Matrix-Degrading Enzymes (AMDE) Matrix-degrading enzymes require zymogen conversion for activation by cleavage of the prosegment to generate a mature enzyme. As discussed above, many matrix-degrading enzymes also require the continued presence of one or more other activating conditions for activity. Exemplary of such activating conditions include, 20 but are not limited to, pH, metal ions, temperature, reducing agents, oxidizing agents and salt concentration. For example, many enzymes require specific pH values or metal ion concentration or salt concentration or the presence of a reducing agent for activity. In one example, lysosomal enzymes require acidic pH conditions for activity. For example, cathepsins of the cysteine and aspartic family of proteases 25 require acidic pH conditions for activity. Heparanase also is a lysosomal enzyme that accumulates in lysosomes for normal processing in the acidic environment. Generally, the acidic environment is provided in the acidic lysosomes where lysosomal proteases are normally localized. Outside of this environment, lysosomal proteases are inactive or less active and require exogenous exposure to acidic pH for 30 activity. In another example, an activating conditions include metal ion concentration. For example, the calpains require sufficient concentration of Ca 2 for activity. Activity of such enzymes is reversible in the absence of the activating condition.

WO 2009/111083 PCT/US2009/001486 - 67 By taking advantage of the requirement for exogenous activating conditions, activatable matrix-degrading enzymes can be made temporally active for a limited duration upon in vivo administration, for example to the ECM. Such activatable matrix-degrading enzymes are active only when exposed to exogenous activating 5 conditions. Since the activating condition is not present at the site of administration and must be applied exogenously, the activating condition will become neutralized or dissipate over time after in vivo administration of an activator supplying the appropriate activating condition. Hence, activation of an AMDE is reversible following in vivo administration as the activator dissipates or is otherwise neutralized. 10 For example, temporal activation of an AMDE can be achieved in the environment of the interstitium of the skin and other tissues by administering the AMDE in the presence of an exogenous activating condition (i.e. an activator) that is not present at the site of administration. Typically, the activating condition is one that is not present in the ECM, prior to administration of an activator providing the activating condition. 15 Thus, exposure of an activatable matrix-degrading enzyme to an activating condition results in enzyme activation for a limited or predetermined time as the activating condition dissipates or is neutralized in the interstitial environment. Hence, provided herein are compositions, combinations and containers containing activatable matrix-degrading enzymes that, upon in vivo administration, 20 permit activation of the enzyme for a limited or predetermined period of time during which the enzyme can exert its biological action. By virtue of the reversible activity of the activatable enzymes, the enzymes become deactivated, thereby controlling the duration of the biological action of such enzymes. The activatable matrix-degrading enzymes are provided in combinations and containers with an activator that provides 25 the activating condition. In addition, the activatable matrix-degrading enzyme and activator also can be combined or provided in combination, such as in containers, with other agents such as any one or more of an antisthetic, alpha adrenergic agent or dispersing agent. The activatable matrix-degrading enzymes are provided in a therapeutically effective amount, that when activated, degrade one or more 30 components of the ECM upon administration, such as upon subcutaneous administration. The resulting activatable matrix-degrading enzymes can be used as therapeutics to treat ECM-mediated diseases or conditions.

WO 2009/111083 PCT/US2009/001486 - 68 Any matrix-degrading enzyme, whether synthetic or isolated from natural sources, such as those set forth in Table 3 or elsewhere herein, allelic or species variants or other variants thereof, or any known to those of skill in the art is intended for use in the compositions, combinations, methods and apparatus provided herein, so 5 long as the enzyme is activatable due to the requirement of an activating condition. The activatable matrix-degrading enzymes are provided in an inactive form either as a zymogen or as an inactive mature polypeptide either in single-chain or two-chain form. For example, cathepsins even in their mature form are inactive and require acidic pH conditions for conformational stability. Activatable matrix-degrading 10 enzymes include lysosomal proteases, such as cathepsins of the cysteine and aspartic family and heparanases. Exemplary activatable matrix-degrading enzymes are any set forth in any of SEQ ID NOS:56, 59, 62, 64, 179, 67, 70, 73, 76, 182, 185, 188, 79, 194, 89, 92, 95 and 155 and mature forms thereof set forth in SEQ ID NOS:57, 60, 1, 65, 180, 68, 71, 74, 77, 183, 186, 189, 80, 195, 90, 93, 96 and 156 or allelic variants 15 or species variants or other variants thereof. One of skill in the art knows or could identify activatable matrix-degrading enzymes. For example, one of skill in the art could use routine assays of enzyme activation, such as any provided herein and known in the art, to assess the requirement of an exogenous activating condition for sustained or reversible activation of any desired enzyme. 20 Activatable matrix-degrading enzymes can be modified to alter any one or more properties or activities. For example, altered properties or activities include, but are not limited to, modification that render the enzyme more stable, alter the substrate specificity and/or confer temperature sensitivity to the enzyme. If desired, enzyme stability also can be increased by pegylation or glycosylation of the enzyme. 25 Modification of polypeptides using standard recombinant DNA techniques is routine to one skilled in the art. For purposes herein, modified matrix-degrading enzymes retain one or more activities of the unmodified enzyme and are activatable. Retained activity can be 40%, 50%, 60%, 70%, 80%, 90%, 95% or more activity of the unmodified enzyme. 30 In one example, a matrix-degrading enzyme, for example, a cathepsin, can be modified such that its prosegment is not inhibitory. Modifications can be made by amino acid replacement, substitution or insertion within the prosegment itself, or within regions of the active site where the inhibitory interactions occur. Hence, a WO 2009/111083 PCT/US2009/001486 - 69 cathepsin could be provided in a zymogen form where autocatalysis occurs under acidic conditions; the cleaved prosegment of such a modified enzyme would not result in inactivation as occurs for wild-type cathepsins if provided in a zymogen form. In another example, an activatable enzyme can be modified to alter its 5 substrate specificity. For example, an enzyme can be modified to have increased specificity for a particular substrate. Thus, for example, cathepsin L, which exhibits substrate specificity for type I and type IV collagen can be modified so that it has increased substrate specificity for type I collagen, and not type IV collagen, and vice versa. Modifications of polypeptides can be achieved by routine molecular biology 10 techniques, and are within the skill of one in the art. Modified enzymes can be tested for their substrate specificity using routine assays for substrate cleavage such as is described herein, or known in the art. For example, substrate cleavage can be assessed on fluorogenic peptides or on purified proteins. Cleavage can be assessed using in vitro or in vivo assays. For example, cleavage can be assessed by incubating 15 the enzyme with the substrate, and then running the mixture on an SDS-PAGE gel. Degradation can be assessed by Western Blot or by using standard protein stains such as Coomasie Blue or Silver Stain reagents. In an additional example, a matrix-degrading enzyme can be modified to have temperature sensitivity. For example, matrix-degrading enzymes that are active at 20 physiological temperature (e.g. 37 *C) can be modified and enzymes selected that are active at lower temperatures (e.g., less than 37 0 C; e.g. at or about 20 *C, 21 *C, 22 *C, 23 0 C, 24 *C, 25 'C, 26 *C, 27 *C, 28 0 C, 29 .C or 30 *C), but that are not active at physiological temperature. Hence, such modified enzymes can be used as activatable matrix-degrading enzymes where the activation condition is low 25 temperature. Administration of the enzymes simultaneously, intermittently, or subsequently with an activating condition providing the cold temperature (e.g. cold buffer) results in activation of the enzyme. The activation of the enzyme is temporally controlled as the in vivo temperature returns to the physiological temperature of 37 *C. 30 1. Activating Conditions and Methods for Activation of Activatable Matrix-Degrading Enzymes Activatable matrix-degrading enzymes are inactive in the absence of an activating condition. Upon in vivo administration, temporal activation of such WO 2009/111083 PCT/US2009/001486 - 70 activatable matrix-degrading enzymes is achieved by exposure (prior to or upon administration subsequently, intermittently or simultaneously) to one or more specific activators that provide an activating condition sufficient for activation of the enzyme. For example, activation can be achieved by exposure of activatable matrix-degrading 5 enzymes to, for example, temperature (e.g. heat or cold), pH, salt, to solutions containing sufficient concentrations of metal ions (e.g., Ca 2 ) for activation, to solutions containing sufficient concentrations of reducing agents or oxidizing agents for activation, or other methods as described herein or known to one of skill in the art. The choice of activator will vary depending upon the choice of enzyme as described 10 herein or known to one of skill in the art. Generally, an amount (e.g. concentration, level or degree) of activator sufficient to generate an active enzyme is used. This amount can be readily determined empirically and is dependent upon the selected enzyme and selected application. By Virtue of the reversible and conditional activation of activatable enzymes, 15 temporary activation is achieved, thereby regulating the duration of enzymatic action on extracellular matrix (ECM) components. This is an advantage of the present methods such that deleterious side effects associated with unwanted prolonged activation of enzymes can be controlled. Temporary activation is achieved because activatable matrix-degrading enzymes require continuous exposure to activating 20 conditions in order to remain active. Activating conditions are not normally present, endogenously, in sufficient amounts for activation of an enzyme at sites where activatable matrix degrading enzymes are administered in vivo. For example, the skin interstitium has a neutral pH, and thus a low pH activating condition is not normally present. In another example, the physiological level of metal ions, such as calcium, in 25 the skin interstitium, are far lower than the effective amounts required for activation of some enzymes. Thus, deactivation of enzymes can occur upon decreasing exposure of the enzyme to the exogenous activating condition as may occur following in vivo administration of an activatable enzyme where the exogenously supplied activating condition gradually dissipates or is neutralized. 30 Thus, activating conditions provided herein are those which are required for activation of an activatable matrix-degrading enzymes, but that are not normally present in sufficient amounts at the site of administration. The requirement for activating conditions for activation of activatable matrix-degrading enzymes permits WO 2009/111083 PCT/US2009/001486 - 71 activation of matrix-degrading enzymes for a limited time, until the activating condition dissipates or is neutralized such that the enzyme becomes inactive or becomes unstable and is degraded. The amount of time an enzyme is active can be for a predetermined time. For example, an activator can be provided containing an 5 amount of activating condition, such as the concentration, effective amount, level or degree, that is chosen such that the enzyme is active for a' set time under the environment and conditions it is exposed to upon in vivo administration. In one example, where acidic pH is the activating condition, the buffering capacity of an acidic buffer can be adjusted to modulate the time of its resistance to changes in pH. 10 The predetermined time at which an activator activates a conditionally activatable matrix-degrading enzyme can be determined empirically and is a function of the disease to be treated, the individual treated, the choice of enzyme and the activator. An activatable matrix-degrading enzyme can be active following in vivo administration in the presence of an activator providing an activating condition for at 15 or about 1 minute, 2 minutes, 3 minutes, 4 minutes, 5 minutes, 10 minutes, 20 minutes, 30 minutes, 40 minutes, 50 minutes, 1 hour, 2 hours, 3 hours, 4 hours, 5 hours, 6 hours or more. Exemplary activating conditions and activators and methods of temporal activation are described herein below. In view of such description, other 20 embodiments will be apparent to one of skill in the art. a. Activating Condition - Acidic pH Compositions and methods for conditional activation of matrix-degrading enzymes whose activity is regulated by pH, and use of such enzymes to treat ECM mediated diseases or conditions are provided herein. Such methods take advantage of 25 proteins having enzymatic activity only at acidic pH, while remaining inactive or becoming unstable and degraded at neutral pH. Such proteins include lysosomal proteases, including, but not limited to, cathepsins of the cysteine and aspartic families, and also heparanase. For example, lysosomes, an acidic intracellular compartment, contain a large variety of hydrolytic enzymes that degrade proteins and 30 other substances internalized by endocytosis. All intralysosomal proteases, for example, cathepsin L, exhibit an acid pH optimum. Exemplary of such proteases are any set forth in any of SEQ ID NOS:57, 60, 1, 65, 180, 68, 71, 74, 77, 183, 186, 189, 80, 195,90,93,96 and 156.

WO 2009/111083 PCT/US2009/001486 - 72 Methods of using matrix-degrading enzymes that are active only upon exposure to certain pH conditions are used herein to take advantage of pH differentials within the skin. Human epidermal systems maintain a pH gradient within the stratified layers of the skin. The outer layers have been reported to exhibit 5 an average pH of 5.5 (W.P. Smith (1994) Cosmetics and Toiletries, 109:41-48). The pH of successive layers of the epidermis increases with depth, reaching a final pH closer to the physiological range (about pH 7.4) at the dermal layer. Hence, it is contemplated herein that activatable matrix-degrading enzymes are employed that exhibit activity at acidic conditions, but are substantially inactive at 10 neutral pH such as exists in the ECM. A substantially inactive enzyme is any exhibiting 10% or less activity of the enzyme at its pH optima, for example, at or about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 9.5% or 10% of activity as present at the enzyme's pH optima. One of skill in the art knows or can determine the pH optima of an enzyme and can assess activity differences at varying pH conditions. 15 For example, the pH optima of cathepsin L is or is about 5.5, but can vary within a range. of 4.5 to 6 depending on the particular species of cathepsin L, buffer condition or ionic strength. Cathepsin L is substantially inactive at or above pH 7.4 (Dehrmann et al. (1995) Arch. Biochem. Biophys., 324:93-98). In another example, the optimal pH value for the activity of cathepsin D is or is about 3.0 to 4.0, and it is substantially 20 inactive at pH values at or about 6.0 or higher (Rojas-Espinosa et al. (1973) Infection and Immunity, 8:1000-1008). Cathepsin S is one of the few lysosomal proteases that is stable at pH 7.0 (Bromme et al. (1993) J Biol. Chem., 268: 4832-4838). For purposes herein, an activatable enzyme is active in pH conditions at or about 3, 3.5, 4, 4.5, 5, 5.5, 6 or 6.5, but is substantially inactive at neutral pH. A pH 25 activity profile can be performed on an enzyme, and relative activity assessed, to determine its pH optima under various conditions (Dehrmann et al. (1995) Arch. Biochem. Biophys., 324:93-98). It is understood that pH optima can be different depending on the substrate used, buffer conditions, ionic strength and species of enzyme. Thus, reference to pH optima herein is for exemplification only. One of 30 skill in the art can empirically determine the pH optima of an enzyme under specific conditions. For example, buffer conditions and ionic strengths can be varied to determine an enzymes activity under various pH conditions. Enzyme assays to determine pH-activity profiles can be performed using fluorogenic substrates such as WO 2009/111083 PCT/US2009/001486 - 73 are described herein and known to one of skill in the art. The choice of fluorogenic substrate used will vary between enzymes, and is known to one of skill in the art or can be empirically determined. Thus, the ability to conditionally activate matrix-degrading enzymes by 5 administration with an activating condition not normally present at the site of administration permits the temporal regulation of, and alteration of, the physiological parameters of organs and tissues, such as the interstitium, exhibiting a neutral pH. Under normal physiological conditions, the pH of the interstitium is neutral. Thus, activatable matrix-degrading enzymes active at low pH, such as lysosomal enzymes 10 described herein, when present in the interstitium would normally be catalytically inactive because of the neutral pH of the interstitium. When the pH of the interstitium is temporarily rendered acidic, for example by administration of a buffered acid solution, lysosomal enzymes with optimal acidic pH when administered to the interstitium will become activated. When the pH of the intersitium turns back 15 towards neutrality, then the matrix-degrading enzymes with requiring acidic pH become inactivated and cease to exert their enzymatic activity. Accordingly, it is contemplated herein that activatable matrix degrading enzymes that are substantially inactive at neutral pH can be administered sub epidermally under the skin (i.e. by subcutaneous, intradermal or intramuscular 20 administration) where the pH is neutral. Other routes of administration of conditionally activatable matrix-degrading enzymes also are contemplated and can be empirically determined based on the pH optima of the particular enzyme such that the activity of the enzyme becomes reversible due to changes in the pH conditions upon administration. Other routes of administration include, but are not limited to, oral, 25 topical and transdermal routes of administration. Since the interstitium of most tissues and organs exhibits a neutral pH, temporary acidification can be achieved by infusing an acidic solution to a tissue or organ interstitium. The acidic buffer is a composition that, when administered, temporarily lowers the pH of the interstitium to less than or about 3.0, 3.5, 4.0, 4.5, 30 5.0, 5.5, 6.0 or 6.5 such that the activatable matrix-degrading enzyme is active. The acid component of the buffer is susceptible to neutralization by the neutral pH of the interstitium. Acidic buffers are known to one of skill in the art. For purposes herein, the acid component of the buffer can be an organic or inorganic acid. Generally, the WO 2009/111083 PCT/US2009/001486 - 74 solution is a solution of a weak acid. Exemplary acids include, but are not limited to, 2-(N-morpholino)ethanesulfonic acid) (MES), acetic acid, citric acid, succinic acid, lactic acid, maleic acid, glycine-hydrochloric acid, citric phosphate and histidine. The effective pH range of acidic buffers is known, and hence, appropriate buffers can be 5 chosen based on the pH optima of the selected enzyme. Exemplary of acidic buffers include, but are not limited to, acetate, citrate, formate, glycine, malate, MES, phosphate, piperazine, propionate, pyridine and succinate buffer. For example, the effective pH range of MES buffer is 5.5 to 6.7. The time period required for neutralization, and subsequent inactivation of the 10 acid activatable matrix-degrading enzyme, depends on the formulation of the acidic buffer. For example, shorter time periods result if the acid and/or buffering agents in the acidic buffer are weak relative to the neutralizing capacity of the interstitium; longer time periods result if a stronger acid is utilized or a stronger buffering agent is employed in the acidic buffer. Hence, the resistance to change in pH is dependent on 15 the buffering capacity of the particular buffer. The higher the ionic strength or concentration of the buffer, the higher the buffer capacity. Thus, in the methods and compositions provided herein, temporal regulation of a matrix-degrading enzyme activated at a given pH can be further controlled by the buffering capacity of the buffer chosen. This is exemplified in Example 7. Determination of desired buffers 20 for given applications is routine and within the level of one of skill in the art. Typically, the acidic solution is infused directly to a site where degradation of one or more ECM components is desired, for example, to treat an ECM-mediated disease or condition. The infusion of the activating condition in the form of an acidic solution activator can be performed simultaneously, sequentially or intermittently 25 with administration of an inactive activatable matrix-degrading enzyme. Where administration occurs simultaneously, the activatable matrix-degrading enzyme and buffered acidic solution can be in the same or separate compositions. When in the same composition, the enzyme and buffered acidic solution can be provided in a composition as a mixture. Activation of the enzyme also can be achieved by addition 30 of the acidic solution to a concentrated liquid solution or suspension or lyophilized or powdered form of the enzyme prior to administration. Generally, where a liquid solution or suspension of an activatable matrix-degrading enzyme is provided, it is a solution or suspension that, when exposed to an activator providing the appropriate WO 2009/111083 PCT/US2009/001486 - 75 activating condition, is amenable to activation of the enzyme by the activating condition. In addition, in the combinations and methods provided herein, an activator having the activating condition (e.g. a buffered acidic solution) and an activatable 5 matrix-degrading enzyme can be provided and administered in combination with any one or more other agents such as any one or more of an anesthetic, alpha adrenergic receptor agonist or dispersing agent. Exemplary of such agents are discussed herein below in the Section entitled "Combination Therapies." The other agents can be administered simultaneously, sequentially or intermittently with the activator and/or 10 matrix-degrading enzyme. In one example of the methods provided herein, a buffered acid solution is administered into the skin interstitium, or other tissue, where an ECM condition or disease is present. The buffered acidic solution can be chosen based on the pH required for activation of the a matrix-degrading enzyme and the desired buffering 15 capacity to achieve activation of limited duration. For example, cathepsin L is an exemplary enzyme for purposes of treating a collagen-mediated disease, such as, for example cellulite. Accordingly, the acidic buffer would be prepared at the optimum pH of 5.5 for activation of cathepsin L. Exemplary of such an acidic buffer is MES. The buffering capacity of the acidic solution also can be experimentally determined as 20 desired, for example, as set forth in Example 7. Generally, the acidic buffer is administered just prior to or together with the matrix-degrading enzyme. For example, if the matrix-degrading enzyme is provided in lyophilized form, the enzyme can be reconstituted with the acidic buffered solution just prior to administration, and the combination of the enzyme and activator administered together. In the presence 25 of the acidic buffer, the enzyme is activated following in vivo administration. Depending on the buffering capacity of the acidic buffer, the pH of the interstitium will return to neutrality after a limited or predetermined time, thereby reversing the degradative effects of the matrix-degrading enzyme. In another example of the methods provided herein, a combination of a 30 anesthetic and vasoconstrictor, for example, lidocaine/epinephrine, is administered prior to administration of the activator and matrix-degrading enzyme. Generally, in the methods, a dispersing agent, such as a hyaluronan degrading enzyme, for example WO 2009/111083 PCT/US2009/001486 - 76 a hyaluronidase, also is administered together with the anesthetic and vasoconstrictor, such as an alpha adrenergic receptor agonist. b. Activating Condition - Metal Cation Concentration Provided herein are composition, combinations, containers and methods 5 containing activatable matrix-degrading enzymes that require exposure to a suitable metal ion, for example Ca 2 +, Mg 2 + or Zn2+, for activation. Exemplary of such an enzyme is calpain (e.g. large subunit set forth in SEQ ID NO:82 (calpain 1) and SEQ IDNO:85 (calpain 2) and small subunit set forth in SEQ ID NO:87, or allelic or species variants or other variants thereof), which requires Ca2+ for activation. The 10 metal ion can be provided in the form of an aqueous composition, for example, as a calcium salt. The inactive enzyme can be provided as a mixture with a metal ion, or can be provided as a separate composition. If provided as a separate composition, such as in the form of a concentrated liquid composition or in lyophilized or powdered form, addition of the metal ion to the enzyme will result in an activated 15 enzyme. Generally, activation is achieved by exposing an inactive enzyme to a metal cation, for example Ca2+, at a concentration sufficient for activation. Precise amounts can be empirically determined or are known to those of skill in the art. For example, in vitro activation of p-calpain and m-calpain require 10-50 and 300-500 PM calcium 20 concentrations, respectively (Hosfield et al. (1999) The EMBO J., 18: 6880-6889.) Assays for enzymatic activity can be performed to determine optimal concentrations. Typically, for purposes herein, activatable matrix-degrading enzymes include those that require sufficient concentration of a metal ion for activation at a concentration that exceeds the physiological level of metal ion present in the interstitium. For the 25 case of p-calpain and m-calpain, the calcium levels required for activation exceed physiological levels (see e.g., U.S. Patent No. 6,620,592; Hosfield et al. (1999) The EMBOJ., 18: 6880-6889.) In general, the inactive enzyme is packaged or provided so that there are insufficient metal ions to trigger enzyme activation. Hence, where the inactive 30 enzyme is provided as a composition separate from the metal ion activator, it might be necessary to add ethylenediaminetetraacetic acid (EDTA) or ethylene glycol tetraacetic acid (EGTA) (concentrations from about 5 to about 100 mM or higher depending on the application) to tie up any Ca 2+ or other metal ion to prevent WO 2009/111083 PCT/US2009/001486 - 77 triggering the activation reaction until desired. The activation reaction then can be triggered by adding Ca 2 + (or other metal cation) at a concentration sufficient to overcome the effects of the chelator. Precise amounts can be empirically determined. Depending on the enzyme, temporary activation can be achieved simply by 5 discontinued exposure to metal ion. For example, sustained activation of calpain requires the presence of calcium. Thus, an inactive form of calpain can be activated by adding Ca 2 , and the resulting mixture, either in the same or separate compositions, can be administered to the interstitum of an organ or tissue. Upon administration, however, the effective concentration of calcium required for continued activation is 10 no longer available; the resulting active enzyme will ultimately return to its inactive state. In other examples, the temporal regulation of an enzyme requiring a metal ion for activation can be controlled by administration of a metal chelator or other reversing agent. c. Activating Condition - Reducing Agent 15 Provided herein are composition, combinations, containers and methods containing activatable matrix-degrading enzymes that require exposure to a suitable thiol or non-thiol containing reducing agent, for example, tris(2 carboxyethyl)phosphine (TCEP) or cysteine, for activation. Exemplary of such an enzyme is cathepsin L, which requires reducing agent for activation. The reducing 20 agent can be provided in the form of an aqueous composition, for example, as cysteine. The inactive enzyme can be provided as a mixture with a reducing agent, or can be provided as a separate composition. If provided as a separate composition, such as in the form of a concentrated liquid composition or in lyophilized or powdered form, addition of the reducing agent to the enzyme will result in an 25 activated enzyme. The reducing agent can be added prior to, simultaneously, subsequently or intermittently upon administration of the enzyme. Generally, activation is achieved by exposing an inactive enzyme to a reducing agent, for example cysteine, at a concentration sufficient for activation. Precise amounts can be empirically determined or are known to those of skill in the 30 art. For example, in vitro activation of cathepsin L generally requires 1-50 mM cysteine. Assays for enzymatic activity can be performed to determine optimal concentrations. Typically, for purposes herein, activatable matrix-degrading enzymes include those that require sufficient concentration of a reducing agent for activation at WO 2009/111083 PCT/US2009/001486 - 78 a concentration that exceeds the physiological level of reducing agent present in the interstitium. In general, the inactive enzyme is packaged or provided so that there is insufficient reducing agent concentration to trigger enzyme activation. The 5 activation reaction then can be triggered by adding cysteine (or other reducing agent) at a concentration sufficient to recover enzyme activity. Precise amounts can be empirically determined. Depending on the enzyme, temporary activation can be achieved simply by discontinued exposure to reducing agent. For example, sustained activation of 10 cathepsin L requires the presence of cysteine or TCEP. Thus, an inactive form of cathepsin L free of its prosegment can be activated by adding cysteine, and the resulting mixture, either in the same or separate compositions, can be administered to the interstitium of an organ or tissue. Upon administration, however, the effective concentration of cysteine required for continued activation is no longer available; the 15 resulting active enzyme will ultimately return to its inactive state. In other examples, the temporal regulation of an enzyme requiring a reducing agent for activation can be controlled by administration of a reversing agent such as oxidized glutathione. d. Activating Condition - Temperature Provided herein are temperature sensitive (ts) enzyme mutants of matrix 20 degrading enzymes (tsAMDE) that degrade one or more components of the extracellular matrix (ECM) in a temperature-dependent manner. In particular, mutants provided herein degrade a collagen. In some examples, the mutants display higher activity at lower temperatures (e.g. 25*C) then at higher temperatures, for example, physiologic temperatures (e.g. 37"C ). In other examples, the mutants 25 display higher activity at physiologic temperatures then at lower temperatures. Thus, the activation of the tsAMDE , for example, tsMMPs, upon administration to the body, can be temporally and conditionally controlled by virtue of changes in temperature. Uncontrolled enzyme activity can be highly disruptive to tissue integrity. By virtue of the conditional activation of activatable tsAMDE, temporary 30 activation is achieved, thereby regulating the duration of enzymatic action on extracellular matrix (ECM) components to reduce deleterious side effects associated with unwanted prolonged activation of enzymes. This is an advantage of the present tsAMDE, for example tsMMPs, over existing collagenase treatments for treating WO 2009/111083 PCT/US2009/001486 - 79 ECM-mediated diseases or conditions. Hence, an advantage of such mutants is that their activity can be regulated, thereby permitting the use of tsAMDE to treat diseases and/or conditions of the ECM. tsAMDEs mutants, for example tsMMPs, provided herein include those that 5 are modified to be temperature sensitive, for example, by amino acid substitution, insertion or replacement. Generally, tsAMDEs contain one or more amino acid replacements in their primary sequence rendering the protein more active at permissive temperatures then at non-permissive temperatures. tsAMDEs provided herein can contain 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 or 10 more amino acid modifications. In particular, tsAMDEs provided herein contain 1, 2, 3, 4, 5 , 6, 7, 8, 9 or 10 amino acids modifications. tsAMDEs, for example tsMMPs, provided herein are activatable at a permissive temperature, but are less active or inactive at other non-permissive temperatures. The tsAMDEs provided herein have a ratio of activity at a permissive 15 temperature compared to a non-permissive temperature that is or is about 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 15, 20, 30, 40, 50 or more. Thus, the activity of the tsAMDEs provided herein at the non-permissive temperature is or is about 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%, 20%, 15%, 10%, 5%, 4%, 3%, 2%, 1%, 0.5% or less of the 20 activity at a permissive temperature. For example, AMDEs that are normally active at physiological temperature (e.g. 37"C) are modified and enzymes selected that are active at lower temperatures (e.g. less than 37*C; e.g. at or about 20"C, 21"C, 22"C, 23"C, 24"C, 25"C, 26"C, 27"C, 28"C, 29"C or 30"C), but that are less active or inactive at physiologic temperature. 25 Such modified enzymes can be used as activatable matrix-degrading enzymes (AMDE) where the activation condition is low temperature. The activation of the enzyme is temporally controlled as the in vivo temperature returns to the physiological temperature of 37"C. Thus, for example, tsAMDEs provided herein are active at a permissive temperature that is at or about 25"C, but are less active at higher 30 temperatures such as at or about 33"C, 34"C, 35"C, 36'C, 37"C, 38*C or 39"C. The tsAMDEs provided herein have a ratio of activity at a low permissive temperature (e.g. less then 37"C, such as at or about 25'C) compared to a non-permissive temperature of at or about 34"C or 37*C, for example, 33"C, 34*C, 35"C, 36"C, 37"C, WO 2009/111083 PCT/US2009/001486 - 80 38"C or 39"C, that is or is about 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 15, 20, 30, 40, 50 or more. Thus, the activity of the tsAMDEs provided herein at the non-permissive temperature of at or about 34*C or 37"C is or is about 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 5 30%, 25%, 20%, 15%, 10%, 5%, 4%, 3%, 2%, 1%, 0.5% or less of the activity at the permissive temperature at or about 25 0 C. tsAMDEs, for example tsMMPs, provided herein retain one or more activities of wild-type enzyme, for example, enzymatic activity for cleavage of an ECM component such as collagen. For example, a tsAMDEs provided herein retains an 10 activity at the permissive temperature that is or is about 30%, 40%, 50%, 60%,70%, 80%, 90%, 100%, 110%, 120%, 140%, 150% or more the activity of wild-type AMDE at the permissive temperature. Generally, tsAMDEs provided herein, however, are less active the then wild-type enzyme at the higher nonpermissive temperature, e.g. physiologic temperature. For example, tsAMDEs provided herein 15 exhibit 95%, 90%, 80%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%, 20%, 15%, 10%, 5%, 4%, 3%, 2%, 1%, 0.5%, generally 40%, 30%, 25%, 20%, 15%, 10%, or 5% residual activity of the wild-type enzyme at physiologic temperature (e.g. 34 or 37"C). Where the activating condition is temperature, an activator can be provided 20 that exposes the tsAMDEs to the permissive temperature required for activation. The exposure to the activator can be in vitro or in vivo. The activator can be exposed to the tsAMDEs prior to, simultaneously, subsequently or intermittently upon in vivo administration. The activator can provide the requisite heat or cold required for activation. For example, where the activating condition is low temperature, the 25 activator can be provided as a cold buffer or as an ice pack to be applied to the site of administration. Where the activating condition is heat, the activator can be provided as a warm buffer or as a heat pack to be applied to the site of administration. The activating condition also can be provided by storage of the tsAMDE at the permissive temperature immediately and just prior to use. The duration of exposure to the 30 activator can be continuous, can be for a predetermined time, or can be intermittent (for example, if the tsAMDEs is reversible). Thus, the time period permitting activation is flexible and can be adapted to the particular enzyme that is used, the disease or condition being treated, the site of administration or other factors. It is WO 2009/111083 PCT/US2009/001486 - 81 within the level of the skilled artisan to determine the duration of exposure to the activator. In the absence of exposure to the activator providing the activating condition, the tsAMDE present at the non-permissive temperature are inactive or substantially 5 inactive compared to the activity at the permissive temperature. The activating condition of a permissive temperature (e.g. low temperature) not normally present at the site of administration permits the temporal regulation of, and alteration of, the physiological parameters of organs and tissues, such as the interstitium that exhibits a physiologic temperature of approximately 37"C. Under normal physiological 10 conditions, the temperature of the interstitium is approximately 37"C. Thus, for example, tsAMDEs active at low temperatures, when present in the interstitium would normally be catalytically inactive because of the physiologic temperature of the interstitium. When the temperature of the interstitium is temporarily rendered cold, for example, by exposure to a cold buffer or to a cold pack administered on the 15 adjacent surface, tsAMDEs when administered to the interstitium will become activated. When the temperature increases and returns to physiological levels, then the tsAMDEs become inactivate or substantially inactive and cease to exert their enzymatic activity. Hence, by taking advantage of the requirement for exogenous activating conditions, tsAMDEs are activatable and can be made temporally active for 20 a limited duration during use, such as upon in vivo administration to the body. The tsAMDEs provided herein include those that are irreversibly inactive following exposure to non-permissive temperatures. Such mutants are active when exposed to permissive temperature conditions (e.g. 25"C), but are less active or inactive when the temperature is altered to a non-permissive temperatures (e.g. 37'C, 25 such as can occur upon in vivo administration to the body and removal of an exogenous activator (e.g. cold pack)). For example, upon return to permissive conditions, irreversible tsAMDEs polypeptides provided herein exhibit at or about 50%, 60%, 70%, 80%, 90%, 100%, 105%, 110%, 115%, or 120% the activity at non permissive temperatures. The activity is not reversible. 30 Also provided herein are tsAMDEs that are reversibly inactive following exposure to a non-permissive temperature. Such mutants are active when exposed to a permissive temperature condition, but are less active or inactive when the temperature is altered to a non-permissive temperatures. Upon renewed exposure to WO 2009/111083 PCT/US2009/001486 - 82 an activating condition providing the permissive temperature (e.g. cold pack), the activity of the tsAMDEs is restored, thereby rendering the enzyme sufficiently active to degrade one or more components of the ECM. For example, upon return to permissive conditions from nonpermissive conditions, reversible tsAMDEs 5 polypeptides provided herein exhibit at or about 120%, 125%, 130%, 140%, 150%, 160%, 170%, 180%, 200% or more the activity at non-permissive temperatures. Typically, tsAMDEs provided herein are zymogens (containing a propeptide) or processed enzymes (lacking a propeptide), or catalytically active forms thereof. As discussed below, most enzymes, including MMPs, are zymogens and require an initial 10 processing event for activity by removal of a propeptide segment from the N-terminal end of the polypeptide. A processing agent, such as a protease or chemical agent, directly or indirectly initiates one or more cleavage events to generate an active enzyme by virtue of removal of the propeptide segment and/or conformational changes that expose the active site of the enzyme. Hence, normally, upon processing 15 of an enzyme to a mature form, the enzyme is active. The activity of a processed enzyme is not reversible, thereby leading to uncontrolled degradation of the ECM upon administration of the processed enzyme to the body. It is contemplated herein that modification of the enzyme to additionally confer temperature sensitivity provides a mechanism to conditionally and temporally control activation of the 20 enzyme to avoid continued activation of the processed form. Any AMDE, whether synthetic or isolated from natural sources, such as those set forth in Table 3 or elsewhere herein, zymogen forms thereof, mature forms thereof lacking the propeptide, and catalytically active forms including polypeptides containing only the catalytically active domain, and allelic or species variants or other 25 variants thereof, or any known to those of skill in the art can be modified to be temperature sensitive and is intended for use in the compositions, combinations, methods and apparatus provided herein, so long as the enzyme is activatable due to the requirement of a temperature activating condition. One of skill in the art knows or could identify tsAMDEs. For example, one of skill in the art could use routine 30 molecular biology techniques to introduce amino acid mutations into a matrix degrading enzyme, and test each for enzyme activation under temperature permissive and non-permissive temperatures to assess the requirement of an exogenous activating WO 2009/111083 PCT/US2009/001486 - 83 condition for sustained or reversible activation of any desired enzyme. Exemplary assays for enzyme activation are provided herein and known in the art, Hence, tsAMDEs provided herein include zymogen forms (e.g. proenzyme), active enzymes lacking a propeptide, and polypeptides containing only the 5 catalytically active domains thereof so long as the tsMMPs exhibits enzymatic activity at the permissive temperature. Hence, modification of the enzyme is in an active form thereof. Exemplary of such a tsAMDEs is a tsMMP-1. tsMMP-1 provided herein contains one or more amino acid modifications in its primary sequence corresponding to amino acid replacements in a wild-type MMP- 1 set forth 10 in SEQ ID NO: 327. Exemplary modifications are described below. The tsMMP-1 mutants provided herein include those that are zymogens or those that are active enzymes lacking a propeptide so long as such forms contain the mutation. The zymogen or active polypeptides provided herein include those that are full-length, include all or a portion of the proline rich linker or the hemopexin binding domain, 15 lack all or a portion of the proline rich linker or the hemopexin binding domain, or polypeptides that include only the catalytically active domains thereof (e.g. corresponding to amino acids 81-242 of the sequence of amino acids set forth in SEQ ID NO: 327) so long as the tsMMP-1 retains enzymatic activity at the permissive temperature. 20 It is understood that when provided in zymogen form, the tsAMDEs are inactive and that processing by a processing agent is required for activity. Generally, the processing of the enzyme is effected prior to use, such as prior to administration in vivo. The processing agent can be applied simultaneously, intermittently or subsequently to exposure of the tsAMDEs to the activating condition (e.g. low 25 temperature) and administration to the body. Generally, the processing agent is chosen that is acceptable for administration to a subject. If desired, the processing agent can be purified away from the enzyme, for example by dialysis or other purification method, before administration. Thus, for zymogen forms of the enzyme, two steps are required for activation: 1) exposure to a processing agent;.and 2) 30 exposure to. an activating condition. Whether in zymogen or processed form, exposure of the tsAMDEs to an activator at the permissive temperature temporally controls activity of a tsAMDE. RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 -84 tsAMDEs can be further modified to alter any one or more properties or activities. For example, altered properties or activities include, but are not limited to, modification that render the enzyme more stable, alter the substrate specificity and/or increase resistance to one or more inhibitors. For example, as described elsewhere 5 herein, tsAMDEs can be modified to alter its substrate specificity. For example, an enzyme can be modified to have increased specificity for a particular substrate. Thus, for example, a tsAMDE, which exhibits substrate specificity for type I and type IV collagen can be modified so that it has increased substrate specificity for type I collagen, and not type IV collagen, and vice versa. If desired, enzyme stability also 10 can be increased by pegylation or glycosylation of the enzyme. Modifications of polypeptides can be achieved by routine molecular biology techniques, and are within the skill of one in the art. For purposes herein, modified tsAMDEs retain one or more activities of the wild-type enzyme at the permissive temperature. Retained activity can be 40%, 50%, 60%, 70%, 80%, 90%, 95%, 100%, 110%, 120%, 130%, 15 140%, 150%, or more activity of the wild-type MMP at the permissive temperature. Modified enzymes can be tested for their substrate specificity using routine assays for substrate cleavage such as is described herein, or known in the art. For example, substrate cleavage can be assessed on fluorogenic peptides or on purified proteins. Cleavage can be assessed using in vitro or in vivo assays. For example, cleavage can 20 be assessed by incubating the enzyme with the substrate, and then running the mixture on an SDS-PAGE gel. Degradation can be assessed by Western Blot or by using standard protein stains such as Coomasie Blue or Silver Stain reagents. The tsAMDEs are provided herein as compositions, combinations and containers. The tsAMDEs are provided in a therapeutically effective amount, that 25 when activated, degrade one or more components of the ECM upon administration, such as upon sub-epidermal administration. The resulting tsAMDEs can be used as therapeutics to treat ECM-mediated diseases or conditions. For example, the tsAMDEs are provided in compositions, combinations and/or containers with an activator that provides the activating condition. In some 30 examples, tsAMDEs also are provided in compositions, combinations and/or containers with a processing agent. The activator and/or processing agent can be in the same composition or in separate compositions and in the same container or separate containers with the tsAMDEs. In addition, the tsAMDEs also can be RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 - 85 combined or provided in combination, such as in containers, with other agents such as any one or more of an anesthetic, alpha-adrenergic agent, dispersing agent, or therapeutic agent. The tsAMDEs can be provided in the same or separate composition as other agents and/or can be provided in the same or separate containers. 5 The tsAMDEs can be provided as a liquid or in lyophilized form at a therapeutically effective concentration. Alternatively, the tsAMDEs can be provided as a concentrated liquid, such that addition of a sufficient amount of activator results in a therapeutically effective concentration of enzyme. The enzymes can be provided as a solution or suspension or encapsulated into a suitable delivery vehicle, such as a 10 liposome, glass particle, capillary tube, drug delivery vehicle, gelatin, gel, tablet, capsule, pill, time release coating, as well as transdermal patch preparation and dry powder inhalers or other such vehicle. The activator typically is provided as a liquid solution or suspension for administration into the interstitium either alone or following reconstitution of and/or exposure to the tsAMDEs. In some examples, the 15 activator is provided exogenously and applied at the site of administration. For example, an activator can be a hot or cold pack that can be applied to the site of administration, e.g. the skin, prior to, simultaneously, subsequently or intermittently following administration of a tsAMDEs. As described below, kits containing these combinations and also articles of manufacture, such as containers, also are provided. 20 Thus, when desired, the tsAMDEs enzyme is subjected to activating conditions in which the enzyme is exposed to an activator to generate an enzyme that is active. Exposure to an activator can be achieved in vitro or in vivo. For example, where an activatable enzyme and activator are separately provided, they can be administered together or separately. Where administered separately, the tsAMDEs 25 can be administered simultaneously, subsequently or intermittently from the activator. In another example, the tsAMDEs, in a lyophilized or concentrated liquid form, can be reconstituted with the activator just prior to use. In such an example, the mixture of the tsAMDEs and activator are administered together. Such methods of activation can be empirically determined by one of skill in the art, and may differ depending on 30 the choice of enzyme and activator, and the method of treatment and treatment regime desired. The activatable matrix-degrading enzyme can be provided in an article or manufacture alone or in combination with the activator. For example, if the enzyme WO 2009/111083 PCT/US2009/001486 - 86 is provided in combination with the activator, an article of manufacture can contain an enzyme, either lyophilized or in liquid form, in one compartment, and an activator in an adjacent compartment. The compartments can be separated by a dividing member. Articles of manufacture can additionally contain a processing agent. Such articles of 5 manufacture are described elsewhere herein. The combinations of tsAMDEs and activator also can further contain other agents, discussed in detail below. For example, in addition to the activator and tsMMP, combinations are provided containing one or more of a anesthetic, vasoconstrictor, dispersing agent or other therapeutic agent. 10 i. Temperature-Sensitive Matrix Metalloprotease Mutants Provided herein are tsMMP polypeptides, for example tsMMP-1 polypeptides, that are temperature sensitive by virtue of modifications-in the primary sequence of the polypeptide compared to an unmodified MMP polypeptide. The tsMMP polypeptide exhibits increased enzymatic activity at a permissive temperature 15 compared with activity of the tsMMP polypeptide at a non-permissive temperature. For example, tsMMP polypeptides provided herein exhibit increased enzymatic activity at a low temperature that is less then 37"C, for example, that is at or about 20 0 C, 21"C, 22"C, 23"C, 24"C, 25"C, 26"C, 27"C, 28 0 C, 29"C or 30"C, in particular at or about 25"C compared to a non-permissive high temperature that is at or about 34"C, 20 35"C, 36"C, 37"C, 38"C or 39"C, in particular at or about 34 0 C or 37"C. Due to the temperature-dependent activity of tsMMP polypeptides, the activity of MMP can be conditionally controlled, thereby temporally regulating activation to prevent prolonged and unwanted degradation of the ECM. In particular, such tsMMP polypeptides can be used in uses, processes or methods to treat diseases or conditions 25 of the ECM, for example, to treat collagen-mediated diseases or conditions such as cellulite. The tsMMP polypeptides provided herein have a ratio of activity at a permissive temperature compared to a non-permissive temperature that is or is about 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 30 8, 8.5, 9, 9.5, 10, 15, 20, 30, 40, 50 or more. Thus, the activity of tsMMP polypeptides provided herein at the non-permissive temperature is or is about 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%, 20%, 15%, 10%, 5%, 4%, 3%, 2%, 1%, 0.5% or less of the activity at a permissive temperature. tsMMPs WO 2009/111083 PCT/US2009/001486 - 87 polypeptides provided herein retain one or more activities of wild-type MMP polypeptide, for example, enzymatic activity for cleavage of an ECM component such as collagen. Typically, such activity is substantially unchanged (less than 1%, 5%, 10%, 20% or 30% changed) compared to a wild-type or starting protein. In other 5 examples, the activity of a modified MMP polypeptide is increased or is decreased as compared to a wild-type or starting MMP-1 polypeptide. Activity is assessed at the permissive temperature and is compared to the activity of a starting, unmodified MMP polypeptide at the permissive temperature or a non-permissive temperature. For example, a tsMMP polypeptide provided herein retains an activity at the 10 permissive temperature that is or is about 10%, 20%, 30%, 40%, 50%, 60%,70%, 80%, 90%, 100%, 110%, 120%, 140%, 150% or more the activity of wild-type MMP I at the permissive temperature or non-permissive temperature. Activity can be assessed in vitro, ex vivo or in vivo and can be compared to that of the unmodified MMP polypeptide, such as for example, an inactive MMP polypeptide set forth in 15 SEQ ID NO: 327 activated by a processing agent, or any other MMP polypeptide known to one of skill in the art that is used as the starting material. As discussed elsewhere herein, it is understood that the zymogen inactive form of an MMP or a modified MMP must be processed to an active form before use or measurement of an activity. 20 Modifications in an MMP polypeptide can be made to any form of an MMP polypeptide, including inactive or active forms, allelic and species variants, splice variants, variants known in the art, or hybrid or chimeric MMP polypeptides. For example, modifications provided herein can be made in any exemplary MMP polypeptide set forth in Table 3, including precursor polypeptides, inactive proenzyme 25 forms, zymogen forms, active forms thereof and allelic or species variants thereof. For example, an exemplary MMP is an precursor MMP-1 polypeptide set forth in SEQ ID NO:98, an inactive pro-enzyme MMP-l containing the propeptide set forth in SEQ ID NO: 327, a mature MMP-1 polypeptide lacking the propeptide set forth in SEQ ID NO: 99, or any species, allelic or modified variant and active fragments 30 thereof that has 40%, 50%, 60%, 70%, 80%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity to any of the MMP-1 polypeptides set forth in SEQ ID NOS: 98-99, 327. Modifications also can be in an MMP polypeptide lacking one or more domains, so long as the MMP polypeptide is temperature sensitive (i.e.

WO 2009/111083 PCT/US2009/001486 - 88 contains the modification) and retains enzymatic activity. For example, modifications can be in an MMP polypeptide that includes only the catalytic domain ( for example in MMP-1 corresponding to amino acids 81-242 of the proenzyme MMP-l polypeptide set forth in SEQ ID NO: 327). Modifications also can be made in an 5 MMP polypeptide lacking all or a portion of the proline rich linker (for example in MMP-1 corresponding to amino acids 243-258 of the proenzyme MMP-l polypeptide set forth in SEQ ID NO: 327) and/or lacking all or a portion of the hemopexin binding domain (for example in MMP-1 corresponding to amino acids 259-450 of the proenzyme MMP-1 polypeptide set forth in SEQ ID NO: 327). Allelic variants of 10 MMP-1 polypeptides include, but are not limited to, any of MMP-1 polypeptide containing any one or more amino acid variant set forth in SEQ ID NO:537. Exemplary species variants for modification herein include, but are not limited to, pig, rabbit, bovine, horse, rat, and mouse, for example, set forth in any of SEQ ID NOS: 527-532. Modifications in an MMP polypeptide provided herein to confer 15 temperature sensitivity can be made to an MMP polypeptide that also contains other modifications, such as those described in the art, including modification of the primary sequence and modifications not in the primary sequence of the polypeptide. It is understood that modifications in an allelic or species variant or other variant include modification in any form thereof such as an active or inactive form, a form 20 including only the catalytic domain, or a form lacking all or a portion of the proline rich linker or the hemopexin binding domain so long as the modified form contains the temperature sensitive modification and is temperature sensitive. As discussed herein below, corresponding MMP-1 modifications can be made to similar forms of other MMP polypeptides. 25 Hence, the resulting modified MMP polypeptides include those that are inactive zymogen proenzymes and those that are active polypeptides. For example, any modified polypeptide provided herein that is a zymogen proenzyme can be activated by a processing agent to generate an active MMP polypeptide. Processing agents include, but are not limited to, any set forth in Table 3A below. Activation of 30 MMP-1 polypeptides are typically exhibited in its active form following cleavage of the propeptide and/or intermolecular and intramolecular processing of the enzyme to remove the propeptide(see e.g. Visse et al. (2003) Cir. Res., 92:827-839; Khan et al. (1998) Protein Science, 7:815-836; Okada et al. (1988) Biochem J., 254:731-741; WO 2009/111083 PCT/US2009/001486 - 89 Okada & Nakanashi (1989) FEBS Lett., 249:353-356; Nagase et al. (1990) Biochemistry, 29:5783-5789; Koklitis et al. (1991) Biochem J., 276:217-221; Springman et al. (1990) PNAS, 87:364-8; Murphy et al. (1997) Matrix Biol., 15:51.1 8). Table 3A. Zymogen Activators Proteolytic Compounds Proteases Plasmin Plasma kallikrein Trypsin-1 (Trypsin I) Trypsin-2 (Trypsin II) Neutrophil elastase Cathepsin G Tryptase Chymase Proteinase-3 Furin uPA MMPs, including MMP-1, MMP-2, MMP-3, MMP 7, MMP-10, MMP-26, and MT1-MMP Non-Proteolytic Compounds Thiol-modifying Agents 4-aminophenylmercuric acetate (AMPA) HgCl 2 N-ethylmaleimide Conformational Perturbants Sodium dodecyl sulfate (SDS) Chaotropic agents Other Chemical Agents Oxidized glutathione (GSSG) Reactive oxygen Au(I) salts Other Activating Conditions Acidic pH Heat 5 Modifications provided herein of a starting, unmodified reference polypeptide include amino acid replacements or substitutions, additions or deletions of amino acids, or any combination thereof. For example, tsMMP polypeptides include those with 1, 2, 3, 4,5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 or more modified 10 positions. Also provided herein are modified tsMMP polypeptides with two or more modifications compared to a starting reference MMP-1 polypeptide. Modified MMP polypeptides include those with 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 or more modified positions. Any modification provided herein can be combined with any other modification known to one of skill in the art so long as the WO 2009/111083 PCT/US2009/001486 - 90 resulting modified MMP polypeptide retains enzymatic activity when it is in its activated form and so long as the enzymatic activity is greater at the permissive temperature compared to the non-permissive temperature. Modified MMP polypeptides provided herein can be assayed for enzymatic activity under various 5 conditions (e.g. permissive and non-permissive temperatures) to identify those that retain enzymatic activity. The modifications provided herein can be made by standard recombinant DNA techniques such as are routine to one of skill in the art. Any method known in the art to effect mutation of any one or more amino acids in a target protein can be 10 employed. Methods include standard site-directed mutagenesis (using e.g. a kit, such as QuikChange available from Stratagene) of encoding nucleic acid molecules, or by solid phase polypeptide synthesis methods. Other modifications that are or are not in the primary sequence of the polypeptide also can be included in a modified MMP polypeptide, or conjugate 15 thereof, including, but not limited to, the addition of a carbohydrate moiety, the addition of a polyethylene glycol (PEG) moiety, the addition of an Fc domain, etc. For example, such additional modifications can be made to increase the stability of half-life of the protein. 1) Exemplary tsMMP-1 Modifications 20 Provided herein are modified MMP-l polypeptides containing one or more amino acid modifications in a starting, unmodified MMP- 1 polypeptide. The amino acid replacement or replacements can be at any one or more positions corresponding to any of the following positions: 84, 85, 95, 98, 99, 100, 103, 104, 105, 106, 109, 110, 111, 112, 118, 123, 124, 126, 147, 150, 151, 152, 153, 155, 156, 158, 159, 170, 25 171,176,178,179, 180, 181, 182,183, 185,187,188,189,190, 191, 192, 194,195, 197,198,206,207,208,210,211,212,218,223,227,228,229,230,233,234,237, 240, 251, 254, 255, 256, 257 and 258 of an unmodified MMP-l polypeptide having a -sequence of amino acids set forth in SEQ ID NO: 327, or at a corresponding position in an allelic or species variant or other variant of an MMP-1 polypeptide that has at 30 least or at least about 60%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to an MMP-1 polypeptide set forth in SEQ ID NO: 327. Amino acid replacements include replacement of amino acids to an acidic (D or E); basic (H, K or R); neutral (C, N, Q, T, Y, S, G) or hydrophobic (F, WO 2009/111083 PCT/US2009/001486 - 91 M, W, I V, L A, P) amino acid residue. For example, amino acid replacements at the noted positions include replacement by amino acid residues E, H, R, C, Q, T, S, G, M, W, I, V, L , A, P , N, F, D, Y or K. Such modified MMP-1 polypeptides include MMP-1 polypeptides that are temperature sensitive by virtue of increased activity at 5 the permissive temperature of 25"C compared to the non-permissive temperatures of 34"C or 37"C. For example, modified MMP-1 polypeptides provided herein can include polypeptides having an amino acid modification corresponding to any one or more modifications of T84F (i.e. replacement of T by F at a position corresponding to 10 position 84 of an MMP-1 polypeptide set forth in SEQ ID NO:327), E85F, L95K, L951, R98D, 199Q, El00V, E100R, E100S, E100T, E100F, E100I, E100N, T103Y, P104A, P104M, D105A, D105F, D105G, D105I, D105L, D105N, D105R, D105S, D105T, D105W, D105E, L106C, L106S, A109H, Dl 10A, VI IR, DI 12S, Al 18T, S123V, N124D, T126S, G147P, R150P, R150V, R150D, R150I, R150H, D151G, 15 N152A, N152S, S153T, F155L, F155A, D156H, D156L, D156A, D156W, D156V, D156K, D156T, D156R, D156M, P158T, P158G, P158K, P158N, G159V, G159T, G159M, G1591, G159W, G159L, G159C, P170D, P170A, G171P, G171E, G171D, A176F, A176W, F178T, F178L, D179N, D179V, D179C, E180Y, E180R, EI80T, E180F, E180G, E180S, E180N, E180D, E181T, D181L, D181K, D181C, D181G, 20 E182T, E182Q, E182M, E182G, E183G, R183S, T185R, T185Y, T185H, T185G, T185V, T185Q, T185A, T185E, T185D, N187R, N187M, N187W, N187F, N187K, N1871, N187A, N187G, N187C, N187H, F188V, R189N, R189T, R189Q, E190G, E190Y, E190D, Y191V, N192H, N192S, N192D, N192C, H194P, R195C, R195W, R195L, R195G, R195Q, R195A, R195D, R195V, A197C, A197V, A198G, A198L, 25 A198M, G206A, G206S, L207R, L207V, L2071, L207G, S208R, S208L, S210V, S210A, T21 IL, D212G, D212H, Y218S, F223C, F223E, F223G, F223A, F223S, F223K, F223M, V227C, V227D, V227E, V227L, V227S, V227W, V227G, V227H, V227Q, V227R, Q228P, L229A, L229T, L291, A230V, D233E, 1234A, 1234T, 1234E, 1234Q, 1237L, 1237W, 1237N, 1240S, 1240A, 1240C, 1251S, 1251W, Q254S, T255H, 30 P256C, K257P, K257T and A258P. Exemplary modified MMP-i polypeptides have a sequence of amino acids set forth in any of SEQ ID NOS: 328-526 and active forms and other forms thereof, and allelic and species variants thereof.

WO 2009/111083 PCT/US2009/001486 - 92 In some examples, such modified MMP-1 polypeptides include polypeptides having an amino acid replacement or replacements at any one or more positions corresponding to any of the following positions: 95, 100, 103, 105, 150, 151, 153, 155, 156, 159, 171, 176, 179, 180, 181, 182, 185, 187, 190, 191,192, 194, 195, 198, 5 206, 207, 210, 212, 218, 223, 227, 228, 229, 230, 233, 234, 237 and 240 of an unmodified MMP- 1 polypeptide having a sequence of amino acids set forth in SEQ ID NO: 327, or at a corresponding position in an allelic or species variant or other variant of an MMP-1 polypeptide that has at least or at least about 60%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more 10 sequence identity to an MMP-1 polypeptide set forth in SEQ ID NO: 327. For example, modified MMP-1 polypeptides provided herein include polypeptides having an amino acid modification corresponding to any one or more modifications of L95K, E100V, T103Y, D105A, D105F, D105G, D105I, D105L, D105N, D105R, D105S, D105T, D105W, R150P, D151G, S153T, F155L, F155A, D156H, D156L, D156A, 15 D156W, D156V, D156K, D156T, D156R, G159V, G159T, G171P, A176F, D179N, E180Y, E180R, E180T, E180F, E181T, D181L, D181K, E182T, E182Q, T185R, T185Y, T185H, T185G, T185V, T185Q, T185A, T185E, N187R, N187M, N187W, N187F, N187K, N1871, N187A, E190G, Y191V, N192H, N192S, N192D, N192C, H194P, R195C, R195W, R195L, R195G, R195Q, R195A, R195D, R195V, A198G, 20 A198L, A198M, G206A, G206S, L207R, L207V, S21OV, D212G, Y218S, F223C, F223E, F223G, F223A, F223S, V227C, V227D, V227E, V227L, V227S, V227W, Q228P, L229A, L229T, L2291, A230V, D233E, 1234A, 1234T, 1234E, 1234Q, 1237L, 1240S, 1240A, and 1240C. Such modified MMP-1 polypeptides exhibit at least 1.2 times or more activity at the permissive temperature of 25"C compared to the non 25 permissive temperatures of 34"C or 37"C, for example, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 15, 20, 30, 40, 50 or more times the activity. Exemplary of such modified MMP- I polypeptides have a sequence of amino acids set forth in any of SEQ ID NOS: 328, 331-340, 345-352, 354-357, 359, 363, 365, 368, 371, 373-374, 377-378, 380, 382-384, 388-395, 397 30 398, 401-419, 421-422, 424-426, 428-430, 433, 435, 437-450, 457-459, 462, 465-472, 477-478, 518, and active forms and other forms thereof, and allelic and species variants thereof.

WO 2009/111083 PCT/US2009/001486 - 93 In other examples, such modified MMP- 1 polypeptides include polypeptides having an amino acid replacement or replacements at any one or more positions corresponding to any of the following positions: 95, 105, 150, 151, 155, 156, 159, 176,179,180,181,182,185,187,195,198,206,210,212,218,223,227,228,229, 5 230, 233, 234, and 240 of an unmodified MMP-1 polypeptide having a sequence of amino acids set forth in SEQ ID NO: 327, or at a corresponding position in an allelic or species variant or other variant of an MMP- I polypeptide that has at least or at least about 60%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to an MMP-1 polypeptide set forth in SEQ ID 10 NO: 327. For example, modified MMP-1 polypeptides provided herein include polypeptides having an amino acid modification corresponding to any one or more modifications of L95K, D105A, D105F, D105G, D105I, D105L, D105N, D105R, D105S, D105T, D105W, R150P, D151G, F155A, D156K, D156T, D156L, D156A, D156W, D156V, D156H, D156R, G159V, G159T, A176F, D179N, E180Y, E180T, 15 E180F, D181L, D181K, E182T, E182Q, T185R, T185H, T185Q, T185A, T185E, N187R, N187M, N187F, N187K, N1871, R195V, A198L, A198M, G206A, G206S, S21OV, Y218S, F223E, V227C, V227E, V227W, Q228P, L229T, L2291, D233E, 1234A, 1234T, 1234E, 1240S, and 1240C. Such modified MMP-1 polypeptides exhibit at least 1.5 times or more activity at the permissive temperature of 25"C compared to 20 the non-permissive temperatures of 34"C or 37"C, for example, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 15, 20, 30, 40, 50 or more times the activity. Exemplary of such modified MMP- I polypeptides have a sequence of amino acids set forth in any of SEQ ID NOS: 328, 331-340, 345-346, 348-352, 534-357, 359, 363, 365, 368, 373-374, 377-378, 382-384, 388-391, 395, 25 397-398,401-402,404,411,415-419,421-422,430,433,437,439-441,443-444, 446-449, and active forms and other forms thereof, and allelic and species variants thereof. In additional examples, modified MMP- 1 polypeptides provide herein include modified MMP-1 polypeptides that are temperature sensitive at the permissive 30 temperature of 25'C and exhibit at least 30%, for example, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, 110%, 120%, 140%, 150% or more activity at 25"C compared to wild-type MMP-1 at 25"C. Such modified MMP-1 polypeptides include polypeptides having an amino acid replacement or replacements at any one or more WO 2009/111083 PCT/US2009/001486 - 94 positions corresponding to any of the following positions: 95, 105, 150, 156, 159, 179, 180, 182, 185, 187, 195, 198, 212, 223, 227, 234, and 240 of an unmodified MMP-1 polypeptide having a sequence of amino acids set forth in SEQ ID NO: 327, or at a corresponding position in an allelic or species variant or other variant of an 5 MMP-1 polypeptide that has at least or at least about 60%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to an MMP-l polypeptide set forth in SEQ ID NO: 327. For example, modified MMP-1 polypeptides provided herein include polypeptides having an amino acid modification corresponding to any one or more modifications L95K, D105A, D105G, D105I, 10 D105L, D105N, D105S, D105W, D105T, R150P, D156K, D156T, D156V, D156H, D156R, G159V, G159T, D179N, E180Y, E180T, E180F, E182T, T185H, T185Q, T185E, N187M, N187K, N1871, R195V, A198L, F223E, V227E, 1234E and 1240S. Exemplary of such modified MMP-1 polypeptides have a sequence of amino acids set forth in any of SEQ ID NOS: 328, 332-335, 337-340, 345, 349-352, 355, 359, 363, 15 368, 373-374, 377, 384, 388-389, 391, 397, 402, 404, 411, 416, 422, 430, 444, 449, or active forms and other forms thereof, and allelic and species variants thereof. In particular, modified MMP-1 polypeptides provided herein have an amino acid replacement or replacements at any one or more positions corresponding to any of the following positions: 95, 105, 150, 156, 159, 179, 180, 182, 185, 187, 198, 227, 20 234 and 240 of an unmodified MMP-1 polypeptide having a sequence of amino acids set forth in SEQ ID NO: 327, or at a corresponding position in an allelic or species variant or other variant of an MMP- 1 polypeptide that has at least or at least about 60%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to an MMP-1 polypeptide set forth in SEQ ID NO: 327. 25 Such modified MMP-1 polypeptides provided herein include polypeptides having an amino acid modification corresponding to any one or more modifications L95K, D105I, D105N, D105L, D105A, D105G, R150P, D156R, D156H, D156K, D156T, G159V, G159T, D179N, E180T, E180F, E182T, T185Q, N1871, A198L, V227E, 1234E and 1240S. More particularly, modified MMP-1 polypeptides provided herein 30 include polypeptides having an amino acid modification corresponding to any one or more modifications L95K, D105N, R150P, D156K, D156T, G159V, D179N, E180T, A198L, V227E, and 1240S.

WO 2009/111083 PCT/US2009/001486 - 95 Modified MMP-1 polypeptides provided herein include those that exhibit reversible or irreversible (also called non-reversible) temperature-dependent activity. In all cases, modified MMP-1 polypeptides provided herein exhibit increased activity at a permissive temperature (e.g. 25 0 C) compared to a non-permissive temperatures 5 (e.g. 34"C or 37"C.) For non-reversible polypeptides, exposure to the non-permissive temperature prior to, subsequently or intermittently from exposure to the permissive temperature renders the polypeptide irreversibly inactive. Thus, a modified MMP-1 polypeptide that is returned to temperature permissive conditions, for example 25 0 C, exhibits the same or similar activity of the MMP-1 polypeptide at non-permissive 10 temperatures, for example, 34"C or 37"C. For example, upon return to permissive conditions, irreversible modified MMP-1 polypeptides provided herein exhibit at or about 50%, 60%, 70%, 80%, 90%, 100%, 105%, 110%, 115%, or 120% the activity at non-permissive temperatures. Exemplary non-reversible modified MMP-1 polypeptides provided herein include polypeptides having an amino acid modification 15 corresponding to any one or more modifications L95K, D105I, D105L, DI05N, D105R, D105W, D151G, F155A, D156K, D156T, D156L, D156A, D156W, D156V, D156H, D156R, G159V, A176F, D179N, D181L, D181K, E182T, E182Q, T185R, N187F, N1871, G206A, G206S, V227C, V227E, Q228E, L229T, D233E, 1234A, 1234T, 1234E, 1240S, for example, any set forth in any of SEQ ID NOS: 328, 331 20 332, 337-339, 346, 348, 349-352, 354-357, 363, 365, 368, 378, 382-384, 390, 401, 404, 417-418, 430, 433, 439-440, 443-444, 446-447, 449 or active forms and other forms thereof, and allelic and species variants thereof. For reversible polypeptides, exposure to the non-permissive temperature prior to, subsequently or intermittently from exposure to the permissive temperature 25 renders the polypeptide reversibly active. Thus, a modified MMP-1 polypeptide that is returned to temperature permissive conditions recovers activity, and thereby exhibits increased activity at the permissive temperature compared to the non permissive temperature. In such examples, the recovered activity can be complete or is partial. Thus, a modified MMP-l polypeptide that is returned to temperature 30 permissive conditions, for example 25'C, exhibits an increased activity compared to activity at non-permissive temperatures, for example, 34"C or 37"C. For example, upon return to permissive conditions, reversible modified MMP- 1 polypeptides provided herein exhibit at or about 120%, 125%, 130%, 140%, 150%, 160%, 170%, WO 2009/111083 PCT/US2009/001486 - 96 180%, 200% or more the activity at non-permissive temperatures. Exemplary non reversible modified MMP-1 polypeptides provided herein include polypeptides having an amino acid modification corresponding to any one or more modifications D105A, D105F, D105G, D105S, D105T, R150P, G159T, E180Y, E180T, E180F, 5 T185H, T185Q, T185A, T185E, N187R, N187M, N187K, R195V, A198L, A198M, S21 OV, Y218S, F223E, V227W, L2291 and 1240C, for example, any set forth in any of SEQ ID NOS: 333-336, 340, 345, 359, 373-374, 377, 388-389, 391, 395, 397-398, 402, 411, 415-416, 419, 421-422, 437, 441, 448, or active forms and other forms thereof, and allelic and species variants thereof. 10 2) Combinations Provided herein are modified MMP-1 polypeptides that contain 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 or more modifications compared to a starting or reference MMP-1 polypeptide. Modified MMP-1 polypeptides provided herein can contain any two or more modifications provided above. For example, 15 modified MMP-1 polypeptides provided herein contain amino acid replacements at aily two or more positions corresponding to any of the following positions: 84, 85, 95, 98,99,100,103,104,105,106,109,110,111,112,118,123,124,126,147, 150, 151, 152, 153, 155, 156, 158, 159, 170, 171, 176, 178, 179, 180, 181, 182, 183, 185, 187, 188, 189, 190, 191, 192, 194, 195, 197, 198, 206, 207, 208,210,211,212,218, 20 223, 227, 228, 229, 230, 233, 234, 237, 240, 251, 254, 255, 256, 257 and 258 of an unmodified MMP-1 polypeptide having a sequence of amino acids set forth in SEQ ID NO: 327, or at a corresponding position in an allelic or species variant or other variant of an MMP-1 polypeptide that has at least or at least about 60%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more 25 sequence identity to an MMP-1 polypeptide set forth in SEQ ID NO: 327. Generally, such combination mutants are temperature sensitive and exhibit increased enzymatic activity at a permissive temperature compared with activity of the tsMMP-1 polypeptide at a non-permissive temperature. Typically, combination mutants also retain activity at the permissive temperature compared to the single mutant MMP-1 30 polypeptides alone or compared to an unmodified MMP-1 polypeptide not containing the amino acid changes (e.g a wild-type MMP-1 polypeptide set forth in SEQ ID NO: 327 or active forms or other forms thereof) at the permissive or non-permissive temperature. RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 - 97 Exemplary MMP-1 combination mutants provided herein contain amino acid replacements at any two or more positions corresponding any of the following positions: 95, 105, 150, 156, 159, 179, 180, 182, 185, 187, 198, 227, 234 and 240 of an unmodified MMP- 1 polypeptide having a sequence of amino acids set forth in 5 SEQ ID NO: 327, or at a corresponding position in an allelic or species variant or other variant of an MMP-1 polypeptide that has at least or at least about 60%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to an MMP-1 polypeptide set forth in SEQ ID NO: 327. For example, modified MMP-1 polypeptides provided herein include polypeptides having 10 amino acid modification corresponding to any two or more modifications L95K, D105I, D105N, D105L, D105A, D105G, R150P, D156R, D156H, D156K, D156T, G159V, G159T, D179N, E180T, E180F, E182T, T185Q, N1871, A198L, V227E, 1234E and 1240S. More particularly, modified MMP-1 polypeptides provided herein include polypeptides having amino acid modification corresponding to any two or 15 more modifications L95K, D105N, R150P, D156K, D156T, G159V, D179N, E180T, A198L, V227E, and 1240S. It is understood that at least two different positions are modified in the combination mutants provided herein. Exemplary MMP- I combination mutant polypeptides provided herein are set forth in Table 27 in Example 29. 20 3) Additional Modifications Any modified MMP, for example any modified MMP-1, polypeptide provided herein also can contain one or more other modifications described in the art. The additional modifications can include, for example, any amino acid substitution, deletion or insertion known in the art. In addition to containing one or modification 25 described above, any modified MMP-1 polypeptide provided herein can contain 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 or more additional modifications, so long as the resulting MMP-1 polypeptides exhibits increased activity at the permissive temperature (e.g. 25*C) compared to the non-permissive temperature (e.g. 34"C or 37"C) and retains activity of wild-type MMP-1 at the 30 permissive or non-permissive temperature. The additional modifications can confer additional properties to the enzyme, for example, increased stability, increased half life and/or increased resistance to inhibitors, for example, TIMP. The additional modifications include modifications to the primary sequence of the polypeptide, as WO 2009/111083 PCT/US2009/001486 - 98 well as other modification such as PEGylation and glycosylation of the polypeptide. Generally, such polypeptides include one or more modifications provided herein and exhibit increased activity at the lower themperature then a higher temperature. Exemplary modifications that can be included in a polypeptide provided herein 5 include, but are not limited to, modifications T4P, QIOP, R30M, R30S, T96R, Al14V, F166C, 1172V, DI81H, R189T, E200A, G214E, D232N, D233G, R243S, Q254P, T286A, 1298T, E314G, F315S, V374M, R386Q, S387T, G391S, and T432A of a polypeptide set forth in SEQ ID NO: 327. 4) Other MMPs 10 Matrix metalloproteases are highly homologous polypeptides and exhibit similar specificities for extracellular matrix components. Exemplary sequences of MMPs are set forth in Table 3, for example, any set forth in SEQ ID NOS: 1, 711, 714, 717, 720, 723, 726, 729, 732, 735, 738, 741, 744, 747, 750, 753, 756, 759, 762, 765, 768, 771, 774 or 777 or zymogen forms, active forms or other forms thereof, or 15 allelic or species variants thereof Figure 1 provides an alignment of the zymogen form of exemplary MMP polypeptides. Thus, any of the modifications provided herein in an MMP-1 can be made in any other MMP polypeptide. Hence, based on the description herein, any MMP, species, allelic variant or other variant, can be made temporally active (reversible or irreversible) by virtue of activity at a permissive 20 temperature (generally a lower temperature) compared to a nonpermissive temperature (generally a higher temperature). Such tsMMP mutants can be used by one of skill in the art and used in compositions, processes or methods for the treatment of ECM-mediated diseases or conditions. It is within the level of one of skill in the art to align various MMPs to MMP-l 25 (for example set forth in SEQ ID NO: 327) and identify corresponding residues. Any of the modifications provided herein can be made in any other MMP at the corresponding residue. One of skill in the art can test the activity of the resulting modified polypeptide for temperature sensitivity at a permissive temperature compared to a non-permissive temperature. In particular, it is understood that 30 conservative amino acid differences at a corresponding position in an MMP are functionally invariant. Thus, where a residue in MMP-1 aligns with a conservative residue thereto in another MMP, it is understood that such a residue is contemplated for modification herein. For example, position 95 in an MMP-1 set forth in SEQ ID WO 2009/111083 PCT/US2009/001486 - 99 NO: 327 is a leucine (L). Alignment of SEQ ID NO: 327 with other MMPs shows that position 95 in other MMPs is a leucine, isoleucine (I) or valine (V) residue (see Figure 1). Each of L, I and V are conservative residues. In particular, provided herein are modified MMP polypeptides that are 5 modified by one or more amino acid replacement to confer temperature sensitivity by effecting a corresponding MMP-1 modification at a corresponding residue in an MMP. Figure 2 depicts exemplary amino acid residues for modification. It is understood that these identified residues are exemplary only and it is within the level of one of skill in the art to effect modification of an MMP at other amino acid 10 residues or other MMP- I corresponding residues to confer temperature sensitivity. Exemplary modifications provided herein include modification of any MMP, for example, an MMP-8, MMP-13, MMP-18, MMP-2, MMP-9, MMP-3, MMP-10, MMP- 11, MMP-7, MMP-26 and MMP-12, at any one or more positions corresponding to any of the following positions: 95, 105, 151, 156, 159, 176, 179, 15 180, 181,182,185,195, 198,206,210,212,218,223,228,229,233,234,and 240of an unmodified MMP-1 polypeptide having a sequence of amino acids set forth in SEQ ID NO: 327. The modification includes any one or more of the modifications provided herein above at the corresponding position to the recited position in MMP- 1. For example, residue 95 in an MMP-1 polypeptide set forth in SEQ ID NO: 327 20 corresponds to residue 113 in an MMP-8 polypeptide set forth in SEQ ID NO: 101. Thus, provided herein are modified MMP-8 polypeptides having an amino acid modification Li 13K of an unmodified MMP-8 polypeptide having a sequence of amino acids set forth in SEQ ID NO:101. Similar modifications are provided herein based on this description. 25 Any modified MMP polypeptide provided herein also can contain one or more other modifications described in the art. The additional modifications can include, for example, any amino acid substitution, deletion or insertion known in the art. In addition to containing one or modification described above, any modified MMP polypeptide provided herein can contain 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 30 16, 17, 18, 19, 20 or more additional modifications, so long as the resulting MMP polypeptides exhibits increased activity at the permissive temperature (e.g. 25*C) compared to the non-permissive temperature (e.g. 34"C or 37"C) and retains activity of wild-type MMP at the permissive or non-permissive temperature. The additional WO 2009/111083 PCT/US2009/001486 -100 modifications can confer additional properties to the enzyme, for example, increased stability, increased half-life and/or increased resistance to inhibitors, for example, TIMP. The additional modifications include modifications to the primary sequence of the polypeptide, as well as other modification such as PEGylation and glycosylation 5 of the polypeptide. Generally, such polypeptides include one or more modifications provided herein and exhibit increased activity at the lower themperature then a higher temperature. Exemplary modifications that can be included in a polypeptide provided herein include, but are not limited to, any modifications set forth in Table 3B, below. Table 3B. Exemplary modifications in MMPs MMP SEQ ID NO Amino Acid Modifications MMP-8 101 S3C; T321; K87E; E154G; D193V; S229T; N246Y; A436V; K460T MMP-13 104 H2L; A8V; F75S; D89H; D390G; 1427T MMP-2 110 A27S; R1OIH; D210Y; A228T; F239L; E404K; A447V; T498M; V6201; V621 L; S6441 MMP-9 113 A20V; N38S; E82K; N127K; L187F; R239H; T2581; Q279R; F571V; P574R; R668Q MMP-3 116 K45E; H113P; R248W MMP-10 119 L4V; V8G; R53K; G65R; E142Q; F226L; G282E; L440F; H475L MMP-11 122 V38A; E44K; P61L; S86P; D166N; F182S; Q323H MMP-7 125 C7W; R77R; S115T; G137D; P241L MMP-26 128 K43E; S46L; 1260M MMP-12 131 N357S; F468L; G469R MMP-19 146 R103C; P245S; P488T; T491M 10 2. Combinations of Matrix-Degrading Enzymes and Activator Combinations of an activatable matrix-degrading enzyme and activator, sufficient for activation of the matrix-degrading enzyme, are provided herein. For purposes herein, the activatable matrix degrading enzyme is provided in an inactive 15 form. Generally, compositions of the activatable matrix-degrading enzyme can be provided separate from the activator. The compositions can be provided separately in the same container or in separate containers. Generally, when packaged by itself, the enzyme is provided so that there are insufficient activating conditions present to render the enzyme active.

WO 2009/111083 PCT/US2009/001486 - 101 The matrix-degrading enzyme can be provided as a liquid or in lyophilized form at a therapeutically effective concentration. Alternatively, the matrix-degrading enzyme can be provided as a concentrated liquid, such that addition of a sufficient amount of activator results in a therapeutically effective concentration of enzyme. 5 The enzymes can be provided as a solution or suspension or encapsulated into a suitable delivery vehicle, such as a liposome, glass particle, capillary tube, drug delivery vehicle, gelatin, tablet, capsule, pill, time release coating, as well as transdermal patch preparation and dry powder inhalers or other such vehicle. The activator typically is provided as a liquid solution or suspension for administration 10 into the interstitium either alone or following reconstitution of and/or exposure to the matrix-degrading enzyme. As described in Section F below, kits containing these combinations and also articles of manufacture, such as containers, also are provided. Thus, when desired, the activatable matrix-degrading enzyme is subjected to activating conditions in which the enzyme is exposed to an activator to generate an 15 active enzyme. Exposure to an activator can be achieved in vitro or in vivo. For example, where an activatable enzyme and activator are separately provided, they can be administered together or separately. Where administered separately, the conditionally activatable matrix-degrading enzyme can be administered simultaneously, subsequently or intermittently from the activator. In another 20 example, the matrix-degrading enzyme, in a lyophilized or concentrated liquid form, can be reconstituted with the activator just prior to use. In such an example, the mixture of the matrix-degrading enzyme and activator are administered together. Such methods of activation can be empirically determined by one of skill in the art, and may differ depending on the choice of enzyme and activator, and the method of 25 treatment and treatment regime desired. The activatable matrix-degrading enzyme can be provided in an article or manufacture alone or in combination with the activator. For example, if the enzyme is provided in combination with the activator, an article of manufacture can contain an enzyme, either lyophilized or in liquid form, in one compartment, and an activator in 30 an adjacent compartment. The compartments can be separated by a dividing member. Such articles of manufacture are described elsewhere herein. The combinations of matrix-degrading enzyme and activator also can further contain other agents, discussed in detail below. For example, in addition to the WO 2009/111083 PCT/US2009/001486 - 102 activator and matrix-degrading enzyme, combinations are provided containing one or more of a anesthetic, vasoconstrictor or dispersing agent. E. Methods of Producing Nucleic Acids Encoding Matrix-Degrading Enzymes and Polypeptides Thereof 5 Polypeptides of matrix-degrading enzymes set forth herein, can be obtained by methods well known in the art for protein purification and recombinant protein expression. Any method known to those of skill in the art for identification of nucleic acids that encode desired genes can be used. Any method available in the art can be used to obtain a full length (i.e., encompassing the entire coding region) cDNA 10 or genomic DNA clone encoding a desired matrix-degrading enzyme, such as from a cell or tissue source. Modified or variant matrix-degrading enzymes, can be engineered from a wildtype polypeptide, such as by site-directed mutagenesis. Polypeptides can be cloned or isolated using any available methods known in the art for cloning and isolating nucleic acid molecules. Such methods include PCR 15 amplification of nucleic acids and screening of libraries, including nucleic acid hybridization screening, antibody-based screening and activity-based screening. Methods for amplification of nucleic acids can be used to isolate nucleic acid molecules encoding a desired polypeptide, including for example, polymerase chain reaction (PCR) methods. A nucleic acid containing material can be used as a starting 20 material from which a desired polypeptide-encoding nucleic acid molecule can be isolated. For example, DNA and mRNA preparations, cell extracts, tissue extracts, fluid samples (e.g. blood, serum, saliva), samples from healthy and/or diseased subjects can be used in amplification methods. Nucleic acid libraries also can be used as a source of starting material. Primers can be designed to amplify a desired 25 polypeptide. For example, primers can be designed based on expressed sequences from which a desired polypeptide is generated. Primers can be designed based on back-translation of a polypeptide amino acid sequence. Nucleic acid molecules generated by amplification can be sequenced and confirmed to encode a desired polypeptide. 30 Additional nucleotide sequences can be joined to a polypeptide-encoding nucleic acid molecule, including linker sequences containing restriction endonuclease sites for the purpose of cloning the synthetic gene into a vector, for example, a protein expression vector or a vector designed for the amplification of the core protein coding WO 2009/111083 PCT/US2009/001486 - 103 DNA sequences. Furthermore, additional nucleotide sequences specifying functional DNA elements can be operatively linked to a polypeptide-encoding nucleic acid molecule. Examples of such sequences include, but are not limited to, promoter sequences designed to facilitate intracellular protein expression, and secretion 5 sequences, for example heterologous signal sequences, designed to facilitate protein secretion. Such sequences are known to those of skill in the art. For example, exemplary heterologous signal sequences include, but are not limited to, human kappa IgG heterologous signal sequence set forth in SEQ ID NO:2. Additional nucleotide residues sequences such as sequences of bases specifying protein binding regions also 10 can be linked to enzyme-encoding nucleic acid molecules. Such regions include, but are not limited to, sequences of residues that facilitate or encode proteins that facilitate uptake of an enzyme into specific target cells, or otherwise alter pharmacokinetics of a product of a synthetic gene. For example, enzymes can be linked to PEG moieties. 15 In addition, tags or other moieties can be added, for example, to aid in detection or affinity purification of the polypeptide. For example, additional nucleotide residues sequences such as sequences of bases specifying an epitope tag or other detectable marker also can be linked to enzyme-encoding nucleic acid molecules. Exemplary of such sequences include nucleic acid sequences encoding a 20 His tag (e.g., 6xHis, HHHHHH; SEQ ID NO:235) or Flag Tag (DYKDDDDK; SEQ ID NO:236). The identified and isolated nucleic acids can then be inserted into an appropriate cloning vector. A large number of vector-host systems known in the art can be used. Possible vectors include, but are not limited to, plasmids or modified 25 viruses, but the vector system must be compatible with the host cell used. Such vectors include, but are not limited to, bacteriophages such as lambda derivatives, or plasmids such as pCMV4, pBR322 or pUC plasmid derivatives or the Bluescript vector (Stratagene, La Jolla, CA). Other expression vectors include the HZ24 expression vector exemplified herein. The insertion into a cloning vector can, for 30 example, be accomplished by ligating the DNA fragment into a cloning vector which has complementary cohesive termini. Insertion can be effected using TOPO cloning vectors (Invitrogen, Carlsbad, CA). If the complementary restriction sites used to fragment the DNA are not present in the cloning vector, the ends of the DNA WO 2009/111083 PCT/US2009/001486 - 104 molecules can be enzymatically modified. Alternatively, any site desired can be produced by ligating nucleotide sequences (linkers) onto the DNA termini; these ligated linkers can contain specific chemically synthesized oligonucleotides encoding restriction endonuclease recognition sequences. In an alternative method, the cleaved 5 vector and protein gene can be modified by homopolymeric tailing. Recombinant molecules can be introduced into host cells via, for example, transformation, transfection, infection, electroporation and sonoporation, so that many copies of the gene sequence are generated. In specific embodiments, transformation of host cells with recombinant DNA 10 molecules that incorporate the isolated protein gene, cDNA, or synthesized DNA sequence enables generation of multiple copies of the gene. Thus, the gene can be obtained in large quantities by growing transformants, isolating the recombinant DNA molecules from the transformants and, when necessary, retrieving the inserted gene from the isolated recombinant DNA. 15 1. Vectors and cells For recombinant expression of one or more of the desired proteins, such as any described herein, the nucleic acid containing all or a portion of the nucleotide sequence encoding the protein can be inserted into an appropriate expression vector, i.e., a vector that contains the necessary elements for the transcription and translation 20 of the inserted protein coding sequence. The necessary transcriptional and translational signals also can be supplied by the native promoter for enzyme genes, and/or their flanking regions. Also provided are vectors that contain a nucleic acid encoding the enzyme. Cells containing the vectors also are provided. The cells include eukaryotic and 25 prokaryotic cells, and the vectors are any suitable for use therein. Prokaryotic and eukaryotic cells, including endothelial cells, containing the vectors are provided. Such cells include bacterial cells, yeast cells, fungal cells, Archea, plant cells, insect cells and animal cells. The cells are used to produce a protein thereof by growing the above-described cells under conditions whereby the 30 encoded protein is expressed by the cell, and recovering the expressed protein. For purposes herein, for example, the enzyme can be secreted into the medium. Provided are vectors that contain a sequence of nucleotides that encodes the proenzyme polypeptide coupled to the native or heterologous signal sequence, as well WO 2009/111083 PCT/US2009/001486 - 105 as multiple copies thereof. The vectors can be selected for expression of the enzyme protein in the cell or such that the enzyme protein is expressed as a secreted protein. The proenzyme (i.e. zymogen) form of the enzyme can be purified for use as a activatable enzyme herein. Alternatively, upon secretion the prosegnent can be 5 cleaved catalytically or autocatalytically to generate a mature enzyme. If necessary, the enzyme can be purified such that the prosegment is removed from the preparation. Such mature forms, if inactive, also can be used herein as activatable enzyme either in a single chain or two-chain form. A variety of host-vector systems can be used to express the protein coding 10 sequence. These include but are not limited to mammalian cell systems infected with virus (e.g. vaccinia virus, adenovirus and other viruses); insect cell systems infected with virus (e.g. baculovirus); microorganisms such as yeast containing yeast vectors; or bacteria transformed with bacteriophage, DNA, plasmid DNA, or cosmid DNA. The expression elements of vectors vary in their strengths and specificities. 15 Depending on the host-vector system used, any one of a number of suitable transcription and translation elements can be used. Any methods known to those of skill in the art for the insertion of DNA fragments into a vector can be used to construct expression vectors containing a chimeric gene containing appropriate transcriptional/translational control signals and 20 protein coding sequences. These methods can include in vitro recombinant DNA and synthetic techniques and in vivo recombinants (genetic recombination). Expression of nucleic acid sequences encoding protein, or domains, derivatives, fragments or homologs thereof, can be regulated by a second nucleic acid sequence so that the genes or fragments thereof are expressed in a host transformed with the recombinant 25 DNA molecule(s). For example, expression of the proteins can be controlled by any promoter/enhancer known in the art. In a specific embodiment, the promoter is not native to the genes for a desired protein. Promoters which can be used include but are not limited to the SV40 early promoter (Bernoist and Chambon, Nature 290:304-310 (1981)), the promoter contained in the 3' long terminal repeat of Rous sarcoma virus 30 (Yamamoto et al. Cell 22:787-797 (1980)), the herpes thymidine kinase promoter (Wagner et al., Proc. Natl. Acad. Sci. USA 78:1441-1445 (1981)), the regulatory sequences of the metallothionein gene (Brinster et al., Nature 296:39-42 (1982)); WO 2009/111083 PCT/US2009/001486 - 106 prokaryotic expression vectors such as the p-lactamase promoter (Jay et al., (1981) Proc. Natl. Acad. Sci. USA 78:5543) or the tac promoter (DeBoer et al., Proc. NatL. Acad. Sci. USA 80:21-25 (1983)); see also "Useful Proteins from Recombinant Bacteria": in Scientific American 242:79-94 (1980)); plant expression vectors 5 containing the nopaline synthetase promoter (Herrar-Estrella et al., Nature 303:209 213 (1984)) or the cauliflower mosaic virus 35S RNA promoter (Gardner et al., Nucleic Acids Res. 9:2871 (1981)), and the promoter of the photosynthetic enzyme ribulose bisphosphate carboxylase (Herrera-Estrella et al., Nature 310:115-120 (1984)); promoter elements from yeast and other fungi such as the Gal4 promoter, the 10 alcohol dehydrogenase promoter, the phosphoglycerol kinase promoter, the alkaline phosphatase promoter, and the following animal transcriptional control regions that exhibit tissue specificity and have been used in transgenic animals: elastase I gene control region which is active in pancreatic acinar cells (Swift et al., Cell 38:639-646 (1984); Ornitz et al., Cold Spring Harbor Symp. Quant. Biol. 50:399-409 (1986); 15 MacDonald, Hepatology 7:425-515 (1987)); insulin gene control region which is active in pancreatic beta cells (Hanahan et al., Nature 315:115-122 (1985)), immunoglobulin gene control region which is active in lymphoid cells (Grosschedl et al., Cell 38:647-658 (1984); Adams et al., Nature 318:533-538 (1985); Alexander et al., Mol. Cell Biol. 7:1436-1444 (1987)), mouse mammary tumor virus control region 20 which is active in testicular, breast, lymphoid and mast cells (Leder et al., Cell 45:485-495 (1986)), albumin gene control region which is active in liver (Pinckert et al., Genes and Devel. 1:268-276 (1987)), alpha-fetoprotein gene control region which is active in liver (Krumlauf et al., Mol. Cell. Biol. 5:1639-1648 (1985); Hammer et al., Science 235:53-58 1987)), alpha-i antitrypsin gene control region which is active 25 in liver (Kelsey et al., Genes and Devel. 1:161-171 (1987)), beta globin gene control region which is active in myeloid cells (Magram et al., Nature 315:338-340 (1985); Kollias et al., Cell 46:89-94 (1986)), myelin basic protein gene control region which is active in oligodendrocyte cells of the brain (Readhead et al., Cell 48:703-712 (1987)), myosin light chain-2 gene control region which is active in skeletal muscle 30 (Shani, Nature 314:283-286 (1985)), and gonadotrophic releasing hormone gene control region which is active in gonadotrophs of the hypothalamus (Mason et al., Science 234:1372-1378 (1986)).

WO 2009/111083 PCT/US2009/001486 - 107 In a specific embodiment, a vector is used that contains a promoter operably linked to nucleic acids encoding a desired protein, or a domain, fragment, derivative or homolog, thereof, one or more origins of replication, and optionally, one or more selectable markers (e.g., an antibiotic resistance gene). Exemplary plasmid vectors 5 for transformation of E. coli cells, include, for example, the pQE expression vectors (available from Qiagen, Valencia, CA; see also literature published by Qiagen describing the system). pQE vectors have a phage T5 promoter (recognized by E. coli RNA polymerase) and a double lac operator repression module to provide tightly regulated, high-level expression of recombinant proteins in E. coli, a synthetic 10 ribosomal binding site (RBS II) for efficient translation, a 6XHis tag coding sequence, to and TI transcriptional terminators, ColE1 origin of replication, and a beta lactamase gene for conferring ampicillin resistance. The pQE vectors enable placement of a 6xHis tag at either the N- or C-terminus of the recombinant protein. Such plasmids include pQE 32, pQE 30, and pQE 31 which provide multiple cloning 15 sites for all three reading frames and provide for the expression of N-terminally 6xHis-tagged proteins. Other exemplary plasmid vectors for transformation of E. coli cells, include, for example, the pET expression vectors (see, U.S patent 4,952,496; available from Novagen, Madison, WI; see, also literature published by Novagen describing the system). Such plasmids include pET 11 a, which contains the T7lac 20 promoter, T7 terminator, the inducible E. coli lac operator, and the lac repressor gene; pET 12a-c, which contains the T7 promoter, T7 terminator, and the E. coli ompT secretion signal; and pET 15b and pET19b (NOVAGEN, Madison, WI), which contain a His-Tag TM leader sequence for use in purification with a His column and a thrombin cleavage site that permits cleavage following purification over the column, 25 the T7-lac promoter region and the T7 terminator. Exemplary of a vector for mammalian cell expression is the HZ24 expression vector. The HZ24 expression vector was derived from the pCI vector backbone (Promega). It contains DNA encoding the Beta-lactamase resistance gene (AmpR), an Fl origin of replication, a Cytomegalovirus immediate-early enhancer/promoter 30 region (CMV), and an SV40 late polyadenylation signal (SV40). The expression vector also has an internal ribosome entry site (IRES) from the ECMV virus (Clontech) and the mouse dihydrofolate reductase (DHFR) gene. 2. Expression WO 2009/111083 PCT/US2009/001486 - 108 Matrix-degrading enzymes can be produced by any method known to those of skill in the art including in vivo and in vitro methods. Desired proteins can be expressed in any organism suitable to produce the required amounts and forms of the proteins, such as for example, needed for administration and treatment. Expression 5 hosts include prokaryotic and eukaryotic organisms such as E. coli, yeast, plants, insect cells, mammalian cells, including human cell lines and transgenic animals. Expression hosts can differ in their protein production levels as well as the types of post-translational modifications that are present on the expressed proteins. The choice of expression host can be made based on these and other factors, such as regulatory 10 and safety considerations, production costs and the need and methods for purification. Many expression vectors are available and known to those of skill in the art and can be used for expression of proteins. The choice of expression vector will be influenced by the choice of host expression system. In general, expression vectors can include transcriptional promoters and optionally enhancers, translational signals, and 15 transcriptional and translational termination signals. Expression vectors that are used for stable transformation typically have a selectable marker which allows selection and maintenance of the transformed cells. In some cases, an origin of replication can be used to amplify the copy number of the vector. Matrix-degrading enzymes also can be utilized or expressed as protein fusions. 20 For example, an enzyme fusion can be generated to add additional functionality to an enzyme. Examples of enzyme fusion proteins include, but are not limited to, fusions of a signal sequence, a tag such as for localization, e.g. a his 6 tag or a myc tag, or a tag for purification, for example, a GST fusion, and a sequence for directing protein secretion and/or membrane association. 25 Generally, matrix-degrading enzymes are expressed in an inactive zymogen form. Zymogen conversion can be achieved by exposure to other proteases or to autocatalysis to generate a mature enzyme. Any form of an enzyme is contemplated herein, so long as it is inactive in the absence of an activator. a. Prokaryotic Cells 30 Prokaryotes, especially E. coli, provide a system for producing large amounts of proteins. Transformation of E. coli is simple and rapid technique well known to those of skill in the art. Expression vectors for E. coli can contain inducible promoters, such promoters are useful for inducing high levels of protein expression WO 2009/111083 PCT/US2009/001486 - 109 and for expressing proteins that exhibit some toxicity to the host cells. Examples of inducible promoters include the lac promoter, the trp promoter, the hybrid tac promoter, the T7 and SP6 RNA promoters and the temperature regulated XPL promoter. 5 Proteins, such as any provided herein, can be expressed in the cytoplasmic environment of E. coli. The cytoplasm is a reducing environment and for some molecules, this can result in the formation of insoluble inclusion bodies. Reducing agents such as dithiothreitol and #-mercaptoethanol and denaturants, such as guanidine-HCl and urea can be used to resolubilize the proteins. An alternative 10 approach is the expression of proteins in the periplasmic space of bacteria which provides an oxidizing environment and chaperonin-like and disulfide isomerases and can lead to the production of soluble protein. Typically, a leader sequence is fused to the protein to be expressed which directs the protein to the periplasm. The leader is then removed by signal peptidases inside the periplasm. Examples of periplasmic 15 targeting leader sequences include the pelB leader from the pectate lyase gene and the leader derived from the alkaline phosphatase gene. In some cases, periplasmic expression allows leakage of the expressed protein into the culture medium. The secretion of proteins allows quick and simple purification from the culture supernatant. Proteins that are not secreted can be obtained from the periplasm by 20 osmotic lysis. Similar to cytoplasmic expression, in some cases proteins can become insoluble and denaturants and reducing agents can be used to facilitate solubilization and refolding. Temperature of induction and growth also can influence expression levels and solubility, typically temperatures between 25 0 C and 37 *C are used. Typically, bacteria produce aglycosylated proteins. Thus, if proteins require 25 glycosylation for function, glycosylation can be added in vitro after purification from host cells. b. Yeast Cells Yeasts such as Saccharomyces cerevisae, Schizosaccharomyces pombe, Yarrowia lipolytica, Kluyveromyces lactis and Pichia pastoris are well known yeast 30 expression hosts that can be used for production of proteins, such as any described herein. Yeast can be transformed with episomal replicating vectors or by stable chromosomal integration by homologous recombination. Typically, inducible promoters are used to regulate gene expression. Examples of such promoters include WO 2009/111083 PCT/US2009/001486 -110 GAL 1, GAL7 and GAL5 and metallothionein promoters, such as CUP 1, AOXI or other Pichia or other yeast promoter. Expression vectors often include a selectable marker such as LEU2, TRP 1, HIS3 and URA3 for selection and maintenance of the transformed DNA. Proteins expressed in yeast are often soluble. Co-expression with 5 chaperonins such as Bip and protein disulfide isomerase can improve expression levels and solubility. Additionally, proteins expressed in yeast can be directed for secretion using secretion signal peptide fusions such as the yeast mating type alpha factor secretion signal from Saccharomyces cerevisae and fusions with yeast cell surface proteins such as the Aga2p mating adhesion receptor or the Arxula 10 adeninivorans glucoamylase. A protease cleavage site such as for the Kex-2 protease, can be engineered to remove the fused sequences from the expressed polypeptides as they exit the secretion pathway. Yeast also is capable of glycosylation at Asn-X Ser/Thr motifs. c. Insect Cells 15 Insect cells, particularly using baculovirus expression, are useful for expressing polypeptides such as matrix-degrading enzymes. Insect cells express high levels of protein and are capable of most of the post-translational modifications used by higher eukaryotes. Baculovirus have a restrictive host range which improves the safety and reduces regulatory concerns of eukaryotic expression. Typical expression 20 vectors use a promoter for high level expression such as the polyhedrin promoter of baculovirus. Commonly used baculovirus systems include the baculoviruses such as Autographa californica nuclear polyhedrosis virus (AcNPV), and the Bombyx mori nuclear polyhedrosis virus (BmNPV) and an insect cell line such as Sf9 derived from Spodoptera frugiperda, Pseudaletia unipuncta (A7 S) and Danaus plexippus (DpN 1). 25 For high-level expression, the nucleotide sequence of the molecule to be expressed is fused immediately downstream of the polyhedrin initiation codon of the virus. Mammalian secretion signals are accurately processed in insect cells and can be used to secrete the expressed protein into the culture medium. In addition, the cell lines Pseudaletia unipuncta (A7S) and Danaus plexippus (DpN1) produce proteins with 30 glycosylation patterns similar to mammalian cell systems. An alternative expression system in insect cells is the use of stably transformed cells. Cell lines such as the Schneider 2 (S2) and Kc cells (Drosophila melanogaster) and C7 cells (Aedes albopictus.) can be used for expression. The WO 2009/111083 PCT/US2009/001486 - 111 Drosophila metallothionein promoter can be used to induce high levels of expression in the presence of heavy metal induction with cadmium or copper. Expression vectors are typically maintained by the use of selectable markers such as neomycin and hygromycin. 5 d. Mammalian Cells Mammalian expression systems can be used to express proteins including matrix-degrading.enzymes. Expression constructs can be transferred to mammalian cells by viral infection such as adenovirus or by direct DNA transfer such as liposomes, calcium phosphate, DEAE-dextran and by physical means such as 10 electroporation and microinjection. Expression vectors for mammalian cells typically include an mRNA cap site, a TATA box, a translational initiation sequence (Kozak consensus sequence) and polyadenylation elements. IRES elements also can be added to permit bicistronic expression with another gene, such as a selectable marker. Such vectors often include transcriptional promoter-enhancers for high-level expression, for 15 example the SV40 promoter-enhancer, the human cytomegalovirus (CMV) promoter and the long terminal repeat of Rous sarcoma virus (RSV). These promoter enhancers are active in many cell types. Tissue and cell-type promoters and enhancer regions also can be used for expression. Exemplary promoter/enhancer regions include, but are not limited to, those from genes such as elastase I, insulin, 20 immunoglobulin, mouse mammary tumor virus, albumin, alpha fetoprotein, alpha I antitrypsin, beta globin, myelin basic protein, myosin light chain 2, and gonadotropic releasing hormone gene control. Selectable markers can be used to select for and maintain cells with the expression construct. Examples of selectable marker genes include, but are not limited to, hygromycin B phosphotransferase, adenosine 25 deaminase, xanthine-guanine phosphoribosyl transferase, aminoglycoside phosphotransferase, dihydrofolate reductase (DHFR) and thymidine kinase. For example, expression can be performed in the presence of methotrexate to select for only those cells expressing the DHFR gene. Fusion with cell surface signaling molecules such as TCR- and FceRI-y can direct expression of the proteins in an 30 active state on the cell surface. Many cell lines are available for mammalian expression including mouse, rat human, monkey, chicken and hamster cells. Exemplary cell lines include but are not limited to CHO, Balb/3T3, HeLa, MT2, mouse NSO (nonsecreting) and other WO 2009/111083 PCT/US2009/001486 -112 myeloma cell lines, hybridoma and heterohybridoma cell lines, lymphocytes, fibroblasts, Sp2/0, COS, NIH3T3, HEK293, 293S, 2B8, and HKB cells. Cell lines also are available adapted to serum-free media which facilitates purification of secreted proteins from the cell culture media. Examples include CHO-S cells 5 (Invitrogen, Carlsbad, CA, cat # 11619-012) and the serum free EBNA-1 cell line (Pham et al., (2003) Biotechnol. Bioeng. 84:332-42.). Cell lines also are available that are adapted to grow in special mediums optimized for maximal expression. For example, DG44 CHO cells are adapted to grow in suspension culture in a chemically defined, animal product-free medium. 10 e. Plants Transgenic plant cells and plants can be used to express proteins such as any described herein. Expression constructs are typically transferred to plants using direct DNA transfer such as microprojectile bombardment and PEG-mediated transfer into protoplasts, and with agrobacterium-mediated transformation. Expression vectors can 15 include promoter and enhancer sequences, transcriptional termination elements and translational control elements. Expression vectors and transformation techniques are usually divided between dicot hosts, such as Arabidopsis and tobacco, and monocot hosts, such as corn and rice. Examples of plant promoters used for expression include the cauliflower mosaic virus promoter, the nopaline synthetase promoter, the ribose 20 bisphosphate carboxylase promoter and the ubiquitin and UBQ3 promoters. Selectable markers such as hygromycin, phosphomannose isomerase and neomycin phosphotransferase are often used to facilitate selection and maintenance of transformed cells. Transformed plant cells can be maintained in culture as cells, aggregates (callus tissue) or regenerated into whole plants. Transgenic plant cells also 25 can include algae engineered to produce matrix-degrading enzymes. Because plants have different glycosylation patterns than mammalian cells, this can influence the choice of protein produced in these hosts. 3. Purification Techniques Method for purification of polypeptides, including matrix-degrading enzymes 30 or other proteins, from host cells will depend on the chosen host cells and expression systems. For secreted molecules, proteins are generally purified from the culture media after removing the cells. For intracellular expression, cells can be lysed and the proteins purified from the extract. When transgenic organisms such as transgenic WO 2009/111083 PCT/US2009/001486 - 113 plants and animals are used for expression, tissues or organs can be used as starting material to make a lysed cell extract. Additionally, transgenic animal production can include the production of polypeptides in milk or eggs, which can be collected, and if necessary, the proteins can be extracted and further purified using standard methods 5 in the art. Generally, matrix-degrading enzymes are expressed and purified to be in an inactive form (zymogen form) for subsequent activation as described in the systems and methods provided herein. In some applications, matrix-degrading enzymes are inactive in their mature form in the absence of an activator as described herein. 10 Hence, following expression, mature forms can be generated by autocatalysis to remove the prosegment. For many enzymes, the autocatalysis requires the presence of the activator. If necessary, additional purification steps can be performed to remove the prosegment from the purified preparation. In some circumstances, such as for use as controls, expressed matrix-degrading enzymes can be purified into an active 15 form, by autocatalysis to remove the prosegment or by addition of an activator. In such examples, autoactivation can occur during the purification process, or by incubating at room temperature for 24-72 hours. The rate and degree of activation is dependent on protein concentration and the specific enzyme, such that for example, a more dilute sample may need to be incubated at room temperature for a longer period 20 of time. Activation can be monitored by SDS-PAGE (e.g., a 3 kilodalton shift) and by enzyme activity (cleavage of a fluorogenic substrate). Where an active enzyme is desired, typically, an enzyme is allowed to achieve >75% activation before purification. Proteins, such as matrix-degrading enzymes, can be purified using standard 25 protein purification techniques known in the art including but not limited to, SDS PAGE, size fraction and size exclusion chromatography, ammonium sulfate precipitation and ionic exchange chromatography, such as anion exchange. Affinity purification techniques also can be utilized to improve the efficiency and purity of the preparations. For example, antibodies, receptors and other molecules that bind 30 matrix-degrading enzymes can be used in affinity purification. Expression constructs also can be engineered to add an affinity tag to a protein such as a myc epitope, GST fusion or His 6 and affinity purified with myc antibody, glutathione resin and Ni-resin, WO 2009/111083 PCT/US2009/001486 - 114 respectively. Purity can be assessed by any method known in the art including gel electrophoresis and staining and spectrophotometric techniques. F. Preparation, Formulation and Administration Of Activatable Matrix Degrading Enzymes 5 The pharmaceutical compositions provided herein contain activatable matrix degrading enzymes provided in an inactive form. Also provided are compositions containing an activator. The compounds can be formulated into suitable pharmaceutical preparations such as solutions, suspensions, gels, tablets, dispersible tablets, pills, capsules, powders, sustained release formulations or elixirs, for oral, 10 parenteral administrate, as well as transdermal patch preparation and dry powder inhalers. Typically, the compounds are formulated into pharmaceutical compositions using techniques and procedures well known in the art (see e.g., Ansel Introduction to Pharmaceutical Dosage Forms, Fourth Edition, 1985, 126). A selected matrix-degrading enzyme is included in an amount sufficient that, 15 when activated, exert a therapeutically useful effect in the absence of undesirable side effects on the patient treated. The composition containing the activatable matrix degrading enzyme can include a pharmaceutically acceptable carrier. Therapeutically effective concentration can be determined empirically by testing the compounds in known in vitro and in vivo systems, such as the assays provided herein. The 20 concentration of a selected matrix-degrading enzyme in the composition depends on absorption, inactivation and excretion rates of the complex, the physicochemical characteristics of the complex, the dosage schedule, and amount administered as well as other factors known to those of skill in the art. For example, it is understood that the precise dosage and duration of treatment is a function of the tissue being treated 25 and may be determined empirically using known testing protocols or by extrapolation from in vivo or in vitro test data. It is to be noted that concentrations and dosage values may also vary with the age of the individual treated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of 30 the person administering or supervising the administration of the formulations, and that the concentration ranges set forth herein are exemplary only and are not intended to limit the scope thereof. The amount of a selected matrix-degrading enzyme to be administered for the treatment of a disease or condition, for example an ECM- WO 2009/111083 PCT/US2009/001486 -115 mediated disease or condition such as cellulite or lymphedema, can be determined by standard clinical techniques. In addition, in vitro assays and animal models can be employed to help identify optimal dosage ranges. The precise dosage, which can be determined empirically, can depend on the particular enzyme, the route of 5 administration, the type of disease to be treated and the seriousness of the disease. Exemplary dosages range from or about 10 pg to 100 mg, particularly 50 pLg to 75 mg, 100 ptg to 50 mg, 250 pLg to 25 mg, 500 pg to 10 mg, 1 mg to 5 mg, or 2 mg to 4 mg. The particular dosage and formulation thereof depends upon the indication and individual. If necessary dosage can be empirically determined. Typically the dosage 10 is administered for indications described herein in a volume of 1-100 ml, particularly, 1-50 ml, 10-50 ml, 10-30 ml, 1-20 ml, or 1-10 ml volumes following reconstitution, such as by addition of an activator. Typically, such dosages are from at or about 100 pg to 50 mg, generally I mg to 5 mg, in a 10-50 ml final volume. A selected activator typically is provided as a buffered solution in an amount 15 that, when exposed to the matrix-degrading enzyme, activates the matrix-degrading enzyme. Typically, the amount of activator in the buffer is one that temporarily alters the physiological amounts of that activator present in the interstitium to a level sufficient to temporarily activate the selected activatable matrix-degrading enzyme. For example, where acidic pH is the activating condition, the activator in the form of 20 an acidic buffer composition contains at least one acid, that when administered to the ECM, together or separate from the matrix-degrading enzyme, temporarily lowers the pH of the ECM below physiological pH, i.e. below neutrality. As described elsewhere herein, the acidic buffer is one that has an effective pH range within the pH optima of the selected enzyme. Neutralization of the acidic buffer will occur upon 25 administration due to the neutral pH environment of the interstitium, and is a function of the buffering capacity. Other buffered solutions also are contemplated herein depending on the selected activatable matrix-degrading enzyme and activator chosen. For example, buffers can be prepared at varying temperatures, or with varying amounts of salt, reducing agent, or metal ions. The buffered activator solution 30 containing the low pH activating condition also can contain a pharmaceutically acceptable carrier or excipient. A matrix degrading enzyme can be administered at once, or can be divided into a number of smaller doses to be administered at intervals of time. Selected WO 2009/111083 PCT/US2009/001486 -116 matrix-degrading enzymes can be administered in one or more doses over the course of a treatment time for example over several hours, days, weeks, or months. In some cases, continuous administration is useful. It is understood that the precise dosage and course of administration depends on the methods and system of activation 5 contemplated. For example, the matrix degrading enzyme can be administered together or separate from the activator. Typically, if administered together, the activator is exposed to the matrix-degrading enzyme just prior to use, for example, by reconstitution of a lyophilized powder. In other presentations, the activator can be a component of the AMDE formulation or can be mixed with a liquid-based dosage 10 form of the AMDE. Also, the AMDE can be diluted with an appropriate diluent prior to mixing the activator. If administered separately, the matrix-degrading enzyme composition can be administered sequentially, simultaneously or intermittently from the activator preparation. Also, it is understood that the precise dosage and duration of treatment is a 15 function of the disease being treated and can be determined empirically using known testing protocols or by extrapolation from in vivo or in vitro test data. It is to be noted that concentrations and dosage values also can vary with the severity of the condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and 20 the professional judgment of the person administering or supervising the administration of the compositions, and that the concentration ranges set forth herein are exemplary only and are not intended to limit the scope or use of compositions and combinations containing them. The compositions can be administered hourly, daily, weekly, monthly, yearly or once. Generally, dosage regimens are chosen to limit 25 toxicity. It should be noted that the attending physician would know how to and when to terminate, interrupt or adjust therapy to lower dosage due to toxicity, or bone marrow, liver or kidney or other tissue dysfunctions. Conversely, the attending physician would also know how to and when to adjust treatment to higher levels if the clinical response is not adequate (precluding toxic side effects). 30 Pharmaceutically acceptable compositions are prepared in view of approvals for a regulatory agency or other agency prepared in accordance with generally recognized pharmacopeia for use in animals and in humans. Compositions can take the form of solutions, suspensions, emulsion, gels, tablets, pills, capsules, powders, WO 2009/111083 PCT/US2009/001486 -117 and sustained release formulations. A composition can be formulated as a suppository, with traditional binders and carriers such as triglycerides. Oral formulation can include standard carriers such as pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium 5 carbonate, and other such agents. The formulation should suit the mode of administration. Pharmaceutical compositions can include carriers such as a diluent, adjuvant, excipient, or vehicle with which an enzyme or activator is administered. Examples of suitable pharmaceutical carriers are described in "Remington's Pharmaceutical 10 Sciences" by E. W. Martin. Such compositions will contain a therapeutically effective amount of the compound, generally in purified form, together with a suitable amount of carrier so as to provide the form for proper administration to the patient. Such pharmaceutical carriers can be sterile liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, 15 mineral oil, and sesame oil. Water is a typical carrier when the pharmaceutical composition is administered intravenously. Saline solutions and aqueous dextrose and glycerol solutions also can be employed as liquid carriers, particularly for injectable solutions. Compositions can contain along with an active ingredient: a diluent such as saline, lactose, sucrose, dextrose, Ringers lactate, dicalcium 20 phosphate, or carboxymethylcellulose; a lubricant, such as magnesium stearate, calcium stearate and talc; and a binder such as starch, natural gums, such as gum acacia gelatin, glucose, molasses, polvinylpyrrolidine, celluloses and derivatives thereof, povidone, crospovidones and other such binders known to those of skill in the art. Suitable pharmaceutical excipients include starch, glucose, lactose, sucrose, 25 maltose, mannose, trehalose, mannitol, sorbitol, gelatin, malt, rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate, talc, sodium chloride, dried skim milk, glycerol, propylene glycol, water, and ethanol. A composition, if desired, also can contain minor amounts of wetting or emulsifying agents, or pH buffering agents, for example, acetate, sodium citrate, maleate, glycinate, histidine, succinate, lactate, 30 cyclodextrin derivatives, sorbitan monolaurate, triethanolamine sodium acetate, triethanolamine oleate, poly ethylene glycol and other such agents. Other excipients in the formulation can include oxidixing or reducing agents such as cysteine, oxidized glutathione or cysteine, reduced glutathione; surfactants such as polysorbate 80, WO 2009/111083 PCT/US2009/001486 - 118 polysorbate 20, pluronic (F68), or preservatives. As noted, for purposes herein, acidic buffering agents can be provided as activators, which generally are provided in combinations separate from the matrix-degrading enzyme until use. Reducing agents can increase the activity of matrix-degrading enzymes, and 5 therefore can be provided in formulations for administration. For example, a reducing agent is required to assay enzyme activity using a fluorogenic peptide substrate (see e.g. Example 25). Also, a reducing agent increases the activity of cathepsin L for substrates such as collagen, HSA and a PH20 composition designated rHuPH20 (see e.g. Example 26). Exemplary reducing agents include, but are not limited to, cysteine 10 or TCEP (tris(2-carboxyethyl)phosphine). Generally, a reducing agent is not included in a liquid formulation for long term storage because this can enhance the auto degradation and make the formulation less stable. It is contemplated herein that a reducing agent is added to a liquid dosage form or is added to reconstitute a lyophilized form of an enzyme prior to use, generally immediately prior to use. For 15 example, a lyophilized enzyme, such as cathepsin L, can be reconstituted with a diluent containing a reducing agent. Alternatively, an enzyme can be formulated as a lyophilized enzyme containing a reducing agent present in the formulation, so long as the resulting protein retains stability of one to two years. In such a formulation, the lyophilized enzyme is reconstituted in a suitable diluent without reducing agent. The 20 amount of reducing agent can be empirically determined and is a function of the particular reducing agent. Exemplary amounts for single dosage administration are from about 1 mM to 30 mM, for example, 1 mM, 2 mM, 5 mM, 6mM, 7 mM, 8 mM, 9 mM, 10 mM, 15 mM, 20 mM, 25 mM or 30 mM. Formulations are provided for administration to humans and animals in unit 25 dosage forms, such as tablets, capsules, pills, powders, granules, sterile parenteral solutions or suspensions, and oral solutions or suspensions, and oil water emulsions containing suitable quantities of the compounds or pharmaceutically acceptable derivatives thereof. Pharmaceutically therapeutically active compounds and derivatives thereof are typically formulated and administered in unit dosage forms or 30 multiple dosage forms. Each unit dose contains a predetermined quantity of therapeutically active compound sufficient to produce the desired therapeutic effect, in association with the required pharmaceutical carrier, vehicle or diluent. Examples of unit dose forms include ampoules, vials and syringes and individually packaged WO 2009/111083 PCT/US2009/001486 -119 tablets or capsules. Unit dose forms can be administered in fractions or multiples thereof. A multiple dose form is a plurality of identical unit dosage forms packaged in a single container to be administered in segregated unit dose form. Examples of multiple dose forms include vials, bottles of tablets or capsules or bottles of pints or 5 gallons. Hence, multiple dose form is a multiple of unit doses that are not segregated in packaging. Generally, dosage forms or compositions containing active ingredient in the range of 0.005% to 100% with the balance made up from non-toxic carrier can be prepared. Compositions can be formulated for administration by any route known to 10 those of skill in the art including intramuscular, intravenous, intradermal, intralesional, intraperitoneal injection, subcutaneous, sub-epidermal, epidural, nasal, oral, vaginal, rectal, topical, local, otic, inhalational, buccal (e.g., sublingual), and transdermal administration or any route. Administration can be local, topical or systemic depending upon the locus of treatment. Local administration to an area in 15 need of treatment can be achieved by, for example, but not limited to, local infusion during surgery, topical application, e.g., in conjunction with a wound dressing after surgery, by injection, by means of a catheter, by means of a suppository, or by means of an implant. Compositions also can be administered with other biologically active agents, either sequentially, intermittently or in the same composition. Administration 20 also can include controlled release systems including controlled release formulations and device controlled release, such as by means of a pump. The most suitable route in any given case depends on a variety of factors, such as the nature of the disease, the progress of the disease, the severity of the disease the particular composition which is used. For purposes herein, it is desired that matrix 25 degrading enzymes and activator are administered so that they reach the interstitium of skin or tissues. Thus, direct administration under the skin, such as by sub epidermal administration methods, is contemplated. These include, for example, subcutaneous, intradermal and intramuscular routes of administration. Thus, in one example, local administration can be achieved by injection, such as from a syringe or 30 other article of manufacture containing a injection device such as a needle. Other modes of administration also are contemplated. Pharmaceutical compositin can be formulated in dosage forms appropriate for each route of administration.

WO 2009/111083 PCT/US2009/001486 - 120 In one example, pharmaceutical preparation can be in liquid form, for example, solutions, syrups or suspensions. If provided in liquid form, the pharmaceutical preparation of an activatable matrix-degrading enzyme can be provided as a concentrated preparation to be diluted to a therapeutically effective 5 concentration upon addition of the activator. The activator can be added to the preparation prior to administration, or the activator can be added simultaneously, intermittently or sequentially with the matrix-degrading enzyme preparation. Such liquid preparations can be prepared by conventional means with pharmaceutically acceptable additives such as suspending agents (e.g., sorbitol syrup, cellulose 10 derivatives or hydrogenated edible fats); emulsifying agents (e.g., lecithin or acacia); non-aqueous vehicles (e.g., almond oil, oily esters, or fractionated vegetable oils); and preservatives (e.g., methyl or propyl-p-hydroxybenzoates or sorbic acid). In another example, pharmaceutical preparations can be presented in lyophilized form for reconstitution with water or other suitable vehicle before use. 15 For example, the pharmaceutical preparations of matrix-degrading enzymes can be reconstituted with a solution containing an appropriate activator. Reconstitution of the preparation yields a mixture containing a therapeutically effective amount of matrix-degrading enzyme in a suitable activator, that can be administered together using any desired route of administration. 20 Administration methods can be employed to decrease the exposure of selected matrix-degrading enzymes to degradative processes, such as proteolytic degradation and immunological intervention via antigenic and immunogenic responses. Examples of such methods include local administration at the site of treatment. Pegylation of therapeutics has been reported to increase resistance to proteolysis, increase plasma 25 half-life, and decrease antigenicity and immunogenicity. Examples of pegylation methodologies are known in the art (see for example, Lu and Felix, Int. J. Peptide Protein Res., 43: 127-138, 1994; Lu and Felix, Peptide Res., 6: 142-6, 1993; Felix et al., Int. J Peptide Res., 46: 253-64, 1995; Benhar et al., J Biol. Chem., 269: 13398 404, 1994; Brumeanu et al., JImmunol., 154: 3088-95, 1995; see also, Caliceti et al. 30 (2003) Adv. Drug Deliv. Rev. 55(10):1261-77 and Molineux (2003) Pharmacotherapy 23 (8 Pt 2):3S-8S). Pegylation also can be used in the delivery of nucleic acid molecules in vivo. For example, pegylation of adenovirus can increase stability and gene transfer (see, e.g., Cheng et al. (2003) Pharm. Res. 20(9): 1444-51).

WO 2009/111083 PCT/US2009/001486 - 121 1. Injectables, solutions and emulsions Parenteral administration, generally characterized by injection, either subcutaneously, intramuscularly or intradermally is contemplated herein. Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, solid 5 forms suitable for solution or suspension in liquid prior to injection, or as emulsions. Suitable excipients are, for example, water, saline, dextrose, glycerol or ethanol. In addition, if desired, the pharmaceutical compositions to be administered may also contain an activator in the form of a solvent such as pH buffering agents, reducing or oxidizing agents, metal ion salts, or other such buffers. The pharmaceutical 10 compositions also may contain other minor amounts of non-toxic auxiliary substances such as wetting or emulsifying agents, pH buffering agents, stabilizers, solubility enhancers, and other such agents, such as for example, sodium acetate, sorbitan monolaurate, triethanolamine oleate and cyclodextrins. Implantation of a slow release or sustained-release system, such that a constant level of dosage is maintained 15 (see, e.g., U. S. Patent No. 3,710,795) is also contemplated herein. The percentage of active compound contained in such parenteral compositions is highly dependent on the specific nature thereof, as well as the activity of the compound and the needs of the subject. Parenteral administration of the compositions generally includes sub 20 epidermal routes of administration such as intradermal, subcutaneous and intramuscular administrations. If desired, intravenous administration also is contemplated. Injectables are designed for local and systemic administration. For purposes herein, local administration is desired for direct administration to the affected interstitium. Preparations for parenteral administration include sterile 25 solutions ready for injection, sterile dry soluble products, such as lyophilized powders, ready to be combined with a solvent just prior to use, including hypodermic tablets, sterile suspensions ready for injection, sterile dry insoluble products ready to be combined with a vehicle just prior to use and sterile mulsions. The solutions may be either aqueous or nonaqueous. If administered intravenously, suitable carriers 30 include physiological saline or phosphate buffered saline (PBS), and solutions containing thickening and solubilizing agents, such as glucose, polyethylene glycol, and polypropylene glycol and mixtures thereof.

WO 2009/111083 PCT/US2009/001486 - 122 Pharmaceutically acceptable carriers used in parenteral preparations include aqueous vehicles, nonaqueous vehicles, antimicrobial agents, isotonic agents, buffers, antioxidants, local anesthetics, suspending and dispersing agents, emulsifying agents, sequestering or chelating agents, amino acids, peptides and other pharmaceutically 5 acceptable substances. Examples of aqueous vehicles include Sodium Chloride Injection, Ringers Injection, Isotonic Dextrose Injection, Sterile Water Injection, Dextrose and Lactated Ringers Injection. Nonaqueous parenteral vehicles include fixed oils of vegetable origin, cottonseed oil, corn oil, sesame oil and peanut oil. Antimicrobial agents in bacteriostatic or fungistatic concentrations can be added to 10 parenteral preparations packaged in multiple-dose containers, which include phenols or cresols, mercurials, benzyl alcohol, chlorobutanol, parabens such as methyl- and propyl-p-hydroxybenzoic acid esters, thimerosal, benzalkonium chloride and benzethonium chloride. Isotonic agents include sodium chloride and dextrose. Buffers include phosphate and citrate. Antioxidants include sodium bisulfate. Local 15 anesthetics include procaine hydrochloride. Suspending and dispersing agents include sodium carboxymethylcelluose, hydroxypropyl methylcellulose and polyvinylpyrrolidone. Emulsifying agents include Polysorbate 80 (TWEEN 80), polysorbate 20 (TWEEN 20), pluronic (F68). A sequestering or chelating agent of metal ions includes EDTA. Pharmaceutical carriers also include ethyl alcohol, 20 polyethylene glycol and propylene glycol for water miscible vehicles and sodium hydroxide, hydrochloric acid, citric acid or lactic acid for pH adjustment. The concentration of the pharmaceutically active compound is adjusted so that an injection provides an effective amount to produce the desired pharmacological effect. The exact dose depends on the age, weight and condition of the patient or 25 animal as is known in the art. The unit-dose parenteral preparations are packaged in an ampoule, a vial or a syringe with a needle. The volume of liquid solution or reconstituted powder preparation, containing the pharmaceutically active compound, is a function of the disease to be treated and the particular article of manufacture chosen for package. For example, for the treatment of cellulite, it is contemplated that 30 for parenteral injection the injected volume is or is about 10 to 50 milliliters. Generally, this volume represents the volume of activator and matrix-degrading enzyme where the two are administered together. Thus, in one example, a dual container or dual-chamber syringe is provided containing a lyophilized enzyme WO 2009/111083 PCT/US2009/001486 - 123 preparation separated from a second compartment containing 10 to 50 milliliters of activator. Following reconstitution of the enzyme with the activator, the mixture can be administered. All preparations for parenteral administration must be sterile, as is known and practiced in the art. The injectable formulation can be stored under 5 appropriate conditions such as at or about -80"C, -40"C, -20"C, 2-8 0 C, 15 0 C, room temperature or controlled room temperature. Lyophilized powders Of interest herein are lyophilized powders, which can be reconstituted for administration as solutions, emulsions and other mixtures. They may also be 10 reconstituted and formulated as solids or gels. The sterile, lyophilized powder is prepared by dissolving a compound of inactive enzyme in a buffer solution. The buffer solution may contain an excipient which improves the stability or other pharmacological component of the powder or reconstituted solution, prepared from the powder. Subsequent sterile filtration of the 15 solution followed by lyophilization under standard conditions known to those of skill in the art provides the desired formulation. Briefly, the lyophilized powder is prepared by dissolving an excipient, such as dextrose, sorbital, fructose, corn syrup, xylitol, glycerin, glucose, sucrose, mannose, sorbitol, trehalose, mannitol, sorbitol, hydroxyethyl starch or other suitable agent, in a suitable buffer, such as citrate, 20 sodium or potassium phosphate or other such buffer known to those of skill in the art. Other excipients that can be added include amino acids such as glycine, alanine, proline, amines such as betaines, trimethylamine N-oxide, and salts of ammonium, sodium or magnesium. Then, a selected enzyme is added to the resulting mixture, and stirred until it dissolves. The resulting mixture is sterile filtered or treated to remove 25 particulates and to insure sterility, and apportioned into vials for lyophilization. Each vial will contain a single dosage (1 mg - I g, generally 1-100 ing, such as 1-5 mg) or multiple dosages of the compound. The lyophilized powder can be stored under appropriate conditions, such as at about 4 'C to room temperature. Reconstitution of this lyophilized powder with a buffer solution provides a 30 formulation for use in parenteral administration. The solution chosen for reconstitution can be any buffer, but typically is a buffer containing the activator. The activator is chosen as a function of the enzyme to be reconstituted. For example, a lyophilized preparation of cathepsin L is reconstituted with an acidic buffer at about WO 2009/111083 PCT/US2009/001486 - 124 pH 5.5. For reconstitution about I ptg -20 mg, preferably 10 ptg- 1 mg, more preferably about 100 pg is added per mL of buffer or other suitable carrier. The precise amount depends upon the indication treated and selected compound. Such amount can be empirically determined. 5 2. Topical administration Topical mixtures are prepared as described for the local and systemic administration. The resulting mixture may be a solution, suspension, emulsions or the like and are formulated as creams, gels, ointments, emulsions, solutions, elixirs, lotions, suspensions, tinctures, pastes, foams, aerosols, irrigations, sprays, 10 suppositories, bandages, dermal patches or any other formulations suitable for topical administration. The compounds or pharmaceutically acceptable derivatives thereof may be formulated as aerosols for topical application, such as by inhalation (see, e.g., U. S. Patent Nos. 4,044,126; 4,414,209; and 4,364,923, which describe aerosols for delivery 15 of a steroid useful for treatment inflammatory diseases, particularly asthma). These formulations for administration to the respiratory tract can be in the form of an aerosol or solution for a nebulizer, or as a microfine powder for insufflation, alone or in combination with an inert carrier such as lactose. In such a case, the particles of the formulation will typically diameters of less than 50 microns, preferably less than 10 20 microns. The compounds may be formulated for local or topical application, such as for topical application to the skin and mucous membranes, such as in the eye, in the form of gels, creams, and lotions and for application to the eye or for intracisternal or intraspinal application. Topical administration is contemplated for transdermal 25 delivery and also for administration to the eyes or mucosa, or for inhalation therapies. Nasal solutions of the active compound alone or in combination with other pharmaceutically acceptable excipients also can be administered. Formulations suitable for transdermal administration are provided. They can be provided in any suitable format, such as discrete patches adapted to remain in 30 intimate contact with the epidermis of the recipient for a prolonged period of time. Such patches contain the active compound in optionally buffered aqueous solution of, for example, 0.1 to 0.2M concentration with respect to the active compound. Formulations suitable for transdermal administration also can be delivered by WO 2009/111083 PCT/US2009/001486 - 125 iontophoresis (see, e.g., Pharmaceutical Research 3(6), 318 (1986)) and typically take the form of an optionally buffered aqueous solution of the active compound. 3. Compositions for other routes of administration Depending upon the condition treated other routes of administration, such as 5 topical application, transdermal patches, oral and rectal administration are also contemplated herein. For example, pharmaceutical dosage forms for rectal administration are rectal suppositories, capsules and tablets for systemic effect. Rectal suppositories include solid bodies for insertion into the rectum which melt or soften at body temperature releasing one or more pharmacologically or therapeutically active 10 ingredients. Pharmaceutically acceptable substances utilized in rectal suppositories are bases or vehicles and agents to raise the melting point. Examples of bases include cocoa butter (theobroma oil), glycerin-gelatin, carbowax (polyoxyethylene glycol) and appropriate mixtures of mono-, di- and triglycerides of fatty acids. Combinations of the various bases may be used. Agents to raise the melting point of suppositories 15 include spermaceti and wax. Rectal suppositories may be prepared either by the compressed method or by molding. The typical weight of a rectal suppository is about 2 to 3 gm. Tablets and capsules for rectal administration are manufactured using the same pharmaceutically acceptable substance and by the same methods as for formulations for oral administration. 20 Formulations suitable for rectal administration can be provided as unit dose suppositories. These can be prepared by admixing the active compound with one or more conventional solid carriers, for example, cocoa butter, and then shaping the resulting mixture. For oral administration, pharmaceutical compositions can take the form of, for 25 example, tablets or capsules prepared by conventional means with pharmaceutically acceptable excipients such as binding agents (e.g., pregelatinized maize starch, polyvinyl pyrrolidone or hydroxypropyl methylcellulose); fillers (e.g., lactose, microcrystalline cellulose or calcium hydrogen phosphate); lubricants (e.g., magnesium stearate, talc or silica); disintegrants (e.g., potato starch or sodium starch 30 glycolate); or wetting agents (e.g., sodium lauryl sulphate). The tablets can be coated by methods well-known in the art. Formulations suitable for buccal (sublingual) administration include, for example, lozenges containing the active compound in a flavored base, usually sucrose WO 2009/111083 PCT/US2009/001486 - 126 and acacia or tragacanth; and pastilles containing the compound in an inert base such as gelatin and glycerin or sucrose and acacia. Pharmaceutical compositions also can be administered by controlled release formulations and/or delivery devices (see, e.g., in U.S. Patent Nos. 3,536,809; 5 3,598,123; 3,630,200; 3,845,770; 3,847,770; 3,916,899; 4,008,719; 4,687,610; 4,769,027; 5,059,595; 5,073,543; 5,120,548; 5,354,566; 5,591,767; 5,639,476; 5,674,533 and 5,733,566). Various delivery systems are known and can be used to administer selected matrix-degrading enzymes, such as but not limited to, encapsulation in liposomes, 10 microparticles, microcapsules, recombinant cells capable of expressing the compound, receptor mediated endocytosis, and delivery of nucleic acid molecules encoding selected matrix-degrading enzymes such as retrovirus delivery systems. Hence, in certain embodiments, liposomes and/or nanoparticles also can be employed with administration of matrix-degrading enzymes. Liposomes are formed 15 from phospholipids that are dispersed in an aqueous medium and spontaneously form multilamellar concentric bilayer vesicles (also termed multilamellar vesicles (MLVs)). MLVs generally have diameters of from 25 nm to 4 pim. Typically, liposomes are also prepared containing cholesterol to stabilize the nanoparticles. Sonication of MLVs results in the formation of small unilamellar vesicles (SUVs) 20 with diameters in the range of 200 to 500 angstroms containing an aqueous solution in the core. Phospholipids can form a variety of structures other than liposomes when dispersed in water, depending on the molar ratio of lipid to water. At low ratios, the liposomes form. Physical characteristics of liposomes depend on pH, ionic strength 25 and the presence of divalent cations. Liposomes can show low permeability to ionic and polar substances, but at elevated temperatures undergo a phase transition which markedly alters their permeability. The phase transition involves a change from a closely packed, ordered structure, known as the gel state, to a loosely packed, less ordered structure, known as the fluid state. This occurs at a characteristic phase 30 transition temperature and results in an increase in permeability to ions, sugars and drugs. Liposomes interact with cells via different mechanisms: endocytosis by phagocytic cells of the reticuloendothelial system such as macrophages and WO 2009/111083 PCT/US2009/001486 - 127 neutrophils; adsorption to the cell surface, either by nonspecific weak hydrophobic or electrostatic forces, or by specific interactions with cell-surface components; fusion with the plasma cell membrane by insertion of the lipid bilayer of the liposome into the plasma membrane, with simultaneous release of liposomal contents into the 5 cytoplasm; and by transfer of liposomal lipids to cellular or subcellular membranes, or vice versa, without any association of the liposome contents. Varying the liposome formulation can alter which mechanism is operative, although more than one can operate at the same time. Nanocapsules can generally entrap compounds in a stable and reproducible way. To avoid side effects due to intracellular polymeric 10 overloading, such ultrafine particles (sized around 0.1 pm) should be designed using polymers able to be degraded in vivo. Biodegradable polyalkyl-cyanoacrylate nanoparticles that meet these requirements are contemplated for use herein, and such particles can be easily made. 4. Combination Therapies 15 Any of the activatable matrix-degrading enzymes and activator combinations described herein can be further co-formulated or co-administered together with, prior to, intermittently with, or subsequent to, other therapeutic or pharmacologic agents or procedures. Such agents include, but are not limited to, other biologics, small molecule compounds, dispersing agents, anesthetics, vasoconstrictors and surgery, 20 and combinations thereof. For example, for any disease or condition, including all those exemplified above, for which other agents and treatments are available, selected activatable matrix-degrading enzyme and activator combination for such diseases and conditions can be used in combination therewith. In another example, a local anesthetic, for example, lidocaine can be administered to provide pain relief. In some 25 examples, the anesthetic can be provided in combination with a vasoconstrictor to increase the duration of the anesthetic effects. Any of the pharmacological agents provided herein can be combined with a dispersion agent that facilitates access into the tissue of pharmacologic agents, for example, following subcutaneous administration. Such substances are known in the art and include, for example, 30 soluble glycosaminoglycanase enzymes such as hyaluronan degrading enzymes, for example, members of the hyaluronidase glycoprotein family (see, e.g., U.S. Publication Nos. 20050260186 and 20060104968).

WO 2009/111083 PCT/US2009/001486 - 128 Compositions of activatable matrix-degrading enzymes provided herein can be co-formulated or co-administered with a local anesthesia. For example, where pH is provided as the activating condition, administration of a local anesthesia is desired to minimize pain associated with exposure to acidic pH. Anesthsias include short-acting 5 and long-lasting local anesthetic drug formulations. Short-acting local anesthetic drug formulations contain lidocaine or a related local anesthetic drug dissolved in saline or other suitable injection vehicle. Typically, local anesthesia with short-acting local anesthetics last approximately 20-30 minutes. Exemplary anesthetics include, for example, non-inhalation local anesthetics such as ambucaines; amoxecaines; 10 amylocaines; aptocaines; articaines; benoxinates; benzyl alcohols; benzocaines; betoxycaines; biphenamines; bucricaines; bumecaines; bupivacaines; butacaines; butambens; butanilicaines; carbizocaines; chloroprocaine; clibucaines; clodacaines; cocaines; dexivacaines; diamocaines; dibucaines; dyclonines; elucaines; etidocaines; euprocins; fexicaines; fomocaines; heptacaines; hexylcaines; hydroxyprocaines; 15 hydroxytetracaines; isobutambens; ketocaines; leucinocaines; lidocaines; mepivacaines; meprylcaines; octocaines; orthocaines; oxethacaines; oxybuprocaines; phenacaines; pinolcaines; piperocaines; piridocaines; polidocanols; pramocaines; prilocaines; procaines; propanocaines; propipocaines; propoxycaines; proxymetacaines; pyrrocaines; quatacaines; quinisocaines; risocaines; rodocaines; 20 ropivacaines; salicyl alcohols; suicaines; tetracaines; trapencaines; and trimecaines; as well as various other non-inhalation anesthetics such as alfaxalones; amolanones; etoxadrols; fentanyls; ketamines; levoxadrols; methiturals; methohexitals; midazolams; minaxolones; propanidids; propoxates; pramoxines; propofols; remifentanyls; sufentanyls; tiletamines; and zolamine. The effective amount in the 25 formulation will vary depending on the particular patient, disease to be treated, route of administration and other considerations. Such dosages can be determined empirically. Due to the short half-life of local anesthetics, it is often desirable to co administer or co-formulate such anesthetics with a vasoconstrictor. Examples of 30 vasoconstrictors include alpha adrenergic receptor agonists including catecholamines and catecholamine derivatives. Particular examples include, but are not limited to, levonordefrin, epinephrine and norepinephrine. For example, a local anesthetic formulation, such as lidocaine, can be formulated to contain low concentrations of WO 2009/111083 PCT/US2009/001486 - 129 epinephrine or another adrenergic receptor agonist such as levonordefrin. Combining local anesthetics with adrenergic receptor agonists is common in pharmaceutical preparations (see e.g., U.S. Patent No. 7,261,889 and 5,976,556). The vasoconstrictor is necessary to increase the half-life of anesthetics. The vasoconstrictor, such as 5 epinephrine, stimulates alpha-adrenergic receptors on the blood vessels in the injected tissue. This has the effect of constriction the blood vessels in the tissue. The blood vessel constriction causes the local anesthetic to stay in the tissue musch longer, resulting in a large increase in the duration of the anesthetic effect. Generally, a vasoconstrictor is used herein in combination with an anesthetic. 10 The anesthetic agent and vasoconstrictor can be administered together as part of a single pharmaceutical composition or as part of separate pharmaceutical compositions so long as the vasoconstrictor acts to constrict the blood vessels in the vicinity of whether the anesthetic agent has been administered to result in a prolonging of anesthesia. In one example, the anesthetic agent and vasoconstrictor are administered 15 together in solution. In addition, the anesthetic agent and vasoconstricter can be formulated together or separate from the activatable matrix-degrading enzyme and activator. Single formulations are preferred. The anesthetic agent and vasoconstrictor can be administered by injection, by infiltration or by topical administration, e.g., as part of a gel or paste. Typically, the anesthetic agent and vasoconstrictor are 20 administered by injection directly into the site to be anesthetized, for example, by subcutaneous administration. The effective amount in the formulation will vary depending on the particular- patient, disease to be treated, route of administration and other considerations. Such dosages can be determined empirically. For example, exemplary amounts of lidocaine is or is about 10 mg to 1000 mg, 100 mg to 500 mg, 25 200 mg to 400 mg, 20 mg to 60 mg, or 30 mg to 50 mg. The dosage of lidocaine administered will vary depending on the individual and the route of administration. Epinephrine can be administered in amounts such as, for example, 10 Ig to 5 mg, 50 ptg to I mg, 50 pg to 500 ptg, 50 pg to 250 pg, 100 pig to 500 pig, 200 jig to 400 jig, I mg to 5 mg or 2 mg to 4 mg. Typically, epinephrine can be combined with lidocaine 30 in a 1:100,000 to 1:200,000 dilution, which means that 100 ml of anesthetic contains 0.5 to 1 mg of epinephrine. Volumes administered can be adjusted depending on the disease to be treated and the route of administration. It is contemplated herein that I 100 ml, 1-50 ml, 10-50 ml, 10-30 ml, 1-20 ml, or 1-10 ml, typically 10-50 ml of an WO 2009/111083 PCT/US2009/001486 - 130 anesthetic/vasoconstrictor formulation can be administered subcutaneously for the treatment of an ECM-mediated disease or condition, such as cellulite. The administration can be subsequently, simultaneously or intermittently with administration of an activatable matrix-degrading enzyme and activator. 5 Compositions of activatable matrix-degrading enzymes provided herein also can be co-formulated or co-administered with a dispersion agent. The dispersion agent also can be co-formulated or co-administered with other pharmacological agents, such as anesthetics, vasoconstrictors, or other biologic agents. Exemplary of dispersion agents are glycosaminoglycanases, such as hyaluronan degrading enzymes, 10 for example, hyaluronidases, that open channels in the interstitial space through degradation of glycosaminoglycans. These channels can remain relatively open for a period of 24-48 hours depending on dose and formulation. Such channels can be used to facilitate the diffusion of exogenously added molecules such as fluids, small molecules, proteins (such as matrix degrading enzymes), nucleic acids and gene 15 therapy vectors and other molecules less than about 500 nm in size. In addition, it is thought that the formation of such channels can facilitate bulk fluid flow within an .interstitial space, which can in turn promote the dispersion or movement of a solute (such as a detectable molecule or other diagnostic agent, an anesthetic or other tissue modifying agent, a pharmacologic or pharmaceutically effective agent, or a cosmetic 20 or other esthetic agent) that is effectively carried by the fluid in a process sometimes referred to as "convective transport" or simply convection. Such convective transport can substantially exceed the rate and cumulative effects of molecular diffusion and can thus cause the therapeutic or other administered molecule to more rapidly and effectively perfuse a tissue. Furthermore, when an agent, such as a matrix degrading 25 enzyme, anesthetic or other agent, is co-formulated or co-administered with a glycosaminoglycanase and both are injected into a relatively confined local site, such as a site of non-intravenous parenteral administration (e.g., intradermal, subcutaneous, intramuscular, or into or around other internal tissues, organs or other relatively confined spaces within the body), then the fluid associated with the administered dose 30. can both provide a local driving force (i.e. hydrostatic pressure) as well as lower impedance to flow (by opening channels within the interstitial matrix), both of which could increase fluid flow, and with it convective transport of the therapeutic agent or other molecule contained within the fluid. As a result, the use of WO 2009/111083 PCT/US2009/001486 - 131 glycosaminoglycanases can have substantial utility for improving the bioavailability as well as manipulating other pharmacokinetic and/or pharmacodynamic characteristics of co-formulated or co-administered agents, such as matrix degrading enzymes. 5 a. Hyaluronan Degrading Enzymes Exemplary of glycosaminoglycanases are hyaluronan-degrading enzymes. Hyaluronan degrading enzymes include any enzyme that degrades hyaluronan. Exemplary hyaluronan degrading enzymes include, but are not limited to hyaluronidases and particular chondroitinases and lyases that have the ability to 10 cleave hyaluronan. Exemplary of hyaluronan degrading enzymes in the compositions, combinations and methods provided herein are soluble hyaluronan degrading enzymes. For example, exemplary of glycosaminoglycanases are hyaluronidases. Hyaluronan-degrading enzymes, such as hyaluronidases, are a family of enzymes that degrade hyaluronic acid. By catalyzing the hydrolysis of hyaluronic acid, a major 15 constituent of the interstitial barrier, hyaluronidase lowers the viscosity of hyaluronic acid, thereby increasing tissue permeability. Hyaluronan, also called hyaluronic acid or hyaluronate, is a non-sulfated glycosaminoglycan that is widely distributed throughout connective, epithelial, and neural tissues. Hyaluronan is an essential component of the extracellular matrix and a 20 major constituent of the interstitial barrier. By catalyzing the hydrolysis of hyaluronan, hyaluronan degrading enzymes lower the viscosity of hyaluronan, thereby increasing tissue permeability and increasing the absorption rate of fluids administered parenterally. As such, hyaluronan degrading enzymes, such as hyaluronidases, have been used, for example, as spreading or dispersing agents in 25 conjunction with other agents, drugs and proteins to enhance their dispersion and delivery. Hyaluronan degrading enzymes act to degrade hyaluronan by cleaving hyaluronan polymers, which are composed of repeating disaccharides units, D glucuronic acid (GlcA) and N-acetyl-D-glucosamine (GlcNAc), linked together via 30 alternating 0-1-> 4 and 0-1-+ 3 glycosidic bonds. Hyaluronan chains can reach about 25,000 disaccharide repeats or more in length and polymers of hyaluronan can range in size from about 5,000 to 20,000,000 Da in vivo. Accordingly, hyaluronan degrading enzymes for the uses and methods provided include any enzyme having the WO 2009/111083 PCT/US2009/001486 - 132 ability to catalyze the cleavage of a hyaluronan disaccharide chain or polymer. In some examples the hyaluronan degrading enzyme cleaves the 0-1-+ 4 glycosidic bond in the hyaluronan chain or polymer. In other examples, the hyaluronan degrading enzyme catalyze the cleavage of the 0-1- 3 glycosidic bond in the hyaluronan chain 5 or polymer. i. Hyaluronidases There are three general classes of hyaluronidases: Mammalian-type hyaluronidases, (EC 3.2.1.35) which are endo-beta-N-acetylhexosaminidases with tetrasaccharides and hexasaccharides as the major end products; Bacterial 10 hyaluronidases (EC 4.2.99.1), degrade hyaluronan and, and to various extents, chondroitin sulfates (CS) and dermatan sulfates (DS), which are endo-beta-N acetylhexosaminidases that operate by a beta elimination reaction that yields primarily disaccharide end products; and Hyaluronidases (EC 3.2.1.36) from leeches, other parasites, and crustaceans that are endo-beta-glucuronidases that generate 15 tetrasaccharide and hexasaccharide end products through hydrolysis of the 3- 1-3 linkage. 1) Mammalian-type hyaluronidases Mammalian-type hyaluronidases have both hydrolytic and transglycosidase activities, and can degrade hyaluronan and chondroitin sulfates (CS), generally C4-S 20 and C6-S. Hyaluronidases of this type include, but are not limited to, hyaluronidases from cows (bovine) (SEQ ID NOS:237, 266 and 272 and BH55 (U.S. Pat. Nos. 5,747,027 and 5,827,721), sheep (ovis aries) (SEQ ID NO:252, 267, 271 and 272), yellow jacket wasp (SEQ ID NOS:238 and 239), honey bee (SEQ ID NO:240), white face hornet (SEQ ID NO:241), paper wasp (SEQ ID NO:242), mouse (SEQ ID 25 NOS:243-245, 257), pig (SEQ ID NOS:246, 247), rat (SEQ ID NOS:248-250, 256), rabbit (SEQ ID NO:251), orangutan (SEQ ID NO:253), cynomolgus monkey (SEQ ID NO:254), guinea pig (SEQ ID NO:255), and human hyaluronidases. Exemplary of hyaluronidases in the compositions, combinations and methods provided herein are soluble hyaluronidases. 30 There are six hyaluronidase-like genes in the human genome, HYALI (SEQ ID NO:262), HYAL2 (SEQ ID NO: 263), HYAL3 (SEQ ID NO:264), HYAL4 (SEQ ID NO:265) and PH20/SPAMI (SEQ ID NO:232). Among hyaluronidases, PH20 is the prototypical neutral active enzyme, while the others exhibit no catalytic activity WO 2009/111083 PCT/US2009/001486 - 133 towards hyaluronan or any known substrates, or are active only under pH conditions. The hyaluronidase-like enzymes can also be characterized by those which are generally locked to the plasma membrane via a glycosylphosphatidyl inositol anchor such as human HYAL2 and human PH20 (Danilkovitch-Miagkova, et al. (2003) Proc 5 Natl Acad Sci USA. 100(8):4580-5), and those which are generally soluble such as human HYAL1 (Frost et al, (1997) Biochem Biophys Res Commun. 236(l):10-5). N linked glycosylation of some hyaluronidases can be very important for their catalytic activity and stability. While altering the type of glycan modifying a glycoprotein can have dramatic affects on a protein's antigenicity, structural folding, solubility, and 10 stability, many enzymes are not thought to require glycosylation for optimal enzyme activity. Hyaluronidases are, therefore, unique in this regard, in that removal of N linked glycosylation can result in near complete inactivation of the hyaluronidase activity. For such hyaluronidases, the presence of N-linked glycans is critical for generating an active enzyme. 15 Hence, mammalian hyaluronidases can be further subdivided into those that are neutral active, predominantly found in testes extracts, and acid active, predominantly found in organs such as the liver. Exemplary neutral active hyaluronidases include PH20, including but not limited to, PH20 derived from different species such as ovine (SEQ ID NO:267), bovine (SEQ ID NO:266) and 20 human (SEQ ID NO:232). Human PH20 (also known as sperm surface protein PH20) is naturally involved in sperm-egg adhesion and aids penetration by sperm of the layer of cumulus cells by digesting hyaluronic acid. The PH20 mRNA transcript (corresponding to nucleotides 1058-2503 of the sequence set forth in SEQ ID NO:224) is normally 25 translated to generate a 509 amino acid precursor protein containing a 35 amino acid signal sequence at the N-terminus (amino acid residue positions 1-35) and a 19 amino acid GPI anchor at the C-terminus (corresponding to amino acid residues 491-509). The precursor sequence is set forth in SEQ ID NO:232. An mRNA transcript containing a mutation of C to T at nucleotide position 2188 of the sequence of amino 30 acids set forth in SEQ ID NO:224 also exists and is a silent mutation resulting in the translated product set forth in SEQ ID NO: 232. The mature PH20 is, therefore, a 474 amino acid polypeptide set forth in SEQ ID NO:233). There are potential N-linked glycosylation sites required for hyaluronidases activity at N82, N166, N235, N254, WO 2009/111083 PCT/US2009/001486 -134 N368, N393, N490 of human PH20 exemplified in SEQ ID NO: 232. Disulfide bonds form between the cysteine residues C60 and C351 and between C224 and C238 (corresponding to amino acids set forth in SEQ ID NO:232) to form the core hyaluronidase domain. However, additional cysteines are required in the carboxy 5 terminus for neutral enzyme catalytic activity such that amino acids 36 to 464 of SEQ ID NO:232 contains the minimally active human PH20 hyaluronidase domain. Bovine PH20 is a 553 amino acid precursor polypeptide (SEQ ID NO:266). Alignment of bovine PH20 with the human PH20 shows only weak homology, with multiple gaps existing from amino acid 470 through to the respective carboxy termini 10 due to the absence of a GPI anchor in the bovine polypeptide (see e.g., Frost GI (2007) Expert Opin. Drug. Deliv. 4: 427-440). No clear GPI anchor is predicted in other PH20 species besides humans. For example, PH20 polypeptides produced from ovine and bovine exist as soluble forms. Though bovine PH20 exists very loosely attached to the plasma membrane, it is not anchored via a phospholipase sensitive 15 anchor (Lalancette et al. (2001) Biol Reprod. 65(2):628-36). This unique feature of bovine hyaluronidase has permitted the use of the soluble bovine testes hyaluronidase enzyme as an extract for clinical use (WydaseTM, HyalaseTM). 2) Bacterial hyaluronidases Bacterial hyaluronidases (EC 4.2.2.1 or EC 4.2.99.1) degrade hyaluronan and, 20 to various extents, chondroitin sulfates and dermatan sulfates. Hyaluronan lyases isolated from bacteria differ from hyaluronidases (from other sources, e.g., hyaluronoglucosaminidases, EC 3.2.1.35) by their mode of action. They are endo-3 N-acetylhexosaminidases that catalyze an elimination reaction, rather than hydrolysis, of the 01-> 4-glycosidic linkage between N-acetyl-beta-D-glucosamine and D 25 glucuronic acid residues in hyaluronan, yielding 3-(4-deoxy--D-gluc-4-enuronosyl) N-acetyl-D-glucosamine tetra- and hexasaccharides, and disaccharide end products. The reaction results in the formation of oligosaccharides with unsaturated hexuronic acid residues at their nonreducing ends. Exemplary hyaluronidases from bacteria for use in the compositions, 30 combinations and methods provided include, but are not limited to, hyaluronan degrading enzymes in microorganisms, including strains of Arthrobacter, Bdellovibrio, Clostridium, Micrococcus, Streptococcus, Peptococcus, Propionibacterium, Bacteroides, and Streptomyces. Particular examples of such WO 2009/111083 PCT/US2009/001486 - 135 enzymes include, but are not limited to Arthrobacter sp. (strain FB24) (SEQ ID NO:275), Bdellovibrio bacteriovorus (SEQ ID NO:276), Propionibacterium acnes (SEQ ID NO:277), Streptococcus agalactiae ((SEQ ID NO:278); 18RS21 (SEQ ID NO:279); serotype Ia (SEQ ID NO:280); serotype III (SEQ ID NO:281), 5 Staphylococcus aureus (strain COL (SEQ ID NO:282); strain MRSA252 (SEQ ID NOS:283 and 284); strain MSSA476 (SEQ ID NO:285); strain NCTC 8325 (SEQ ID NO:286); strain bovine RF122 (SEQ ID NOS:287 and 288); strain USA300 (SEQ ID NO:289), Streptococcus pneumoniae ((SEQ ID NO:290); strain ATCC BAA-255 / R6 (SEQ ID NO:291); serotype 2, strain D39 / NCTC 7466 (SEQ ID NO:292), 10 Streptococcus pyogenes (serotype M1) (SEQ ID NO:293); serotype M2, strain MGAS10270 (SEQ ID NO:294); serotype M4, strain MGAS10750 (SEQ ID NO:295); serotype M6 (SEQ ID NO:296); serotype M12, strain MGAS2096 (SEQ ID NOS:297 and 298); serotype M12, strain MGAS9429 (SEQ ID NO:299); serotype M28 (SEQ ID NO:300); Streptococcus suis (SEQ ID NOS:301-303); Vibriofischeri 15 (strain ATCC 700601/ ES 114 (SEQ ID NO:304)), and the Streptomyces hyaluronolyticus hyaluronidase enzyme, which is specific for hyaluronic acid and does not cleave chondroitin or chondroitin sulfate (Ohya, T. and Kaneko, Y. (1970) Biochim. Biophys. Acta 198:607). 3) Hyaluronidases from leeches, other parasites 20 and crustaceans Hyaluronidases from leeches, other parasites, and crustaceans (EC 3.2.1.36) are endo-#l-glucuronidases that generate tetra- and hexasaccharide end-products. These enzymes catalyze hydrolysis of 01-- 3-linkages between O-D-glucuronate and N-acetyl-D-glucosamine residues in hyaluronate. Exemplary hyaluronidases from 25 leeches include, but are not limited to, hyaluronidase from Hirudinidae (e.g., Hirudo medicinalis), Erpobdellidae (e.g., Nephelopsis obscura and Erpobdella punctata,), Glossiphoniidae (e.g., Desserobdella picta, Helobdella stagnalis, Glossiphonia complanata, Placobdella ornata and Theromyzon sp.) and Haemopidae (Haemopis marmorata) (Hovingh et al. (1999) Comp Biochem Physiol B Biochem Mol Biol. 30 124(3):319-26). An exemplary hyaluronidase from bacteria that has the same mechanism of action as the leech hyaluronidase is that from the cyanobacteria, Synechococcus sp. (strain RCC307, SEQ ID NO:305). ii. Other hyaluronan degrading enzymes WO 2009/111083 PCT/US2009/001486 - 136 In addition to the hyaluronidase family, other hyaluronan degrading enzymes can be used in conjunction with the activatable matrix degrading enzymes in the compositions, combinations and methods provided. For example, enzymes, including particular chondroitinases and lyases, that have the ability to cleave hyaluronan can be 5 employed. Exemplary chondroitinases that can degrade hyaluronan include, but are not limited to, chondroitin ABC lyase (also known as chondroitinase ABC), chondroitin AC lyase (also known as chondroitin sulfate lyase or chondroitin sulfate eliminase) and chondroitin C lyase. Methods for production and purification of such enzymes for use in the compositions, combinations, and methods provided are known 10 in the art (e.g., U.S. Patent No. 6,054,569; Yamagata, et al. (1968) J. Biol. Chem. 243(7):1523-1535; Yang et al. (1985) J. Biol. Chem. 160(30):1849-1857). Chondroitin ABC lyase contains two enzymes, chondroitin-sulfate-ABC endolyase (EC 4.2.2.20) and chondroitin-sulfate-ABC exolyase (EC 4.2.2.21) (Hamai et al. (1997) JBiol Chem. 272(14):9123-30), which degrade a variety of 15 glycosaminoglycans of the chondroitin-sulfate- and dermatan-sulfate type. Chondroitin sulfate, chondroitin-sulfate proteoglycan and dermatan sulfate are the preferred substrates for chondroitin-sulfate-ABC endolyase, but the enzyme also can act on hyaluronan at a lower rate. Chondroitin-sulfate-ABC endolyase degrades a variety of glycosaminoglycans of the chondroitin-sulfate- and dermatan-sulfate type, 20 producing a mixture of A4-unsaturated oligosaccharides of different sizes that are ultimately degraded to A4-unsaturated tetra- and disaccharides. Chondroitin-sulfate ABC exolyase has the same substrate specificity but removes disaccharide residues from the non-reducing ends of both polymeric chondroitin sulfates and their oligosaccharide fragments produced by chondroitin-sulfate-ABC endolyase (Hamai, 25 A. et al. (1997) J. Biol. Chem. 272:9123-9130). A exemplary chondroitin-sulfate ABC endolyases and chondroitin-sulfate-ABC exolyases include, but are not limited to, those from Proteus vulgaris and Flavobacterium heparinum (the Proteus vulgaris chondroitin-sulfate-ABC endolyase is set forth in SEQ ID NO: 306 (Sato et al. (1994) Apple. Microbiol. Biotechnol. 41(1):39-46). 30 Chondroitin AC lyase (EC 4.2.2.5) is active on chondroitin sulfates A and C, chondroitin and hyaluronic acid, but is not active on dermatan sulfate (chondroitin sulfate B). Exemplary chondroitinase AC enzymes from the bacteria include, but are not limited to, those from Flavobacterium heparinum and Victivallis vadensis, set WO 2009/111083 PCT/US2009/001486 - 137 forth in SEQ ID NOS:307 and 308, respectively, and Arthrobacter aurescens (Tkalec et al. (2000) Applied and Environmental Microbiology 66(1 ):29-3 5; Ernst et al. (1995) Critical Reviews in Biochemistry and Molecular Biology 30(5):387-444). Chondroitinase C cleaves chondroitin sulfate C producing tetrasaccharide plus 5 an unsaturated 6-sulfated disaccharidec(delta Di-6S). It also cleaves hyaluronic acid producing unsaturated non-sulfated disaccharide (delta Di-OS). Exemplary chondroitinase C enzymes from the bacteria include, but are not limited to, those from Streptococcus and Flavobacterium (Hibi et al. (1989) FEMS-Microbiol-Lett. 48(2):121-4; Michelacci et al. (1976) J Biol. Chem. 251:1154-8; Tsuda et al. (1999) 10 Eur. J. Biochem. 262:127-133). iii. Soluble hyaluronan degrading enzymes Soluble hyaluronan degrading enzymes, including soluble hyaluronidases can be used in the methods, combinations or compositions provided herein for co administration or co-formulation with matrix degrading enzymes, activators, 15 anesthetics, vasoconstrictors, other pharmacologic or therapeutic agents, or combinations thereof, to permit the diffusion into tissues. Soluble hyaluronan degrading enzymes include any hyaluronan degrading enzymes that exist in soluble form, including, but not limited to, hyaluronidases such as bovine PH20 and ovine PH20, allelic variants thereof and other variants. Also included among soluble 20 hyaluronan degrading enzymes are any hyaluronan degrading enzymes that have been modified to be soluble. For example, hyaluronan degrading enzymes that contain a GPI anchor can be made soluble by truncation of and removal of all or a portion of the GPI anchor. In one example, the human hyaluronidase PH20, which is normally membrane anchored via a GPI anchor, can be made soluble by truncation of and 25 removal of all or a portion of the GPI anchor at the C-terminus. Soluble hyaluronan degrading enzymes also include neutral active and acid active hyaluronidases. Depending on factors, such as, but not limited to, the desired level of activity of the enzyme following administration and/or site of administration, neutral active and acid active hyaluronidases can be selected. In a particular example, 30 the hyaluronan degrading enzyme for use in the compositions, combinations and methods is a soluble neutral active hyaluronidase. Exemplary of a soluble hyaluronidase is PH20 from any species, such as any set forth in any of SEQ ID NOS:232, 233, 266, 251, 267, 255, 257, 271-274, or WO 2009/111083 PCT/US2009/001486 - 138 truncated forms thereof lacking all or a portion of the C-terminal GPI anchor, so long as the hyaluronidase is soluble and retains hyaluronidase activity. Also included among soluble hyaluronidases are allelic variants or other variants of any of SEQ ID NOS:232, 233, 266, 251, 267, 255, 257, 271-274, or truncated forms thereof. Allelic 5 variants and other variants are known to one of skill in the art, and include polypeptides having 60%, 70%, 80%, 90%, 91%, 92%, 93%, 94%, 95% or more sequence identity to any of SEQ ID NOS:232, 233, 266, 251, 267, 255, 257, 271-274, or truncated forms thereof. Typically, for use in the compositions, combinations, and methods herein, a 10 soluble human PH20 is used. Although PH20 from other animals can be utilized, such preparations are potentially immunogenic, since they are animal proteins. For example, a significant proportion of patients demonstrate prior sensitization secondary to ingested foods, and since these are animal proteins, all patients have a risk of subsequent sensitization. Thus, non-human preparations may not be suitable for 15 chronic use. If non-human preparations are desired, it is contemplated herein that such polypeptides can be prepared to have reduced immunogenicity. Such modifications are within the level of one of skill in the art and can include, for example, removal and/or replacement of one or more antigenic epitopes on the molecule. 20 Hyaluronan degrading enzymes, including hyaluronidases (e.g., PH20), used in the methods herein can be recombinantly produced or can be purified or partially purified from natural sources, such as, for example, from testes extracts. Methods for production of recombinant proteins, including recombinant hyaluronan degrading enzymes, are provided elsewhere herein and are well known in the art. 25 1) Soluble Human PH20 . For example, soluble forms of recombinant human PH20 have been produced and can be used in the methods described herein for co-administration or co formulation with matrix degrading enzymes, activators, anesthetics, vasoconstrictors, other pharmacologic or therapeutic agents, or combinations thereof, to permit the 30 diffusion into tissues. The production of such soluble forms of PH20 is described in related Application Serial Nos. 11/065,716 and 11/238,171, and in Examples 12-15 below. Soluble forms include, but are not limited to, any having C-terminal truncations to generate polypeptides containing amino acid I to amino acid 347, 372, WO 2009/111083 PCT/US2009/001486 - 139 394, 413, 430, 447, 467, 477, 478, 479, 480, 481, 482 and 483 of the sequence of amino acids set forth in SEQ ID NO:232. When expressed in mammalian cells, the 35 amino acid N-terminal signal sequence is cleaved during processing, and the mature form of the protein is secreted. Thus, the mature soluble polypeptides contain 5 amino acids 36 to 347, 372, 394, 413, 430, 447, 467, 477, 478, 479, 480, 481, 482 and 483 of SEQ ID NO:232. Deletion mutants ending at amino acid position 477 to 483 (corresponding to the precursor polypeptide set forth in SEQ ID NO:232) exhibit higher secreted hyaluronidase activity than the full length GPI-anchored form. Hence, soluble forms include, but are not limited to, any having C-terminal 10 truncations to generate polypeptides containing amino acid 1 to amino acid 442, 443, 444, 445, 446 and 447 of the sequence of amino acids set forth in any of SEQ ID NOS 226-231, respectively, or allelic or species variants or other variants thereof. Generally soluble forms of PH20 are produced using protein expression systems that facilitate correct N-glycosylation to ensure the polypeptide retains activity, since 15 glycosylation is important for the catalytic activity and stability of hyaluronidases. Such cells include, for example Chinese Hamster Ovary (CHO) cells (e.g. DG44 CHO cells). 2) rHuPH20 Recombinant soluble forms of human PH20 have been generated and can be 20 produced and purified using the methods described herein. The generation of such soluble forms of recombinant human PH20 are described in related Application Serial Nos. 11/065,716 and 11/238,171, and in Examples 12-15 below. Exemplary of such a polypeptide are those generated from a nucleic acid molecule encoding amino acids 1 482 set forth in SEQ ID NO:225. The generation, production and purification of this 25 PH20 is described in Examples 12-15 below. Resulting purified rHuPH20 can be heterogeneous due to peptidases present in the culture medium upon production and purification. As produced in the culture medium there is heterogeneity at the C terminus so that the product, called rHuPH20, includes a mixture of species that can include any one or more of SEQ ID NOS. 226-231 in various abundance. Generally 30 soluble forms of PH20, such as rHuPH20, are produced using protein expression systems that facilitate correct N-glycosylation to ensure the polypeptide retains activity, since glycosylation is important for the catalytic activity and stability of WO 2009/111083 PCT/US2009/001486 -140 hyaluronidases. Such cells include, for example Chinese Hamster Ovary (CHO) cells (e.g. DG44 CHO cells). Hyaluronan degrading enzymes, such as any hyaluronidase, in particular a soluble PH20 such as rHuPH20, can be administered by any suitable route as 5 described elsewhere herein. Typically, administration is by parenteral administration, such as by intradermal, intramuscular, subcutaneous or intravascular administration. The compounds provided herein can be formulated for parenteral administration by injection, e.g., by bolus injection or continuous infusion. Formulations for injection can be presented in unit dosage form, e.g., in ampoules or in multi-dose containers, 10 with an added preservative. The compositions can be suspensions, solutions or emulsions in oily or aqueous vehicles, and can contain formulatory agents such as suspending, stabilizing and/or dispersing agents. Alternatively, the active ingredient can be in powder form for reconstitution with a suitable vehicle, e.g., sterile pyrogen free water or other solvents, before use. For example, provided herein are parenteral 15 formulations containing an effective amount of soluble PH20, such as 10 Units to 500,000 Units, 100 Units to 100,000 Units, 500 Units to 50,000 Units, 1000 Units to 10,000 Units, 5000 Units to 7500 Units, 5000 Units to 50,000 Units, or 1,000 Units to 10,000 Units, generally 10,000 to 50,000 Units, in a stabilized solution or suspension or a lyophilized from. The formulations can be provided in unit-dose forms such as, 20 but not limited to, ampoules, syringes and individually packaged tablets or capsules. The dispersing agent can be administered alone, or with other pharmacologically effective agents in a total volume of 1-100 ml, 1-50 ml, 10-50 ml, 10-30 ml, 1-20 ml, or 1-10 ml, typically 10-50 ml. In one example of a combination therapy, it is contemplated herein that a 25 anesthetic, vasoconstrictor and dispersion agent are co-administered or co-formulated with an activatable matrix-degrading enzyme and/or activator to be administered subsequently, simultaneously or intermittently therewith. An exemplary formulation is one containing lidocaine, epinephrine and a soluble PH20, for example, a soluble PH20 set forth in SEQ ID NO:226. Soluble PH20 can be mixed directly with 30 lidocaine (Xylocaine), and optionally with epinephrine. The formulation can be prepared in a unit dosage form, such as in a syringe. For example, the lidocaine/epinephrine/soluble PH20 formulation can be provided in a volume, such as WO 2009/111083 PCT/US2009/001486 - 141 1-100 ml, 1-50 ml, 10-50 ml, 10-30 ml, 1-20 ml, or 1-10 ml, typically 10-50 ml, prepackaged in a syringe for use. In the combination therapies, the other pharmacologic agents, such as a lidocaine/epinephrine/soluble PH20 formulation, can be co-administered together 5 with or in close temporal proximity to the administration of an activatable matrix degrading enzyme (and activator). Typically it is preferred that an anesthetic and/or dispersion agent be administered shortly before (e.g. 5 to 60 minutes before) or, for maximal convenience, together with the pharmacologic agent. As will be appreciated by those of skill in the art, the desired proximity of co-administration depends in 10 significant part on the effective half lives of the agents in the particular tissue setting, and the particular disease being treated, and can be readily optimized by testing the effects of administering the agents at varying times in suitable models, such as in suitable animal models. iv. Modifications of hyaluronan degrading enzymes to improve 15 their pharmacokinetic properties Hyaluronan degrading enzymes can be modified to improve their pharmacokinetic properties, such as increasing their half-life in vivo and/or activities. The modification of hyaluronan degrading enzymes for use in the compositions, combinations and/or methods provided can include attaching, directly or indirectly via 20 a linker, such as covalently or by other stable linkage, a polymer, such as dextran, a polyethylene glycol (pegylation(PEG)) or sialyl moiety, or other such polymers, such as natural or sugar polymers. Pegylation of therapeutics is known to increase resistance to proteolysis, increase plasma half-life, and decrease antigenicity and immunogenicity. Covalent or 25 other stable attachment (conjugation) of polymeric molecules, such as polyethylene glycol moiety (PEG), to the hyaluronan degrading enzyme thus can impart beneficial properties to the resulting enzyme-polymer composition. Such properties include improved biocompatibility, extension of protein (and enzymatic activity) half-life in the blood, cells and/or in other tissues within a subject, effective shielding of the 30 protein from proteases and hydrolysis, improved biodistribution, enhanced pharmacokinetics and/or pharmacodynamics, and increased water solubility. Exemplary polymers that can be conjugated to the hyaluronan degrading enzyme, include natural and synthetic homopolymers, such as polyols (i.e. poly-OH), WO 2009/111083 PCT/US2009/001486 - 142 polyamines (i.e. poly-NH2) and polycarboxyl acids (i.e. poly-COOH), and further heteropolymers i.e. polymers comprising one or more different coupling groups e.g. a hydroxyl group and amine groups. Examples of suitable polymeric molecules include polymeric molecules selected from among polyalkylene oxides (PAO), such as 5 polyalkylene glycols (PAG), including polypropylene glycols (PEG), methoxypolyethylene glycols (mPEG) and polypropylene glycols, PEG-glycidyl ethers (Epox-PEG), PEG-oxycarbonylimidazole (CDI-PEG) branched polyethylene glycols (PEGs), polyvinyl alcohol (PVA), polycarboxylates, polyvinylpyrrolidone, poly-D,L-amino acids, polyethylene-co-maleic acid anhydride, polystyrene-co-maleic 10 acid anhydride, dextrans including carboxymethyl-dextrans, heparin, homologous albumin, celluloses, including methylcellulose, carboxymethylcellulose, ethylcellulose, hydroxyethylcellulose, carboxyethylcellulose and hydroxypropylcellulose, hydrolysates of chitosan, starches such as hydroxyethyl starches and hydroxypropyl-starches, glycogen, agaroses and derivatives thereof, guar 15 gum, pullulan, inulin, xanthan gum, carrageenan, pectin, alginic acid hydrolysates and bio-polymers. Typically, the polymers are polyalkylene oxides (PAO), such as polyethylene oxides, such as PEG, typically mPEG, which, in comparison to polysaccharides such as dextran, pullulan and the like, have few reactive groups capable of cross-linking. 20 Typically, the polymers are non-toxic polymeric molecules such as (m)polyethylene glycol (mPEG) which can be covalently conjugated to the hyaluronan degrading enzyme (e.g., to attachment groups on the protein surface) using a relatively simple chemistry. Suitable polymeric molecules for attachment to the hyaluronan degrading 25 enzyme include, but are not limited to, polyethylene glycol (PEG) and PEG derivatives such as methoxy-polyethylene glycols (mPEG), PEG-glycidyl ethers (Epox-PEG), PEG-oxycarbonylimidazole (CDI-PEG), branched PEGs, and polyethylene oxide (PEO) (see e.g. Roberts et al., Advanced Drug Delivery Review 2002, 54: 459-476; Harris and Zalipsky, S (eds.) "Poly(ethylene glycol), Chemistry 30 and Biological Applications" ACS Symposium Series 680, 1997; Mehvar et al., J Pharm. Pharmaceut. Sci., 3(1):125-136, 2000; Harris, Nature Reviews 2:215 et seq. (2003); and Tsubery, JBiol. Chem 279(37):38118-24, 2004). The polymeric molecule can be of a molecular weight typically ranging from about 3 kDa to about WO 2009/111083 PCT/US2009/001486 - 143 60 kDa. In some embodiments the polymeric molecule that is conjugated to a protein, such as rHuPH20, has a molecular weight of 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60 or more than 60 kDa. Various methods of modifying polypeptides by covalently attaching 5 (conjugating) a PEG or PEG derivative (i.e. "PEGylation") are known in the art (see e.g., U.S. Patent Nos. 5,672,662 and U.S. 6,737,505; and U.S. Publication Nos. 2006/0104968 and 2004/0235734). Techniques for PEGylation include, but are not limited to, specialized linkers and coupling chemistries (see e.g., Harris, Adv. Drug Deliv. Rev. 54:459-476, 2002), attachment of multiple PEG moieties to a single 10 conjugation site (such as via use of branched PEGs; see e.g., Veronese et al., Bioorg. Med. Chem. Lett. 12:177-180, 2002), site-specific PEGylation and/or mono PEGylation (see e.g., Chapman et al., Nature Biotech. 17:780-783, 1999), and site directed enzymatic PEGylation (see e.g., Sato, Adv. Drug Deliv. Rev., 54:487-504, 2002) (see, also, for example, Lu and Felix (1994) Int. J Peptide Protein Res. 15 43:127-138; Lu and Felix (1993) Peptide Res. 6:142-6, 1993; Felix et al. (1995) Int. J. Peptide Res. 46:253-64; Benhar et al. (1994) J. Biol. Chem. 269:13398-404; Brumeanu et al. (1995) JImmunol. 154:3088-95; see also, Caliceti et al. (2003) Adv. Drug Deliv. Rev. 55(10):1261-77 and Molineux (2003) Pharmacotherapy 23 (8 Pt 2):3S-8S). Methods and techniques described in the art can produce proteins having 20 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more than 10 PEG or PEG derivatives attached to a single protein molecule (see e.g., U.S. Publication No. 2006/0104968). Numerous reagents for PEGylation have been described in the art. Such reagents include, but are not limited to, N-hydroxysuccinimidyl (NHS) activated PEG, succinimidyl mPEG, mPEG2-N-hydroxysuccinimide, mPEG succinimidyl 25 alpha-methylbutanoate, mPEG succinimidyl propionate, mPEG succinimidyl butanoate, mPEG carboxymethyl 3-hydroxybutanoic acid succinimidyl ester, homobifunctional PEG-succinimidyl propionate, homobifunctional PEG propionaldehyde, homobifunctional PEG butyraldehyde, PEG maleimide, PEG hydrazide, p-nitrophenyl-carbonate PEG, mPEG-benzotriazole carbonate, 30 propionaldehyde PEG, mPEG butryaldehyde, branched mPEG2 butyraldehyde, mPEG acetyl, mPEG piperidone, mPEG methylketone, mPEG "linkerless" maleimide, mPEG vinyl sulfone, mPEG thiol, mPEG orthopyridylthioester, mPEG orthopyridyl disulfide, Fmoc-PEG-NHS, Boc-PEG-NHS, vinylsulfone PEG-NHS, WO 2009/111083 PCT/US2009/001486 - 144 acrylate PEG-NHS, fluorescein PEG-NHS, and biotin PEG-NHS (see e.g., Monfardini et al., Bioconjugate Chem. 6:62-69, 1995; Veronese et al., J. Bioactive Compatible Polymers 12:197-207, 1997; U.S. 5,672,662; U.S. 5,932,462; U.S. 6,495,659; U.S. 6,737,505; U.S. 4,002,531; U.S. 4,179,337; U.S. 5,122,614; U.S. 5 5,183,550; U.S. 5,324, 844; U.S. 5,446,090; U.S. 5,612,460; U.S. 5,643,575; U.S. 5,766,581; U.S. 5,795, 569; U.S. 5,808,096; U.S. 5,900,461; U.S. 5,919,455; U.S. 5,985,263; U.S. 5,990, 237; U.S. 6,113,906; U.S. 6,214,966; U.S. 6,258,351; U.S. 6,340,742; U.S. 6,413,507; U.S. 6,420,339; U.S. 6,437,025; U.S. 6,448,369; U.S. 6,461,802; U.S. 6,828,401; U.S. 6,858,736; U.S. 2001/0021763; U.S. 2001/0044526; 10 U.S. 2001/0046481; U.S. 2002/0052430; U.S. 2002/0072573; U.S. 2002/0156047; U.S. 2003/0114647; U.S. 2003/0143596; U.S. 2003/0158333; U.S. 2003/0220447; U.S. 2004/0013637; US 2004/0235734; U.S. 2005/000360; U.S. 2005/0114037; U.S. 2005/0171328; U.S. 2005/0209416; EP 01064951; EP 0822199; WO 00176640; WO 0002017; WO 0249673; WO 9428024; and WO 0187925). 15 In one example, the hyaluronan degrading enzyme for use in the methods, compostions, and combinations provided is a soluble hyaluronidase that is PEGylated. In a particular example, the soluble hyaluronidase is a PEGylated PH20 hyaluronidase. In another particular example, the soluble hyaluronidase is PEGylated rHuPH20. 20 G. Packaging and Articles of Manufacture of Activatable Matrix-Degrading Enzymes Pharmaceutical compounds of selected matrix-degrading enzymes or nucleic acids encoding selected matrix-degrading enzymes, or a derivative or variant thereof can be packaged as articles of manufacture containing packaging material, a 25 pharmaceutical composition which is effective for treating the disease or disorder, and a label that indicates that selected matrix-degrading enzyme or nucleic acid molecule is to be used for treating the disease or disorder. Combinations of a selected matrix degrading enzyme, or derivative or variant thereof and an activator also can be packaged in an article of manufacture. 30 The articles of manufacture provided herein contain packaging materials. Packaging materials for use in packaging pharmaceutical products are well known to those of skill in the art. See, for example, U.S. Patent Nos. 5,323,907, 5,052,558 and 5,033,252, each of which is incorporated herein in its entirety. Examples of WO 2009/111083 PCT/US2009/001486 - 145 pharmaceutical packaging materials include, but are not limited to, blister packs, bottles, tubes, inhalers, pumps, bags, vials, containers, syringes, bottles, and any packaging material suitable for a selected formulation and intended mode of administration and treatment. The articles of manufacture can include a needle or 5 other injection device so as to facilitate administration (e.g. sub-epidermal administration) for local injection purposes. A wide array of formulations of the compounds and compositions provided herein are contemplated as are a variety of treatments for any ECM-mediated disease or disorder. The choice of package depends on the matrix-degrading enzyme and activator, 10 and whether such compositions will be packaged together or separately. In general, the packaging is non-reactive with the compositions contained therein such that activation of the activatable matrix-degrading enzyme does not occur prior to addition of the activator. In one example, the activatable matrix-degrading enzyme can be packaged as a mixture with the activator. Thus, for example, a lysosomal enzyme 15 (e.g., cathepsin L) that requires low pH for activation can be packaged as a mixture with a buffered acidic solution. In another example, the components can be packaged as separate compositions that, upon mixing, result in activation of the matrix-degrading enzyme. For example, a composition containing a matrix-degrading enzyme can be provided separately 20 from, and for use with, a separate composition containing an activator, such as a buffered acidic solution. Thus, in such examples, the activatable matrix-degrading enzyme is packaged in a separate container from the activator, and activation is achieved by exposure to the activator at the users will. Exposure to the activator can occur at any time preceding administration by addition of the activator to the enzyme. 25 For example, the container can have a single compartment containing the matrix degrading enzyme and being amenable to addition of the activator by the user, for example through an opening in the compartment. Any container or other article of manufacture that is amenable to having a defining space for containment of the matrix-degrading enzyme and that is amenable to simple manipulation to permit 30 addition of the final components necessary for activation is contemplated. The activator is added prior to use. Exposure to the activator also can occur following administration to the interstitium. For example, if heat is the activator, a matrix degrading enzyme can be administered and the local injection site subjected to heat.

WO 2009/111083 PCT/US2009/001486 - 146 In an alternate example, an acidic buffered solution can be administered to the interstitium followed by administration of a matrix-degrading enzyme, for example any requiring acidic pH for activation such as a cathepsin. In other examples, the activatable matrix-degrading enzyme is packaged in a 5 container with the activator such that activation of the matrix-degrading enzyme is amenable to activation by the user at will in the container. Generally, examples of such containers include those that have an enclosed, defined space that contains the matrix-degrading enzyme, and a separate enclosed, defined space containing the activator such that the two spaces are separated by a readily removable membrane 10 which, upon removal, permits the components to mix and thereby react, resulting in activation of the protease. Any container or other article of manufacture is contemplated, so long as the matrix-degrading enzyme is separated from the activator. Exposure of the activator to the matrix-degrading enzyme is prior to use. For example, the physical separation means are those that are readily removed by the user, 15 to permit mixing, resulting in activation of the enzyme. For example, an article of manufacture can contain a matrix-degrading enzyme in one compartment and an activator in an adjacent compartment. The compartments are separated by a dividing member, such as a membrane, that, upon compression of the article or manufacture ruptures permitting separated components to mix. For suitable embodiments see e.g, 20 containers described in U.S. Patent Nos. 3,539,794 and 5,171,081. Following are some examples of the packaging requirements of various end uses of activatable matrix-degrading enzymes. These are offered as examples only and in no way are intended as limiting. 1. Single Chamber Apparatus 25 Among the simplest embodiments herein, are those in which the apparatus contains a single chamber or container and, if needed, -ejection means. Single chamber housings or containers include any item in which a matrix-degrading enzyme is included in the container. The matrix-degrading enzyme is housed in the vessel in liquid phase or as a powder or other paste or other convenient composition. The 30 activator component is introduced just prior to use. Prior to use the activator, typically provided as a buffered solution, is added and contacted with the matrix degrading enzyme to permit mixing and/or reconstitution of the matrix-degrading enzyme. For example, when desired and depending on the matrix-degrading enzyme, WO 2009/111083 PCT/US2009/001486 - 147 a liquid containing Ca 2 +, such as a mixture containing the Ca 2 + in an appropriate buffer, or an acidic buffered solution, or other solution containing an activating condition, is added to the container. Kits containing the item and the activator also are provided. 5 2. Dual Chamber Apparatus An example of an apparatus contemplated for use herein is a dual chamber container. In general, this apparatus has two chambers or compartments thereby maintaining the matrix-degrading enzyme separate from the activator until activation is desired. The apparatus can include a mixing chamber to permit mixing of the 10 components prior to dispensing from the apparatus. Alternatively, mixing can occur by ejection of the activator from one chamber into a second chamber containing the activatable matrix-degrading enzyme. For example, the activatable matrix-degrading enzyme can be provided in lyophilized form, and reconstitution can be achieved by ejection of the activator, such as an acidic buffered solution, from a first chamber into 15 the second chamber containing the lyophilized enzyme. In one embodiment, a dual chamber apparatus employs a mechanical pump mechanism in it operation. In such an example, the dispensing apparatus maintains the components in separate chambers. A pump mechanism operated to withdraw the contents from each chamber and into a mixing chamber, or from one chamber into the 20 second chamber. Upon mixing, the mixed composition is activated by reaction of the components in the chambers. The pump mechanism can be manually operated, for example, by a plunger. Exemplary of such dual chamber apparatus include dual chamber syringes (see e.g., U.S. Patent Nos. 6,972,005, 6,692,468, 5,971,953, 4,529,403, 4,202,314, 4,214,584, 4,983,164, 5,788,670, 5,395,326; and International 25 Patent Application Nos. W02007006030 and W02001047584). Another embodiment of a dual chamber fluid dispensing apparatus contemplated for use herein takes the form of a compressible bottle or tube or other similar device. The device has two compartments within it that keep the components separated. The cap of the device can serve as a mixing chamber, a mixing chamber 30 can be positioned between the two chambers and the cap, or mixing can be achieved within one of the chambers. The components are forced by compression from the separate compartments into the mixing chamber. They are then dispensed from the mixing chamber. For example, the mixed contents can be removed from the device WO 2009/111083 PCT/US2009/001486 - 148 by attaching a plunger/syringe apparatus to the dispensing end and withdrawing the contents therethrough. Such devices are known in the art (see e.g., International Patent Application. No. W01994015848). 3. Kits 5 Selected matrix-degrading enzymes, activators and/or articles of manufacture thereof also can be provided as kits. Kits can include a pharmaceutical composition described herein and an item for administration provided as an article of manufacture. For example a selected matrix-degrading enzyme can be supplied with a device for administration, such as a syringe, an inhaler, a dosage cup, a dropper, or an applicator. 10 The compositions can be contained in the item for administration or can be provided separately to be added later. Generally, kits contain an item with a matrix-degrading enzyme, and an activator composition containing the activating condition. The kit can, optionally, include instructions for application including dosages, dosing regimens and instructions for modes of administration. Kits also can include a 15 pharmaceutical composition described herein and an item for diagnosis. For example, such kits can include an item for measuring the concentration, amount or activity of the selected protease in a subject. H. Methods of Assessing Activity of Matrix-Degrading Enzymes 1. Methods of Assessing Enzymatic Activity 20 Activatable matrix-degrading enzymes can be tested for their enzymatic activity against known substrates. Activity assessment can be performed in the presence or absence of an activator. Activity assessment also can be performed under varying conditions, for example, by varying the amount of activator used for activation. In one example, pH profiles can be be performed to determine the relative 25 activity of an enzyme under various pH conditions (see e.g., Dehrmann et al. (1995) Arch. Biochm. Biophys., 324:93-98). Activity assessments can be performed on conditioned medium or other supernatants or on purified protein. Enzymatic activity can be assessed by assaying for substrate cleavage using known substrates of the enzyme. The substrates can be in the form of a purified 30 protein or provided as peptide substrates. For example, enzymatic activity of cathepsin L can be assessed by cleavage of purified proteins like Azocasein, collagen, elastin, human serum albumin and rHuPH20 either by incubating them individually with the ADME or as a mixture of two or more purified proteins. Cleavage of a WO 2009/111083 PCT/US2009/001486 - 149 purified protein by an enzyme can be assessed using any method of protein detection, including, but not limited to, HPLC, CE, Mass spectrometry, SDS-PAGE analysis, ELISA, Western blotting, immunohistochemistry, immunoprecipitation, NH2 terminal sequencing, and protein labeling. 5 The use of fluorogenic groups on the substrates facilitates detection of cleavage. For example, substrates can be provided as fluorogenically tagged tetrapeptides of the peptide substrate, such as an ACC- or 7-amino-4-methyl courmarin (AMC)-tetrapeptide. Other fluorogenic groups are known and can be used and coupled to protein or peptide substrates. These include, for example, 7-amino-4 10 methyl-2-quinolinone (AMeq), 2-naphthylamine (NHNap) and 7-amino-4 methylcoumarin (NHMec) and fluorescein-5-isothiocyanate (FITC) (Sarath et al. "Protease Assay Methods," in Proteolytic Enzymes: A Practical Approach. Ed. Robert J. Beynon and Judith S. Bond. Oxford University Press, 2001. pp. 45-76). Peptide substrates are known to one of skill in the art, as are exemplary fluorogenic 15 peptide substrates. For example, exemplary substrates for cathepsin B include, N aBZ-Phe-Val-Arg-p-NA, DNA-Phe-Arg-Nph-Leu, Z-Ala-Arg-Arg-F 3 MCA, Z-Arg Arg-MBNA, Z-Arg-Arg-NHMec, Z-Phe-Arg-NHMec, and Z-Leu-Arg-AMC and variations thereof such as with different flurogenic groups. In another example, an exemplary substrate for cathepsin L includes Z-Phe-Arg-NHMec and Z-Leu-Arg 20 AMC, and Z-His-Arg-Tyr-Arg-AMC, and variations thereof such as with different fluorgenic groups. Thus, since cathepsin B and cathepsin L share the same substrate, for example, Z-Phe-Arg-NHMec and Z-Leu-Arg-AMC, activity assessment of cathepsin L can be performed in the presence of a specific inhibitor to cathepsin B. Exemplary of such an inhibitor is CA-074. This is exemplified in Example 9 herein. 25 Enzymes assays to measure enzymatic activity by fluorescence intensity are standard, and are typically performed as a function of incubation time of the enzyme and substrate (see e.g., Dehrmann et al. (1995) Arch. Biochem. Biophys., 324:93-98; Barrett et al. (1981) Methods Enzymol., 80:536-561). While detection of fluorogenic compounds can be accomplished using a 30 fluorometer, detection can be accomplished by a variety of other methods well known to those of skill in the art. Thus, for example, when the fluorophores emit in the visible wavelengths, detection can be simply by visual inspection of fluorescence in response to excitation by a light source. Detection also can be by means of an image WO 2009/111083 PCT/US2009/001486 - 150 analysis system utilizing a video camera interfaced to a digitizer or other image acquisition system. Detection also can be by visualization through a filter, as under a fluorescence microscope. The microscope can provide a signal that is simply visualized by the operator. Alternatively, the signal can be recorded on photographic 5 film or using a video analysis system. The signal also can simply be quantified in real time using either an image analysis system or a photometer. Thus, for example, a basic assay for enzyme activity of a sample involves suspending or dissolving the sample in a buffer (at the pH and ionic strength optima of the particular protease being assayed) adding to the buffer a fluorogenic enzyme 10 peptide indicator, and monitoring the resulting change in fluorescence using a spectrofluorometer at a specific temperature for incubation as shown in e.g., Harris et al., (1998) JBiol Chem 273:27364. The spectrofluorometer is set to excite the fluorophore at the excitation wavelength of the fluorophore and detect signal at the emission wavelength of the fluorophore. The fluorogenic enzyme indicator is a 15 substrate sequence of a enzyme (e.g. of a protease) that changes in fluorescence due to a protease cleaving the indicator. Enzymatic activity is typically expressed as standard units/ml based on a calibration curve generated with varying concentration of the fluorogenic substrate, and specific activity is represented as units/mg protein. 2. Methods of Assessing ECM Degradation 20 The degradation of extracellular matrix proteins by matrix-degrading enzymes, including, but not limited to, those described above, such as cathepsin L, can be assessed in vitro or in vivo.. Assays for such assessment are known to those of skill in the art, and can be used to test the activities of a variety of matrix-degrading enzymes on a variety of extracellular matrix proteins, including, but not limited to 25 collagen (I, II, III and IV), fibronectin, vitronectin and proteoglycans. a. In vitro assays Exemplary in vitro assays include assays to assess the degradation products of extracellular matrix proteins following incubation with a matrix-degrading enzyme. In some examples, the assays detect a single, specific degradation product. In other 30 examples, the assays detect multiple degradation products, the identity of which may or may not be known. Assessment of degradation products can be performed using methods well known in the art including, but not limited to, HPLC, CE, Mass spectrometry, SDS-PAGE analysis, ELISA, Western blotting, immunohistochemistry, WO 2009/111083 PCT/US2009/001486 - 151 immunoprecipitation, NH2-terminal sequencing, and protein labeling. Extracellular matrix degradation products can be visualized, for example, by SDS-PAGE analysis following incubation with matrix-degrading enzymes for an appropriate amount of time at an appropriate temperature. For example, collagen can be incubated with 5 activated cathepsin L and subjected to SDS-PAGE using, for example, a 4-20% Tris/glycine gel to separate the products. Coomassie staining of the gel facilitates visualization of smaller degradation products, or disappearance of collagen bands, compared to intact collagen. Immunoblotting using, for example, a polyclonal Ig specific to the extracellular matrix protein also can be used to visualize the 10 degradation products following separation with SDS-PAGE. Assays that specifically detect a single product following degradation of an extracellular matrix protein also are known in the art and can be used to assess the ability of a matrix-degrading enzyme to degrade an extracellular matrix protein. For example, the hydroxyproline (HP) assay can be used to measure degradation of 15 collagen. 4-hydroxyproline is a modified imino acid that makes up approximately 12% of the weight of collagen. HP assays measure the amount of solubilized collagen by determining the amount of HP in the supernatant following incubation with a matrix-degrading enzyme, such as activated cathepsin L (see e.g., Example 2, below, and Reddy and Enwemeka (1996) Clinical Biochemistry 29:225-229). Measurement 20 of HP can be effected by, for example, colorimetric methods, high performance liquid chromatography, mass spectrometry and enzymatic methods (see e.g., Edwards et al., (1980) Clin. Chim. Acta 104:161-167; Green (1992) Anal. Biochem. 201:265-269; Tredget et al., (1990) Anal. Biochem. 190:259-265; Ito et al., (1985) Anal. Biochem. 151:510-514; Garnero et al. (1998) J Biol. Chem 273:32347-32352). 25 The collagen source used in such in vitro assays can include, but is not limited to, commercially available purified collagen, bone particles, skin, cartilage and rat tail tendon. Collagenolytic activity of a matrix-degrading enzyme such as cathepsin L can be assessed by incubating the activated enzyme with an insoluble collagen suspension, followed by hydrolysis, such as with HCl. The amount of hydroxyproline 30 derived from the solubilized (degraded) collagen can be determined by spectrophotometric methods, such as measuring the absorbance at 550 nm following incubation with Ehrlich's reagent. In some examples, the collagen source is rat or pig skin explant that is surgically removed from anesthetized animals and then perfused WO 2009/111083 PCT/US2009/001486 - 152 with first an acidic solution and then the matrix-degrading enzyme, such as cathepsin L (see e.g. Examples 3-4, below). HP levels in the perfusates can then be assessed. In a modification of this method, the effect of, for example, cathepsin L on the fibrous septae in the explants can be assessed (see e.g. Example 5). Briefly, following 5 perfusion with the matrix degrading enzyme, the explants are cut into small pieces and embedded in paraffin and analyzed by microscopy following Masson's Trichrome staining for visualization of collagen. The number of collagen fibrous septae can be visualized and compared to tissue that has not been treated with a matrix degrading enzyme. 10 Assays to detect degradation of specific collagens also are known in the art. Such assays can employ immunological methods to detect a degradation product unique to the specific collagen. For example, the degradation of collagen I by some matrix-degrading enzymes releases telopeptides with different epitopes that can be detected using immunoassays. Such assays detect the cross-linked N-telopeptides 15 (NTx) and the cross-linked C-telopeptides (CTx and ICTP), each of which contain unique epitopes. Typically, CTx assays utilize the CrossLaps (Nordic Biosciences) antibodies that recognize the 8 amino acid sequence EKAHD-#-GGR octapeptide, where the aspartic acid is in -isomerized configuration, in the C-terminal telopeptide region of the al chain (Eastell (2001) Bone Markers: Biochemical and Clinical 20 Perspectives, pg 40). Immunoassays to detect ICTP also are known in the art and can be used to detect degradation of collagen I (US Patent No. 5,538,853). In other examples, immunoassays, such as, for example, ELISAs, can be used to detect NTx following incubation of collagen type I with proteases such as Cathepsins K, S, L and B (Atley et al., (2000) Bone, 26:241-247). Other antibodies and assays specific for 25 degraded collagens are known in the art and can be used to detect degradation by matrix-degrading enzymes. These include antibodies and assays specific for degraded collagen I (Hartmann et al (1990) Clin. Chem. 36:421-426), collagen II (Hollander et al (1994) J. Clin. Invest. 93:1722-1732), collagen III (U.S. Patent No. 5,34,2756), and collagen IV (Wilkinson et al (1990) Anal. Biochem. 185:294-6). 30 b. In vivo assays Assays to detect the in vivo degradation of ECM also are known in the art. Such assays can utilize the methods described above to detect, for example, hydroxyproline and N- and C-telopeptides and degraded collagens or other ECM in WO 2009/111083 PCT/US2009/001486 - 153 biological samples such as urine, blood, serum and tissue. Detection of degraded ECM can be performed following administration to the patient of one or more matrix degrading enzymes. Detection of pyridinoline (PYD) and deoxypyridinoline (DPYD), also can be used to assess degradation of collagen. Also known as 5 hydroxylysylpyridinoline and lysylpyridinoline, respectively, PYD and DPYD are the two nonreducible trivalent cross-links that stabilize type I collagen chains and are released during the degradation of mature collagen fibrils. Pyridinoline is abundant in bone and cartilage, whereas deoxypyridinoline is largely confined to bone. Type III collagen also contains pyridinoline cross-links at the amino terminus. Total PYD and 10 DPYD can be measured, for example, in hydrolyzed urine samples or serum by fluorimetric detection after reversed-phase HPLC (Hata et al (1995) Clin. Chimica. Acta. 235:221-227). c. Non-human animal models Non-human animal models can be used to assess the activity of matrix 15 degrading enzymes. For example, non-human animals can be used as models for a disease or condition. Non-human animals can be injected with disease and/or phenotype-inducing substances prior to administration of matrix-degrading enzymes. Genetic models also are useful. Animals, such as mice, can be generated which mimic a disease or condition by the overexpression, underexpression or knock-out of 20 one or more genes. For example, animal models are known in the art for conditions including, but not limited to, Peyronie's Disease (Davila et al. (2004) Biol. Reprod., 71:1568-1577), tendinosis (Warden et al., (2006) Br. J. Sports Med. 41:232-240) and scleroderma (Yamamoto (2005) Cur. Rheum. Rev. 1:105-109). Non-human animals also can be used to test the activity of matrix-degrading 25 enzymes in vivo in a non-diseased animal. For example, matrix-degrading enzymes can be administered to, non-human animals, such as, a mouse, rat or pig, and the level of ECM degradation can be determined. In some examples, the animals are used to obtain explants for ex vivo assessment of ECM degradation, such as that described above and in Examples 3-5, below. In other examples, ECM degradation is assessed 30 in vivo. In one example, collagen degradation of the skin of anesthetized rats is assessed (see e.g. Example 6 below). Briefly, a matrix degrading enzyme, such as cathepsin L in a buffer with a pH of 5, is perfused via insertion of a needle into the dermal layer of the skin of the tail. Perfusate fractions are collected from the tail skin WO 2009/111083 PCT/US2009/001486 - 154 and analyzed for collagen degradation by hydroxyproline analysis. Other methods can be used to detect degradation including, but not limited to, any of the assays described above, such as immunoassays to detect specific degradation products. The effect of administering an acidic solution, such as the buffer containing cathepsin L that 5 facilitates optimal activity, to the skin also can be assessed in a non-human animal model (see e.g. Example 7). Dyes sensitive to pH change, such as phenol red, can be used for these purposes. I. Exemplary Methods of Treating Diseases or Defects of ECM The activatable matrix degrading enzymes provided herein can be used for 10 treatment of any condition mediated by any one or more ECM components. This section provides exemplary uses of, and administration methods for, activatable matrix-degrading enzymes. These described therapies are exemplary and do not limit the applications of enzymes. Such methods include, but are not limited to, methods of treatment of any ECM condition or disease that is caused by excess, aberrant or 15 accumulated expression of any one or more ECM component. Exemplary of diseases or conditions to be treated are any mediated by collagen, elastin, fibronectin, or a glycosaminoglycan such as a proteoglycan. For example, exemplary of collagen mediated diseases or disorders include, but are not limited to, cellulite, Dupuytren's disease (also called Dupuytren's contracture), Peyronie's disease, frozen shoulder, 20 chronic tendinosis or scar tissue of the tendons, localized scleroderma and lymphedema. It is within the skill of a treating physician to identify such diseases or conditions. The particular disease or condition to be treated dictates the activatable matrix-degrading enzyme that is selected. For example, treatment of a collagen 25 mediated disease or disorder can be effected by administration of matrix-degrading enzyme that cleaves collagen. Such matrix-degrading enzymes are listed above in Table 3, and/or known to one of skill in the art. Activatable matrix-degrading enzymes, and systems and methods for activation can be chosen accordingly to treat a particular disease or condition. For example, cathepsins of the cysteine and aspartic 30 families can be made temporally active by acidic pH conditions as described herein. Thus, in one example, a cathepsin that cleaves a collagen, for example, cathepsin L, can be administered in the presence of an activating condition, such as acidic pH, to treat a collagen-mediated disease or condition.

WO 2009/111083 PCT/US2009/001486 - 155 Treatment of diseases and conditions with activatable matrix-degrading enzymes can be effected by any suitable route of administration using suitable formulations as described herein including, but not limited to, subcutaneous injection, intramuscular, intradermal, oral, and topical and transdermal administration. As 5 described above, a route of administration of activatable matrix-degrading enzymes typically is chosen that results in administration under the skin directly to the affected site. Exemplary of such routes of administration include, but are not limited to, subcutaneous, intramuscular, or intradermal. If necessary, a particular dosage and duration and treatment protocol can be 10 empirically determined or extrapolated. For example, exemplary doses of recombinant and native active matrix-degrading enzymes or activatable matrix degrading enzymes can be used as a starting point to determine appropriate dosages. Dosage levels can be determined based on a variety of factors, such as body weight of the individual, general health, age, the activity of the specific compound employed, 15 sex, diet, time of administration, rate of excretion, drug combination, the severity and course of the disease, and the patient's disposition to the disease and the judgment of the treating physician. The amount of active ingredient that can be combined with the carrier materials to produce a single dosage form will vary depending upon the particular matrix-degrading enzyme, the host treated, the particular mode of 20 administration, and the activating condition required for activation, and/or the predetermined or length of time in which activation is desired. The pharmaceutical compositions typically should provide a dosage of from about I ptg/ml to about 20 mg/ml. Generally, dosages are from or about 10 pg/ml to 1 mg/ml, typically about 100 pg/ml, per single dosage administration. It is understood that the amount to 25 administer will be a function of the activatable matrix-degrading enzyme and the activating condition chosen, the indication treated, and possibly side effects that will be tolerated. Dosages can be empirically determined using recognized models for each disorder. Also, as described elsewhere herein, activatable matrix-degrading enzymes can be administered in combination with other agents sequentially, 30 simultaneously or intermittently. Exemplary of such agents include, but are not limited to, lidocaine, epinephrine, a dispersing agent such as hyaluronidase and combinations thereof.

WO 2009/111083 PCT/US2009/001486 - 156 Upon improvement of a patient's condition, a maintenance dose of a compound or compositions can be administered, if necessary; and the dosage, the dosage form, or frequency of administration, or a combination thereof can be modified. In some cases, a subject can require intermittent treatment on a long-term 5 basis upon any recurrence of disease symptoms. Descriptions of the involvement of collagen to collagen-mediated diseases or conditions is provided below as an example of the role of ECM components in diverse disease and conditions. Such descriptions are meant to be exemplary only and are not limited to a particular activatable matrix-degrading enzyme or to a particular ECM 10 mediated diseases or conditions. One of skill in the art can select an activatable matrix-degrading enzyme and activating condition for activation thereof, to be used in the treatment of any desired ECM-mediated disease, based on the ability of a particular enzyme to cleave or degrade an ECM component involved in the particular disease or condition. The particular treatment and dosage can be determined by one 15 of skill in the art. Considerations in assessing treatment include, for example, the disease to be treated, the ECM component involved in the disease, the severity and course of the disease, whether the activatable matrix-degrading enzyme is administered for preventive or therapeutic purposes, previous therapy, the patient's clinical history and response to therapy, and the discretion of the attending physician. 20 1. Collagen-mediated Diseases or Conditions Collagen is a major structural constituent of mammalian organisms and makes up a large portion of the total protein content of the skin and other parts of the animal body. Numerous diseases and conditions are associated with excess collagen deposition, for example, due to erratic accumulation of fibrous tissue rich in collagen 25 or other causes. Collagen-mediated diseases or conditions (also referred to as fibrotic tissue disorders) are known to one of skill in the art (see e.g., published U.S. Application No. 20070224183; U.S. Patent Nos. 6,353,028; 6,060,474; 6,566,331; 6,294,350). Excess collagen has been associated with diseases and conditions, such as, but not limited to, fibrotic diseases or conditions resulting in scar formation, 30 cellulite, Dupuytren's syndrome, Peyronie's disease, frozen shoulder, localized scleroderma, lymphedema, Interstitial cystitis (IC), Telangrectase, Barrett's metaplasia, Pneumatosis cytoides intestinalis, collagenous colitis. For example, disfiguring conditions of the skin, such as wrinkling, cellulite formation and WO 2009/111083 PCT/US2009/001486 - 157 neoplastic fibrosis result from excessive collagen deposition, which produces unwanted binding and distortion of normal tissue architecture. Activatable matrix-degrading enzymes described herein, including but not limited to cathepsin L, can be used to treat collagen-mediated diseases or conditions. 5 Exemplary of activatable matrix degrading enzymes for treatment of diseases and conditions described herein are those that are active at neutral pH, and require sustained acidic conditions for activity. For example, temporary acidification of the extracellular matrix, such as the skin interstitium, can be achieved by infusing a buffered acidic solution directly at the affected site. In one example, a buffered acid 10 solution can be administered via sub-epithelium administration, i.e. under the skin, such that administration is effected directly at the site where ECM components are present and accumulated. Other methods of activation can be employed, and are known to one of skill in the art in view of the descriptions herein. a. Cellulite 15 Activatable matrix-degrading enzymes, such as those described herein, including cathepsin L, can be used to treat cellulite. In normal adipose tissues, a fine mesh of blood vessels and lymph vessels supplies the tissue with necessary nutrients and oxygen, and takes care of the removal of metabolized products. For example, triglycerides are stored in individual adipocytes that are grouped into capillary rich 20 lobules. Each fat lobule is composed of adipocytes. Vertical strands of collagen fibers named fibrous septae separate the fat lobules and tether the overlying superficial fascia to the underlying muscle. Cellulite is typically characterized by dermal deterioration due to a breakdown in blood vessel integrity and a loss of capillary networks in the dermal and subdermal 25 levels of the skin. The vascular deterioration tends to decrease the dermal metabolism. This decreased metabolism hinders protein synthesis and repair processes, which results in dermal thinning. The condition is further characterized by fat cells becoming engorged with lipids, swelling and clumping together, as well as excess fluid retention in the dermal and subdermal regions of the skin. The 30 accumulation of fat globules or adipose cells creates a need for a bigger blood supply to provide extra nourishment. To provide the blood to tissues, new capillaries are formed, which release more filtrate resulting in a saturation of tissues with interstitial fluid causing edema in the adipose tissues. Abundant reticular fibers in the interstitial WO 2009/111083 PCT/US2009/001486 - 158 tissues accumulate and thicken around the aggregated adipose cells; they form capsules or septa, which gradually transform into collagen fibers and are felt as nodules. The formation of these septa further occludes fat cells. Collagen fibers are also laid down in the interstitial tissue spaces, rendering the connective tissue sclerotic 5 (hard). Hence, as the condition further progresses, hard nodules of fat cells and clumps of fats surrounded by septa form in the dermal region. This leads to the surface of the skin displaying considerable heterogeneity and being characterized as having a "cottage cheese" or "orange peel" appearance. The dimpling occurs when 10 the fibrous septae that connect the skin to the dermis and deeper tissue layers tighten and pull in the skin. Thus, the "orange peel" appearance of cellulite is due to the deformation of the fat lobules as a result of outward forces on the adipose tissue. The fat lobules can be large, for example up to 1 cm wide, and easily protrude into the overlying dermis, causing a visible deformation on the surface of the skin. The net 15 result is the undulating appearance of the out er skin as the fat pushes upwards. As the connective septae run in the same direction as these outward forces, they can offer no counter force to keep the adipose from protruding into the dermis. Cellulite is more prevalent among females than males. The prevalence of cellulite is estimated between 60% and 80% of the female population and its severity 20 tends to worsen with obesity. Recently, a published study showed by in vivo magnetic resonance imaging that women with cellulite have a higher percentage of perpendicular fibrous septae than women without cellulite or men (Querleux et al., (2002) Skin Research and Technology, 8:118-124). Cellulite occurs most often on the hips, thighs and upper arms. For example, premenopausal females tend to accumulate 25 fat subcutaneously, primarily in the gluteal/thigh areas where cellulite is most common. Clinically, cellulite is accompanied by symptoms that include thinning of the epidermis, reduction and breakdown of the microvasculature leading to subdermal accumulations of fluids, and subdermal agglomerations of fatty tissues. b. Dupuytren's Disease 30 Activatable matrix-degrading enzymes, such as those described herein, can be used to treat Dupuytren's syndrome (also called Dupuytren's contracture). Dupuytren's contracture (also known as Morbus Dupuytren) is a fixed flexion contracture of the hand where the fingers bend towards the palm and cannot be fully WO 2009/111083 PCT/US2009/001486 - 159 extended. A similar lesion sometimes occurs in the foot. The connective tissue within the hand becomes abnormally thick and is accompanied by the presence of nodules containing fibroblasts and collagen, particularly type III collagen. The fibrous cord of collagen is often interspersed with a septa-like arrangement of adipose 5 tissue. These present clinically as mattress-type "lumps" of varying sized and in Dupuytren's disease are termed nodules. This can cause the fingers to curl, and can result in impaired function of the fingers, especially the small and ring fingers. Dupuytren's disease occurs predominantly in men. It is generally found in middle aged and elderly persons, those of Northern European ancestry, and in those with 10 certain chronic illnesses such as diabetes, alcoholism and smoking. Dupuytren's disease is a slowly progressive disease that occurs over many years causing fixed flexion deformities in the metacarpophalangeal (MP) and proximal interphalangeal (PIP) joints of the fingers. The small and ring fingers are the most often affected. The disease progresses through three stages (Luck et al. 15 (1959) J Bone Joint Surg., 41A:635-664). The initial proliferative stage is characterized by nodule formation in the palmar fascia in which a cell known as the myofibroblast appears and begins to proliferate. The involutional or mid-disease stage involves myofibroblast proliferation and active type III collagen formation. In the last or residual phase, the nodule disappears leaving acellular tissue and thick 20 bands of collagen. The ratio of type III collagen to type I collagen increases. Treatment of Dupuytren's disease with an activatable-matrix degrading enzyme is typically in the mid-disease and residual disease stages. c. Peyronie's Disease Activatable matrix-degrading enzymes, such as those described herein, can be 25 used to treat Peyronie's disease. Peyronie's disease is a connective tissue disorder involving the growth of fibrous plaques in the soft tissue of the penis affecting as many as 1-4% of men. Collagen is the major component of the plaque in Peyronie's disease. Specifically, the fibrosing process occurs in the tunica albuginea, a fibrous envelope surrounding the penile corpora cavernosa. The pain and disfigurement 30 associated with Peyronie's disease relate to the physical structure of the penis in which is found two erectile rods, called the corpora cavernosa, a conduit (the urethra) through which urine flows from the bladder, and the tunica which separates the cavernosa from the outer layers of skin of the penis. A person exhibiting Peyronie's WO 2009/111083 PCT/US2009/001486 - 160 disease will have formation(s) of plaque or scar tissue between the tunica and these outer layers of the skin (referred to as "sub-dermal" in this application). The scarring or plaque accumulation of the tunica reduces its elasticity causes such that, in the affected area, it will not stretch to the same degree (if at all) as the surrounding, 5 unaffected tissues. Thus, the erect penis bends in the direction of the scar or plaque accumulation, often with associated pain of some degree. In all but minor manifestations of Peyronie's disease, the patient has some degree of sexual dysfunction. In more severe cases, sexual intercourse is either impossible, or is so painful as to be effectively prohibitive. 10 Empirical evidence indicates an incidence of Peyronie's disease in approximately one percent of the male population. Although the disease occurs mostly in middle-aged men, younger and older men can acquire it. About 30 percent of men with Peyronie's disease also develop fibrosis (hardened cells) in other elastic tissues of the body, such as on the hand or foot. Common examples of such other 15 conditions include Dupuytren's contracture of the hand and Ledderhose Fibrosis of the foot. d. Ledderhose Fibrosis Activatable matrix-degrading enzymes, such as those described herein, can be used to treat Ledderhose fibrosis. Ledderhose fibrosis is similar to Dupuytren's 20 disease and Peyronie's disease, except that the fibrosis due to fibroblast proliferation and collagen deposition occurs in the foot. Ledderhose disease is characterized by plantar fibrosis over the medial sole of the foot, and is sometimes referred to as plantar fibrosis. e. Stiff joints 25 Activatable matrix-degrading enzymes, such as those described herein, can be used to treat stiff joints, for example, frozen shoulder. Frozen shoulder (adhesive capsulitis) is a chronic fibrozing condition of the capsule of the joint characterized by pain and loss of motion or stiffness in the shoulder. It affects about 2% of the general population. Frozen shoulder results from increased fibroblast matrix synthesis. The 30 sythesis is caused by an excessive inflammatory response resulting in the overproduction of cytokines and growth factors. Fibroblasts and myofibroblasts lay down a dense matrix of collagen in particular, type-I and type-III collagen within the WO 2009/111083 PCT/US2009/001486 - 161 capsule of the shoulder. This results in a scarred contracted shoulder capsule and causes joint stiffness. Other examples of stiff joints include, but are not limited to, those caused by capsular contractures, adhesive capsulitis and arthrofibrosis, which result from 5 musculoskeletal surgery. Such stiff joints can occur in joints, including, for example, joints of the knees, shoulders, elbows, ankles and hips. Like frozen shoulder, such joint diseases are caused by increased matrix synthesis and scar formation. The stiff joints inevitably can cause abnormally high forces to be transmitted to the articular cartilage of the affected area. Over time, these forces result in the development of 10 degenerative joint disease and arthritis. For example, in arthrofibrosis and capsular contracture, fibroblasts form excessive amounts of matrix in response to local trauma, such as joint dislocation. f. Existing Scars Activatable matrix-degrading enzymes, such as those described herein, can be 15 used to treat existing scars. Collagen is particularly important in the wound healing process and in the process of natural aging, where it is produced by fibroblast cells. In some cases, however, an exaggerated healing response can result in the production of copious amounts of healing tissue (ground substance), also termed scar tissue. For example, various skin traumas such as bums, surgery, infection, wounds and accident 20 are often characterized by the erratic accumulation of fibrous tissue rich in collagen. There also is often an increased proteoglycan content. In addition to the replacement of the normal tissue that has been damaged or destroyed, excessive and disfiguring deposits of new tissue sometimes form during the healing process. The excess collagen deposition has been attributed to a disturbance in the balance between 25 collagen synthesis and collagen degradation. Including among scars are, for example, chronic tendinosis or scar tissue of the tendons, surgical adhesions, keloids, hypertrophic scars, and depressed scars. i. Surgical adhesions Surgical adhesions are attachments of organs or tissues to each other through 30 scar formation, which can cause severe clinical problems. The formation of some scar tissue after surgery or tissue injury is normal. In some cases, however, the scar tissue overgrows the region of injury and creates surgical adhesions, which tend to restrict the normal mobility and function of affected body parts. In particular, WO 2009/111083 PCT/US2009/001486 - 162 fibroblast proliferation and matrix synthesis is increased locally following such soft tissue injury. Adhesions then form when the body attempts to repair tissue by inducing a healing response. For example, this healing process can occur between two or more otherwise healthy separate structures (such as between loops of bowel 5 following abdominal surgery). Alternately, following local trauma to a peripheral nerve, fibrous adhesions can form, resulting in severe pain during normal movement. ii. Keloids Keloids are scars of connective tissue containing hyperplastic masses that occur in the dermis and adjacent subcutaneous tissue, most commonly following 10 trauma. Keloids generally are fibrous nodules that can vary in color from pink or red to dark brown. Keloids form in scar tissue as a result of overgrowth of collagen, which participates in wound repair. Keloid lesions are formed when local skin fibroblasts undergo vigorous hyperplasia and proliferation in response to local stimuli. The resulting lesion can result in a lump many times larger than the original scar. In 15 addition to occur as a result of wound or other trauma, keloids also can form from piercing, pimples, a scratch, severe acne, chickenpox scarring, infection at a wound site, repeated trauma to an area, or excessive skin tension during wound closure. iii. Hypertrophic scars Hypertrophic scars are raised scars that form at the site of wounds. They 20 generally do not grow beyond the boundaries of the original wound. Like keloid scars, hypertrophic scars are a result of the body overproducing collagen. iv. Depressed scars Depressed scars generally result from an inflammatory episode and are characterized by contractions of the skin, and leave a cosmetically displeasing and 25 permanent scar. The most common example is scarring that occurs following inflammatory acne. The depression occurs as a normal consequence of wound healing, and the scar tissue causing the depression is predominantly made up of collagen resulting from fibroblast proliferation and metabolism. g. Scleroderma 30 Activatable matrix-degrading enzymes, such as those described herein, can be used to treat scleroderma. Scleroderma is characterized by a thickening of the collagen. The more common form of the disease, localized scleroderma, affects only the skin, usually in just a few places, and sometimes the face. It is sometimes referred WO 2009/111083 PCT/US2009/001486 - 163 to as CREST syndrome. Symptoms include hardening of the skin and associated scarring. The skin also appears reddish or scaly, and blood vessels can be more visible. In more serious cases, scleroderma can affect the blood vessels and internal organs. Diffuse scleroderma can be fatal as a result of heart, kidney lung or intestinal 5 damage, due to musculoskeletal, pulmonary, gastrointestinal, renal and other complications. The condition is characterized by collagen buildup leading to loss of elasticity. The overproduction of collagen has been attributed to autoimmune dysfunction, resulting in accumulation of T cells and production of cytokines and other proteins 10 that stimulate collagen deposition from fibroblasts. h. Lymphedema Activatable matrix-degrading enzymes, such as those described herein, can be used to treat lymphedema. Lymphedema is an accumulation of lymphatic fluid that causes swelling in the arms and legs. Lymphedema can progress to include skin 15 changes such as, for example, lymphostatic fibrosis, sclerosis and papillomas (benign skin tumors) and swelling. Tissue changes associated with lymphedema include proliferation of connective tissue cells, such as fibroblasts, production of collagen fibers, an increase in fatty deposits and fibrotic changes. These changes occur first at the lower extremities, i.e. the fingers and toes. Lymphedema can be identified based 20 on the degree of enlargement of the extremities. For example, one method to assess lymphedema is based on identification of 2-cm or 3-cm difference between four comparative points of the involved and uninvolved extremities. i. Collagenous colitis Activatable matrix-degrading enzymes, such as those described herein, can be 25 used to treat collagenous colitis. Collagenous colitis was first described as chronic watery diarrhea (Lindstrom et al. (1976) Pathol. Eur., 11:87-89). Collagenous colitis is characterized by collagen deposition, likely resulting from an imbalance between collagen production by mucosal fibroblasts and collagen degradation. It results in secretory diarrhea. The incidence of collagenous colitis is similar to primary biliary 30 cirrhosis. The disease has an annual incidence of 1.8 per 100,000 and a prevalence of 15.7 per 100,000, which is similar to primary biliary cirrhosis (12.8 per 100,000) and lower than ulcerative colitis (234 per 100,000), Crohn's disease (146 per 100,000) or celiac disease (5 per 100,000). In patients with chronic diarrhea, about 0.3 to 5% WO 2009/111083 PCT/US2009/001486 -164 have collagenous colitis. Collagenous colitis is an inflammatory disease resulting in increased production of cytokines and other agents that stimulate the proliferation of fibroblasts, resulting in increased collagen accumulation. 2. Spinal Pathologies 5 Diseases of the ECM or involving the ECM also include spinal pathologies, typically referred to as herniated disc or bulging discs, that can be treated using the methods herein. These include protruded and extruded discs. A protruded disc is one that is intact but bulging. In an extruded disk, the fibrous wrapper has torn and the nucleus pulposus (NP) has oozed out, but is still connected to the disk. While the NP 10 is not the cause of the herniation, the NP contributes to pressure on the nerves causing pain. The NP contains hyaluronic acid, chondrocytes, collagen fibrils, and proteoglycan aggrecans that have hyaluronic long chains which attract water. Attached to each hyaluronic chain are side chains of chondroitin sulfate and keratan sulfate. 15 Herniated discs have been treated with chemonucleolytic drugs, such as chymopapain and a collagenase, typically by local introduction of the drug into the disc. A chemonucleolytic drug degrades one or more components of the NP, thereby relieving pressure. Chemonucleolysis is effective on protruded and extruded disks. Chemonucleolysis has been used treat lumbar (lower) spine and cervical (upper 20 spine) hernias. For the methods herein, any enzyme that degrades a component of the NP and that is conditionally activated can be administered. These enzymes include cathepsin L. In addition, any of the hyaluronidases, collagenases, chondroitinases that are not conditionally activatable, can be modified to render them so. For example, temperature sensitive enzymes, as described herein, including 25 modified MMPs, such as MMP-1 modified as described herein can be employed in the methods herein. J. EXAMPLES The following examples are included for illustrative purposes only and are not intended to limit the scope of the invention. 30 EXAMPLE 1 Preparation of Activated Recombinant Cathepsin-L WO 2009/111083 PCT/US2009/001486 - 165 Histidine (His)-tagged purified recombinant human cathepsin-L was purchased from R&D systems (Minneapolis, MN. Cat# 952-CY) and was formulated at a concentration of 0.9 mg/mL in 50 mM Acetate, pH 4.0, 100 mM NaCl. Aliquots of 500 pL were stored at -80*C until they were used. 5 Concentration and buffer exchange were performed on stored aliquots before use. Briefly, 2 mL of 0.9 mg/mL cathepsin-L was thawed on ice and 500 PL transferred to 4 microcon centrifugal filter membrane tubes having a 30 KDa cut-off (Millipore; Bedford, MA, Cat#4241 0). The microcon tubes were spun at 9000 rpm for 5 minutes resulting in a final volume of 50 pl. 450 pL of cold concentration 10 buffer (100 mM Na-Formate pH 4, 100 mM NaCl, 5 mM DTT, 10 mM EDTA) was added to each micron tube. The addition of 5 mM DTT during processing converts cathepsin-L to a single chain protein of approximately 36 KDa as assessed by SDS PAGE. The concentration and buffer exchange steps remove the inhibitory 10-16 KDa pro-peptide. In addition, the DTT and EDTA added during concentration and 15 buffer exchange minimize proteolytic degradation of cathepsin-L. The centrifugation procedure was repeated three times. Tubes and concentration solutions were chilled to minimize degradation, since cathepsin-L is sensitive to temperature. After the final spin, the microcon tubes were inverted and the liquid was collected in the retentate cup by centrifugation at 5000 rpm for 5 minutes. The final volume recovered was 400 20 ptL, resulting in a five-fold concentration. The concentrated cathepsin-L was aliquoted in volumes of 67 pL, which contained approximately 300 pg of activated enzyme. Aliquots were stored at -80*C, and thawed on ice prior to use. Before use, cathepsin-L was formulated at its optimal pH of 5 by adding one aliquot to 3 mL of MES buffer solution (2-(N-morpholino)ethanesulfonic acid) at pH 25 5, resulting in a final concentration of 100 pg/mL of activated cathepsin-L. As a control, cathepsin-L was formulated in HEPES buffer at pH 7.4 where the enzyme is minimally active. Example 2 Hydroxyproline Assay 30 A hydroxyproline assay was used to measure collagen content changes in skin samples following perfusion with cathepsin-L. While the hydroxyproline content of other proteins is negligible, collagen contains hydroxyproline at a concentration of 8% (TV. Burjanadze, Hydroxyproline content and location in relation to collagen thermal WO 2009/111083 PCT/US2009/001486 - 166 stability. Biopolymers 18: 4931-4938 (2002)). The hydroxyproline (HP) assay used was a modification of the procedure of Reddy and Enwemeka (Clinical Biochemistry 29:225-229 (1996)). In particular, the volumes of the reagents were modified for completion of the 5 reaction in 8-well 0.2 mL strip tubes (Brandtech, Essex, CT) in a standard thermocycler (Eppenforf Mastercycler, Westbury, NY). All steps including hydrolyzation, acidification and detection with Ehrlich's reagent were carried out in the 0.2 mL tubes. All chemicals were purchased from Sigma (St. Louis, MO). Briefly, perfusate samples from perfusion experiments were extracted by precipitation 10 with 5 volumes of 200 proof ethanol and centrifuged. The volumes of perfusate collected were measured using 1 mL or 200 pL pipettes. The perfusates were transferred to labeled 15 mL conical centrifuge tubes. The ethanol perfusate mixtures were stored in a -80'C freezer for 30 minutes before being centrifuged at 3000 rpm for 10 minutes in an Eppendorf swinging bucket centrifuge. Following 15 centrifugation, the precipitate was dissolved in 150-400 PL of 2N NaOH depending on the size of the pellet. The supernatant was dried in a lyophilizer, and dissolved in 150-200 ptL of 2N NaOH. Following dissolution in NaOH, samples were transferred to 8-well strip tubes at a volume of 200 pL or less per tube and hydrolyzed at 99'C for 12 hours in a thermocycler to allow for complete hydrolysis of collagen and 20 hydroxyproline release. Samples were acidified with concentrated HCl (5.2 PL of HCl per every 25 pL of hydrolyzed sample). 60 ptL of Chloramine-T (Sigma; Cat# C9887) were added to an equal volume of acidified hydrolysate to complete hydroxyproline oxidation. After complete oxidation, 120 pL of Ehrlich's reagent (Sigma, Saint Louis, MO, Cat# 39070(Fluka) ) was added and incubated at 65*C for 25 25 minutes, resulting in a purple color. The intensity of the coloration is dependent on the amount of hydroxyproline derived from the collagen released in the perfusate. Samples were read in the visible range at 550 nm in a Spectramax 2E plate reader (Molecular Devices, Sunnyvale, CA). A standard curve was established using purified hydroxyproline solution (Sigma, Saint Louis, MO, Cat# H54409), and 30 hydroxyproline content in skin samples were determined from the standard curve. Example 3 Degradation of Collagen by Perfusion of Ex Vivo Rat Skin Explants with Activated Cathepsin-L WO 2009/111083 PCT/US2009/001486 - 167 Skin explants (2 cm x 2 cm) were surgically removed from the dorsolateral site of 3-month old male Sprague-Dawley rats (Harlan Sprague Dawley, Indianapolis, IN) anesthetized with 2% isofluorane. Explants were pinned down with needles to a Styrofoam pad glued to a 100 mm Petri dish and kept at 37*C with a heating pad. 5 Using an infusion pump (Thermo Orion, model M361, Boston, MA), 6 mL of a solution containing MES buffer (2-(N-morpholino-ethanesulfonic acid) at pH 5 and rHuPH20 at 2500 Units/mL (rHuPH20 Halozyme internal manufacturing lot# 056 100; specific activity: 124,000 U/mL and protein content of 1.05 mg/mL) were first perfused for 35 minutes through the skin explants via a 27-gauge butterfly needle 10 inserted into the dermal layer of the explants. After completion of the acidic perfusion, the skin explants were perfused for approximately 30 minutes with or without 100 ptg/mL of activated cathepsin-L in MES buffer, pH 5 or control cathepsin-L in HEPES buffer, pH 7.4. Fractions were collected by aspirating with a 200 pL micropipette and collecting the contents in 1.5 mL Eppendorf tubes at time 15 intervals of 5-10 minutes during the entire perfusion procedure. The fractions were pooled in Eppendorf tubes and rapidly frozen until hydroxyproline (HP) analysis was performed as described in Example 2. The results of three different experiments show that HP levels were significantly increased only in samples perfused with activated cathepsin-L at the 20 optimum pH of 5. Average (n=3) HP levels increased from less than I pig /mLof perfusate at approximately 6 minutes to more than 30 pg /mL of perfusate at approximately 30 minutes. None or little HP was measured in the perfusates from infusions with MES buffer pH 5 only; HEPES buffer pH 7.4 only; and control cathepsin-L at pH 7.4. 25 Example 4 Degradation of Collagen by Perfusion of Ex Vivo Pig Skin Explants with Activated Cathepsin-L Three-month old female Yorkshire pigs (S and S Farm, Ramona, CA) were fasted overnight and anesthetized by intramuscular injection of Ketamine (20 30 mg/kg)/Xylazine (2 mg/kg) and atropine (0.04 mg/kg). Animals were then intubated and anesthesia was maintained with 2% inhaled isoflurane (Baxter, Deerfield, IL) in oxygen (Airgas, San Diego, CA). Whole skin explants (5 cm x 5 cm) were surgically removed from the back of the animals, placed in phosphate buffered saline (PBS) at WO 2009/111083 PCT/US2009/001486 - 168 4"C, and used within 2 hours following excision. Perfusion of explants and hydroxyproline analysis were carried out essentially as described in Example 3, except that the pig skin explants were perfused with MES buffer pH 5, or MES buffer pH 5 containing 100 pig/ml of cathepsin-L without PH20. Initially, explants were 5 perfused with 6 mL of MES buffer pH 5 for approximately 30 minutes, and fractions were collected every 5-10 minutes. Thereafter, explants were perfused with 3 mL of 100 pg/ml of cathepsin-L in MES buffer pH 5 or buffer alone as a control collected every 5 minutes for approximately 25 minutes. HP analysis showed a time-dependent increase in HP levels in the samples perfused with cathepsin-L. No detectable HP 10 could be measured in samples perfused with MES buffer pH 5 without cathepsin-L. Highest levels of HP were measured at time 15 minutes. HP levels measured at 25 minutes were similar to those measured at 15 minutes. Example 5 Decrease in Fibrous Septae in the Subcutaneous Space 15 by Perfusion of Pig Explants with Activated Cathepsin-L Pig skin explants were processed essentially as described in Example 4 by perfusion with MES buffer, pH 5 containing 2500 U/mL rHuPH20, at a rate of 0.17 mL per minute for 30 minutes, followed by perfusion with 3 mL of 100 pg/ml cathepsin-L in MES buffer pH 5 without rHuPH20 at 0.12 mL/min for 25 minutes. 20 Following infusion with cathepsin-L, the explants were trimmed into small pieces that were fixed in 4% buffered formalin overnight. Control untreated pig explants were processed similarly. Tissues were washed in PBS, dehydrated in graded ethanol and xylene solutions, and embedded in paraffin. Blocks were cut in 4 pm thin sections that were transferred to microscope slides and stained with Masson's Trichrome 25 staining for visualization of collagen. Briefly, sections were deparaffinized, hydrated in distilled water and treated with mordant in Bouin's solution (Sigma, Cat #HT10 132) for 15 to 30 minutes at 56*C. The sections were cooled and washed in running water until the yellow color disappeared and rinsed in distilled water. The sections were then stained in Weigert's Iron Hematoxylin Working solution (Sigma Cat # 30 HT107 and HT109) for 5 minutes and washed in running water for 10 minutes. Sections were rinsed in deionized water for 5 minutes and placed in Biebrich Scarlet Acid Fuchsin (Sigma, Cat # HT1 51) for 5 minutes. The sections were transferred to Working Phosphotungstic/Phosphomolybdic Acid solution (Sigma Cat # HT1 52 and WO 2009/111083 PCT/US2009/001486 - 169 HT153) and finally stained in Aniline Blue Solution (Sigma Cat # HT154) for 5 minutes and differentiated in 1% Acetic Acid for 2 minutes. Sections were rinsed in distilled water, dehydrated in 95% alcohol and absolute alcohol, and cleared in xylene with two changes. Sections were mounted and observed in a Nikon inverted 5 microscope. Images were obtained using a 20x objective in a Nikon fluorescent microscope coupled to a camera scanner (Diagnostic Instrument Inc., Sterling Heights, MI) containing the SPOT advance imaging program. The hypodermis predominantly contains adipose tissue. Dense connective tissue strands made of collagen fibrous septae extend from the dermis deep into the 10 hypodermis and anchor the skin to underlying structures. The histology results shows that fibrous septae separating the fat cell chambers are visible throughout the hypodermis in the non-treated sample. Following treatment with cathepsin-L in MES buffer, pH 5, the number of collagen fibrous septae was substantially lower than in untreated samples, indicating that treatment with cathepsin-L dramatically alters the 15 collagen network organization in the hypodermis. Example 6 A. Collagen Degradation in the Skin of Live Anesthetized Rats Perfusion experiments were performed on three month old male Sprague Dawley rats (Harlan Sprague-Dawley, Inc. Indianapolis, IN) kept under 2% isoflurane 20 anesthesia. Perfusion experiments were performed using cathepsin-L at pH 5, and as a control for specificity, in HEPES buffer at pH 7.4. Briefly, using a infusion pump, about 15 mL of a solution containing either 25 mM MES buffer pH 5, or 25 mM HEPES buffer pH 7.4, and 2500 Units/ml of rHuPH20 (Halozyme internal manufacturing lot # 056-100 with specific activity of 124,000 U/mL and protein 25 content of 1.05 mg/mL), were first perfused for approximately 60 minutes via the tail skin using a 27-gauge butterfly needle inserted into the dermal layer of the skin. Thereafter a 3 mL solution containing cathepsin-L or buffer control was perfused for 25 min. Cat-L containing perfusion solutions contained 100 pIg /mL of activated Cat L either at its optimum pH of 5 in 5 mM MES or at the control pH of 7.4 in 20 mM 30 HEPES. The ionic strength of pH 5 buffer was reduced from 25 mM to 5 mM to facilitate neutralization of the pH by the local tissue environment and thereby limit the spread of the active enzyme. In case of Cat-L in HEPES buffer at pH 7.4 an ionic strength of at least 20 mM was maintained to ensure that the added Cat-L, activated WO 2009/111083 PCT/US2009/001486 - 170 and formulated in a high ionic strength buffer at pH 4, would not substantially alter the pH of the HEPES buffer (pH7.4). A small aliquot of the Cat-L added to 20 mM HEPES pH 7.4 was checked with pH paper to ensure that pH of the resulting solution, after Cat-L has been added, was indeed close to pH 7.4. Buffer control solutions used 5 for perfusion were 5 mM MES pH 5 or 20 mM HEPES pH 7.4, with no added enzyme. Perfusate fractions were collected from the tail skin at regular time intervals, i.e at 20, 40 and 60 minutes during the initial perfusion and at 8 and 25 minutes during perfusion with Cat-L. The fractions were pooled in Eppendorf tubes and rapidly frozen to prevent further enzymatic action. Hydroxyproline analysis was 10 performed as described in Example 2. The results show that HP could be measured only in the samples perfused with activated cathepsin-L. The highest levels of HP were measured in the 25 minute perfusate samples. There was no detectable HP in the samples perfused with MES buffer pH 5 only, or with HEPES buffer pH 7.4 only, or with cathepsin-L in HEPES buffer pH 7.4. 15 B. Cathepsin-L Treatment Leads to pH-dependent Collagen Degradation in vitro Cathepsins B, D, L and S and bacterial collagenase were assessed for degradation towards rat collagen at pH 5.0 and pH 8.0. Cathepsins B, D, L and S were purchased from R&D systems and each enzyme was activated based on 20 individual specifications from the enzyme manufacture. Bacterial collagenase was purchased from Sigma Chemicals, and does not require activation. Soluble rat tail collagen Type I was digested for 1 hour at 370 C by incubation with activated cathepsin B, D, L or S or bacterial collagenase, in the manufacture's specified buffers or in Tris pH 8.0 buffered saline, followed by SDS-Page gels and Coomassie Blue 25 staining. Other cathepsins were not tested at pH 5, but at manufacture specified pH and buffer. The results show that cathepsin-L was the only enzyme that was active at pH 5.0, but not at pH 8.0. Cathepsins B, D and S showed some slight degradation of rat collagen at the manufacture specified pH and no degradation of rat collagen at pH 8.0, while bacterial collagenase degraded rat collagen at both pH 5.0 and pH 8.0. 30 Example 7 A. Return to Neutrality Following Acidification of the Skin in a Live Rat When a dilute aqueous acid solution is injected into the skin interstitium, the change in pH is temporary and the neutral skin pH is rapidly restored due to the WO 2009/111083 PCT/US2009/001486 - 171 significant buffering capacity of interstitium. Phenol red was used as a visual indicator of interstitial pH. The sodium salt of phenol red is widely used in cell culture medium to identify changes from neutral to acidic pH values. A solution of phenol red has a yellow color at a pH of 6.4 or below, orange color at pH 7.0, red 5 color at pH 7.4 and above, and purple color at pH 7.8. Three month old male Sprague-Dawley rats (Harlan Sprague Dawley, Indianapolis, IN) were kept under 2% isoflurane anesthesia. Skin was shaven for easy visualization of phenol red dye. 2-2.5 mL of 25 mM MES, pH 5 containing 500 U/ml of rHuPH20 were perfused into the tail skin via a 27-gauge butterfly needle 10 inserted into the dermal layer. This was-followed by a solution of 1-1.5 mL of 0.05% phenol red (Sigma-Aldrich, St. Louis, MO, Cat # P0290) in 10 mM, 25 mM, 50 mM and 100 mM MES buffer, pH 5. MES (2-(N-morpholino-ethanesulfonic acid (CI6Hl3NO4A)) has a molecular weight of 195.2. No rHuPH20 was included in the phenol red solution. Using microcalipers, the phenol red front was measured at 15 different time points, in two dimensions, and the areas were calculated using the formula: Area = (Dl x D2) x 7r/4. The change in color was observed and time to return to neutrality was recorded. The results of Table 4A summarize the average time in minutes to return to neutrality and indicate that return to neutrality can be modulated by the ionic strength of the buffer. Table 4A - Average time to neutrality Buffer Initial % % % % Average strength area of reduction reduction reduction reduction time to solution Phenol after 5 after 10 after 15 after 20 neutrality in mM Red minutes minutes minutes minutes In min id MES 10;n=3 80 71 86 98 - 10 25;n=3 123 59 78 91 - 10 50;n=2 115 38 100 100 - 10 100;n=2 191 15 38 55 71 20 20 B. Return to Neutrality Following Acidification of Mouse Skin The time period to return to neutralization, and subsequent inactivation of cathepsin-L depends on the strength of the injected buffer. The intrinsic buffering capacity of the interstitium was assessed by measuring the time to return to 25 neutralization using a phenol red indicator dye at pH 5.0 with increasing buffer WO 2009/111083 PCT/US2009/001486 - 172 strength (10-100 mM MES) in nude mice. Anesthetized nude mice were injected with 0.125 mL of MES buffer (10 mM to 100 mM), pH 5 containing phenol red. The time to phenol red neutralization in the dermis was measured visually. The results are depicted in Table 4B below. TABLE 4B: Measurement of Interstitial Buffering Capacity in Mouse Skin Buffer Ionic pH Time to SD Strength Neutralization (mM) (minutes) Phosphate 10 7.4 0 MES 10 5.0 0 MES 25 5.0 0 MES 50 5.0 7.3 1.25 MES 100 5.0 7.8 2.1 5 SD: standard deviation Thus, by intradermal injection of pH indicators in increasing buffer strengths (10-100 mM MES pH 5.0), it was established that an acidic temporal-spatial extracellular environment from 1-20 minutes/100mm2 injection could be obtained. Example 8 10 Engineering of Recombinant Human Liver Cathepsin-L Human Cat-L cDNA SEQ ID NO: 9 (encoded by a sequence of nucleotides set forth in SEQ ID NO:10) and Cat-L-His cDNA SEQ ID NO: 12 (encoded by a sequence of nucleotides set forth in SEQ ID NO: 13), were PCR amplified from human liver cDNA (Clonetech QUICK-Clone cDNA 637205) using primers that were 15 designed according to the published sequence data for human kidney procathepsin-L cDNA. 5' NheI and 3' BamHI restriction sites were added as part of the PCR primer synthesis. The primers used in the amplification are set forth in Table 5. TABLE 5: Primers Primer Sequence SEQ Tm length Match ID length NO Human 5' 5'- 16 64*C 42 mer 22 AAGGCCGCTAGCCACCATGGATCC Cat- L TACACTCATCCTTGCTGC-3' WO 2009/111083 PCT/US2009/001486 - 173 3' (with 5'- 17 65*C 35 mer 20 GAGCACGGATCCTCATCACACAGT GGGGTAGCTGG-3' stop codons) Cat-L-His 5' 5'- 16 64*C 42 mer 22 AAGGCCGCTAGCCACCATGGATCC TACACTCATCCTTGCTGC-3' 3' (with 5'- 18 57*C '49 mer 16 .i CCTGCCGGATCCTCAATGATGATGA 6xHis

TGATGATGCACAGTGGGGTAGCTG

tag) 3' Both cDNA based constructs have the second amino acid of the native Cat-L secretory leader peptide mutated by a single base to form a consensus Kozak sequence, thereby changing the second amino acid from N to D (as set forth in SEQ 5 ID NO: 9 and 12). The identity of the clones was verified by standard agarose gel electrophoresis and DNA sequencing analysis The resulting amplified product was introduced for cloning into the HZ24 (b/s) expression vector. The expression vector is a CMV-based bi-cistronic cassette for expression of both the cathepsin-L protein and the murine DHFR gene separated 10 by an internal ribosomal entry site (IRES) from the encephalomyocarditis virus. The resulting sequence of the HZ24-Cat-L expression vector is set forth in SEQ ID NO: 11. The resulting sequence of the HZ24-Cat-L-His expression vector is set forth in SEQ ID NO:14. Both Cat-L and Cat-L-His expression plasmids were introduced into CHO-S 15 cells (CHO-KI cells adapted to serum free suspension culture, Invitrogen, Carlsbad, CA, cat # 11619-012) by transfection using Genejuice transfection reagent (EMD Biosciences, San Diego, CA, cat # 70967). The expression plasmids also were introduced into DG44 CHO cells (obtained by license from Dr. Lawrence Chasin, Columbia University), which were adapted to grow in suspension culture in a 20 chemically defined, animal product-free medium (Invitrogen, Cat # 10743-029) by electroporation. For electroporation, greater than 100 ptg of Clal linearized plasmid was used for each electroporation of each of the plasmids. Twenty million DG44 CHO cells per electroporation, at 350 Volts constant voltage were transfected. The electroporation buffer contained 2X HeBS (40 mM HEPES, pH 7.0; 274 mM NaCI; WO 2009/111083 PCT/US2009/001486 - 174 10 mM KCl; 1.4 mM Na2HPO4; 12 mM dextrose). Transfected cells were cloned by limiting dilution 72 hours after electroporation in standard CD-CHO media (Invitrogen #12610-010 ) without sodium hypoxanthine and thymidine to select for cells carrying the DHFR plasmid. Selected clones growing without sodium 5 hypoxanthine and thymidine were further sub-cloned, with amplification using methotrexate to increase insert copy number. A mock transfection served as a negative control. Supernatants were harvested 72 hours post transfection and spun at 1500 rpm for 5 minutes. Cell free supernatants from CHO-S and CHO-DG44 cells transfected 10 with his-Cat-L, Cat-L and mock were applied to I OkDa cutoff micron centrifugal concentrators (Millipore; Bedford, MA. Cat# 42407) and concentrated approximately 10-fold by centrifugation at 12000 rpm at 4' C. Recombinant Human Cathepsin-L secreted into tissue culture supernatants was screened by capture ELISA (Calbiochem Cathepsin-L ELISA Kit #QIA94), Western Blot analysis using the monoclonal Mab 15 33/1 (Bender MedSystems, Burlingame, CA) as described in Example 10 and for enzymatic activity using the fluorescent peptide substrate (Z-L-R-AMC) as described in Example 9. Example 9 Determination of Enzymatic Activity of cathepsin-L 20 using a fluorogenic peptide substrate Enzymatic activity of cathepsin-L was assayed using a commercially available fluorogenic substrate, designated as Z-Leu-Arg-AMC (Z=:N-carbobenzyloxy; AMC: 7-Amino-4-Methyl Coumarin, R&D Systems, Minneapolis, MN, Cat# ES008). The peptide substrate contains a highly fluorescent 7-amino-4-methyl coumarin group 25 (AMC) that is quenched by the amide bond formed between its amino group and the carboxyl group of the Arg residue. Activated cathepsin-L cleaves this amide bond resulting in an increase in released fluorescence. While the peptide substrate can be cleaved by other cathepsins, prominent among which is cathepsin-B, cathepsin-L activity was specifically determined by using suitable specific inhibitors for the 30 cathepsin-B and measuring activity in the presence and absence of the inhibitor. Specifically the selective cathepsin-B inhibitor CA-074 (Calbiochem, San Diego, CA, Cat# 205530) was used at a final concentration of 1 pM and samples were assayed in presence and absence of CA-074. Cell culture supernatants from 72 hours post WO 2009/111083 PCT/US2009/001486 - 175 transfection in CHO cells were adjusted to pH 5 by adding concentrated MES buffer at pH 5 and incubated on ice for 30 minutes. This acid activation step cleaves the pro peptide and generates mature cathepsin-L. To dilute the propeptide fragment which is a potent inhibitor of cathepsin-L enzyme activity (Carmona, E. et al. Potency and 5 selectivity of the cathepsin-L propeptide as an inhibitor of cysteine proteases. Biochemistry 35: 8149-8157 (1996)), the samples were concentrated and buffer exchanged with 50 mM MES pH5 buffer on a 30 KDa microcon tube three times. Samples were then assayed for enzyme activity by the fluorogenic peptide substrate assay on the Z-AMC substrate, 10 - A commercial preparation of cathepsin-L (R&D Systems; Cat# 952-CY) was activated in a manner similar to that of the samples, and was used as a standard by serial dilution. Following activation, samples and standards were serially diluted in 100 mM MES buffer pH 5 containing 5 mM DTT and 10 mM EDTA, in an opaque bottom microplate and incubated with the fluorogenic peptide substrate Z-AMC at 15 37'C for 30 minutes. Z-AMC substrate was used at a final concentration of 10 ptM in a total volume of 200 pL when combined with samples or standards. The resulting fluorescence was read at the recommended optimum excitation emission (380 nm-460 nm) band for the substrate in a fluorescent plate reader (Molecular Devices, SpectraMax 3, Sunnyvale, CA). Sample values were derived 20 from the standard curve drawn from the relative fluorescence unit (RFU) values obtained from the dilution series of the standard. After a 4-parameter fit with the Softmax@ software (Molecular Devices, SpectraMax 3, Sunnyvale, CA), the standard curve was pseudo-linear between the concentration ranges of 10-100 ng/mL. The results are shown in Table 6 below. The activity of cathepsin-L from CHO-S 25 transfected cells was at least 10-20 fold higher than background activity from mock transfected host cells and by assaying in presence of the selective cathepsin-B inhibitor CA-074. The increased enzymatic activity in cathepsin-L transfected tissue culture medium can thus be assigned to Cat-L specific activity. Table 6: Cat-L enzyme activity measurements in presence of cathepsin B inhibitor by Z-AMC assay in transfected cells 72 hours post transfection Clone Mock transfected Cat-L transfected His Cat-L description CHO-S CHO-S transfected CHO-S WO 2009/111083 PCT/US2009/001486 -176 ng/mL of Cat-L 20 723 248 activity Example 10 Western Blot Analysis of Expressed Human Recombinant Cathepsin-L Following expression and concentration of cell free supernatants as described 5 in Example 8, Western Blot analysis was performed to confirm expression. Briefly, for each of the 6 different samples (cat-L, cat-L-His and mock from each of CHO-S or CHO-DG44 cells), 30 pL of concentrated supernatants were mixed with 10 PL of 4X (instead of gel loading sample buffer) for SDS-PAGE (EMD Bioscience, San Diego, CA, cat# 70607-3) and 2 ptL of 100 mM DTT and incubated at 80 0 C for 20 minutes. 10 As a positive control, 750 ng of commercial purified recombinant cathepsin-L (R&D Systems) in 30 pL of 1X PBS was included and processed identically. The total volume (42 pL) of samples were loaded onto 4-20% Tris-Glycine gels (Invitrogen, Carlsbad, CA, Cat# EC6028BOX) and electrophoresis was carried out in Tris-Glycine SDS running buffer until the dye front of the prestained molecular weight marker 15 (Invitrogen, Cat# LC5925) reached the bottom of the gel. The proteins were transferred onto PVDF membrane by the I-Blot semi dry blotting apparatus (Invitrogen, Cat# IB1001) according to manufacturer's instructions. Transfer was verified by the almost complete absence of color of the prestained marker bands on the gel. The membrane was blocked in blocker buffer consisting of 5% non fat dry 20 milk in PBS for 2 hours at room temperature. Cathepsin-L was detected with a mouse monoclonal antibody (Mab 33/1) to human cathepsin-L (Bender MedSystems, Burlingame, CA, Cat# BMS 166) used at 1 pg/mL final concentration in blocker and incubated overnight at 4'C followed by a HRP conjugated goat anti-mouse IgG (Calbiochem, San Diego, CA, Cat# DC02L) used at a concentration of 33 ng/mL in 25 blocker for 1 hr at room temperature. The HRP signal was developed by the TMB Insoluble (Calbiochem, Cat# 613548) membrane development solution and the reaction was stopped after 30 minutes at room temperature. Western blot analysis showed protein bands specific for Cat-L. No specific band was detected in the mock transfected cells. The expression level of Cat-L and 30 His-Cat-L appeared to be higher in CHO-S cells than in DG44 cells, probably due to transfection efficiency in the two cell lines. The Western blot analysis results were WO 2009/111083 PCT/US2009/001486 - 177 consistent with results using enzyme activity assay with the fluorogenic peptide substrate Z-AMC as described in Example 9. The molecular weight of cathepsin-L expressed in CHO-S and DG44 is 44-45 KDa which corresponds to the expected size of the protein still containing the propeptide. The molecular weight of commercial 5 cathepsin used as a positive control (R&D Systems) was 36 KDa for mature cathepsin-L. The difference in size between the protein expressed in transfected CHO-S and CHO-DG44 cells and the commercial cathepsin-L may be due to different host cell specific glycosylation or to the removal of the propeptide from the commercial Cat-L. 10 Example 11 A. Generation of Synthetic Cathepsin-L and Cathepsin-L-His A DNA construct encoding mature human cathepsin-L, (amino acids 18-333 of GenBank Accession No. EAW62736; SEQ ID NO: 1) was synthesized using codon optimization for CHO cells. Codon optimization was based on codon optimization 15 table for Cricetulus griseus, listed by Blue Heron Biotech (blueheronbio.com). The construct was synthesized to contain a heterologous signal peptide designed from the .human kappa IgG gene family (SEQ ID NO:2) to permit secretion of the recombinant protein into tissue culture supernatant. The nucleotide sequence of the optimized cathepsin-L construct is set forth in SEQ ID NO: 3 and encodes a polypeptide set 20 forth in SEQ ID NO:4. A 5' Nhe I restriction site and a 3' BamH I restriction site were incorporated as part of the construct synthesis. The synthetic construct was then introduced into the HZ24 (b/s) expression vector, as described in Example 8. The synthetic Cat-L expression vector was designated HZ24 (B/S) - CAT-L and is set forth in SEQ ID NO:5. Another Cat-L construct containing a C-terminal 6 Histidine 25 tag separated by a linker (GGGGSG; SEQ ID NO: 15) also was synthesized. The nucleotide sequence of the synthesized Cat-L-His construct is set forth in SEQ ID NO:6 and encodes a polypeptide set forth in SEQ ID NO:7. This construct also contained a 5' Nhe I and a 3' BamH I restriction site, incorporated as part of the construct synthesis, and was introduced into the HZ24 (b/s) expression vector. The 30 synthetic Cat-L-His expression vector was designated HZ24 (B/S) - CAT-L-His and is set forth in SEQ ID NO: 8. The synthetic Cat-L expression vector set forth in SEQ ID NO:5 and the synthetic Cat-L-His expression vector set forth in SEQ ID NO:8 were transfected into WO 2009/111083 PCT/US2009/001486 - 178 CHO-DG44 cells by electroporation, as described in Example 8. Supernatants were harvested for 72 hours post-transfection and were processed as described in Example 8 (without pH adjustment) to generate non-activated cathepsin-L. Tissue culture supernatants also were processed to result in the activation of 5 cathepsin-L. This was achieved using a low pH, resulting in cleavage of the pro peptide of cathepsin-L, resulting in the activation of the enzyme. Supernatants from cells transfected with the synthetic construct and un-transfected control cells were adjusted to pH 4 by adding concentrated acidic buffer (1000 mM Formate pH 4, 1000 mM NaCl, 50 mM DTT, 100 mM EDTA) to the supernatants in a ratio of 1:10, 10 respectively. The supernatants were incubated on ice for 30 minutes to allow for complete activation. They were then concentrated by centrifuging through a 30 KDa molecular weight cutoff centrifugal concentration device (Microcon 30, Millipore, Bedford, MA. Cat# 42410), which allowed the cleaved propeptide (with a predicted size of approximately 12-14 KDa) to pass through, while retaining the mature protein 15 (predicted size about 36-40 kDa). Following concentration, activated and non activated supernatants were run on a 4-12% SDS-PAGE gel followed by analysis by Western Blot using the monoclonal Mab 33/1 as described in Example 10. Synthetic Cathepsin-L and Cat-L-His were detected in tissue culture supernatants of transfected cells at similar levels. The molecule weight of the Cathepsin-L and Cat-L-His in non 20 activated supernatants was about 44 kDa, compared to about 36 to 40 kDa for the activated supernatants, due to the absence of the pro-peptide. Activated supernatants also were screened for Cathepsin-L enzymatic activity using the fluorescent peptide substrate (Z-L-R-AMC) as described in Example 9. Cat-L enzyme activity was measured in the presence of the cathepsin-B inhibitor (to 25 block host cathepsin-B-like enzyme activity) by Z-AMC assay in transfected CHO DG44 cells 72 hours post transfection. The results are set forth in Table 7 below. The activity of cathepsin-L from CHO-DG44 transfected cells 72 hours post transfection was about 6-17 fold higher than background activity from mock transfected host cells. By assaying in the presence of the selective cathepsin-B 30 inhibitor CA-074, the contribution from host cathepsin-B like enzyme activity was blocked. Thus, the increased enzymatic activity in cathepsin-L transfected tissue culture medium can be assigned to Cat-L specific activity expressed from the transfected Cat-L clones.

WO 2009/111083 PCT/US2009/001486 - 179 TABLE: 7 Clone description Mock Cat-L His Cat-L transfected transfected transfected ng/mL of Cat-L Less than 100 1700 600 activity B. Selection of synthetic Cathepsin-L clones in methotrexate The synthetic Cathepsin-L cells, produced as described in section A, above, were cloned by limiting dilution after electroporation in standard CD-CHO media 5 without sodium hypoxanthine and thymidine to select for cells carrying a plasmid with the DHFR gene, then further sub-cloned and expanded in the presence of 50 mM methotrexate to increase insert copy number. Subsequent rounds of sub-cloning and expansion in 200 mM and 1000 mM were then performed to identify methotrexate amplified cells lines suitable for use in large scale production of cathepsin L. 10- 1. Cloning and identification of Cat-L cell clones in no methotrexate To select cells and identify Cat-L cell clones that grew in the absence of methotrexate, cells from the transfection described above were collected and washed twice with standard CD-CHO media (GIBCO; Invitrogen) containing 4 mM GlutaMAXTM-I (GIBCO; Invitrogen), and without hypoxanthine and thymidine 15 supplements, by brief centrifugation at 500 x g. After the final wash, cell were counted, and diluted to 10,000 to 20,000 viable cells per mL. A 0.1 mL aliquot of the cell suspension was transferred to each well of ten, 96 well round bottom tissue culture plates. All plates were supplemented with an additional 0.1 mL of the same. Cells were allowed to grow at 37 0 C, 5% CO 2 in a humidified incubator. 20 Wells containing growing colonies of cells under selection without hypoxanthine and thymidine were identified by a combination of Cathepsin-L enzyme assay and visual appearance of cell growth in culture wells. Enzyme activity in the tissue culture supernatant of each well was assessed as described in Example 9. Twenty clones were identified (Table 7a). Table 7a. Clone Relative Clone Relative (Plate/well) ID Cat-L activity (Plate/well) ID Cat-L activity (rfu) (rfu) WO 2009/111083 PCT/US2009/001486 - 180 IC5 8957 6E3 9393 1F6 9161 6G11 5214 2F2 8722 7B2 6792 2C8 8487 7G9 9619 3E4 4952 8E4 3124 3F8 8599 8D7 3085 4F4 9540 9A5 6226 4D10 3374 9E12 7653 5B2 10065 10D3 2053 5B10 11709 10F6 3895 The identified clones were expanded into individual wells of 24-well tissue culture plates, containing 1 mL of CD-CHO media supplemented with 4 mM GlutaMAXTM-I, and without hypoxanthine and thymidine. The cells were grown at 5 37'C, 5% CO 2 in a humidified incubator. The cells were further expanded into T-75 tissue culture flasks in the same media. Three vials of each clone were archived by freezing in 10% DMSO, 45% conditioned media. 2. Cloning and identification of cells in 50 nM methotrexate The 20 cell line sub-clones demonstrating proliferation and expression of Cat 10 L enzymatic activity were sub-cloned from 24 well plates into 96-well round bottom tissue culture plates, using a two-dimensional infinite dilution strategy, in which the cells are diluted I in 3 across the plate, and I in 2 down the plate. Diluted sub-clones were grown in a background of 500 non-transfected DG44 CHO cells per well, to provide necessary growth factors for the initial days in culture. Five plates were made 15 per sub-clone, containing a final concentration of 50 nM methotrexate in CD-CHO media supplemented with 4 mM GlutaMAXTM-I, and without hypoxanthine and thymidine. Cells were grown at 37'C, 5% CO 2 in a humidified incubator. The sub-clones growing in 50 nM methotrexate that expressed recombinant human (synthetic) Cat-L were identified by measuring Cat-L enzyme activity as 20 described in Example 9. Wells demonstrating substantially higher enzymatic activity were compared to the neighboring wells microscopically, and high expressing outlier clones were chosen for expansion. A total of 96 individual clones were expanded into WO 2009/111083 PCT/US2009/001486 - 181 12-well tissue culture plates containing a final concentration of 50 nM methotrexate in CD-CHO media supplemented with 4 mM GlutaMAXTM-I, and without hypoxanthine and thymidine. The cells were grown at 37-C, 5% CO 2 in a humidified incubator. These 96 sub-clones were tested for secreted Cat-L enzymatic activity as 5 described in Example 9 at two different times points, 7 days apart. The sub-clones demonstrating the greatest increases in Cat-L enzymatic activity over the 7 day period and healthy microscopic appearance were chosen for propagation. The 7 sub-clones that were propagated included 9E12 (#16), 7G9 (#50), 1C5 (#69), 4F4 (#76), 1F6 (#77), 5B 10 (#90) and 2F2 (#92). These sub-clones were expanded in the presence of 10 50 nM methotrexate into T-25 and T-75 flasks and archived by freezing. 3. Cloning and identification of cells in 200 nM methotrexate Sub-clones 9E12 (#16), 7G9 (#50), 1C5 (#69), 4F4 (#76), 1F6 (#77), 5B10 (#90) and 2F2 (#92) were then sub-cloned into media containing 200 nM methotrexate. Five, 96-well round bottom tissue culture plates were set-up using the 15 two-dimensional infinite dilution strategy for each of the seven sub-clones. Diluted sub-clones were grown in a background of 500 non-transfected DG44 CHO cells per well in CD-CHO media supplemented with 200 nM methotrexate and 4 mM GlutaMAX

TM

-I (without hypoxanthine and thymidine). The 35 plates were incubated at 37*C, 5% CO 2 in a humidified incubator. 20 The sub-clones expressing high levels of rHuCat-L while being grown in 200 nM methotrexate were identified by measuring Cat-L enzyme activity in the cell culture supernatant, as described in Example 9. A total of 35 sub-clones (5 from each of 9E12 (#16), 7G9 (#50), 1C5 (#69), 4F4 (#76), 1F6 (#77), 5B10 (#90) and 2F2 (#92) were selected and expanded into 24-well tissue culture plates in CD-CHO 25 media supplemented with 200 nM methotrexate and 4 mM GlutaMAXTM-I (without hypoxanthine and thymidine). The sub-clones were incubated at 37'C, 5% CO 2 in a humidified incubator. The 35 sub-clones were assayed for Cat-L activity, and the 10 sub-clones expressing the highest levels of secreted enzymatic activity were propagated to 6-well 30 tissue culture plates. The 10 clones, and the clones from which they were derived in Table 7b. These 10 sub-clones were subsequently expanded into T75 tissue culture flasks and then into shaker flasks in CD-CHO media supplemented with 200 nM WO 2009/111083 PCT/US2009/001486 - 182 methotrexate and 4 mM GlutaMAXTM-I (without hypoxanthine and thymidine). Shaker flasks growing the subclones were expanded, and cells archived by freezing. Four sub-clones, 9E12-3D3 and 7G9-2F2, 7G9-3F1 and 7G9-5F2, demonstrating early rapid cell expansion (shorter doubling times) in small shaker 5 flasks for greater than 7 passages were expanded for inoculation of 4 x 10 L controlled Bioreactors for comparative expression and production studies. The four sub-clones also were continuously expanded and passaged in 1 L shaker flasks containing CD-CHO media supplemented with 200 nM methotrexate and 4 mM GlutaMAXTM-I. Cell density and viability were measured every other day, with cell 10 free retains stored at 4C for later evaluation of enzyme activity. Table 7b. 50 nM methotrexate sub- 200 nM methotrexate Primary Clone clones sub-clones IC5 1C5-3 3-2F2 IC5 1C5-3 3-1F2 2F2 2F2-7 7-5F3 4F4 4F4-4 4-3C3 4F4 4F4-4 4-4B3 7G9 7G9-2 2-2F2 7G9 7G9-2 2-3F1 7G9 7G9-2 2-5F2 9E12 9E12-1 1-3D3 9E12 9E12-1 1-1C2 4. Cloning and identification of cells in 1000 nM methotrexate The 9E12-1-3D3 and 1C5-3-2F2 were sub-cloned for a third time into 1000 nM methotrexate containing media on July 1, 2008. Five, 96-well round bottom 15 tissue culture plates were set-up using the two-dimensional infinite dilution strategy for each of the two sub-clones. The diluted sub-clones were grown in a background of 500 non-transfected DG44 CHO cells per well at 37'C, 5% CO 2 in a humidified incubator, CD-CHO media containing 1000 nM methotrexate and 4 mM GlutaMAXTM-I (without hypoxanthine and thymidine).

WO 2009/111083 PCT/US2009/001486 - 183 Wells containing sub-clones growing in 1000 nM methotrexate were identified by visual and microscopic examination. Twenty wells containing growing cells diluted from the 9E12-1-3D3 and 1C5-3-2F2 sub-clones (10 wells per subclone) were then assayed for rHuCat-L expression by Western Blot. All 20 sub-clones were 5 expanded to 12-well tissue culture plates in CD-CHO media containing 1000 nM methotrexate and 4 mM GlutaMAXTM-I (without hypoxanthine and thymidine) and incubated at 37 0 C, 5% CO 2 in a humidified incubator. Table 7c sets forth the 20 sub clones, and the sub-clones from which they were derived. The clones able to grow in 1000 nM methotrexate are then expanded and assayed for Cat-L enzymatic activity, 10 and archived by freezing in liquid nitrogen. Table 7c. 50 nM 200 nM 1000 nM methotrexate sub- methotrexate sub- methotrexate sub Primary Clone clones clones clones 9E12 9E12-1 1-3D3 IF5 9E12 9E12-1 1-3D3 1E2 9E12 9E12-1 1-3D3 2D4 9E12 9E12-1 1-3D3 2G8 9E12 9E12-1 1-3D3 3E3 9E12 9E12-1 1-3D3 3G2 9E12 9E12-1 1-3D3 4D4 9E12 9E12-1 1-3D3 4F3 9E12 9E12-1 1-3D3 5D2 9E12 9E12-1 1-3D3 5F2 IC5 IC5-3 3-2F5 1D4 1C5 1C5-3 3-2F5 1G2 1C5 1C5-3 3-2F5 2E2 1C5 1C5-3 3-2F5 2E3 1C5 1C5-3 3-2F5 3D6 IC5 IC5-3 3-2F5 3G3 1C5 1C5-3 3-2F5 4E4 IC5 1C5-3 3-2F5 4G2 WO 2009/111083 PCT/US2009/001486 - 184 IC5 1C5-3 3-2F5 5F4 IC5 1C5-3 3-2F5 5G5 B. Large Scale Production and Purification of Cathepsin L To purify the synthetic Cathepsin-L in large quantities, unactivated pro Cathepsin L cell culture supernatant from the cell line 9E12-1-3D3, produced as 5 described above, was cultured in a 36 L bioreactor. Following incubation in the bioreactor, the cell culture was clarified by harvest filters, concentrated and buffer exchanged using tangential flow filtration, viral-inactivated by solvent/detergent, and then purified by sequential chromatography on Q Sepharose Fast Flow (GE Healthcare) anion exchange chromatography and Ceramic Hydroxyapatite 10 chromatography (Biorad, Richmond, CA). Following treatment at reduced pH (pH 4.5), activated Cathepsin-L was further purified by SP Sepharose Fast Flow (GE Healthcare) cation exchange chromatography, viral filtration and tangential flow filtration. The 9E12-1-3D3 cell line was first expanded through a series of flasks. 15 Briefly, 35 mL of culture at passage 6, with 6 x10 5 cell/mL and a viability of 73% was expanded to 200 mL with CD CHO media (Invitrogen) supplemented with 40 mL/L GlutaMAXTM-I (Invitrogen; stock solution 200 mM) and 200 nM methotrexate. At four days, it was expanded to 1200 mL in a 6L sparged spinner using CD CHO media supplemented with 40 mL/L GlutaMAXTM-I. In the 6L spinner, the culture was 20 then expanded to 2200 mL on day 11, to 3500 mL on day 15, and finally to 5000 mL on day 18, each time using CD CHO media supplemented with 40 mL/L GlutaMAXTM-. The 36 L bioreactor, containing 20 L CD CHO medium supplemented with 800 mL GlutaMAX

TM

-I, 100 mg of recombinant human insulin (rHulnsulin), and 30 25 mL Gentamicin, was inoculated with an initial seeding density of 4.6 x 105 cells/mL. To provide smooth mixing and a slight vortex in the culture, the agitation set point was 80 RPM, the temperature setpoint was 37'C, the pH setpoint was pH 7.15, and the dissolved oxygen setpoint was 25%. The bioreactor vessel received filtered air overlay and an air/oxygen/CO 2 sparge, as controlled by an Applikon ADI 1030 30 controller. A constant air sparge of 0.1-0.2 slpm was provided, with the 02 solenoid WO 2009/111083 PCT/US2009/001486 - 185 valve as a slave to the DO controller, such that the 02 flow automatically supplemented the constant air sparge as needed. During the bioreactor run, the culture was supplemented with feed media at various intervals to supplement nutrients and glucose throughout the bioreactor run, as 5 well as providing additional basal medium concentrate and GlutaMAXTM-I in the early, growth phase of the cells, in order to maximize the growth rate and peak cell density. Additional protein digest (Yeastolate Utlrafiltrate 50x (200g/L); Invitrogen) and sodium butyrate were added in the late, production phase of the bioreactor run maximize expression and secretion of product. The feed media was sterile filtered into 10 the bioreactor via peristaltic pump. On days 7, 10, 12, 13, 14 and 16, 500 mL of Feed #1-6, respectively, were added to the bioreactor cell cure. Feed #1 and Feed #2 contained 48.6 g/L powdered CD CHO AGTT M media, 200 mL/L GlutaMAXTM-I (final concentration 8 mM), 200 mL/L Yeastolate Utlrafiltrate 50x (final concentration 8 g/L), 50 g D-Glucose (Dextrose; Invitrogen), and 1.1 g sodium 15 butyrate. Feed #3 through Feed #6 contained 48.6 g/L powdered CD CHO AGT TM media, 100 mL/L GlutaMAXTM-I (final concentration 4 mM), 300 mL/L Yeastolate Utlrafiltrate 50x (final concentration 12 g/L), 40 g D-Glucose (Dextrose; Invitrogen), and 1.6 g sodium butyrate. The cell culture was sampled before each feeding and prior to harvest (day 19) to test for viable cell density (VCD) and % viability by 20 hemocytometer with Trypan Blue staining, and residual glucose. Table 8 sets forth the results of the testing. Table 7d. Hours post VCD % viability Cell Glucose Feed inoculation x 10 5 culture cells/mL volume (L) 0 4.6 87 26 8280 72 16.3 93 26 4690 115 37.6 93 26 4230. 165 43.1 83 26 1830 Feed #1 234 45.7 78 26.5 1040 Feed #2 264 49.7 78 27 1320 WO 2009/111083 PCT/US2009/001486 - 186 287 42.2 78 27 800 Feed #3 312 39.8 74 27.5 1180 Feed#4 336 39.1 73 27.5 1390 Feed #5 386 28.3 58 28 1360 Feed #6 409 24.5 50 28.5 1810 432 20.5 36 28.5 1530 448 18.9 31 28.5 1190 Harvest The bioreactor was harvested on day 19, and the cell culture (approximately 28.5 L) was clarified by filtration to remove cells and cell debris. The cell removal and clarification filtration consisted of Millipore Pod filters DOHC (0.5 M 2 ) and 5 AlHC (0.1 M2). The Millipore Pods were first flushed with water for injection (WFI) followed by equilibration with PBS, before the harvest was added. Following clarification, the harvested cell culture fluid (HCCF) was filtered into storage bags via small capsule filters (Sartobran 300, 0.45 ptm, Sartorius). The HCCF (31.6 L, consisting of 28.5 L of culture supernatant and 3.1 L of PBS flush volume) was 10 supplemented to yield 50 mM Tris and stored at 2-8'C. The HCCF was then concentrated and diafiltered by tangential flow filtration (TFF), consisting of 5 x 1 ft 2 of PES membrane with a 30 kDa molecular weight cut off. The membrane was first equilibrated in 20 mM Bis-Tris, 50 mM NaCl, pH 7.0. The 31.6 L HCCF was added to the TFF system concentrated 1 Ox to 3 L, then 15 dialfiltered with 28 L of 20 mM Bis-Tris, 50 mM NaCl, pH 7.0. The concentrated HCCF was filtered through a 0.2 pm filter, yielding a final volume of 3 L. Viral inactivation was effected by treating the concentrated/buffer exchanged harvest with 1% Triton X-100 and 0.3 % tri-n-butyl phosphate for 90 minutes at room temperature. A Q Sepharose Fast Flow (GE Healthcare) anion exchange column was 20 prepared. Post sanitization, charging, and neutralization, the column was equilibrated with five column volumes of 20 mM Bis-Tris, pH 7.0. Following viral inactivation, the concentrated, buffer exchanged harvest was loaded onto the Q column using a five minute residence time for all steps (407 cm/hr). The column was sequentially washed with five column volumes of 20 mM Bis-Tris, pH 7.0 and five column volumes of 20 WO 2009/111083 PCT/US2009/001486 - 187 mM Bis-Tris, 50 mM NaCl, pH 7.0. The protein was eluted with 20 mM Bis-Tris, 160 mM NaCl, pH 7.0. A ceramic hydroxyapatite (CHT) column (BioRad) was equilibrated with 5 mM sodium phosphate, pH 7.0 post sanitization, charging, and neutralization. The Q 5 Sepharose purified protein was loaded onto the CHT column using a five minute residence time for all steps (257 dm/hr). The column was sequentially washed with five column volumes of 5 mM sodium phosphate, pH 7.0 and five column volumes 10 mM sodium phosphate, pH 7.0. The protein was eluted with 70 mM sodium phosphate, pH 7.0. 10 Pro-cathepsin L was then activated to Cathepsin L by adjusting the pH to 4.5 with 0.5 M sodium acetate, pH 4.0. Following activation, the Cathepsin L was further purified by SP Sepharose Fast Flow chromatography. A SP Sepharose Fast Flow (GE Healthcare) ion exchange column was prepared and equilibrated with five column volumes of 50 mM sodium acetate, pH 4.5 post sanitization, charging, and 15 neutralization. Prior to loading, the activated Cathepsin L was diluted two-fold with 50 mM sodium acetate, pH 4.5. The activated Cathepsin L was loaded onto the SPFF column using a five minute residence time for all steps (253 cm/hr). The column was washed with five column volumes of 50 mM sodium acetate, pH 4.5. The protein was eluted with 50 mM sodium acetate, 50 mM NaCl, pH 5.0. The purified protein is then 20 filtered to remove viruses, and concentrated, such as to between 1-20 mg/mL. EXAMPLE 12 Generation of a soluble recombinant human PH20 (rHuPH20) Expressing Cell Line The HZ24 plasmid (set forth in SEQ ID NO:224) was used to transfect 25 Chinese Hamster Ovary (CHO cells). The DNA encoding the soluble rHuPH20 construct contains an NheI site and a Kozak consensus sequence prior to the DNA encoding the methionine at amino acid position 1 of the native signal leader of human PH20 hyaluronidase, and a stop codon following the DNA encoding the tyrosine at amino acid position 482 of human PH20 hyaluronidase, followed by a BamHI 30 restriction site. The construct pCI-PH20-IRES-DHFR-SV40pa (HZ-24), therefore, results in a single mRNA species driven by the CMV promoter that encodes amino acids 1-482 of PH20 (set forth in SEQ ID NO:225) and amino acids 1-187 of the dihydrofolate reductase (set forth in SEQ ID NO:261), separated by an internal WO 2009/111083 PCT/US2009/001486 - 188 ribosomal entry site (IRES). Non-transfected DG44 CHO cells were grown in GIBCO Modified CD-CHO media for DHFR(-) cells, supplemented with 4 mM Glutamax' and 18 ml Plurionic F68/L (Gibco), and were seeded at 0.5 x 106 cells/ml in a shaker flask in preparation 5 for transfection. Cells were grown at 37* C in 5% CO 2 in a humidified incubator, shaking at 120 rpm. Exponentially growing non-transfected DG44 CHO cells were tested for viability prior to transfection. Sixty million viable cells of the non-transfected DG44 CHO cell culture were pelleted and resuspended to a density of 2 x10 7 cells in 0.7 mL of 2x transfection 10 buffer (2x HeBS: 40 mM Hepes, pH 7.0, 274 mM NaCl, 10 mM KCl, 1.4 mM Na 2

HPO

4 , 12 mM dextrose). To each aliquot of resuspended cells, 0.09 mL (250 pg) of the linear HZ24 plasmid (linearized by overnight digestion with Cla I (New England Biolabs); linear HZ24 plasmid set forth in SEQ ID NO: 19) was added, and the cell/DNA solutions were transferred into 0.4 cm gap BTX (Gentronics) 15 electroporation cuvettes at room temperature. A negative control electroporation was performed with no plasmid DNA mixed with the cells. The cell/plasmid mixes were electroporated with a capacitor discharge of 330 V and 960 pF or at 350 V and 960 piF. The cells were removed from the cuvettes after electroporation and transferred 20 into 5 mL of Modified CD-CHO media for DHFR(-) cells, supplemented with 4 mM Glutamine and 18 ml Plurionic F68/L (Gibco), and allowed to grow in a well of a 6 well tissue culture plate without selection for 2 days at 370 C in 5% CO 2 in a humidified incubator. Two days post-electroporation, 0.5 mL of tissue culture media was removed 25 from each well and tested for the presence of hyaluronidase activity (see Example 16). The results are set forth in Table 8 below. Table 8: Initial Hyaluronidase Activity of HZ24 Transfected DG44 CHO cells at 40 hours post-transfection Dilution Activity Units/ml Transfection 1 to 10 0.25 1 330V Transfection 1 to 10 0.52 2 WO 2009/111083 PCT/US2009/001486 - 189 350V Negative 1 to 10 0.015 Control Cells from Transfection 2 (350V) were collected from the tissue culture well, counted and diluted to I x104 to 2 x 104 viable cells per mL. A 0.1 mL aliquot of the cell suspension was transferred to each well of five, 96 well round bottom tissue 5 culture plates. One hundred microliters of CD-CHO media (GIBCO) containing 4 mM GlutaMAXTM-1 supplement (GIBCOTM, Invitrogen Corporation) and without hypoxanthine and thymidine supplements were added to the wells containing cells (final volume 0.2 mL). Ten clones were identified from the 5 plates grown without methotrexate (see 10 Table 9). Table 9 Plate/Well ID Relative Hyaluronidase 1C3 261 2C2 261 3D3 261 3E5 243 3C6 174 2G8 103 11B9 304 2D9 273 4D10 302 Six HZ24 clones were expanded in culture and transferred into shaker flasks as single cell suspensions. Clones 3D3, 3E5, 2G8, 2D9, 1E 11, and 4D10 were plated 15 into 96-well round bottom tissue culture plates using a two-dimensional infinite dilution strategy in which cells were diluted 1:2 down the plate, and 1:3 across the plate, starting at 5000 cells in the top left hand well. Diluted clones were grown in a background of 500 non-transfected DG44 CHO cells per well, to provide necessary growth factors for the initial days in culture. Ten plates were made per subclone, with 20 5 plates containing 50 nM methotrexate and 5 plates without methotrexate.

WO 2009/111083 PCT/US2009/001486 - 190 Clone 3D3 produced 24 visual subclones (13 from the no methotrexate treatment, and 11 from the 50 nM methotrexate treatment.) Significant hyaluronidase activity was measured in the supernatants from 8 of the 24 subclones (>50 Units/mL), and these 8 subclones were expanded into T-25 tissue culture flasks in the presence of 5 50 nM methotrexate where appropriate. Clone 3D3 50 nM was further expanded in 500 nM methotrexate giving rise to clones producing in excess of 1,000 Units/ml in shaker flasks (clone 3D35M; generation I or Geni 3D35M). Example 13 Production and Purification of Gen1 Human sPH20 10 A. 5 L Bioreactor Process A vial of 3D35M was thawed and expanded from shaker flasks through I L spinner flasks in CD-CHO media (Invitrogen, Carlsbad Calif.) supplemented with 100 nM Methotrexate and GlutaMAXTM-1 (Invitrogen). Cells were transferred from spinner flasks to a 5 L bioreactor (Braun) at an inoculation density of 4 x1 05 viable 15 cells per ml. Parameters were temperature Setpoint 37'C, pH 7.2 (starting Setpoint), with Dissolved Oxygen Setpoint 25% and an air overlay of 0-100 cc/min. At 168 hrs, 250 ml of Feed #1 Medium (CD CHO with 50 g/L Glucose) was added. At 216 hours, 250 ml of Feed #2 Medium (CD CHO with 50 g/L Glucose and 10 mM Sodium Butyrate) was added, and at 264 hours 250 ml of Feed #2 Medium was added. This 20 process resulted in a final productivity of 1600 Units per ml with a maximal cell density of 6 X106 cells/ml. The addition of sodium butyrate was to dramatically enhance the production of soluble rHuPH20 in the final stages of production. Conditioned media from the 3D35M clone was clarified by depth filtration and tangential flow diafiltration into 10 mM Hepes pH 7.0. Soluble rHuPH20 was 25 then purified by sequential chromatography on Q Sepharose (Pharmacia) ion exchange, Phenyl Sepharose (Pharmacia) hydrophobic interaction chromatography, phenyl boronate (Prometics) and Hydroxapatite Chromatography (Biorad, Richmond, CA). Soluble rHuPH20 bound to Q Sepharose and eluted at 400 mM NaCI in the 30 same buffer. The eluate was diluted with 2M ammonium sulfate to a final concentration of 500 mM ammonium sulfate and passed through a Phenyl Sepharose (low sub) column, followed by binding under the same conditions to a phenyl boronate resin. The soluble rHuPH20 was eluted from the phenyl sepharose resin in WO 2009/111083 PCT/US2009/001486 -191 Hepes pH 6.9 after washing at pH 9.0 in 50 mM bicine without ammonium sulfate. The eluate was loaded onto a ceramic hydroxyapatite resin at pH 6.9 in 5 mM potassium phosphate and 1 mM CaCl 2 and eluted with 80 mM potassium phosphate, pH 7.4 with 0.1 mM CaCl 2 . 5 The resultant purified soluble rHuPH20 possessed a specific activity in excess of 65,000 USP Units/mg protein by way of the microturbidity assay (Example 16) using the USP reference standard. Purified sPH20 eluted as a single peak from 24 to 26 minutes from a Pharmacia 5RPC styrene divinylbenzene column with a gradient between 0.1% TFA/H 2 0 and 0.1% TFA/90% acetonitrile/10% H 2 0 and resolved as a 10 single broad 61 kDa band by SDS electrophoresis that reduced to a sharp 51 kDa band upon treatment with PNGASE-F. N-terminal amino acid sequencing revealed that the leader peptide had been efficiently removed. B. Upstream Cell Culture Expansion Process into 100 L Bioreactor Cell Culture A scaled-up process was used to separately purify soluble rHuPH20 from four 15 different vials of 3D35M cell to produce 4 separate batches of sHuPH20; HUA0406C, HUA041 OC, HUA0415C and HUA0420C. Each vial was separately expanded and cultured through a 125 L bioreactor, then purified using column chromatography. Samples were taken throughout the process to assess such parameters as enzyme yield. The description of the process provided below sets forth representative 20 specifications for such things as bioreactor starting and feed media volumes, transfer cell densities, and wash and elution volumes. The exact numbers vary slightly with each batch, and are detailed in Tables 3 to 10. Four vials of 3D35M cells were thawed in a 37*C water bath, CD CHO containing 100 nM methotrexate and 40 mL/L GlutaMAX was added and the cells 25 were centrifuged. The cells were re-suspended in a 125 mL shake flask with 20 mL of fresh media and placed in a 37'C, 7% CO 2 incubator. The cells were expanded up to 40 mL in the 125 mL shake flask. When the cell density reached 1.5 - 2.5 x 106 cells/mL, the culture was expanded into a 125 mL spinner flask in a 100 mL culture volume. The flask was incubated at 37*C, 7% CO 2 . When the cell density reached 30 1.5 - 2.5 x 106 cells/mL, the culture was expanded into a 250 mL spinner flask in 200 mL culture volume, and the flask was incubated at 37'C, 7% CO 2 . When the cell density reached 1.5 - 2.5 x 106 cells/mL, the culture was expanded into a 1 L spinner flask in 800 mL culture volume and incubated at 37*C, 7% CO 2 . When the cell WO 2009/111083 PCT/US2009/001486 - 192 density reached 1.5 - 2.5 x 106 cells/mL, the culture was expanded into a 6 L spinner flask in 5 L culture volume and incubated at 37'C, 7% CO 2 . When the cell density reached 1.5 - 2.5 x 106 cells/mL, the culture was expanded into a 36 L spinner flask in 20 L culture volume and incubated at 37*C, 7% CO 2 . 5 A 125 L reactor was sterilized with steam at 121 0 C, 20 PSI and 65 L of CD CHO media was added. Before use, the reactor was checked for contamination. When the cell density in the 36 L spinner flasks reached 1.8 -2.5 x 106 cells/mL, 20 L cell culture were transferred from the 36L spinner flasks to the 125 L bioreactor (Braun), resulting a final volume of 85 L and a seeding density of approximately 4 x 10 10 5 cells/mL. Parameters were temperature setpoint, 37*C; pH: 7.2; Dissolved oxygen: 25% ± 10%; Impeller Speed 50 rpm; Vessel Pressure 3 psi; Air Sparge I L/ min.; Air Overlay: 1 L/min. The reactor was sampled daily for cell counts, pH verification, media analysis, protein production and retention. Nutrient feeds were added during the run. At Day 6, 3.4 L of Feed #1 Medium (CD CHO + 50 g/L 15 Glucose + 40 mL/L GlutaMAXTM-1) was added, and culture temperature was changed to 36.5*C. At day 9 , 3.5 L of Feed #2 (CD CHO + 50 g/L Glucose + 40 mL/L GlutaMAXTM- 1 + 1.1 g/L Sodium Butyrate) was added, and culture temperature was changed to 36*C. At day 11, 3.7 L of Feed #3 (CD CHO + 50 g/L Glucose + 40 mL/L GlutaMAX T M -1 + 1.1 g/L Sodium Butyrate) was added, and the 20 culture temperature was changed to 35.5*C. The reactor was harvested at 14 days or when the viability of the cells dropped below 50%. The process resulted in production of soluble rHuPH20 with an enzymatic activity of 1600 Units/ml with a maximal cell density of 8 million cells/mL. At harvest, the culture was sampled for mycoplasma, bioburden, endotoxin, and virus in vitro and in vivo, transmission 25 electron microscopy (TEM) for viral particles, and enzyme activity. The one hundred liter bioreactor cell culture harvest was filtered through a series of disposable capsule filters having a polyethersulfone medium (Sartorius): first through a 8.0 um depth capsule, a 0.65 ptm depth capsule, a 0.22 ptm capsule, and finally through a 0.22 pm Sartopore 2000 cm2 filter and into a 100 L sterile storage 30 bag. The culture was concentrated 1 Ox using two TFF with Spiral Polyethersulfone 30 kDa MWCO filters (Millipore) , followed by a 6x buffer exchange with 10 mM HEPES, 25 mM Na 2

SO

4 , pH 7.0 into a 0.22 pim final filter into a 20 L sterile storage WO 2009/111083 PCT/US2009/001486 - 193 bag. Table 10 provides monitoring data related to the cell culture, harvest, concentration and buffer exchange steps. Table 10. Monitoring data for cell culture, harvest, concentration and buffer exchange steps. Parameter HUA0406C HUA04010C HUA0415C HUA0420C Time from thaw to inoculate 21 19 17 18 100 L bioreactor (days) 100 L inoculation density (x 0.45 0.33 0.44 0.46 106 cells/mL) Doubling time in logarithmic 29.8 27.3 29.2 23.5 growth (hr) Max. cell density (x 106 5.65 8.70 6.07 9.70 cells/mL) Harvest viability (%) 41 48 41 41 Harvest titer (U/ml) 1964 1670 991 1319 Time in 100-L bioreactor 13 13 12 13 (days) Clarified harvest volume (mL) 81800 93300 91800 89100 Clarified harvest enzyme 2385 1768 1039 1425 assay (U/mL) Concentrate enzyme assay 22954 17091 8561 17785 (U/mL) Bufferexchanged 15829 11649 9915 8679 concentrate enzyme assay (U/mL) Filtered buffer exchanged 21550 10882 9471 8527 concentrate enzyme assay (U/mL) Buffer exchanged concentrate 10699 13578 12727 20500 volume(mL) Ratio enzyme units 0.87 0.96 1.32 1.4 concentration/harvest 5 A Q Sepharose (Pharmacia) ion exchange column (3 L resin, Height = 20 cm, Diameter = 14 cm) was prepared. Wash samples were collected for a determination of pH, conductivity and endotoxin (LAL) assay. The column was equilibrated with 5 column volumes of 10 mM Tris, 20 mM Na 2

SO

4 , pH 7.5. The concentrated, 10 diafiltered harvest was loaded onto the Q column at a flow rate of 100 cm/hr. The column was washed with 5 column volumes of 10 mM Tris, 20 mM Na 2

SO

4 , pH 7.5 and 10 mM Hepes, 50 mM NaCl, pH 7.0. The protein was eluted'with 10 mM Hepes, 400 mM NaCl, pH 7.0 and filtered through a 0.22 pm final filter into a sterile bag. Phenyl-Sepharose (Pharmacia) hydrophobic interaction chromatography was 15 next performed. A Phenyl-Sepharose (PS) column (9.1 L resin, Height = 29 cm, WO 2009/111083 PCT/US2009/001486 -194 Diameter = 20cm) was prepared. The column was equilibrated with 5 column volumes of 5 mM potassium phosphate, 0.5 M ammonium sulfate, 0.1 mM CaC 2 , pH 7.0. The protein eluate from above was supplemented with 2M ammonium sulfate, I M potassium phosphate and 1 M CaCl 2 stock solutions to final concentrations of 5 5 mM, 0.5 M and 0.1 mM, respectively. The protein was loaded onto the PS column at a flow rate of 100 cm/hr. 5 mM potassium phosphate, 0.5 M ammonium sulfate and 0.1 mM CaCl 2 pH 7.0 was added at 100 cm/hr. The flow through was passed through a 0.22 pm final filter into a sterile bag. The PS-purified protein was the loaded onto an aminophenyl boronate column 10 (ProMedics) (6.3 L resin, Height = 20 cm, Diameter = 20cm) that had been equilibrated with 5 column volumes of 5 mM potassium phosphate, 0.5 M ammonium sulfate. The protein was passed through the column at a flow rate of 100 cm/hr, and the column was washed with 5 mM potassium phosphate, 0.5 M ammonium sulfate, pH 7.0. The column was then washed with 20 mM bicine, 100 mM NaCl, pH 9.0 and 15 the protein eluted with 50 mM Hepes, 100 mM NaCl pH 6.9 through a sterile filter and into a 20 L sterile bag. The eluate was tested for bioburden, protein concentration and enzyme activity. A hydroxyapatite (HAP) column (BioRad) (1.6 L resin, Height = 10 cm, Diameter = 14 cm) was equilibrated with 5 mM potassium phosphate, 100 mM NaCl, 20 0.1 mM CaC 2 pH 7.0. Wash samples were collected and tested for pH, conductivity and endotoxin (LAL assay. The aminophenyl boronate purified protein was supplemented with potassium phosphate and CaCl 2 to yield final concentrations of 5 mM potassium phosphate and 0.1 mM CaCl 2 and loaded onto the HAP column at a flow rate of 100 cm/hr. The column was washed with 5 mM potassium phosphate 25 pH 7.0, 100 mM NaCI, 0.1 mM CaCl 2 , then 10 mM potassium phosphate pH 7.0, 100 mM NaCl, 0.1 mM CaCl 2 pH. The protein was eluted with 70 mM potassium phosphate pH 7.0 and filtered through a 0.22 pm filter into a 5 L sterile storage bag. The eluate was tested for bioburden, protein concentration and enzyme activity. The HAP-purified protein was then pumped through a 20 nM viral removal 30 filter via a pressure tank. The protein was added to the DV20 pressure tank and filter (Pall Corporation), passing through an Ultipor DV20 Filter with 20 nm pores (Pall Corporation) into a sterile 20 L storage bag. The filtrate was tested for protein concentration, enzyme activity, oligosaccharide, monosaccharide and sialic acid WO 2009/111083 PCT/US2009/001486 - 195 profiling, and process-related impurities. The protein in the filtrate was then concentrated to 1 mg/mL using a 10 kD molecular weight cut off (MWCO) Sartocon Slice tangential flow filtration (TFF) system (Sartorius). The filter was first prepared by washing with a Hepes/saline solution (10 mM Hepes, 130 mM NaCl, pH 7.0) and 5 the permeate was sampled for pH and conductivity. Following concentration, the concentrated protein was sampled and tested for protein concentration and enzyme activity. A 6x buffer exchange was performed on the concentrated protein into the final buffer: 10 mM Hepes, 130 mM NaCl, pH 7.0. The concentrated protein was passed though a 0.22 pm filter into a 20 L sterile storage bag. The protein was 10 sampled and tested for protein concentration, enzyme activity, free sulfhydryl groups, oligosaccharide profiling and osmolarity. Tables 11 to 17 provide monitoring data related to each of the purification steps described above, for each 3D35M cell lot. Table 11. Q sepharose colunm data Parameter HUA0406C HUA0410C HUA0415C HUA0420C Load volume (mL) 10647 13524 12852 20418 Load Volume/Resin 3.1 4.9 4.5 7.3 Volume ratio Column Volume (mL) 2770 3840 2850 2880 Eluate volume (mL) 6108 5923 5759 6284 Protein Conc. of Eluate 2.8 3.05 2.80 2.86 (mg/mL) Eluate Enzyme Assay 24493 26683 18321 21052 (U/mL) Enzyme Yield (%) 65 107 87 76 15 Table 12. Phenyl Sepharose column data Parameter HUA0406C HUA0410C HUA0415C HUA0420C Volume Before Stock 5670 5015 5694 6251 Solution Addition (mL) Load Volume (mL) 7599 6693 7631 8360 Column Volume (mL) 9106 9420 9340 9420 Load Volume/Resin 0.8 0.71 0.82 0.89 Volume ratio Eluate volume (mL) 16144 18010 16960 17328 Protein Cone of Eluate 0.4 0.33 0.33 0.38 (mg/mL) Eluate Enzyme Assay 8806 6585 4472 7509 (U/mL) Protein Yield (%) 41 40 36 37 Enzyme Yield (%) 102 88 82 96 RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 - 196 Table 13. Amino Phenyl Boronate column data Parameter HUA0406C HUA0410C HUA0415C HUA0420C Load Volume (mL) 16136 17958 16931 17884 Load Volume/Resin 2.99 3.15 3.08 2.98 Volume ratio Column Volume (mL) 5400 5700 5500 5300 Eluate volume (mL) 17595 22084 20686 19145 Protein Conc. of Eluate 0.0 0.03 0.03 0.04 (mg/mL) Protein Conc. of not tested 0.03 0.00 0.04 Filtered Eluate (mg/mL) Eluate Enzyme Assay 4050 2410 1523 4721 (U/mL) Protein Yield (%) 0 11 11 12 Enzyme Yield (%) not 41 40 69 determined Table 14. Hydroxyapatite column data Parameter HUA0406C HUA0410C HUA0415C HUA0420C Volume Before Stock 16345 20799 20640 19103 Solution Addition (mL) Load Volume/Resin 10.95 13.58 14.19 12.81 Volume ratio Column Volume (mL) 1500 1540 1462 1500 Load volume (mL) 16429 20917 20746 19213 Eluate volume (mL) 4100 2415 1936 2419 Protein Conc. of Eluate not tested 0.24 0.17 0.23 (mg/mL) Protein Conc. of NA NA 0.17 NA Filtered Eluate (mg/mL) Eluate Enzyme Assay 14051 29089 20424 29826 (U/mL) Protein Yield (%) Not tested 93 53 73 Enzyme Yield (%) 87 118 140 104 5 Table 15. DV20 filtration data Parameter HUA0406C HUA0410C HUA0415C HUA0420C Start volume (mL) 4077 2233 1917 2419 Filtrate Volume (mL) 4602 3334 2963 3504 Protein Conc. of 0.1 NA 0.09 NA Filtrate (mg/mL) Protein Conc. of NA 0.15 0.09 0.16 Filtered Eluate (mg/mL) Protein Yield (%) not tested 93 82 101 Table 16. Final concentration data WO 2009/111083 PCT/US2009/001486 - 197 Parameter HUA0406C HUA0410C HUA0415C HUA0420C Start volume (mL) 4575 3298 2963 3492 Concentrate Volume 562 407 237 316 (mL) Protein Conc. of 0.9 1.24 1.16 1.73 Concentrate (mg/mL) Protein Yield (%) 111 102 103 98 Table 17. Buffer Exchange into Final Formulation data Parameter HUA0406C HUA0410C HUA0415C HUA0420C Start Volume (mL) 562 407 237 316 Final Volume Buffer 594 516 310 554 Exchanged Concentrate (mL) Protein Conc. of 1.00 0.97 0.98 1.00 Concentrate (mg/mL) Protein Conc. of 0.95 0.92 0.95 1.02 Filtered Concentrate (mg/mL) Protein Yield(%) 118 99 110 101 The purified and concentrated soluble rHuPH20 protein was asceptically filled 5 into sterile vials with 5 mL and 1 mL fill volumes. The protein was passed though a 0.22 ptm filter to an operator controlled pump that was used to fill the vials using a gravimetric readout. The vials were closed with stoppers and secured with crimped caps. The closed vials were visually inspected for foreign particles and then labeled. Following labeling, the vials were flash-frozen by submersion in liquid nitrogen for 10 no longer than 1 minute and stored at s1 5 0 C (-20 ± 5 0 C). EXAMPLE 14 Production of Gen2 Cells Containing Soluble human PH20 (rHuPH20) The GenI 3D35M cell line described in Example 12 was adapted to higher methotrexate levels to produce generation 2 (Gen2) clones. 3D35M cells were 15 seeded from established methotrexate-containing cultures into CD CHO medium containing 4mM GlutaMAX-lTM and 1.0 pM methotrexate. The cells were adapted to a higher methotrexate level by growing and passaging them 9 times over a period of 46 days in a 37*C, 7% CO 2 humidified incubator. The amplified population of cells was cloned out by limiting dilution in 96-well tissue culture plates containing medium 20 with 2.0 ptM methotrexate. After approximately 4 weeks, clones were identified and clone 3E10B was selected for expansion. 3E10B cells were grown in CD CHO medium containing 4 mM GlutaMAX-1TM and 2.0 iM methotrexate for 20 passages.

WO 2009/111083 PCT/US2009/001486 - 198 A master cell bank (MCB) of the 3E1 OB cell line was created and frozen and used for subsequent studies. Amplification of the cell line continued by culturing 3E1OB cells in CD CHO medium containing 4 mM GlutaMAX-1TM and 4.0 ptM methotrexate. After the 12 th 5 passage, cells were frozen in vials as a research cell bank (RCB). One vial of the RCB was thawed and cultured in medium containing 8.0 pM methotrexate. After 5 days, the methotrexate concentration in the medium was increased to 16.0 ptM, then 20.0 pM 18 days later. Cells from the 8 th passage in medium containing 20.0 pM methotrexate were cloned out by limiting dilution in 96-well tissue culture plates 10 containing CD CHO medium containing 4 mM GlutaMAX-1TM and 20.0 pM methotrexate. Clones were identified 5-6 weeks later and clone 2B2 was selected for expansion in medium containing 20.0 pM methotrexate. After the 11th passage, 2B2 cells were frozen in vials as a research cell bank (RCB). The resultant 2B2 cells are dihydrofolate reductase deficient (dhfr-) DG44 15 CHO cells that express soluble recombinant human PH20 (rHuPH20). The soluble PH20 is present in 2B2 cells at a copy number of approximately 206 copies/cell. Southern blot analysis of Spe I-, Xba I- and BamH I/Hind Ill-digested genomic 2B2 cell DNA using a rHuPH20-specific probe revealed the following restriction digest profile: one major hybridizing band of-7.7 kb and four minor hybridizing bands 20 (-13.9, -6.6, -5.7 and -4.6 kb) with DNA digested with Spe I; one major hybridizing band of-5.0 kb and two minor hybridizing bands (-13.9 and -6.5 kb) with DNA digested with Xba I; and one single hybridizing band of-1.4 kb observed using 2B2 DNA digested with BamH I/Hind III. Example 15 25 A. Production of Gen2 soluble rHuPH20 in 300 L Bioreactor Cell Culture A vial of HZ24-2B2 was thawed and expanded from shaker flasks through 36L spinner flasks in CD-CHO media (Invitrogen, Carlsbad, CA) supplemented with 20 pM methotrexate and GlutaMAX-1TM (Invitrogen). Briefly, the a vial of cells was thawed in a 37'C water bath, media was added and the cells were centrifuged. The 30 cells were re-suspended in a 125 mL shake flask with 20 mL of fresh media and placed in a 37 0 C, 7% CO 2 incubaor. The cells were expanded up to 40 mL in the 125 mL shake flask. When the cell density reached greater than 1.5 x 106 cells/mL, the WO 2009/111083 PCT/US2009/001486 - 199 culture was expanded into a 125 mL spinner flask in a 100 mL culture volume. The flask was incubated at 37*C, 7% CO 2 . When the cell density reached greater than 1.5 x 106 cells/mL, the culture was expanded into a 250 mL spinner flask in 200 mL culture volume, and the flask was incubated at 37*C, 7% CO 2 . When the cell density 5 reached greater than 1.5 x 106 cells/mL, the culture was expanded into a 1 L spinner flask in 800 mL culture volume andincubated at 37 0 C, 7% CO 2 . When the cell density reached greater than 1.5 x 106 cells/mL the culture was expanded into a 6 L spinner flask in 5000 mL culture volume and incubated at 37 0 C, 7% CO 2 . When the cell density reached greater than 1.5 x 106 cells/mL the culture was expanded into a 10 36 L spinner flask in 32 L culture volume and incubated at 37*C, 7% CO 2 . A 400 L reactor was sterilized and 230 mL of CD-CHO media was added. Before use, the reactor was checked for contamination. Approximately 30 L cells were transferred from the 36L spinner flasks to the 400 L bioreactor (Braun) at an inoculation density of 4.0 x 105 viable cells per ml and a total volume of 260L. 15 Parameters were temperature setpoint, 37 0 C; Impeller Speed 40-55 RPM; Vessel Pressure: 3 psi; Air Sparge 0.5- 1.5 L/Min.; Air Overlay: 3 L/ min.. The reactor was sampled daily for cell counts, pH verification, media analysis, protein production and retention. Also, during the run nutrient feeds were added. At 120 hrs (day 5), 10.4L of Feed #1 Medium (4x CD-CHO + 33 g/L Glucose + 160 mL/L Glutamax-I TM + 83 20 mL/L Yeastolate + 33 mg/L rHuInsulin) was added. At 168 hours (day 7), 10.8 L of Feed #2 (2x CD-CHO + 33 g/L Glucose + 80 mL/L Glutamax-I TM + 167 mL/L Yeastolate + 0.92 g/L Sodium Butyrate) was added, and culture temperature was changed to 36.5 0 C. At 216 hours (day 9), 10.8 L of Feed #3 (1x CD-CHO + 50 g/L Glucose + 50 mL/L Glutamax-1TM + 250 mL/L Yeastolate + 1.80 g/L Sodium 25 Butyrate) was added, and culture temperature was changed to 360 C. At 264 hours (day 11), 10.8 L of Feed #4 (1x CD-CHO + 33 g/L Glucose + 33 mL/L Glutamax-1TM + 250 mL/L Yeastolate + 0.92 g/L Sodium Butyrate) was added, and culture temperature was changed to 35.5* C. The addition of the feed media was observed to dramatically enhance the production of soluble rHuPH20 in the final stages of 30 production. The reactor was harvested at 14 or 15 days or when the viability of the cells dropped below 40%. The process resulted in a final productivity of 17,000 Units per ml with a maximal cell density of 12 million cells/mL. At harvest, the culture was WO 2009/111083 PCT/US2009/001486 - 200 sampled for mycoplasma, bioburden, endotoxin and viral in vitro and in vivo, Transmission Electron Microscopy (TEM) and enzyme activity. The culture was pumped by a peristaltic pump through four Millistak filtration system modules (Millipore) in parallel, each containing a layer of diatomaceous earth 5 graded to 4-8 pm and a layer of diatomaceous earth graded to 1.4-1.1 pm, followed by a cellulose membrane, then through a second single Millistak filtration system (Millipore) containing a layer of diatomaceous earth graded to 0.4-0.11 pm and a layer of diatomaceous earth graded to <0.1 Im, followed by a cellulose membrane, and then through a 0.22 pm final filter into a sterile single use flexible bag with a 350 10 L capacity. The harvested cell culture fluid was supplemented with 10 mM EDTA and 10 mM Tris to a pH of 7.5. The culture was concentrated I Ox with a tangential flow filtration (TFF) apparatus using four Sartoslice TFF 30 kDa molecular weight cut-off (MWCO) polyether sulfone (PES) filter (Sartorious) , followed by a I Ox buffer exchange with 10 mM Tris, 20mM Na 2

SO

4 , pH 7.5 into a 0.22 ptm final filter 15 into a 50 L sterile storage bag. The concentrated, diafiltered harvest was inactivated for virus. Prior to viral inactivation, a solution of 10% Triton X- 100, 3% tri (n-butyl) phosphate (TNBP) was prepared. The concentrated, diafiltered harvest was exposed to 1% Triton X- 100, 0.3% TNBP for 1 hour in a 36 L glass reaction vessel immediately prior to 20 purification on the Q column. B. Purification of Gen2 soluble rHuPH20 A Q Sepharose (Pharmacia) ion exchange column (9 L resin, H= 29 cm, D= 20 cm) was prepared. Wash samples were collected for a determination of pH, conductivity and endotoxin (LAL) assay. The column was equilibrated with 5 25 column volumes of 10 mM Tris, 20 mM Na2SO4, pH 7.5. Following viral inactivation, the concentrated, diafiltered harvest was loaded onto the Q column at a flow rate of 100 cm/hr. The column was washed with 5 column volumes of 10 mM Tris, 20 mM Na2SO4, pH 7.5 and 10 mM Hepes, 50 mM NaCl, pH7.0. The protein was eluted with 10 mM Hepes, 400 mM NaCl, pH 7.0 into a 0.22 pm final filter into 30 sterile bag. The eluate sample was tested for bioburden, protein concentration and hyaluronidase activity. A 280 absorbance reading were taken at the beginning and end of the exchange..

WO 2009/111083 PCT/US2009/001486 - 201 Phenyl-Sepharose (Pharmacia) hydrophobic interaction chromatography was next performed. A Phenyl-Speharose (PS) column (19-21 L resin, H=29 cm, D= 30 cm) was prepared. The wash was collected and sampled for pH, conductivity and endotoxin (LAL assay). The column was equilibrated with 5 column volumes of 5 5 mM potassium phosphate, 0.5 M ammonium sulfate, 0.1 mM CaCl2, pH 7.0. The protein eluate from the Q sepharose column was supplemented with 2M ammonium sulfate, I M potassium phosphate and 1 M CaCl 2 stock solutions to yield final concentrations of 5 mM, 0.5 M and 0.1 mM, respectively. The protein was loaded onto the PS column at a flow rate of 100 cm/hr and the column flow thru collected. 10 The column was washed with 5 mM potassium phosphate, 0.5 M ammonium sulfate and 0.1 mM CaCl2 pH 7.0 at 100 cm/hr and the wash was added to the collected flow thru. Combined with the column wash, the flow through was passed through a 0.22 pm final filter into a sterile bag. The flow through was sampled for bioburden, protein concentration and enzyme activity. 15 An aminophenyl boronate column (Promtics) was prepared. The wash was collected and smpled for pH, conductivity and endotoxin (LAL assay). The column was equilibrated with 5 column volumes of 5 mM potassium phosphate, 0.5 M ammonium sulfate. The PS flow through containing purified protein was loaded onto the aminophenyl boronate column at a flow rate of 100 cm/hr. The column was 20 washed with 5 mM potassium phosphate, 0.5 M ammonium sulfate, pH 7.0. The column was washed with 20 mM bicine, 0.5 M ammonium sulfate, pH 9.0. The column was washed with 20 mM bicine, 100 mM sodium chloride, pH 9.0. The protein was eluted with 50 mM Hepes, 100 mM NaCl, pH 6.9 and passed through a sterile filter into a sterile bag. The eluted sample was tested for bioburden, protein 25 concentration and enzyme activity. The hydroxyapatite (HAP) column (Biorad) was prepared. The wash was collected and test for pH, conductivity and endotoxin (LAL assay). The column was equilibrated with 5 mM potassium phosphate, 100 mM NaCl, 0.1mM CaC 2 , pH 7.0. The aminophenyl boronate purified protein was supplemented to final concentrations 30 of 5 mM potassium phosphate and 0.1 mM CaCl 2 and loaded onto the HAP column at a flow rate of 100 cm/hr. The column was washed with 5 mM potassium phosphate, pH 7, 100 mM NaCl, 0.1 mM CaCl 2 . The column was next washed with 10 mM potassium phosphate, pH 7, 100 mM NaCl, 0.1 mM CaC 2 . The protein was eluted WO 2009/111083 PCT/US2009/001486 - 202 with 70 mM potassium phosphate, pH 7.0 and passed through a 0.22pm sterile filter into a sterile bag. The eluted sample was tested for bioburden, protein concentration and enzyme activity. The HAP purified protein was then passed through a viral removal filter. The 5 sterilized Viosart filter (Sartorius) was first prepared by washing with 2 L of 70 mM potassium phosphate, pH 7.0. Before use, the filtered buffer was sampled for pH and conductivity. The HAP purified protein was pumped via a peristaltic pump through the 20 nM viral removal filter. The filtered protein in 70 mM potassium phosphate, pH 7.0 was passed through a 0.22 pm final filter into a sterile bag. The viral filtered 10 sample was tested for protein concentration, enzyme activity, oligosaccharide, monosaccharide and sialic acid profiling. The sample also was tested for process related impurities. The protein in the filtrate was then concentrated to 10 mg/mL using a 10 kD molecular weight cut off (MWCO) Sartocon Slice tangential flow filtration (TFF) 15 system (Sartorius). The filter was first prepared by washing with 10 mM histidine, 130 mM NaCl, pH 6.0 and the permeate was sampled for pH and conductivity. Following concentration, the concentrated protein was sampled and tested for protein concentration and enzyme activity. A 6x buffer exchange was performed on the concentrated protein into the final buffer:. 10 mM histidine, 130 mM NaCl, pH 6.0. 20 Following buffer exchange, the concentrated protein was passed though a 0.22 pm filter into a 20 L sterile storage bag. The protein was sampled and tested for protein concentration, enzyme activity, free sulfhydryl groups, oligosaccharide profiling and osmolarity. The sterile filtered bulk protein was then asceptically dispensed at 20 mL into 25 30 mL sterile Teflon vials (Nalgene). The vials were then flash frozen and stored at 20 ± 5 0 C. C. Comparison of production and purification of Gen1 soluble rHuPH20 and Gen2 soluble rHuPH20 The production and purification of Gen2 soluble rHuPH20 in a 300L 30 bioreactor cell culture contained some changes in the protocols compared to the production and purification Geni soluble rHuPH20 in a IOOL bioreactor cell culture (described in Example 13.B). Table 18 sets forth exemplary differences, in addition to simple scale up changes, between the methods. RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 - 203 Table 18 Process Difference Gen1 soluble rHuPH20 Gen2 soluble rHuPH20 Cell line 3D35M 2B2 Media used to expand Contains 0.10 pM Contains 20 pM cell inoculum methotrexate (0.045 methotrexate (9 mg/L) mg/L) Media in 6L cultures Contains 0.10 pM Contains no onwards methotrexate methotrexate 36 L spinner flask No instrumentation Equipped with instrumentation that monitors and controls pH, dissolved oxygen, sparge and overlay gas 20 L operating volume. flow rate. 32 L operating volume Final operating volume Approx. 100 L in a 125 L Approx. 300L in a 400L in bioreactor bioreactor bioreactor (initial culture (initial culture volume + volume + 260L) 65 L) Culture media in final No rHulnsulin 5.0 mg/L rHulnsulin bioreactor Media feed volume Scaled at 4% of the Scaled at 4% of the bioreactor cell culture bioreactor cell culture volume i.e. 3.4, 3.5 and volume i.e. 10.4, 10.8, 3.7 L, resulting in a 11.2 and 11.7 L, target bioreactor volume resulting in a target of -92 L. bioreactor volume of -303L. Media feed Feed #1 Medium: CD Feed #1 Medium: 4x CD CHO + 50 g/L Glucose + CHO + 33 g/L Glucose 8mM GlutaMAX

TM

-1 + 32 mM Glutamax + 16.6 g/L Yeastolate + 33 Feed #2 (CD CHO + 50 mg/L rHulnsulin g/L Glucose + 8 mM GlutaMAX + 1.1 g/L Feed #2: 2x CD CHO + Sodium Butyrate 33 g/L Glucose + 16 mM Glutamax + 33.4 g/L Feed #3: CD CHO + 50 Yeastolate + 0.92 g/L g/L Glucose + 8 mM Sodium Butyrate GlutaMAX + 1.1 g/L Sodium Butyrate Feed #3: 1 x CD CHO + 50 g/L Glucose + 10 mM Glutamax + 50 g/L Yeastolate + 1.80 g/L Sodium Butyrate Feed #4:1 x CD CHO + WO 2009/111083 PCT/US2009/001486 -204 33 g/L Glucose + 6.6 mM Glutamax + 50 g/L Yeastolate + 0.92 g/L Sodium Butyrate Filtration of bioreactor Four polyethersulfone 1 sT stage - Four modules cell culture filters (8.0 pm, 0.65 pm, in parallel, each with a 0.22 pm and 0.22 pm) in layer of diatomaceous series earth graded to 4-8 pm and a layer of diatomaceous earth graded to 1.4-1.1 pm, followed by a cellulose membrane. 2 nd stage -single module containing a layer of diatomaceous earth graded to 0.4-0.11 pm and a layer of diatomaceous earth graded to <0.1 pm, followed by a cellulose membrane. 100 L storage bag 3 rd stage - 0.22 pm polyethersulfone filter 300L storage bag Harvested cell culture is supplemented with 10 mM EDTA, 10 mM Tris to a pH of 7.5. Concentration and Concentrate with 2 TFF Concentrate using four buffer exchange prior to with Millipore Spiral Sartorius Sartoslice TFF chromatography Polyethersulfone 30K 30K MWCO Filter MWCO Filter Buffer Exchange the Buffer Exchange the Concentrate 6x with 10 Concentrate 1 Ox with 10 mM Hepes, 25 mM mM Tris, 20 mM NaCl, pH 7.0 Na2SO4, pH 7.5 20L sterile storage bag 50L sterile storage bag Viral inactivation prior to None Viral inactivation chromatography performed with the addition of a 1 % Triton X-100, 0.3% Tributyl Phosphate, pH 7.5, 1 ist purification step (Q No absorbance reading A280 measurements at WO 2009/111083 PCT/US2009/001486 - 205 sepharose) the beginning and end Viral filtration after Pall DV-20 filter (20 nm) Sartorius Virosart filter chromatography (20 nm) Concentration and Hepes/saline pH 7.0 Histidine/saline, pH 6.0 buffer exchange after buffer buffer chromatography Protein concentrated to Protein concentrated to 1 mg/ml 10 mg/ml Example 16 Determination of hyaluronidase activity of soluble rHuPH20 Hyaluronidase activity of soluble rHuPH20 in samples such as cell cultures, 5 purification fractions and purified solutions was determined using a tubidometric assay, which based on the formation of an insoluble precipitate when hyaluronic acid binds with serum albumin. The activity is measured by incubating soluble rHuPH20 with sodium hyaluronate (hyaluronic acid) for a set period of time (10 minutes) and then precipitating the undigested sodium hyaluronate with the addition of acidified 10 serum albumin. The turbidity of the resulting sample is measured at 640 nrm after a 30 minute development period. The decrease in turbidity resulting from enzyme activity on the sodium hyaluronate substrate is a measure of the soluble rHuPH20 enzymatic activity. The method is run using a calibration curve generated with dilutions of a soluble rHuPH20 assay working reference standard, and sample activity 15 measurements are made relative to this calibration curve. Dilutions of the sample were prepared in Enzyme Dilurent Solutions. The Enzyme Diluent Solution was prepared by dissolving 33.0 ± 0.05 mg of hydrolyzed gelatin in 25.0 mL of the 50 mM PIPES Reaction Buffer (140 mM NaCl, 50 mM PIPES, pH 5.5) and 25.0 mL of SWFI, and diluting 0.2 mL of 25% Buminate solution 20 into the mixture and vortexing for 30 seconds. This was performed within 2 hours of use and stored on ice until needed. The samples were diluted to an estimated 1-2 U/mL. Generally, the maximum dilution per step did not exceed 1:100 and the initial sample size for the first dilution was not be less than 20 ptL. The minimum sample volumes needed to perform the assay were: In-process Samples, FPLC Fractions: 80 25 pL; Tissue Culture Supernatants: 1 mL; Concentrated Material 80 pL; Purified or Final Step Material: 80 pL. The dilutions were made in triplicate in a Low Protein WO 2009/111083 PCT/US2009/001486 - 206 Binding 96-well plate, and 30 ptL of each dilution was transferred to Optilux black/clear bottom plates (BD BioSciences). Dilutions of known soluble rHuPH20 with a concentration of 2.5 U/mL were prepared in Enzyme Diluent Solution to generate a standard curve and added to the 5 Optilux plate in triplicate. The dilutions included 0 U/mL, 0.25 U/mL, 0.5 U/mL, 1.0 U/mL, 1.5 U/mL, 2.0 U/mL, and 2.5 U/mL. "Reagent blank" wells that contained 60 tL of Enzyme Diluent Solution were included in the plate as a negative control. The plate was then covered and warmed on a heat block for 5 minutes at 37 0 C. The cover was removed and the plate was shaken for 10 seconds. After shaking, the plate was 10 returned to the plate to the heat block and the MULTIDROP 384 Liquid Handling Device was primed with the warm 0.25mg/mL sodium hyaluronate solution (prepared by dissolving 100 mg of sodium hyaluronate (LifeCore Biomedical) in 20.0 mL of SWFI. This was mixed by gently rotating and/or rocking at 2-8*C for 2-4 hours, or until completely dissolved). The reaction plate was transferred to the MULTIDROP 15 384 and the reaction was initiated by pressing the start key to dispense 30 pL sodium hyaluronate into each well. The plate was then removed from the MULTIDROP 384 and shaken for 10 secondsbefore being transferred to a heat block with the plate cover replaced. The plate was incubated at 37C for 10 minutes The MULTIDROP 384 was prepared to stop the reaction by priming the 20 machine with Serum Working Solution and changing the volume setting to 240 /pL. (25 mL of Serum Stock Solution [1 volume of Horse Serum (Sigma) was diluted with 9 volumes of 500 mM Acetate Buffer Solution and the pH was adjusted to 3.1 with hydrochloric acid] in 75 mL of 500 mM Acetate Buffer Solution). The plate was removed from the heat block and placed onto the MULTIDROP 384 and 240 pL of 25 serum Working Solutions was dispensed into the wells. The plate was removed and shaken on a plate reader for 10 seconds. After a further 15 minutes, the turbidity of the samples was measured at 640 nm and the enzyme activity (in U/mL) of each sample was determined by fitting to the standard curve. Specific activity (U/mg) was calculated by dividing the enzyme activity 30 (U/ml) by the protein concentration (mg/mL). EXAMPLE 17 Cathepsin-L Severs Fibrous Septae in the Subcutaneous Space of Zucker Rats WO 2009/111083 PCT/US2009/001486 - 207 Zucker rats were treated by administration of 90 pg/ml cathepsin-L in MES buffer, pH 5.3 and histology performed on skin sections to visualize the fibrous septae. As a control, rats were treated with MES buffer, pH 5.3 alone. Sections were fixed and stained with Masson's Trichrome staining for visualization of collagen as 5 described in Example 5. Sections also were stained with Hemotoxylin and Eosin. Briefly, sections were deparaffinized and hydrated to water. If the sections were Zenker-fixed, the mercuric chloride crystals were removed with iodine and cleared with sodium thiosulphate. Samples were stained with Mayer's hematoxylin for 15 minutes, followed by washing in running tap water for 20 minutes. The sections were 10 counter-stained with eosin for 15 seconds to 2 minutes depending on the age of the eosin, and the depth of the counterstain desired. For even staining results, the slides were dipped several times before allowing them to set in the eosin. The sections were dehydrated in 95% and absolute alcohols with two changes of two minutes each until excess eosin was removed. The slides were checked under a microscope before being 15 cleared in xylene with two changes of two minutes each. Sections were mounted in Permount or Histoclad. The results show that in control animals treated with acidic buffer only, the hypodermal adipose lobules were separated by a complex network of collagen fibrous septae extending perpendicularly to the skin surface. Treatment of rats with cathepsin-L results in degradation of the hypodermis fibrous septae. 20 The organization of the fibrous septae was further visualized with a rabbit anti-collagen antibody following treatment with MES buffer, pH 5.3 without cathepsin-L, with 90 pg/ml cathepsin-L or with 90 pg/ml bacterial collagenase in 50 mM HEPES buffer, pH 7.4. The results show a normal collagen distribution in control rats treated with acidic MES buffer only. Treatment of rats with cathepsin-L 25 showed a decreased staining for collagen evidencing degradation of collagen. The degradation of collagen, however, was much more pronounced by treatment of rats with bacterial collagenase. These results demonstrate that cathepsin-L has a greater temporal control of collagen degradation compared to bacterial collagenase. EXAMPLE 18 30 Duration of Enzymatic Action of Cathepsin-L in Zucker Rat Dermis The duration of the enzymatic action of cathepsin-L was assessed in the dermis of Zucker rat using two complementary methods: Western blots and enzymatic activity. Rats were injected in the dermis with 1 mL of 1200 units/ml of RECTIFIED SHEET (RULE 91) ISA/EP WO 2009/111083 PCT/US2009/001486 - 208 rHuPH20, pH 5.3, containing epinephrine (2.5 ug/mL) to induce vascular contraction. This was immediately followed by an injection of 1 mL of 100 pg/mL of recombinant cathepsin-L, pH 5.3, in 50 mM MES buffer. Incisions were made in the injection site and interstitium perfusate was collected from 3 to 70 minutes post-injection with a 20 5 pL and 200 pL Eppendorf pipet. The fluid was analyzed by Western blot analysis for collagen degradation as described in Example 10 and by measuring the enzymatic activity of cathepsin-L as determined from the rate of hydrolysis of a commercially available fluorogenic substrate, which activity is expressed as relative fluorescence units (RFU)/minute, designated as Z-Leu-Arg-AMC, over one hour as described in 10 Example 9. pH values of the interstitial fluid perfusate was recorded using pH indicator strips (EMD Chemicals, Inc., Gibbstown, NJ, Cat#9588). The data are shown in Table 19. Maximal enzymatic activity was measured within 10 minutes post treatment. Activity decreased by about 50% at 30 min and about 70% at 60 min following the 15 administration in the dermis. Table 19. Time after administration in relation with cathepsin-L activity and pH of the interstitium fluid following administration of 100 tg/mL of recombinant cathepsin-L, pH 5.3. Time Cathepsin-L activity pH of the perfusate (min post injection) (RFU/min) 9 1930 5-5.5 12 1917 5-5.5 15 1759 5-5.5 18 1261 5-5.5 21 1165 5-5.5 25 1115 5.5 30 950 5.5-6 40 669 5.5-6 60 636 6 EXAMPLE 19 Dose-response Effect of Cathepsin-L on Collagen Degradation 20 in Zucker Rat Dermis WO 2009/111083 PCT/US2009/001486 - 209 Following administration of 1 ml of 1200 U/ml of rHuPH20, pH 5.3 in the dermis of Zucker rats, 1 ml of cathepsin-L doses ranging from 1 tg/mL to 500 pg/mL were administered into the dermis of Zucker rats. Twenty minutes post-injection, biopsies were collected, fixed in Bouin's fixative, and processed for histology. 5 Sections were stained with Hematoxylin and Eosin, and Masson's Trichrome for visualization of collagen as described in Example 5. Incisions were made with a scalper in the injection site and interstitium fluid was collected. Histological analysis of the treated skin and Western blot analysis of the perfusates were carried out as described in Examples 5 and 10, respectively. An 10 aliquot of 25 pL of interstitium fluid was mixed with 5 pL of 6X gel loading sample buffer for SDS-PAGE. The total volume of samples were loaded onto 4-12% Tris Glycine gels (Invitrogen, Carlsbad, CA, Cat# EC6038) and electrophoresis was carried out in Tris-Glycine SDS running buffer until the dye front of the prestained molecular weight markers (Invitrogen, Cat# LC5925) reached the bottom of the gel. 15 The proteins were transferred onto a nitrocellulose membrane (Invitrogen, Cat#LC2001) using the XCell II Blot module (Invitrogen, Cat# IB 1001) at 20V for 1.5 hours at 4*C in a buffer of 20% Methanol, 25 mM Tris, and 220 mM Glycine. Transfer was verified by the almost complete absence of color of the prestained marker bands on the gel. The membrane was blocked in a buffer consisting of 2% non 20 fat dry milk in PBST (phosphate-buffered saline (PBS) solution (137 mM NaCl, 2.7 mM KCl, 10 mM phosphate, pH 7.4), with the detergent Tween 20 (0.05% v/v) for use as a wash buffer and diluent for ELISA) for 30 minutes at room temperature. Collagen I was detected with a rabbit polyclonal antibody to human collagen I (Abcam, Cambridge, MA, Cat#ab34710) used at I pg/mL final concentration in 25 PBST and incubated at room temperature for 1 hour followed by a HRP conjugated goat anti-rabbit IgG (Calbiochem, San Diego, CA, Cat#DC03L) used at a concentration of 33 ng/mL in PBST for I hr at room temperature. The HRP signal was developed by the TMB Insoluble (Calbiochem, Cat# 613548) membrane development solution and the reaction was stopped by rinsing in ddH20 after 5-10 30 minutes at room temperature. Histological and western blot analysis showed that increased doses of cathepsin-L resulted in dose dependent collagen degradation. Western blot analysis indicated that higher concentrations of cathepsin-L resulted in more extensive WO 2009/111083 PCT/US2009/001486 -210 collagen degradation as judged by the presence of numerous low molecular weight bands in the samples treated with 100 tg/mL. EXAMPLE 20 Dose-dependent Effect of Cathepsin-L on Fibrous Septae Disruption 5 Following administration of 1 mL of 1200 U/ml of rHuPH20 in 50 mM MES, 150 mM NaCl, pH 5.3, Zucker rats were administered 1 mL of human recombinant cathepsin-L doses ranging from 1, 10, 50, 100, 250, and 500 pg/mL in MES buffer, pH 5.3, to the dermis. As a control, rats were treated with MES buffer, pH 5.3, alone. Twenty minutes post injection, the interstitium perfusates were collected from the 10 injection sites as described in Example 18. Skin biopsies were collected, fixed in Bouin's fixative and processed for histology. Deparaffined sections were stained with Hematoxylin and Eosin, and Masson's Trichrome for visualization of collagen as described in Example 5. Western blots were carried out as described in Example 10. Results from histology and Western blot analysis showed that recombinant 15 cathepsin-L degradation of collagen in the Zucker rat was dose dependent. Disruption of the fibrous septae was clearly visible in the skin treated with 10 pg/mL of cathepsin-L. EXAMPLE 21 Effect of Ionic Strength on the Effect of Cathepsin-L in Zucker Rat Dermis 20 The time period of cathepsin-L enzymatic activity injected in the dermis was studied as a function of the ionic strength of the buffer and epinephrine. Zucker rats were injected with 1 mL of 1200 U/ml rHuPH20 followed by I mL of 25 jig/mL cathepsin-L in 1, 5, 10 and 50 mM of MES buffer, 150 mM NaCl, pH 5.3. The interstitium perfusate was collected at 20 minutes post administration. 25 pH values of the interstitial fluid perfusate was recorded using pH indicator strips (EMD Chemicals, Inc., Gibbstown, NJ, Cat#9588) and cathepsin-L enzymatic activity in the dermis was measured as described in Example 9. pH values of the dermal perfusate was 7.5 for the low ionic buffer strength (1, 5, and 10 mM MES, pH5.3). pH value of the dermal perfusate was 6.5 when cathepsin-L was delivered in 50 mM 30 MES, pH 5.3. No measurable enzymatic activity was detected when cathepsin-L was delivered in low ionic buffer strength (1, 5, and 10 mM MES). Robust enzymatic activity was detected in the perfusate of injection site administered with cathepsin-L WO 2009/111083 PCT/US2009/001486 -211 formulated in 50 mM MES. These results indicated that the enzymatic activity of cathepsin-L can be tightly modulated by the ionic strength of the buffer. EXAMPLE 22 Disruption of Fibrous Septae by Cathepsin-L Injected into Zucker Rat 5 Subdermis The effect of one single dose of cathepsin-L injected into the subdermis of Zucker rat was assessed in 22 Male Zucker rats treated with either 10 or 100 ptg/mL cathepsin-L in 50 mM MES buffer, 150 mM NaCl, pH 5.3 following administration of 1200 U/ml of rHuPH20 in 50 mM MES, 150 mM NaCl, pH 5.3. Biopsies were 10 taken once a week for a period of 20 weeks and analyzed histologically as described. in Example 5. A single treatment with either 10 pg/ml or 100 pg/ml dose of cathepsin-L resulted in rapid disruption of the fibrous septae as described in Example 17. Histological analysis of biopsies taken at week 4 indicated that the number of fibrous septae was lower in the treated areas than in the nontreated areas. From week 15 20 on, the typicalvertical orientation of the fibrous septae was not seen in the treated areas. Rather, the orientation of the collagen in the hypodermis was horizontal and parallel to the skin surface, consistent with tissue remodeling. EXAMPLE 23 Administration of Cathepsin-L is Not Associated with Adverse Effects 20 Safety study of cathepsin L injected intravascularly shows no obvious adverse effects. 25 g Male balb/c mice (Charles River) and 200g male Sprague Dawley rats (Harlan Laboratories) were administered recombinant cathepsin L in 50 mM MES, 150 mM NaCl, pH 5.3 at concentrations up to 12 mg/kg in the tail vein. Animals were observed for one week for adverse effects. No adverse effect recorded by cage side 25 observation. EXAMPLE 24 Cathepsin-L Alters the Structure of the Fibrous Septae Microarchitecture in the Pig Hypodermis Anesthetized Yorkshire pigs (SNS farms, Ramona, Ca) received 5 mL of 30 50mM MES, 150 mM NaCl buffer at pH 5.3 containing 1200 U/mL of rHuPH20 through a 23-gauge butterfly needle (Terumo, Leuven, Belgium Cat#CEO197) inserted into the hypodermis of the flank, immediately followed by i) 5 mL of 50 WO 2009/111083 PCT/US2009/001486 -212 pig/ml cathepsin-L in 50 mM MES, 150 mM NaCl buffer, pH 5.3; or ii) 50 jg bacterial collagenase in 50 mM HEPES, 150 mM NaCI buffer, pH 7.4. Controls were 50 mM MES buffer, 150 mM NaCl pH 5.3; rHuPH20 alone pH 5.3; and cathepsin-L at pH 7.4. Full thickness biopsies were harvested at 2 hours, 24 hours and seven days 5 post treatment and fixed in Bouin's fixative. Six mm histological sections were cut and stained with Hematoxylin and Eosin or with Mason Trichrome collagen stain. Gross changes characterized by intense brown discoloration were observed in the collagenase injected sites, but to a much lesser degree in the cathepsin-L treated site. No gross changes were seen at the sites injected with the controls or in the untreated 10 skin. These results show that treatment with cathepsin-L is accompanied with minimal bleeding compared to bacterial collagenase injection. Gross changes typically correlated with histological findings of substantial subcutaneous injection site bleeding with collagenase, but minimal bleeding with cathepsin-L. The micro-architecture of fibrous septae was characterized by 15 longitudinal splitting, disintegration and angulation of the collagen fibers in the skin injected with cathepsin-L and bacterial collagenase, compared to the densely packed collagen septae in the MES buffer only treated skin. The histology results, however, did show a more severe change in the micro architecture of the septae in the collagenase-treated site compared to the cathepsin-L treated site, consistent with the 20 hemorrhage results. In addition, treatment with doses of bacterial collagenase as low as 5 jig /mL resulted in serious rhabdomyolysis. These results demonstrate that while cathepsin-L degrades collagen and alters the structure of the fibrous septae, its effects are more controlled then bacterial collagenase because cathepsin-L is rapidly inactivated at physiological pH whereas collagenase is active for a prolonged period 25 of time at physiological pH. In another study, pigs received 5 mL of 120/ml U rHuPH20 at pH 5.3 followed by 5 mL of recombinant cathepsin-L in doses ranging from 5 to 1000 jig/mL (5, 25, 50, 100, 200, 500, and 1000 pg /mL) in 50 mM MES, 150 mM NaCl, pH 5.3. Full thickness skin biopsies were harvested at 2 and 24 hr post treatment, fixed in 30 Bouin's fixative and processed for H&E or with Masson's Trichrome for collagen stain as described in Example 5. Visual examination of the skin excised 2 hours and 24 hours after injection showed that there was a moderate bleeding at the injection site treated with doses of 25 pg /mL and above. Rhamdomyolysis was observed only in WO 2009/111083 PCT/US2009/001486 -213 the injection sites area at the high doses of 500 pg /mL and 1000 pg /mL of recombinant cathepsin-L. Example 25 Effect of Reducing Conditions on Enzymatic Activity of Cathepsin-L for a 5 Fluorogenic Substrate The effect of reducing agents on the enzymatic activity of cathepsin-L was assayed using a custom manufactured fluorogenic substrate, designated Z-His-Arg Tyr-Arg-AMC (SEQ ID NO: 536; Z=:N-carbobenzyloxy; AMC: -7-Amino-4-Methyl Coumarin) (Biomatik Corp., Wilmington, DE). Cathepsin-L activity in RFU/Sec was 10 determined in the presence of cysteine (Spectrum Chemical, Gardena, CA; Catalog # C1473) or TCEP (tris (2-carboxyethyl)phosphine) (Sigma Aldrich, St. Louis, MO Cat#C4706). Activatated cathepsin-L at a stock concentration of 7.85 mg/mL containing 5 mM Cysteine was used. 2 ng/ml cathepsin-L was incubated with 20 PM fluorogenic 15 peptide substrate Z-His-Arg-Tyr-Arg-AMC at 37"C for 30 minutes at 37"C in a total volume of 200 pl 50 mM Sodium Citrate buffer pH 6.5, 2% DMSO, 0.01% Brij-35 containing the appropriate concentration of cysteine or TCEP as indicated in Table 19A. Incubations were performed in an opaque-bottom microplate. The resulting fluorescence was read at the optimum excitation emission 360nm - 460 nm for the 20 substrate in a fluorescent plate reader (Molecular Devices, Spectramax M5, Sunnyvale, CA). After sigmoidal dose response fits in Graphpad Prizm software (Graphpad Software, La Jolla, CA), the curve fits had R 2 values >0.998. The results shown in Table 19A below indicate that the presence of a reducing agent increases the activity of cathepsin-L 25 TABLE 19A: Effect of Reducing Agents on Cathepsin-L activity pM Reductant Activity % Max (Cysteine) RFU/Second Activity 10000 413.577 99.7%. 3333 414.853 100.0% 1111 303.383 73.1% 370 101.905 24.6% 123 17.821 4.3% 41 3.310 0.8% 14 1.384 0.3% WO 2009/111083 PCT/US2009/001486 - 214 Activity % Max pM Reductant (TCEP) RFU/Second Activity 10000 358.5 88.4% 3333 405.4 100.0% 1111 399.5 98.5% 370 385.1 95.0% 123 388.9 95.9% 41 331.9 81.9% 14 172.1 42.5% 4.6 26.7 6.6% 1.5 0.7 0.2% Example 26 Enzymatic Activity of Cathepsin-L on Substrates Cathepsin-L at a concentration of 0.25 mg/ml was incubated with either one of 5 the following three proteins (Collagen Type I at 0.5 mg/ml; HSA at 0.25 mg/ml; and PH20 at 0.25 mg/ml) or as a mixture of two or three at 37"C for up to 16 hours in a buffer containing either 50mM sodium acetate pH 5, 50mM sodium acetate pH 6 or 50 mM Hepes pH 7. At various time points (0, 15 min, 30 min, 60 min, 120 min, 240 min, and overnight), aliquots of samples were taken and analyzed by SDS-PAGE 10 using blue staining. Protein degradation by cathepsin-L was dose-dependent and was observed for each of the substrates tested by a visual decrease in the intensity of the intact protein. Degradation of collagen Type I, HAS and PH20 by cathepsin L was more complet at pH 5. The degradation diminished at pH 6 and above. At neutral pH, the degradation of collagen Type I, HAS and PH20 by cathepsin L was minimal. 15 Since cathepsin L is stable at pH 5, adding a reducing agent to the buffer had little or no effect on the degradation of collagen, HAS and PH20 by cathepsin L at pH 5. Since cathepsin L undergoes autocatalysis as the pH is increased to neutral, adding a reducing agent at neutral pH decreased the autocatalysis of cathepin L and thereby increased the degradation of collagen, HAS and PH20. 20 Example 27 Cloning and Expression of hMMP-1 A. Cloning and High-Throughput Expression of hMMP-1 Library In this example, a human matrix metalloprotease 1 (hMMP-1) library was created by cloning DNA encoding human MMP-l into a plasmid followed by 25 transformation and protein growth/isolation. The library was created by introducing WO 2009/111083 PCT/US2009/001486 - 215 mutations in a parent human MMP- 1 DNA sequence having the sequence of nucleotides set forth in SEQ ID NO: 534, which encodes the inactive zymogen proMMP-1 (set forth in SEQ ID NO: 327), to generate single amino acid variants of MMP-1 across the catalytic domain and proline rich linker domain of the polypeptide. 5 The hMMP-1 library was designed to contain at least 15 amino acid variants at each of 178 amino acids positions within the catalytic domain (amino acids 81-242 of SEQ ID NO: 327) and the linker region (amino acids 243-258 of SEQ ID NO: 327) of human MMP-1 (See Table 20, below). Table 20: hMMP-1 Library Amino Amino Acid Substitutions Acid E; H; R; C; Q; T; S; G; M; W; I; V; L; F81 A; P R; C; N; Q; T; Y; S; G; F; M; W; I; L; V82 A; P D; E; H; R; C; Q; T; Y; S; G; M; W; I; L83 A; P D; E; H; R; C; Q; Y; S; G; F; I; V; L; A; T84 P K; R; C; N; Q; T; Y; S; G; F; M; V; L; E85 A; P D; H; K; C; N; T; Y; S; F; M; W; I; V; G86 L; P E; H; R; C; Q; Y; S; G; F; M; I; V; L; N87 A; P D; E; H; K; R; C; Q; T; Y; G; W; I; V; P88 L;A E; H; K; N; T; Y; S; G; F; M; W; V; L; R89 A; P E; H; R; N; Q; T; S; G; F; M; I; V; L; A; W90 P D; H; R; C; N; T; Y; S; G; F; W; I; V; E91 L;A E; K; R; N; T; Y; S; G; F; W; I; V; L; Q92 A; P D; E; K; R; N; S; G; F; M; W; I; V; L; T93 A; P D; E; R; N; T; S; G; F; M; W; I; V; L; H94 A; P D; E; H; K; R; C; T; Y; S; G; W; I; V; L95 A; P T96 E; H; R; C; N; Q; S; G; F; W; I; V; L; WO 2009/111083 PCT/US2009/001486 -216 Table 20: hMMP-1 Library Amino Amino Acid Substitutions Acid A; P D; E; H; K; R; N; Q; T; S; G; W; V; L; Y97 A; P D; E; H; K; C; Y; S; G; F; M; W; V; L; R98 A; P E; H; R; C; N; Q; T; Y; S; G; F; W; V; 199 L; A; P D; H; R; N; T; Y; S; G; F; M; W; I; V; E100 L;P D; H; K; R; C; T; Y; S; F; M; W; V; L; N101 A; P D; E; K; R; C; N; Q; S; G; F; M; V; L; Y102 A; P D; E; K; R; C; N; Q; Y; S; G; W; V; L; T103 A; P D; E; H; R; C; Q; T; Y; S; G; F; M; V; P104 L; A E; R; C; N; T; S; G; F; M; W; I; V; L; D105 A; P D; H; R; C; N; T; Y; S; G; F; M; I; V; L106 A;P D; K; R; C; T; Y; S; G; F; M; W; I; V; P107 L; A E; K; C; N; T; Y; S; G; F; W; I; V; L; R108 A; P D; E; H; R; N; Q; T; Y; S; G; M; W; I; A109 V; L; H; R; C; Q; T; Y; S; G; F; M; I; V; L; D110 A; P D; E; K; R; C; Q; T; Y; S; G; W; I; L; Vi1 A; P H; K; R; C; Q; T; Y; S; G; F; M; W; I; D112 V; L; A; P D; E; R; N; T; Y; S; G; F; M; W; V; L; H113 A; P E; R; C; N; Q; T; S; G; F; M; W; I; V; A114 L; P D; E; H; K; R; C; Q; T; S; G; F; W; V; 1115 L;P D; H; K; R; C; N; Q; S; G; F; M; I; L; E116 A;P D; E; H; R; N; Q; T; Y; S; G; F; W; L; K117 A; P D; E; H; K; R; Q; T; S; G; F; W; I; V; A118 L; P WO 2009/111083 PCT/US2009/001486 -217 Table 20: hMMP-1 Library Amino Amino Acid Substitutions Acid E; H; K; R; C; N; T; Y; S; G; W; V; L; F119 A; P D; E; H; K; R; C; N; T; Y; G; M; W; V; Q120 A; P E; H; K; R; C; N; Q; T; S; G; F; I; V; A; L121 P E; H; K; R; N; Q; T; Y; S; G; F; V; L; W122 A; P D; H; K; R; C; N; Q; T; Y; G; F; M; W; S123 I; V; L; A; P D; K; R; C; T; S; G; F; M; W; I; V; L; N124 A; P D; E; H; R; C; Q; T; Y; S; G; F; M; W; V125 A; P E; H; K; R; N; Q; S; G; F; M; W; V; L; T126 A; P E; H; K; R; C; Q; T; S; F; M; W; I; V; P127 L; A D; K; R; C; Q; T; S; G; F; M; W; I; V; L128 A; P E; H; K; R; C; Y; S; G; F; M; I; V; L; T129 A; P E; H; K; R; C; N; T; Y; S; G; I; V; L; A; F130 P D; E; H; R; C; Q; Y; S; G; F; M; I; L; T131 A; P D; E; H; R; T; Y; S; G; F; M; I; V; L; A; K132 P D; E; H; K; R; C; N; T; S; G; M; W; L; V133 A; P D; E; H; K; R; C; N; Q; T; Y; G; V; L; S134 A;P D; H; R; N; Q; T; S; F; M; W; I; V; L; E135 A; P D; E; H; R; C; N; T; S; M; W; I; V; L; G136 A; P E; H; K; R; C; N; T; Y; S; G; F; W; L; Q137 A; P D; E; H; R; C; Q; T; S; G; M; W; I; V; A138 L; P E; H; R; C; N; Y; S; G; F; M; W; I; V; D139 L; A; P D; E; H; K; R; C; T; Y; G; F; M; W; V; 1140 L; A M141 D; E; H; R; C; N; T; Y; S; G; W; I; L; WO 2009/111083 PCT/US2009/001486 -218 Table 20: hMMP-1 Library Amino Amino Acid Substitutions Acid A; P K; R; N; Q; T; Y; S; G; F; M; W; V; L; 1142 A; P E; H; R; C; N; Q; T; Y; G; M; W; I; L; S143 A;P E; H; K; R; C; N; Q; T; S; G; M; W; V; F144 L; P D; E; H; K; R; C; N; Q; T; S; G; W; L; V145 A; P D; E; H; K; C; N; Q; T; Y; S; F; V; L; R146 A; P E; H; R; C; Q; T; S; F; M; W; I; V; L; G147 A; P E; K; R; C; N; T; S; G; M; W; I; V; L; D148 A; P E; R; C; N; Q; T; Y; S; G; W; I; V; L; H149 A; P D; E; H; K; N; T; S; G; M; W; I; V; L; R150 A; P K; R; N; Q; T; Y; S; G; F; M; W; V; L; D151 A;P D; H; K; R; C; T; Y; S; G; F; W; I; L; N152 A;P D; H; K; R; C; Q; T; Y; G; F; I; V; L; S153 A;P H; K; R; C; N; Q; T; Y; S; F; W; I; V; P154 L; A E; H; R; N; Q; T; Y; S; G; M; W; V; L; F155 A;P E; H; K; R; C; T; Y; S; G; M; W; V; L; D156 A; P D; H; K; R; N; Q; T; Y; S; F; M; V; L; G157 A; P D; K; R; C; N; Q; T; Y; S; G; F; W; I; P158 V;L;A E; K; R; C; Q; T; Y; S; M; W; I; V; L; G159 A; P E; H; R; C; N; Q; T; S; M; W; I; V; L; G160 A; P E; H; R; C; Q; T; Y; S; G; F; W; I; V; L; N161 P D; E; R; C; Q; T; Y; S; G; F; M; W; I; L162 A;P E; K; R; C; N; Q; T; Y; S; G; F; I; V; L; A163 P WO 2009/111083 PCT/US2009/001486 - 219 Table 20: hMMP-1 Library Amino Amino Acid Substitutions Acid E; K; R; C; N; Q; Y; S; G; F; M; V; L; H164 A; P D; H; K; R; N; Q; T; S; G; F; M; W; V; A165 L; P E; H; K; R; C; N; S; G; M; W; I; V; L; F166 A; P D; E; K; R; N; T; Y; S; G; F; M; V; L; Q167 A; P D; H; R; C; N; T; S; G; F; M; W; I; V; P168 L; A D; E; H; R; C; Q; T; S; M; W; I; V; L; G169 A; P D; H; K; R; C; Q; T; S; G; F; M; W; I; P170 L; A D; E; H; K; R; C; N; Q; Y; S; M; W; L; G171 A; P D; E; R; C; N; Q; T; Y; G; M; W; V; L; 1172 A;P D; K; R; C; N; T; Y; S; F; M; W; V; L; G173 A; P D; E; H; R; N; T; Y; S; F; M; W; V; L; G174 A; P E; H; R; C; N; Q; T; Y; S; G; F; I; V; L; D175 A;P D; E; K; R; C; N; Q; T; S; G; F; W; V; A176 L; P D; R; C; N; Q; T; Y; S; G; W; I; V; L; H177 A; P E; H; K; R; C; Q; T; Y; S; G; W; I; V; F178 L;A;P E; K; R; C; N; Q; T; S; G; W; I; V; L; D179 A; P D; K; R; C; N; Q; T; Y; S; G; F; M; I; E180 A; P E; K; R; C; Q; T; Y; S; G; F; M; V; L; D181 A;P D; R; C; Q; T; Y; S; G; F; M; W; I; L; E182 A;P E; H; K; C; N; T; S; G; M; W; I; V; L; R183 A; P E; H; R; N; Q; T; S; G; F; M; I; V; L; A; W184 P D; E; H; R; C; N; Q; Y; S; G; W; V; L; T185 A; P N186 D; E; H; R; C; Q; T; Y; S; G; F; V; L; WO 2009/111083 PCT/US2009/001486 - 220 Table 20: hMMP-1 Library Amino Amino Acid Substitutions Acid A; P D; H; K; R; C; T; S; G; F; M; W; I; L; N187 A;P D; E; H; K; R; N; Q; S; G; W; I; V; L; F188 A;P D; E; H; K; C; N; Q; T; Y; G; W; V; L; R189 A; P D; H; K; R; C; T; Y; S; G; M; I; V; L; E190 A;P D; E; H; K; R; C; Q; T; S; G; W; V; L; Y191 A;P D; H; K; R; C; Q; T; S; G; M; W; V; L; N192 A; P D; E; K; R; N; Q; T; Y; S; G; F; W; I; L193 A; P E; K; Q; T; Y; S; G; F; M; W; I; V; L; H194 A; P D; E; K; C; Q; T; Y; S; G; F; W; V; L; R195 A; P D; E; H; K; R; Q; T; Y; S; G; M; I; L; V196 A; P E; H; R; C; N; Q; T; Y; S; G; W; I; V; A197 L; P D; E; H; K; R; T; Y; S; G; F; M; W; V; A198 L;P E; K; R; C; N; T; S; G; M; W; I; V; L; H199 A; P D; R; C; N; T; Y; S; G; F; M; W; I; V; E200 A; P D; E; K; R; N; Q; T; S; G; M; W; I; V; L201 A;P D; E; H; K; R; C; T; Y; S; M; I; V; L; G202 A; P D; E; R; C; N; Q; T; Y; S; G; I; V; L; A; .H203 P D; H; K; R; N; Q; T; Y; G; W; I; V; L; S204 A; P D; E; R; C; N; Q; T; S; G; M; W; I; V; L205 A;P D; E; H; R; C; Q; T; S; M; W; I; V; L; G206 A; P D; H; K; R; N; Q; Y; S; G; M; W; I; V; L207 A; P D; E; K; R; C; N; Q; T; G; F; W; V; L; S208 A; P WO 2009/111083 PCT/US2009/001486 -221 Table 20: hMMP-1 Library Amino Amino Acid Substitutions Acid D; R; C; N; Q; T; Y; S; G; F; W; V; L; H209 A; P H; K; R; C; N; Q; T; G; F; W; I; V; L; S210 A;P D; H; K; R; N; Q; S; G; F; M; W; V; L; T211 A;P E; H; K; R; N; Q; T; Y; S; G; F; V; L; D212 A;P D; E; H; K; R; C; N; Q; T; S; G; F; M; 1213 V; L; A; P D; E; R; C; Q; T; Y; S; F; M; I; V; L; A; G214 P D; H; K; R; C; N; Q; T; S; G; M; W; I; A215 V; L; P D; E; K; R; C; Q; T; S; G; M; W; I; V; L216 A; P D; H; K; R; C; N; Q; T; Y; S; G; I; L; M217 A; P D; E; R; C; N; Q; S; G; F; W; I; V; L; Y218 A;P D; E; H; K; R; C; Q; T; S; G; F; W; V; P219 L; A E; H; K; R; N; Q; T; G; F; M; I; V; L; S220 A;P E; K; R; C; N; Q; T; S; G; M; W; V; L; Y221 A;P D; H; R; C; N; Y; S; G; F; M; W; I; V; T222 L; A; P E; H; K; R; C; N; Q; T; Y; S; G; M; L; F223 A; P D; H; K; R; C; Q; T; G; M; W; I; V; L; S224 A; P D; E; H; K; R; C; N; Q; T; S; M; W; V; G225 A; P E; H; R; C; N; T; S; G; M; W; I; V; L; D226 A; P D; E; H; K; R; C; Q; T; Y; S; G; W; L; V227 A; P D; E; H; K; R; N; T; Y; S; G; M; W; L; Q228 A; P D; E; H; R; C; Q; T; Y; G; M; W; I; V; L229 A;P D; H; R; C; N; T; Y; S; G; M; W; I; V; A230 L; P Q231 D; H; R; C; Y; S; G; F; M; W; I; V; L; WO 2009/111083 PCT/US2009/001486 - 222 Table 20: hMMP-1 Library Amino Amino Acid Substitutions Acid A; P E; H; K; R; N; Q; T; Y; S; G; F; W; V; D232 L; P E; K; R; N; Q; T; S; G; M; W; I; V; L; D233 A; P D; E; H; C; N; Q; T; Y; G; M; W; V; L; 1234 A; P E; H; R; C; N; Q; T; Y; S; G; I; V; L; A; D235 P D; E; K; R; C; N; T; Y; S; F; M; I; V; L; G236 P D; E; K; R; C; N; Q; T; Y; S; G; W; L; 1237 A; P E; H; K; R; C; N; T; Y; S; G; F; W; I; L; Q238 P D; H; K; R; C; Q; T; Y; S; G; F; W; I; A239 V; L; P D; K; R; C; Q; T; Y; S; G; F; M; V; L; 1240 A; P D; H; R; N; Q; T; S; G; M; W; I; V; L; Y241 A; P E; H; K; R; N; T; Y; S; F; W; I; V; L; G242 A; P D; H; K; C; N; Q; T; Y; S; G; I; V; L; R243 A; P D; E; H; R; Q; T; Y; G; F; M; W; V; L; S244 A; P E; H; K; R; C; T; S; G; F; M; W; I; V; Q245 L; P D; K; R; C; Q; T; Y; S; G; F; W; I; V; N246 L; A; P D; E; H; K; R; N; Q; T; S; G; F; I; V; L; P247 A E; H; K; R; C; Q; T; Y; S; G; F; M; W; V248 I; L; A E; H; K; R; C; N; T; Y; G; W; I; V; L; Q249 A; P D; K; R; N; Q; T; Y; S; G; F; M; W; V; P250 L; A D; E; K; R; C; Q; T; Y; S; G; W; V; L; 1251 A; P D; E; H; K; R; C; T; S; F; M; W; I; V; G252 L; A; P E; K; R; C; N; Q; T; Y; G; M; W; I; V; P253 L; A WO 2009/111083 PCT/US2009/001486 - 223 Table 20: hMMP-1 Library Amino Amino Acid Substitutions Acid D; E; R; C; T; Y; S; G; F; W; I; V; L; A; Q254 P E; H; K; R; C; N; Q; S; G; F; I; V; L; A; T255 P E; K; R; C; N; Q; Y; S; G; F; M; I; V; P256 L; A E; R; C; N; T; S; G; F; M; W; I; V; L; K257 A; P D; E; R; N; Q; T; Y; G; F; M; W; I; V; A258 L; P The cDNA encoding each individual hMMP- I mutant was generated by changing the wild type codon, encoding each of the 178 amino acids positions identified in Table 21 below, to a codon encoding the desired amino acid substitution. 5 The wild type codons are set forth in SEQ ID NO:534. SEQ ID NO: 534 also depicts the encoded amino acids. The amino acids substitutions and corresponding mutated codons are listed in Table 21, below. Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon F81C TGT T84L TTG N87S AGT W90H CAT F81E GAG T84D GAT N871 ATT W90M ATG F811 ATT T84R CGG N87C TGT W90R CGG F81L CTG T841 ATT N87A GCG W90E GAG F81P CCT T84S TCT N87G GGT W90N AAT F81S TCT T84G GGT N87Y TAT W90Q CAG F81A GCG T84Q CAG N87E GAG E91N AAT F81M ATG T84P CCT N87H CAT E91R CGG F81G GGG T84A GCG N87Q CAG E91W TGG F81T ACG T84C TGT P88C TGT E91G GGG F81Q CAG T84Y TAT P88K AAG E91V GTG F81R CGT T84F TTT P88W TGG E91Y TAT F81W TGG E85L CTG P88G GGG E91C TGT F81H CAT E85Q CAG P88L CTG E91H CAT F81V GTG E85P CCT P88Q CAG E91T ACG V821 ATT E85T ACT P88A GCG E91S AGT V82C TGT E85K AAG P88T ACG E91A GCG V82A GCG E85M ATG P88Y TAT E911 ATT V82P CCG E85G GGT P88R CGG E91D GAT V82Y TAT E85R CGT P88H CAT E91F TTT V82M ATG E85S TCT P881 ATT E91L TTG WO 2009/111083 PCT/US2009/001486 - 224 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon V82Q CAG E85C TGT P88V GTG Q92V GTT V82F TTT E85Y TAT P88E GAG Q92Y TAT V82W TGG E85A GCG P88D GAT Q92L CTG V82N AAT E85N AAT R89V GTG Q92N AAT V82R CGT E85V GTG R89W TGG Q92E GAG V82G GGT E85F TTT R89M ATG Q921 ATT V82S TCG G86L CTT[ R89A GCG Q92T ACT V82L TTG G86P CCG R89T ACG Q92G GGT V82T ACT G861 ATT R89G GGG Q92P CCG L83A GCG G86T ACT R89S TCT Q92W TGG L83C TGT G86H CAT R89K AAG Q92F TTT L83D GAT G86D GAT R89F TTT Q92S TCG L83E GAG G86N AAT R89Y TAT Q92R CGG L83G GGT G86S AGT R89N AAT Q92K AAG L83H CAT G86K AAG R89H CAT Q92A GCT L831 ATT G86W TGG R89L TTG T93A GCG L83M ATG G86Y TAT R89E GAG T93L CTT L83P CCG G86V GTT R89P CCT T93M ATG L83Q CAG G86C TGT W90L TTG T93N AAT L83R CGG G86M ATG W90G GGG T93V GTG L83S AGT G86F TTIT W90P CCG T931 ATT L83T ACG N87M ATG W90T ACT T93D GAT L83W TGG N87L CTG W90S TCG T93S TCG L83Y TAT N87P CCG W90V GTG T93R CGG T84V GTT N87V GTT W901 ATT T93W TGG T84E GAG N87R CGT W90A GCT T93F TTT T84H CAT N87F TTT W90F TTT T93P CCT T93G GGG Y97R CGT E1OOL CTG T103R CGG T93K AAG Y97V GTG E100H CAT T103Y TAT T93E GAG Y97A GCT ElOOD GAT T103N AAT H94L CTG Y97P CCT ElOOM ATG T103C TGT H94S TCG Y97L CTT ElOOG GGT T103Q CAG H94M ATG Y97T ACG E1OOW TGG T103W TGG H94R CGG Y97K AAG E100Y TAT T103P CCG H94E GAG Y97W TGG ElOOR CGT T103A GCG H941 ATT Y97H CAT E100S TCT T103G GGG H94D GAT Y97S TCG ElOOT ACG T103K AAG H94P CCG Y97E GAG E1OOF TTT P104G GGG H94A GCG Y97D GAT E100I ATT P104E GAG H94N AAT Y97N AAT ElOON AAT P104T ACT H94F TTT Y97G GGT N101M ATG P104F TTT H94G GGG Y97Q CAG N101F TTT P104R CGT H94T ACT R98H CAT N101L TTG P104D GAT H94V GTG R98K AAG N101V GTG P104C TGT H94W TGG R98C TGT N101H CAT P104Q CAG WO 2009/111083 PCT/US2009/001486 -225 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon L95E GAG R98L CTG N101R CGG P104V GTG L95Y TAT R98M ATG N1O1C TGT P104Y TAT L95R CGG R98F TTT N101T ACT P104H CAT L95A GCT R98W TGG N101P CCT P104L TTG L95G GGG R98Y TAT N101W TGG P104S TCG L95K AAG R98P CCT N101K AAG P104A GCG L95S AGT R98E GAG N101S TCG P104M ATG L95T ACG R98A GCG N101D GAT D105A GCT L95H CAT R98G GGG N101A GCG D105C TGT L95W TGG R98V GTT N101Y TAT D105F TTT L95V GTG R98S TCG Y102R CGT D105G GGT L95C TGT R98D GAT Y102K AAG D1051 ATT L95P CCT 199C TGT Y102V GTG D105L CTG L95D GAT 199E GAG Y102M ATG D105M ATG L951 ATT 199G GGG Y102P CCG D105N AAT T96E GAG 199H CAT Y102N AAT D105P CCT T96R CGG 199N AAT Y102G GGG D105R CGG T96P CCG 199P CCT Y102L CTG D105S TCG T96S TCG 199T ACG Y102D GAT D105T ACG T96A GCG 199V GTT Y102S TCG D105V GTT T96L TTG 199A GCG Y102F TTT D105W TGG T96W TGG 199F TTT Y102A GCT D105E GAG T96N AAT 199L CTG Y102E GAG L106P CCG T96G GGT 199R CGT Y102Q CAG L106D GAT T96F TTT 199S TCG Y102C TGT L106N AAT T96Q CAG 199Q CAG T103E GAG L106G GGT T96H CAT 199W TGG T103D GAT L106M ATG T96V GTT 199Y TAT T103S AGT L106A GCT T961 ATT E100V GTT T103L CTG L106R CGG T96C TGT ElOOP CCG T103V GTT L106Y TAT L106T ACG A109V GTT D1121 ATT E116A GCG L106V GTG A109E GAG D112Y TAT E116C TGT L106H CAT A109L CTT D112L TTG E116D GAT L106F TTT A109H CAT H113T ACT E116F TTT L1061 ATT D110P CCT H113L CTG E116G GGT L106C TGT D11OF TTT H113M ATG E116H CAT L106S TCT D110Q CAG H113S TCG E1161 ATT P107L TTG D11OR CGG H113N AAT E116K AAG P107W TGG D110M ATG H113R AGG E116L CTG P107T ACT D110H CAT H113A GCT E116M ATG P107S TCG D110I ATT H113E GAG E116N AAT P107R CGG D110L CTT H113V GTG E116P CCG P107Y TAT D11OV GTG H113Y TAT E116Q CAG P107M ATG D110T ACG H113F TTT E116R AGG P107V GTG D110S TCG H113D GAT E116S TCT WO 2009/111083 PCT/US2009/001486 - 226 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon P107D GAT D110Y TAT H113W TGG K117H CAT P107A GCG D11OG GGT H113G GGG K117T ACG P107C TGT D110C TGT H113P CCG K117Q CAG P107K AAG D110A GCG A114E GAG K117E GAG P107F TTT V111E GAG A114S TCG K117A GCG P1071 ATT V111A GCT A1141 ATT K117F TTT P107G GGT VilS TCT A114P CCT K117D GAT R108P CCT V111W TGG A114N AAT K117N AAT R108G GGT V11IG GGT A114L CTT K117G GGT R108T ACG VillY TAT A114T ACT K117W TGG R108E GAG ViliP CCG A114F TTT K117Y TAT R108A GCG V111L CTG A114V GTT K117L TTG R108Y TAT V111D GAT A114G GGT K117S AGT R108K AAG V111K AAG A114C TGT K117P CCG R108C TGT V111T ACT A114M ATG K117R AGG R108S TCT V111Q CAG A114R AGG A118G GGG R108F TTT V111I ATT A114W TGG A118R CGT R108W TGG ViliC TGT A114Q CAG A118W TGG R1081 ATT V111R CGT 1115F TTT A118K AAG R108L CTT D112A GCG 1115T ACT A118P CCT R108N AAT D112M ATG 1115H CAT A118V GTG R108V GTT D112V GTT 1115G GGT A118L TTG A109S TCG D112R CGG 1115K AAG A118D GAT A109R CGG D112K AAG 1115E GAG A118S AGT A109T ACG D112P CCT 1115S AGT A118F TTT A109W TGG D112Q CAG 1115P CCT A1181 ATT A1091 ATT D112F TTT 1115C TGT A118H CAT A109Q CAG D112G GGG 1115L CTT A118E GAG A109N AAT D112C TGT 1115Q CAG A118Q CAG A109Y TAT D112W TGG 1115R CGG A118T ACT A109G GGG D112T ACT 1115W TGG F119G GGG A109M ATG D112H CAT 1115V GTT F119T ACT A109D GAT D112S TCT 1115D GAT F119R CGG F119L TTG W122G GGG V125T ACG L128A GCG F119N AAT W122S TCG V125A GCT L128D GAT F1 19S AGT W122V GTT V125C TGT L128V GTG F119C TGT W122H CAT V125D GAT L128W TGG F119P CCG W122F TTT V125W TGG L128C TGT F119W TGG W122Y TAT V125R CGG L128K AAG F119K AAG W122K AAG V125E GAA T129G GGT F119H CAT W122Q CAG V125F TTT T129A GCT F119A GCG W122E GAG V125H CAT T129C TGT F119V GTT S123D GAT T126K AAG T129K AAG F119Y TAT S123L TTG T126V GTG T129F TTT F119E GAG S123A GCT T126G GGG T129Y TAT WO 2009/111083 PCT/US2009/001486 - 227 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon Q120K AAG S123C TGT T126R CGG T129S TCG Q120N AAT S1231 ATT T126L TTG T129R CGG Q120A GCG S123K AAG T126H CAT T129V GTT Q120V GTG S123N AAT T126M ATG T129L CTT Q120D GAT S123F TTT T126P CCG T129H CAT Q120R CGG S123Y TAT T126A GCG T129P CCT Q120P CCT S123M ATG T126N AAT T129E GAG Q120W TGG S123H CAT T126E GAG T1291 ATT Q120Y TAT S123R CGG T126F TTT T129M ATG Q120C TGT S123W TGG T126W TGG F130L CTG Q120H CAT S123T ACG T126Q CAG F130P CCT Q120T ACT S123P CCT T126S AGT F130C TGT Q120M ATG S123G GGG P127C TGT F130R CGG Q120E GAG S123Q CAG P127F TTT F130Y TAT Q120G GGT S123V GTT P127T ACG F130H CAT L121E GAG N124G GGT P127E GAG F1301 ATT L121Q CAG N124C TGT P127W TGG F130V GTT L121P CCT N124V GTG P127A GCT F130K AAG L121R CGG N124L CTT. P127S AGT F130T ACT L121C TGT N124T ACG P127H CAT F130E GAG L121G GGG N124R CGT P127Q CAG F130A GCG L121K AAG N124M ATG P127K AAG F130N AAT L121F TTT N124S TCG P127R CGG F130G GGT L1211 ATT N124P CCT P1271 ATT F130S AGT L121S TCG N124A GCG P127V GTG T131F TTT L121V GTT N124K AAG P127L CTG T131P CCG L121H CAT N124F TTT P127M ATG T131A GCG L121T ACT N124W TGG L128F TTT T131S TCT L121A GCT N1241 ATT L128M ATG T131G GGT L121N AAT N124D GAT L128T ACT T1311 ATT W122R CGT V125G GGG L128R CGT T131L CTT W122A GCG V125Q CAG L128S TCG T131H CAT W122N AAT V125S TCG L128G GGT T131Q CAG W122P CCG V125P CCG L1281 ATT T131D GAT W122T ACG V125M ATG L128Q CAG T131E GAG W122L CTT V125Y TAT L128P CCT T131C TGT T131R CGT E135V GTT A138C TGT M141S AGT T131Y TAT E135M ATG A138T ACG M141C TGT T131M ATG E135S TCG A138S TCT M141L CTG K132G GGT E135D GAT A138R CGT M141A GCG K132V GTG E135T ACG A138G GGG M141D GAT K132L TTG E135L CTG A138E GAG M141W TGG K132A GCT E135A GCG A138H CAT M141G GGT K132P CCG E135W TGG A138M ATG M141H CAT K132F TTT E135F TTT A138Q CAG M141Y TAT WO 2009/111083 PCT/US2009/001486 - 228 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon K132R CGG E135P CCG A1381 ATT M141N AAT K1321 ATT E135R CGG A138D GAT 1142L CTG K132H CAT E135N AAT A138W TGG 1142M ATG K132S TCT E135H CAT D139R CGT 1142G GGT K132M ATG E135Q CAG D139V GTT 1142K AAG K132D GAT E1351 ATT D139M ATG 1142A GCT K132T ACT G136V GTG D139C TGT 1142N AAT K132Y TAT G136W TGG D139P CCT 1142W TGG K132E GAG G136D GAT D139S TCT 1142P CCG V133G GGG G136M ATG D139L CTT 1142Q CAG V133E GAG G136N AAT D1391 ATT 1142Y TAT V133T ACT G136A GCG D139H CAT 1142V GTG V133N AAT G136L TTG D139A GCG 1142T ACT V133A GCG G136C TGT D139G GGG 1142R CGG V133H CAT G136P CCG D139F TTT 1142S AGT V133P CCG G136T ACG D139N AAT 1142F TTT V133K AAG G136R CGT D139W TGG S143P CCG V133R CGG G136S TCG D139Y TAT S143C TGT V133L CTT G1361 ATT D139E GAG S143E GAG V133W TGG G136H CAT 1140D GAT S143G GGT V133C TGT G136E GAG 1140K AAG S143H CAT V133D GAT Q137A GCT 1140A GCT S143R CGT V133M ATG Q137R CGG 1140G GGG S143L TTG V133S AGT Q137G GGG 1140C TGT S143Q CAG S134V GTT Q137K AAG 1140Y TAT S143N AAT S134H CAT Q137H CAT 1140V GTT S143W TGG S134P CCT Q137P CCT 1140W TGG S143A GCT S134G GGG Q137S TCG 1140F TTT S143T ACT S134N AAT Q137L CTG 1140H CAT S143Y TAT S134R CGT Q137W TGG 1140L CTG S143M ATG S134L CTG Q137F TTT 1140R CGG S1431 ATT S134Q CAG Q137T ACG 1140E GAG F144K AAG S134E GAG Q137C TGT 1140M ATG F144M ATG S134Y TAT Q137Y TAT 1140T ACT F144E GAG S134A GCG Q137N AAT M141E GAG F144S AGT S134K AAG Q137E GAG M1411 ATT F144L CTG S134D GAT A138V GTT M141R CGG F144W TGG S134T ACG A138L CTT M141T ACG F144P CCG S134C TGT A138P CCG M141P CCG F144R CGG F144N AAT G147V GTT R150H CAT P154L CTT F144C TGT G147Q CAG D151R CGT P154C TGT F144G GGT G147M ATG D151F TTT P154S TCT F144T ACT G147P CCT D151P CCG P154K AAG F144Q CAG D148R CGG D151W TGG P1541 ATT F144H CAT D1481 ATT D151Q CAG P154A GCT WO 2009/111083 PCT/US2009/001486 -229 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon F144V GTG D148T ACG D151L CTT P154T ACG V145A GCG D148G GGT D151S TCG P154H CAT V145T ACG D148L CTG D151G GGT P154Y TAT V145L CTG D148V GTT D151A GCT P154N AAT V145P CCG D148A GCG D151N AAT P154F TTT V145K AAG D148W TGG D151K AAG P154R CGT V145N AAT D148P CCG D151Y TAT P154Q CAG V145D GAT D148S TCG D151V GTT F155S TCT V145H CAT D148K AAG D151T ACT F155T ACT V145R CGG D148E GAG D151M ATG F155G GGT V145Q CAG D148M ATG N152G GGG F155N AAT V145S TCT D148N AAT N152C TGT F155R CGG V145G GGG D148C TGT N152F TTT F155W TGG V145W TGG H149W TGG N152L TTG F155L CTG V145C TGT H149A GCG N152P CCG F155Q CAG V145E GAG H149L TTG N152R CGG F155M ATG R146T ACG H149C TGT N152H CAT F155E GAG R146L CTG H149Q CAG N152T ACG F155A GCG R146N AAT H149T ACT N152Y TAT F155P CCT R146H CAT H149Y TAT N152K AAG F155V GTT R146Q CAG H149P CCG N152D GAT F155H CAT R146K AAG H149V GTT N152W TGG F155Y TAT R146C TGT H149R CGG N1521 ATT D156H CAT R146S AGT H149G GGT N152A GCG D156L CTT R146D GAT H149E GAG N152S TCT D156E GAG R146A GCT H149S AGT S1531 ATT D156A GCT R146Y TAT H1491 ATT S153R CGG D156W TGG R146P CCT H149N AAT S153K AAG D156C TGT R146V GTT R150S TCG S153C TGT D156P CCT R146E GAG R150E GAG S153G GGG D156V GTT R146F TTT R150G GGG S153H CAT D156K AAG G147R CGT R150M ATG S153L CTT D156S TCT G147F TTT R150P CCG S153V GTT D156G GGG G1471 ATT R150T ACG S153T ACG D156T ACT G147L CTG R150W TGG S153P CCT D156Y TAT G147A GCG R150A GCG S153A GCG D156R CGT G147E GAG R150N AAT S153F TTT D156M ATG G147H CAT R150K AAG S153D GAT G157K AAG G147W TGG R150L TTG S153Q CAG G157D GAT G147T ACG R150V GTT S153Y TAT G157F TTT G147C TGT R150D GAT P154V GTT G157R CGT G147S TCT R1501 ATT P154W TGG G157H CAT G157L TTG G160M ATG A163E GAG F166C TGT G157N AAT G160C TGT A163T ACG F166E GAG G157Y TAT G160Q CAG A163Q CAG Q167D GAT WO 2009/111083 PCT/US2009/001486 - 230 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon G157S TCG G160V GTT A1631 ATT Q167R CGG G157T ACG G160S AGT A163N AAT Q167A GCG G157A GCT G160E GAG H164L CTT Q167S AGT G157Q CAG G160L CTT H164M ATG Q167F TTT G157P CCG G160T ACG H164K AAG Q167Y TAT G157V GTG N161S AGT H164P CCG Q167P CCG G157M ATG N161C TGT H164C TGT Q167T ACT P158S TCT N161L TTG H164R CGT Q167V GTG P158Y TAT N161R CGT H164A GCG Q167L CTG P158R CGG N161G GGT H164V GTG Q167M ATG P158L CTT N161W TGG H164S TCG Q167N AAT P158V GTG N161Y TAT H164N AAT Q167G GGG P158C TGT N161E GAG H164G GGG Q167K AAG P158A GCG N161P CCT H164F TTT Q167E GAG P158W TGG N161T ACG H164Y TAT P168N AAT P1581 ATT N161H CAT H164Q CAG P168F TTT P158F TTT N1611 ATT H164E GAG P168R CGG P158Q CAG N161V GTG A165W TGG P168W TGG P158T ACT N161F TTT A165V GTT P168A GCT P158G GGT N161Q CAG A165G GGG P168T ACG P158K AAG L162A GCT A165K AAG P168V GTT P158N AAT L162G GGG A165L TTG P168G GGG P158D GAT L162C TGT A165P CCT P168C TGT G159R CGG L162P CCG A165Q CAG P168M ATG G159S AGT L162R CGG A165D GAT P168H CAT G159Q CAG L1621 ATT A165H CAT P168L CTT G159P CCT L162S TCT A165F TTT P168S AGT G159V GTG L162D GAT A165S AGT P1681 ATT G159K AAG L162M ATG A165T ACT P168D GAT G159A GCG L162E GAG A165R CGG G169H CAT G159Y TAT L162T ACT A165N AAT G169A GCG G159E GAG L162Y TAT A165M ATG G169E GAG G159T ACG L162F TTT F166G GGG G169C TGT G159M ATG L162W TGG F166S TCG G169S TCG G1591 ATT L162Q CAG F166L CTT G169L CTG G159W TGG A163R CGT F166V GTG G169V GTT G159L CTG A163G GGG F166P CCT G169T ACG G159C TGT A163Y TAT F166N AAT G169R CGG G160A GCG A163P CCT F166R CGT G169W TGG G160H CAT A163S AGT F166A GCG G169M ATG G160N AAT A163L CTT F166K AAG G1691 ATT G160W TGG A163C TGT F166H CAT G169P CCG G160R CGG A163K AAG F166W TGG G169D GAT G160P CCG A163V GTG F1661 ATT G169Q CAG G1601 ATT A163F TTT F166M ATG P170L CTT WO 2009/111083 PCT/US2009/001486 -231 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon P170R CGG G173S AGT A176L CTG D1791 ATT P1701 ATT G173A GCG A176P CCT D179R CGT P170T ACG G173R AGG A176N AAT D179N AAT P170F TTT G173N AAT A176G GGT D179W TGG P170Q CAG G173T ACG A176S TCT D179Q CAG P170G GGG G173D GAT A176R CGT D179V GTG P170S TCT G173V GTT A176K AAG D179C TGT P170H CAT G173F TTT A176D GAT E180M ATG P170C TGT G173M ATG A176W TGG E180P CCT P170M ATG G173Y TAT H177T ACG E180K AAG P170K AAG G173P CCG H177P CCG E180Y TAT P170W TGG G174R CGT H177Q CAG E180Q CAG P170D GAT G174A GCG H177A GCG E180R CGG P170A GCG G174E GAG H177S TCG E180A GCG G171S TCT G174F TTT H177G GGG E180T ACT G171M ATG G174H CAT H177W TGG E1801 ATT G171N AAT G174T ACT H177L CTG E180F TTT G171P CCT G174D GAT H177V GTT E180C TGT G171R CGG G174S AGT H1771 ATT E180G GGG G171Y TAT G174P CCG H177R CGG E180S TCG G171A GCT G174W TGG H177N AAT E180N AAT G171Q CAG G174V GTT H177Y TAT E180D GAT G171H CAT G174N AAT H177C TGT D181S TCG G171L CTT G174Y TAT H177D GAT D181Q CAG G171W TGG G174M ATG F178G GGT D181P CCT G171C TGT G174L CTT F178C TGT D181Y TAT G171K AAG D1751 ATT F178W TGG D181R CGT G171E GAG D175T ACG F178R CGG D181V GTT G171D GAT D175N AAT F178K AAG D181F TTT 1172Y TAT D175V GTT F178S AGT D181A GCT 1172T ACG D175S TCG F178H CAT D181T ACG 1172P CCT D175R CGG F178P CCT D181L TTG 1172A GCG D175G GGG F178V GTT D181E GAG 1172L CTT D175A GCG F178A GCT D181K AAG 1172Q CAG D175F TTT F178Q CAG D181M ATG 1172E GAG D175C TGT F178Y TAT D181C TGT 1172C TGT D175Q CAG F1781 ATT D181G GGT 1172M ATG D175Y TAT F178T ACT E182C TGT 1172D GAT D175L CTG F178L CTG E182P CCT 1172V GTT D175H CAT F178E GAG E182S AGT 1172R CGT D175P CCG D179P CCT E182T ACG 1172G GGG D175E GAG D179L TTG E182R CGG 1172W TGG A176F TTT D179E GAG E182D GAT 1172N AAT A176Q CAG D179G GGG E182A GCT G173C TGT A176V GTG D179S AGT E182F TT WO 2009/111083 PCT/US2009/001486 - 232 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon G173L CTG A176E GAG D179A GCT E182L CTT G173K AAG A176T ACT D179K AAG E1821 ATT G173W TGG A176C TGT D179T ACT E182Y TAT E182Q CAG T185D GAT R189K AAG N192S TCG E182W TGG N186G GGG R189P CCG N192W TGG E182M ATG N186A GCT R189E GAG N192G GGG E182G GGT N186T ACT R189V GTT N192D GAT R183P CCT N186R CGT R189D GAT N192V GTG R183K AAG N186L TTG R189Y TAT N192A GCT R183W TGG N186P CCG R189C TGT N192T ACT R183E GAG N186S AGT R189A GCT N192K AAG R183A GCT N186V GTG R189H CAT N192C TGT R183T ACG N186Q CAG R189W TGG N192M ATG R183L CTT N186H CAT R189N AAT L193P CCG R183N AAT N186C TGT R189T ACT L193G GGG R183H CAT N186E GAG R189Q CAG L193F TTT R183V GTG N186F TTT E190A GCG L193S TCG R183C TGT N186Y TAT E190H CAT L193W TGG R183M ATG N186D GAT E190V GTG L193A GCT R1831 ATT N187R CGG E190P CCG L193R CGT R183G GGT N187M ATG E190C TGT L193Q CAG R183S TCT N187S TCT E190G GGT L193E GAG W184G GGG N187T ACG E190R CGG L193K AAG W184H CAT N187L CTG E1901 ATT L193N AAT W184L CTG N187W TGG E190S TCG L1931 ATT W184E GAG N187F TTT E190T ACT L193T ACT W184P CCT N187K AAG E190M ATG L193D GAT W184N AAT N1871 ATT E190L TTG L193Y TAT W184A GCG N187A GCT E190K AAG H194S AGT W184T ACT N187P CCG E190Y TAT H194E GAG W184R CGG N187D GAT E190D GAT H194K AAG W184Q CAG N187G GGG Y191T ACT H194Q CAG W184V GTG N187C TGT Y191H CAT H194V GTT W184S TCT N187H CAT Y191G GGG H194T ACT W184M ATG F188P CCG Y191L TTG H194L CTG W1841 ATT F1881 ATT Y191P CCT H194Y TAT W184F TTT F188N AAT Y191Q CAG H194F TTT T185R CGT F188S AGT Y191K AAG H194G GGT T185Y TAT F188Q CAG Y191D GAT H1941 ATT T185W TGG F188K AAG Y191A GCG H194W TGG T185H CAT F188G GGG Y191W TGG H194M ATG T185G GGG F188W TGG Y191S TCT H194A GCT T185P CCT F188E GAG Y191V GTT H194P CCT T185S TCG F188H CAT Y191E GAG R195C TGT T185V GTT F188D GAT Y191R CGT R195F TTT WO 2009/111083 PCT/US2009/001486 - 233 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon T185Q CAG F188A GCG Y191C TGT R195W TGG T185N AAT F188L CTT N192R CGG R195T ACT T185C TGT F188R CGT N192L CTG R195L CTG T185L CTT F188V GTT N192Q CAG R195G GGT T185A GCG R189L TTG N192P CCT R195Q CAG T185E GAG R189G GGG N192H CAT R195K AAG R195S TCT A198F TTT L201N AAT L205S TCT R195A GCT A198W TGG G202T ACG L205G GGT R195D GAT A198Y TAT G202Y TAT L205P CCT R195P CCT A198D GAT G202E GAG L205E GAG R195Y TAT H1991 ATT G202V GTG L205V GTG R195E GAG H199P CCG G202S TCT L205M ATG R195V GTG H199G GGT G202L CTG L205N AAT V196T ACG H199N AAT G2021 ATT L205C TGT V196D GAT H199S TCG G202M ATG L2051 ATT V196G GGG H199L TTG G202H CAT L205A GCG V196E GAG H199M ATG G202C TGT L205R CGG V196A GCG H199A GCG G202R CGT L205W TGG V196S AGT H199C TGT G202P CCT L205Q CAG V196Q CAG H199K AAG G202A GCT G2061 ATT V196P CCG H199R CGT G202K AAG G206V GTG V196R CGT H199V GTG G202D GAT G206A GCG V196H CAT H199W TGG H203Y TAT G206C TGT V196Y TAT H199T ACT H203E GAG G206S TCG V1961 ATT H199E GAG H203R CGG G206P CCG V196L CTG E200P CCG H203Q CAG G206L TTG V196K AAG E200G GGG H203P CCG G206D GAT V196M ATG E200A GCT H203G GGG G206M ATG A197G GGT E200T ACG H203T ACT G206R CGG A197S AGT E2001 ATT H203D GAT G206Q CAG A197L CTT E200W T.GG H203L TTG G206E GAG A197P CCG E200R CGG H203N AAT G206H CAT A197V GTG E200F TTT H203A GCT G206T ACG A197Y TAT E200M ATG H203S TCT G206W TGG A197Q CAG E200D GAT H203V GTT L207S TCT A197R CGG E200V GTG H2031 ATT L207Y TAT A197T ACT E200C TGT H203C TGT L207A GCG A1971 ATT E200S TCT S204R CGG L207R CGT A197H CAT E200Y TAT S204N AAT L207P CCG A197E GAG E200N AAT S204A GCG L207Q CAG A197W TGG L201A GCG S204T ACT L207N AAT A197N AAT L201R CGG S204Y TAT L207K AAG A197C TGT L201E GAG S204V GTG L207M ATG A198T ACG L201P CCT S204L CTT L207W TGG A198K AAG L201G GGT S204H CAT L207H CAT WO 2009/111083 PCT/US2009/001486 - 234 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon A198S TCG L201V GTT S204D GAT L207D GAT A198H CAT L201T ACG S204Q CAG L207V GTT A198G GGT L2011 ATT S204G GGG L2071 ATT A198E GAG L201S TCT S204W TGG L207G GGT A198P CCG L201W TGG S2041 ATT S208D GAT A198L TTG L201Q CAG S204K AAG S208V GTT A198R CGT L201D GAT S204P CCT S208P CCT A198V GTT L201M ATG L205T ACG S208G GGT A198M ATG L201K AAG L205D GAT S208A GCG S208K AAG T211Q CAG G214A GCT M217A GCG S208N AAT T211S TCG G214D GAT M217H CAT S208F TTT T211A GCG G214F TTT M2171 ATT S208Q CAG T211F TTT G214Y TAT M217D GAT S208W TGG T211D GAT G214M ATG Y218C TGT S208T ACG T211W TGG G214C TGT Y218F TTT S208E GAG T211L CTG A215L CTG Y218W TGG S208C TGT D212E GAG A215Q CAG Y218L CTG S208R CGT D212A GCG A215M ATG Y218A GCG S208L CTT D212K AAG A215G GGT Y218P CCG H209T ACG D212R CGG A215W TGG Y218R CGG H209Y TAT D212T ACG A215S AGT Y218N AAT H209R CGG D212N AAT A215T ACG Y218V GTG H209Q CAG D212G GGG A215V GTT Y218Q CAG H209A GCT D212S TCT A215N AAT Y2181 ATT H209G GGG D212P CCG A215P CCG Y218D GAT H209N AAT D212Q CAG A215H CAT Y218S TCG H209P CCT D212V GTT A215K AAG Y218G GGG H209W TGG D212L TTG A2151 ATT Y218E GAG H209V GTT D212F TTT A215R CGT P219L TTG H209D GAT D212H CAT A215C TGT P219C TGT H209S AGT D212Y TAT A215D GAT P219V GTG H209F TTT 1213Q CAG L216A GCT P219D GAT H209L CTG 1213T ACT L216C TGT P219F TTT H209C TGT 1213C TGT L216D GAT P219A GCG S210C TGT 1213P CCT L216E GAG P219T ACT S21OG GGT 1213H CAT L216G GGG P219E GAG S2101 ATT 1213A GCG L2161 ATT P219Q CAG S21OR CGT 1213V GTT L216K AAG P219R CGG S210L CTG 1213G GGG L216M ATG P219H CAT S210V GTG 1213N AAT L216P CCT P219G GGG S210H CAT 1213L CTT L216Q CAG P219K AAG S21ON AAT 1213S AGT L216R CGG P219S TCG S21OF TTT 1213M ATG L216S TCT P219W TGG S210P CCG 1213R CGG L216T ACT S220R CGT S21OW TGG 1213K AAG L216V GTG S220A GCG WO 2009/111083 PCT/US2009/001486 -235 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon S210Q CAG 1213F TTT L216W TGG S220Q CAG S210T ACG 1213D GAT M217P CCT S220T ACT S210K AAG 1213E GAG M217Y TAT S220L CTT S210A GCG G214L TTG M217T ACG S220K AAG T211P CCG G214Q CAG M217C TGT S220G GGG T211R CGT G214S TCT M217S AGT S220H CAT T211K AAG G214T ACT M217L CTG S220E GAG T211G GGG G214V GTG M217N AAT S220M ATG T211M ATG G2141 ATT M217R CGG S220V GTT T211N AAT G214R CGT M217Q CAG S220P CCG T211V GTG G214P CCG M217K AAG S2201 ATT T211H CAT G214E GAG M217G GGG S220F TTT S220N AAT S224T ACG V227K AAG A230S TCG Y221W TGG S224Q CAG V227L CTG A230C TGT Y221K AAG S224R CGG V227P CCT A230V GTT Y221Q CAG S224P CCG V227S TCT A230T ACT Y221C TGT S2241 ATT V227T ACT A230Y TAT Y221N AAT S224V GTT V227W TGG A230M ATG Y221P CCT S224L TTG V227Y TAT A230N AAT Y221V GTT S224C TGT V227G GGG A230H CAT Y221A GCG S224K AAG V227H CAT Q2311 ATT Y221G GGG S224D GAT V227Q CAG Q231A GCT Y221R CGG S224H CAT V227R CGT Q231F TTT Y221S TCG S224M ATG Q228A GCT Q231P CCT Y221M ATG S224A GCT Q228D GAT Q231Y TAT Y221T ACG S224W TGG Q228E GAG Q231R CGT Y221L CTT G225D GAT Q228G GGT Q231L CTG Y221E GAG G225R CGT Q228H CAT Q231D GAT T222L TTG G225Q CAG Q228K AAG Q231G GGT T222Y TAT G225M ATG Q228L CTG Q231V GTT T222R CGT G225P CCT Q228M ATG Q231W TGG T222V GTT G225W TGG Q228N AAT Q231S AGT T222P CCT G225S TCT Q228P CCG Q231H CAT T222S AGT G225E GAG Q228R CGG Q231C TGT T222A GCT G225V GTT Q228S TCT Q231M ATG T222H CAT G225T ACG Q228T ACG D232H CAT T222G GGG G225K AAG Q228W TGG D232G GGG T222M ATG G225N AAT Q228Y TAT D232R CGT T222F TTT G225C TGT L229R CGG D232P CCT T222C TGT G225H CAT L229A GCG D232Y TAT T2221 ATT G225A GCG L229T ACG D232N AAT T222N AAT D226S TCT L229Q CAG D232S TCG T222W TGG D226W TGG L229P CCT D232F TTT T222D GAT D226R CGG L229E GAG D232V GTG F223L TTGI D226A GCT L229W TGG D232K AAG WO 2009/111083 PCT/US2009/001486 - 236 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon F223T ACG D226N AAT L229M ATG D232W TGG F223C TGT D226T ACT L2291 ATT D232Q CAG F223R CGT D226E GAG L229G GGT D232E GAG F223N AAT D226L CTT L229C TGT D232T ACT F223P CCT D226P CCT L229Y TAT D232L CTG F223E GAG D226H CAT L229D GAT D233Q CAG F223G GGG D226G GGT L229H CAT D233P CCG F223Q CAG D2261 ATT L229V GTG D233S TCT F223A GCG D226M ATG A230L TTG D233T ACG F223S TCT D226V GTG A230G GGT D233A GCG F223Y TAT D226C TGT A230W TGG D233W TGG F223H CAT V227A GCT A230P CCG D233G GGT F223K AAG V227C TGT A230D GAT D233R CGT F223M ATG V227D GAT A230R CGT D233E GAG S224G GGG V227E GAG A2301 ATT D233N AAT D233V GTG G236N AAT 1240G GGG R243L CTT D233M ATG G236F TTT 1240Q CAG R243A GCG D233L CTG 1237S TCG 1240P CCG R243H CAT D233K AAG 1237L CTG 1240R CGG R243Q CAG D2331 ATT 1237R CGT 1240S TCG R243S AGT 1234A GCT 1237Q CAG 1240K AAG R2431 ATT 1234T ACG 1237K AAG 1240V GTG R243C TGT 1234V GTT 1237D GAT 1240D GAT R243N AAT 1234W TGG 1237A GCG 1240A GCG R243Y TAT 1234E GAG 1237T ACG 1240C TGT R243G GGG 1234G GGT 1237E GAG 1240L CTT R243D GAT 1234L CTT 1237C TGT 1240F TTT R243V GTG 1234H CAT 1237G GGG 1240Y TAT S244P CCG 1234M ATG 1237P CCT 1240M ATG S244L CTT 1234N AAT 1237Y TAT 1240T ACG S244W TGG 1234Y TAT 1237W TGG Y241V GTT S244M ATG 1234P CCT 1237N AAT Y241A GCT S244V GTT 1234D GAT Q238G GGG Y241G GGG S244Q CAG 1234Q CAG Q238H CAT Y241H CAT S244D GAT 1234C TGT Q238S TCG Y241R CGG S244E GAG D235H CAT Q238Y TAT Y241P CCG S244T ACG D235G GGG Q238F TTT Y241Q CAG S244H CAT D235A GCG Q238E GAG Y241L TTG S244G GGT D235P CCG Q238L TTG Y241T ACG S244A GCT D235L CTT Q238W TGG Y241S AGT S244F TTT D235V GTG Q238P CCG Y241W TGG S244Y TAT D235E GAG Q238R AGG Y241N AAT S244R CGT D235R CGT Q238C TGT Y241M ATG Q245P CCT D235Q CAG Q238N AAT Y2411 ATT Q2451 ATT D235T ACG Q2381 ATT Y241D GAT Q245F TTT WO 2009/111083 PCT/US2009/001486 -237 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon D235C TGT Q238T ACG G242A GCG Q245V GTT D235S TCG Q238K AAG G242F TTT Q245M ATG D235N AAT A239S TCT G242L CTT Q245T ACT D235Y TAT A239Q CAG G242N AAT Q245E GAG D2351 ATT A239T ACG G242P CCT Q245S TCG G236M ATG A239P CCT G242W TGG Q245R CGG G236R CGG A239V GTG G242T ACG Q245G GGT G236D GAT A239L CTG G242R CGT Q245H CAT G236S TCT A239Y TAT G242V GTT Q245L CTT G236T ACT A2391 ATT G242S TCG Q245K AAG G236C TGT A239C TGT G2421 ATT Q245W TGG G236K AAG A239G GGG G242Y TAT Q245C TGT G236E GAG A239W TGG G242H CAT N246W TGG G236P CCG A239F TTT G242E GAG N246R CGG G2361 ATT A239K AAG G242K AAG N246A GCG G236Y TAT A239H CAT R243P CCG N246F TTT G236L CTG A239R CGT R243K AAG N246G GGT G236V GTT A239D GAT R243T ACG N246P CCT N246V GTT Q249G GGT G252P CCT T255L TTG N246Q CAG Q249N AAT G252H CAT T255H CAT N246Y TAT Q249K AAG G252C TGT P256S AGT N246C TGT Q2491 ATT G252V GTT P256V GTG N2461 ATT Q249Y TAT G2521 ATT P256F TTT N246L TTG Q249V GTG P253C TGT P256Y TAT N246S TCT Q249L TTG P253G GGT P2561 ATT N246T ACT Q249H CAT P253Q CAG P256A GCT N246K AAG P250L CTG P2531 ATT P256L CTT N246D GAT P250S TCG P253L CTG P256G GGT P247A GCG P250R CGG P253R CGG P256N AAT P247D GAT P250Y TAT P253A GCT P256R CGG P247E GAG P250M ATG P253E GAG P256Q CAG P247F TTT P250F TTT P253Y TAT P256E GAG P247G GGG P250A GCT P253W TGG P256K AAG P247H CAT P250K AAG P253M ATG P256M ATG P2471 ATT P250G GGT P253V GTG P256C TGT P247K AAG P250N AAT P253T ACT K257C TGT P247L CTG P250T ACT P253K AAG K257M ATG P247N AAT P250W TGG P253N AAT K257V GTT P247Q CAG P250D GAT Q254R CGT K257A GCT P247R CGT P250V GTG Q254G GGG K257E GAG P247S TCG P250Q CAG Q254W TGG K257S TCT P247T ACG 1251A GCG Q254T ACT K257L CTT P247V GTT 1251Q CAG Q254A GCT K2571 ATT V248W TGG 1251G GGG Q254F TTT K257G GGG V248L CTG 1251L CTG Q254D GAT K257N AAT WO 2009/111083 PCT/US2009/001486 - 238 Table 21. Codons encoding each amino acid substitution Mutation Codon Mutation Codon Mutation Codon Mutation Codon V248Q CAG 1251K AAG Q254P CCG K257F TTT V248M ATG 1251R CGT Q254L CTG K257W TGG V248Y TAT 1251E GAG Q254C TGT K257R CGG V248G GGG 1251D GAT Q254Y TAT K257P CCG V248C TGT 1251T ACG Q2541 ATT K257T ACT V248R CGG 1251C TGT Q254E GAG A258Q CAG V248A GCG 1251Y TAT Q254V GTG A258Y TAT V248H CAT 1251P CCT Q254S TCT A258W TGG V2481 ATT 1251S TCT T2551 ATT A258G GGG V248T ACT 1251W TGG T255Q CAG A258L TTG V248K AAG 1251V GTT T255P CCG A258F TTT V248S TCG G252F TTT T255R CGT A258M ATG V248F TTT G252W TGG T255C TGT A258N AAT V248E GAG G252A GCG T255N AAT A258V GTG Q249T ACT G252R CGG T255S AGT A258T ACG Q249W TGG G252L CTT T255V GTG A2581 ATT Q249R CGG G252E GAG T255E GAG A258D GAT Q249E GAG G252D GAT T255G GGG A258R CGT Q249A GCT G252K AAG T255K AAG A258E GAG Q249P CCG G252S TCG T255A GCT A258P CCG Q249C TGT G252T ACG T255F TTT T255L TTG The DNA encoding each individual library member was generated according to standard DNA synthesis protocols and expressed using routine molecular biology techniques. Briefly, the DNA was ligated into vector pET303CTHis (Invitrogen, SEQ 5 ID NO: 533) using routine molecular biology techniques. Plasmid containing one individual hMMP-1 mutant was transformed into BL21 (DE3) E.coli cells (Tigen, Beiging, China) using manufacturers recommendations. The process was repeated for all library members. The transformation culture was used to inoculate I mL LB medium containing ampicillin additives. The culture was grown at 37*C with shaking 10 for 16 hours. Protein expression was induced by the addition of 1 mM isopropyl-O-D thiogalactoside (IPTG) and the culture was incubated at 25"C with shaking. After 6 hours, the cells were pelleted by centrifugation at 6,000g for 10 minutes and the supernatant was removed. The periplasmic protein was enriched by incubating the cells in 50 pl OS buffer (200 mM Tris-HCV, pH 7.5, 20% sucrose, 1 mM EDTA) 15 with 4 pl DNAse (10 ig/ml), 4 pl RNAse (10 ptg/ml), and 4 il lysozyme (10 pg/ml) for 10 minutes at 25"C. 50 pl of water was added to each well followed by centrifugation at 6000 g for 10 minutesto remove cell debris. The supernatant, WO 2009/111083 PCT/US2009/001486 - 239 containing the hMMP- 1 protein, was stored at -20"C. Activity of supernatants were screened as described in the following examples. B. Cloning and Expression of wild type hMMP-1 In this example, wild type hMMP-1 was individually expressed in both E. coli 5 and CHO-S cells. 1. Expression in E. coli Wild type hMMP-1 (clone BAP006_10, having a sequence of nucleotides set forth in SEQ ID NO: 534) was cloned into vector pET303CTHis (Invitrogen, SEQ ID NO:533) and grown in BL21(DE3) E. coli. The pET303CTHis vector contained a C 10 terminal His tag (SEQ ID NO:235). Protein expression was induced upon the addition of 1 mM isopropyl-3-D-thiogalactoside (IPTG) as described above. Following expression, the protein was enriched as described in Example 27A, and subsequently purified using a HiTrap Ni 2 + column (GE Healthcare) according to standard molecular biology protocols. Expression and purification were monitored by 15 SDS/PAGE and Western blot analysis. 2. Expression in CHO-S cells Wild type hMMP-1 (clone BAP006_2, having a sequence of nucleotides set forth in SEQ ID NO: 534) was expressed in CHO-S cells and secreted into the medium. The wild type hMMP-1 protein was purified using a HiTrap Ni 2 + column 20 (GE Healthcare) according to standard molecular biology protocols Example 28 Determination of Enzymatic Activity of the hMMP-1 Mutants using a fluorogenic peptide substrate In this example, the hMMP-1 mutant library, generated in Example 27, was 25 screened using a high throughput fluorescence activity assay to identify temperature sensitive hMMP-1 mutants. To screen for temporally sensitive hMMP-1 mutants, the enzymtic activity of each individual mutant was determined at 25 *C and 37 'C and/or 34"C, using a commercially available fluorogenic substrate, peptide IX, designated as Mca-K-P-L-G-L-Dpa-A-R-NH 2 (SEQ ID NO: 535; Mca=(7-Methoxycoumarin-4 30 yl)acetyl; Dpa=N-3-(2,4,-Dinitrophenyl)-L-2,3-diaminopropionyl; R&D Systems, Minneapolis, MN, Cat# ESOlO). The peptide substrate contains a highly flurorescent 7-methoxycoumarin group that is quenched by resonance energy transfer to the 2,4 dinitrophenyl group. Activated hMMP-1 cleaves the amide bond between glycine and WO 2009/111083 PCT/US2009/001486 - 240 leucine resulting in an increase in released fluorescence. Reactions were initially performed in a 96-well assay and confirmed using a 14 ml tube format. A. 96-well assay Prior to assessing activity of the supernatants, supernatants were treated with a 5 processing agent to activate the inactive zymogen form into an active enzyme. Briefly, 4ptl of each hMMP- 1 mutant supernatant generated in Example 27 was added to 100 pl of TCNB (50 nM Tris, 10 mM CaCl 2 , 150 mM NaCl, 0.05% Brij 35, pH 7.5) with 1 mM of the processing agent p-aminophenylmercuric acetate (APMA) in a 96-well plate. The solution was incubated at the reaction temperature (either 25 'C or 10 37 C) for 2 hours. This activation step cleaves the pro-peptide and generates mature hMMP-l. Following activation, 1.6 pl of TCNB containing 620ptM Mca-K-P-L-G-L Dpa-A-R-NH 2 fluorescent substrate was added to each well to a final concentration of 10 ptM, at the indicated reaction temperature (either 25 *C or 37 C) for 1 hour. 15 Fluorescence was detected by measuring fluorescence in a fluorescent plate reader at 320 nrim exitation/405 nm emission. Relative fluorescence units (RFU) were determined. Supernatant from wild type hMMP-1 and plasmid/vector transformed cells were used as positive and negative controls. Duplicate reactions were performed for each sample, reaction temperature, and positive and negative control. 20 From the initial screen of 2687 hMMP-1 mutants, 199 putative primary hits were identified (see Table 22) with reduced activity at 37 'C. These hMMP-1 mutants were rescreened, using the same assay, and 104 primary hits were confirmed (see Table 23, below). hMMP-1 mutants that were active at 25 *C and had at least a 16 % decrease in activity at 37 *C (e.g., the ratio of the activities at 25 *C or 37 'C 25 (25*C/37 0 C) is greater than or equal to 1.2) were deemed to be confirmed primary temperature sensitive hits. Table 22, below, lists the hMMP-1 mutation, the average RFU at 25 *C and 37 *C, and the ratio of the activities (25 0 C/37*C). The Table also lists the temperature phenotype: DOWN, indicates the ratio (25 0 C/37*C) of the activity of the mutant is decreased compared to the ratio (25*C/37 0 C) of the activity 30 of the wild-type, i.e. decreased greater than 16 % the activity of the wild type; NEUTRAL, indicates the ratio (25 0 C/37*C) of the activity of the mutant is similar to the ratio (25*C/37*C) of the activity of wild-type, i.e. within 16 % of the activity of the wild type; and UP, indicates the ratio (25*C/37*C) of the activity of the mutant is WO 2009/111083 PCT/US2009/001486 - 241 increased compared to the ratio (25*C/37*C) of the activity of the wild-type, i.e. increased more than 16 % the activity of the wild type. Table 22, below, also lists the residual activities at 25 *C and 37 *C, as compared to wild type hMMP-1. The residual activity is the ratio of the hMMP-1 5 mutant activity versus the wildtype hMMP- I activity at the indicated temperature, either 25 *C or 37 *C. Several of the hMMP-1 mutants had activities that were comparable to, or greater than, wildtype hMMP-1 at 25 *C while they all exhibited decreased activities at 37 'C, thereby reconfirming their decreased activity at elevated temperatures. Table.22. Results of Initial Screen for Temperature Sensitive hMMP-1 mutants Temp. hMMP-1 SEQ Avg. Avg. Ratio Res. Res. Act. Phenotype mutation ID NO RFU RFU 25 0 C/ Act. Mut/wt 25 *C 37 *C 37 0 C Mut/wt 37 *C 25 *C Neutral T84F 479 6312.72 6453.46 0.98 1.10 1.27 Neutral E85F 480 6092.47 6362.37 0.96 1.06 1.26 Up L95K 328 1333.28 1191.46 1.12 0.15 0.14 Down L951 329 1707.98 2294.02 0.74 0.30 0.45 Down R98D 481 2905.96 3867.31 0.75 0.33 0.47 Down 199Q 482 3318.21 4623.91 0.72 0.37 0.56 Down E100V 457 3980.72 5009.20 0.79 1.26 1.01 Neutral ElOOR 451 7410.11 7964.52 0.93 0.83 0.96 Neutral E100S 454 3768.09 4664.58 0.81 0.42 0.56 Neutral E100T 453 6985.28 7478.12 0.93 0.79 0.90 Neutral E100F 455 6709.27 7436.60 0.90 0.75 0.90 Neutral E100I 456 8824.19 8458.79 1.04 0.99 1.02 Neutral El00N 452 8809.68 8215.63 1.07 0.99 0.99 Neutral T103Y 458 1181.09 1423.76 0.83 0.37 0.29 Neutral P104A 484 8861.30 8360.82 1.06 1.00 1.01 Up P104M 483 6709.44 7118.65 0.94 0.88 0.75 Up D105A 340 2674.16 1227.06 2.18 0.65 0.24 Up D105F 336 2009.56 1221.58 1.65 0.49 0.24 Up D105G 335 2407.89 1686.68 1.43 0.58 0.34 Up D105I 338 ~1732.38 1105.99 1.57 0.42 0.22 Up D105L 339 1563.61 859.56 1.82 0.38 0.17 Up D105N 332 3766.72 1475.08 2.55 0.91 0.29 Up D105R 331 3892.02 2016.90 1.93 0.94 0.40 Up D105S 334 3646.49 2727.22 1.34 0.88 0.54 Up D105T 333 2513.64 1729.46 1.45 0.61 0.34 Up D105W 337 2565.93 1855.05 1.38 0.62 0.37 Neutral D105E 330 4000.92 3366.64 1.19 0.59 0.45 Neutral L106C 485 2995.56 3678.33 0.81 0.34 0.44 Neutral L106S 486 2730.64 2899.36 0.94 0.31 0.35 WO 2009/111083 PCT/US2009/001486 - 242 Neutral A109H 487 7206.01 7536.96 0.96 0.81 0.91 Neutral DI1OA 488 4179.59 5112.44 0.82 0.47 0.62 Neutral V1IIR 489 2401.69 2925.16 0.82 0.27 0.35 Neutral D112S 490 7203.69 7600.93 0.95 0.81 0.92 Neutral Al 18T 491 745.83 665.63 1.12 0.13 0.13 Down S123V 492 3220.29 4504.25 0.71 0.41 0.60 Neutral N124D 493 6218.73 6620.92 0.94 0.92 0.88 Neutral T126S 494 7114.42 6856.69 1.04 1.06 0.91 Up G147P 495 494.94 392.93 1.26 0.07 0.05 Up R150P 345 2291.14 828.28 2.77 0.31 0.12 Neutral R150V 344 6869.28 6604.61 1.04 1.20 1.30 Neutral R150D 341 7230.41 6033.28 1.20 1.26 1.19 Down R150I 343 3120.05 4082.34 0.76 0.39 0.55 Neutral R150H 342 8281.04 8056.17 1.03 1.05 1.08 Up D151G 346 1073.32 733.89 1.46 0.20 0.11 Neutral N152A 497 6669.94 5660.16 1.18 1.17 1.12 Down N152S 496 4607.85 8096.31 0.57 0.58 1.08 Neutral S153T 459 10530.07 8798.72 1.20 1.44 1.24 Up F155L 347 1322.13 864.19 1.53 0.25 0.13 Up F155A 348 1250.93 760.12 1.65 0.23 0.11 Up D156H 349 2722.09 2081.55 1.31 0.51 0.31 Up D156L 356 2548.30 1597.53 1.60 0.48 0.24 Up D156A 357 2679.29 1734.45 1.54 0.50 0.26 Up D156W 354 1575.39 1268.36 1.24 0.30 0.19 Up D156V 355 1400.88 766.80 1.83 0.26 0.11 Up D156K 350 1292.89 966.62 1.34 0.24 0.14 Up D156T 352 2871.09 1843.03 1.56 0.54 0.27 Up D156R 351 2431.23 1545.89 1.57 0.46 0.23 Up D156M 353 817.96 502.82 1.63 0.12 0.07 Neutral P158T 500 4204.23 3507.76 1.20 0.53 0.47 Neutral P158G 501 6277.86 5496.27 1.14 0.79 0.73 Neutral P158K 498 6860.82 6680.30 1.03 0.87 0.89 Neutral P158N 499 3656.04 3874.48 0.94 0.46 0.52 Up G159V 363 2453.98 732.46 3.35 0.34 0.10 Up G159T 359 5059.91 1734.12 2.92 0.69 0.24 Up G159M 360 5905.06 4874.00 1.21 0.75 0.65 Neutral G1591 362 5725.99 5357.20 1.07 0.72 0.72 Neutral G159W 361 6787.40 6287.71 1.08 0.86 0.84 Neutral G159L 364 8231.62 7638.64 1.08 1.04 1.02 Neutral G159C 358 2897.77 3053.86 0.95 0.37 0.41 Neutral P170D 502 1434.38 1462.91 0.98 0.25 0.29 Neutral P170A 503 2733.72 2793.24 0.98 0.48 0.55 Up G171P 462 1570.74 1204.39 1.30 0.27 0.17 Neutral G171E 461 1154.96 1199.65 0.96 0.20 0.24 Neutral G171D 460 791.81 690.33 1.15 0.14 0.14 Up A176F 365 10486.82 6516.31 1.61 1.31 0.78 Neutral A176W 366 482.38 414.85 1.16 0.06 0.06 WO 2009/111083 PCT/US2009/001486 - 243 Neutral F178T 504 560.54 487.01 1.15 0.10 0.10 Up F178L 505 1788.95 1314.38 1.36 0.31 0.26 Up D179N 368 2433.73 812.01 3.00 0.26 0.10 Up D179V 369 604.63 490.35 1.23 0.11 0.10 Up D179C 367 613.81 503.76 1.22 0.11 0.10 Up E180Y 374 6655.19 5379.42 1.24 0.72 0.63 Neutral E180R 371 6932.51 6309.81 1.10 0.75 0.74 Up E180T 373 3718.16 2425.13 1.53 0.40 0.29 Up E180F 377 7014.78 5382.78 1.30 0.76 0.63 Up E180G 376 5952.65 4547.28 1.31 1.04 0.90 Up E180S 375 5217.80 3977.60 1.31 0.91 0.78 Up E180N 372 6534.65 4843.84 1.35 1.14 0.96 Up E180D 370 7738.70 6277.22 1.23 1.35 1.24 Neutral D181T 380 6867.00 6057.09 1.13 0.74 0.71 Up D181L 382 1727.20 1274.09 1.36 0.19 0.15 Up D181K 378 1087.36 696.83 1.56 0.12 0.08 Up D181C 379 549.29 447.40 1.23 0.10 0.09 Up D181G 381 2764.20 2056.56 1.34 0.48 0.41 Up E182T 384 2995.97 1779.42 1.68 0.32 0.21 Up E182Q 383 1393.28 804.84 1.73 0.15 0.09 Up E182M 386 649.73 524.43 1.24 0.11 0.10 Neutral E182G 385 604.92 543.78 1.11 0.11 0.11 Up R183G 507 7326.36 6021.39 1.22 1.28 1.19 Up R183S 506 7896.17 6240.74 1.27 1.38 1.23 Up T185R 390 1728.04 851.07 2.03 0.20 0.10 Up T185Y 392 937.75 540.66 1.73 0.11 0.07 Up T185H 389 1448.04 783.89 1.85 0.17 0.10 Up T185G 393 3922.30 1990.15 1.97 0.46 0.24 Up T185V 394 1648.14 897.66 1.84 0.19 0.11 Up T185Q 391 1594.81 583.93 2.73 0.19 0.07 Up T185A 395 1599.64 711.08 2.25 0.19 0.09 Up T185E 388 1324.02 703.76 1.88 0.16 0.09 Neutral T185D 387 485.86 418.67 1.16 0.06 0.06 Up N187R 398 1042.36 709.74 1.47 0.12 0.09 Up N187M 402 1731.67 995.07 1.74 0.20 0.12 Neutral N187W 403 1694.86 1425.68 1.19 0.20 0.17 Up N187F 401 1240.41 731.98 1.69 0.15 0.09 Up N187K 397 2331.93 1140.19 2.05 0.27 0.14 Up N1871 404 1444.98 683.03 2.12 0.17 0.08 Up N187A 405 4379.80 2616.49 1.67 0.52 0.32 Neutral N187G 400 535.06 514.10 1.04 0.07 0.07 Neutral N187C 399 1804.28 1860.67 0.97 0.23 0.25 Neutral N187H 396 1143.07 1071.67 1.07 0.14 0.14 Up F188V 508 7116.29 5860.00 1.21 1.24 1.16 Neutral R189N 509 7842.39 6675.36 1.17 1.37 1.32 Neutral R189T 511 7610.10 6459.94 1.18 1.33 1.27 Neutral jR189Q 510 7465.37 6396.79 1.17 1.30 1.26 WO 2009/111083 PCT/US2009/001486 - 244 Up E190G 465 5313.99 4365.93 1.22 0.75 0.48 Up E190Y 464 7243.54 5742.33 1.26 1.27 1.13 Up E190D 463 7910.21 6468.78 1.22 1.38 1.28 Up Y191V 466. 1553.58 1254.11 1.24 0.19 0.14 Up N192H 468 2274.24 1058.80 2.15 0.32 0.12 Up N192S 470 2043.65 1630.74 1.25 0.29 0.18 Up N192D 467 4213.33 2216.40 1.90 0.59 0.24 Up N192C 469 1310.46 987.31 1.33 0.18 0.11 Neutral H194P 471 5264.79 5058.19 1.04 0.74 0.56 Up R195C 407 4231.32 1853.20 2.28 0.60 0.20 Neutral R195W 410 5099.23 4524.84 1.13 0.72 0.50 Neutral R195L 412 5073.57 4520.73 1.12 0.72 0.50 Up R195G 409 5269.21 3025.93 1.74 0.74 0.33 Up RI95Q 408 1958.69 1361.83 1.44 0.28 0.15 Up R195A 413 5605.90 3852.81 1.46 0.79 0.42 Up R195D 406 2724.53 1907.81 1.43 0.38 0.21 Up R195V 411 1711.48 1037.62 1.65 0.24 0.11 Up A197C 512 4012.80 3140.52 1.28 0.70 0.62 Neutral A198G 414 2610.82 2368.26 1.10 0.37 0.26 Up A198L 416 1339.94 726.74 1.84 0.19 0.08 Up A198M 415 1384.46 999.55 1.39 0.20 0.11 Up G206A 418 4554.61 2702.11 1.69 0.47 0.30 Up G206S 417 1226.37 919.66 1.33 0.13 0.10 Up L207R 472 3476.88 1332.44 2.61 0.36 0.15 Neutral L207V 475 656.95 550.54 1.19 0.08 0.07 Neutral L2071 474 645.37 550.32 1.17 0.08 0.07 Up L207G 473 610.01 484.35 1.26 0.08 0.06 Neutral S208R 513 7639.06 6465.10 1.18 1.34 1.28 Up S208L 514 7811.78 6354.14 1.23 1.37 1.25 Up S21OV 419 1190.35 856.63 1.39 0.29 0.17 Neutral S21OA 420 1682.05 1546.97 1.09 0.25 0.21 Neutral T211L 515 2376.23 2102.07 1.13 0.35 0.28 Up D212G 477 1011.62 657.28 1.54 0.24 0.13 Neutral D212H 476 4696.49 4001.41 1.17 0.70 0.53 Up Y218S 421 3702.49 3099.73 1.19 0.58 0.43 Up F223C 424 3115.11 2488.91 1.25 0.53 0.35 Up F223E 422 7194.34 5884.03 1.22 1.22 0.83 Up F223G 426 3236.56 2599.04 1.25 0.55 0.36 Up F223A 428 5226.86 3982.92 1.31 0.89 0.56 Up F223S 425 6006.80 4916.07 1.22 1.02 0.69 Neutral F223K 423 4021.97 3712.91 1.08 0.60 0.49 Neutral F223M 427 525.66 441.29 1.19 0.08 0.06 Up V227C 433 4040.96 3278.65 1.23 0.68 0.46 Up V227D 429 1190.09 731.34 1.63 0.20 0.10 UP V227E 430 5381.63 2605.20 2.07 0.91 0.37 UP V227L 438 4883.98 4000.68 1.22 0.83 0.56 Up V227S 435 3863.33 3131.47 1.23 0.65 0.44 WO 2009/111083 PCT/US2009/001486 - 245 Up V227W 437 1845.46 1374.06 1.34 0.31 0.19 Neutral V227G 436 1040.74 883.01 1.18 0.15 0.12 Up V227H 431 689.20 504.65 1.37 0.10 0.07 Up V227Q 434 696.97 506.11 1.38 0.10 0.07 Neutral V227R 432 664.31 561.06 1.18 0.10 0.07 Up Q228P 439 2862.74 1291.55 2.22 1.33 0.44 Up L229A 442 2627.78 2118.07 1.24 1.22 0.72 Up L229T 440 3780.54 1464.25 2.58 1.75 0.50 Up L2291 441 1158.56 828.94 1.40 0.54 0.28 Up A230V 478 5030.94 3433.18 1.47 2.33 1.17 Up D233E 443 2881.17 1918.57 1.50 1.33 0.65 Up 1234A 447 1458.10 1018.50 1.43 0.31 0.18 Up 1234T 446 1451.51 1188.67 1.22 0.31 0.21 Up 1234E 444 1301.06 840.09 1.55 0.27 0.15 Up 1234Q 445 1095.18 837.53 1.31 0.23 0.15 Up 1237L 518 2880.14 2240.61 1.29 0.61 0.39 Down 1237W 517 4188.38 5663.94 0.74 0.62 0.75 Neutral 1237N 516 5368.49 6271.59 0.86 0.80 0.83 Up 1240S 449 2033.91 1204.66 1.69 0.32 0.15 Neutral 1240A 450 2099.13 1776.41 1.18 0.33 0.23 Up 1240C 448 970.78 650.04 1.49 0.15 0.08 Neutral 1251S 519 8445.88 7160.96 1.18 1.07 0.96 Neutral 1251W 520 7305.95 6974.26 1.05 0.92 0.93 Neutral Q254S 521 7768.13 8801.19 0.88 1.15 1.17 Neutral T255H 522 8243.01 7352.60 1.12 1.22 0.98 Neutral P256C 523 4674.45 4633.67 1.01 0.69 0.62 Neutral K257P 525 8039.60 7464.88 1.08 1.19 0.99 Neutral K257T 524 9346.88 8849.42 1.06 1.39 1.18 Neutral A258P 526 10414.06 9178.82 1.13 1.55 1.22 TABLE 23: Reconfirmed HITs Temperature hMMP-1 SEQ ID Phenotype mutation NO Up L95K 328 Down E100V 457 Neutral T103Y 458 Up D105A 340 Up D105F 336 Up D105G 335 Up D105I 338 Up D105L 339 Up D105N 332 Up D105R 331 Up D105S 334 Up D105T 333 WO 2009/111083 PCT/US2009/001486 - 246 Up D105W 337 Up R150P 345 Up D15IG 346 Neutral S153T 459 Up F155L 347 Up F155A 348 Up D156H 349 Up D156L 356 Up D156A 357 Up D156W 354 Up D156V 355 Up D156K 350 Up D156T 352 Up D156R 351 Up G159V 363 Up G159T 359 Up G171P 462 Up A176F 365 Up D179N 368 Up E180Y 374 Neutral E180R 371 Up E180T 373 Up E180F 377 Neutral D181T 380 Up D181L 382 Up D181K 378 Up E182T 384 Up E182Q 383 Up T185R 390 Up T185Y 392 Up T185H 389 Up T185G 393 Up T185V 394 Up T185Q 391 Up T185A 395 Up T185E 388 Up N187R 398 Up N187M 402 Neutral N187W 403 Up N187F 401 Up N187K 397 Up N1871 404 Up N187A 405 Up E190G 465 Up Y191V 466 Up N192H 468 Up N192S 470 WO 2009/111083 PCT/US2009/001486 - 247 Up N192D 467 Up N192C 469 Neutral H194P 471 Up R195C 407 Neutral R195W 410 Neutral R195L 412 Up R195G 409 Up R195Q 408 Up R195A 413 Up R195D 406 Up R195V 411 Neutral A198G 414 Up A198L 416 Up A198M 415 Up G206A 418 Up G206S 417 Up L207R 472 Up S210V 419 Up D212G 477 Up Y218S 421 Up F223C 424 Up F223E 422 Up F223G 426 Up F223A 428 Up F223S 425 Up V227C 433 Up V227D 429 Up V227E 430 Up V227L 438 Up V227S 435 Up V227W 437 Up Q228P 439 Up L229A 442 Up L229T 440 Up L2291 441 Up A230V 478 Up D233E 443 Up 1234A 447 Up 1234T 446 Up 1234E 444 Up 1234Q 445 Up 1237L 518 Up I240S 449 Neutral 1240A 450 Up 1240C 448 WO 2009/111083 PCT/US2009/001486 - 248 B. 14-mL protein expression In this example, the hMMP-1 mutants that were identified as temperature sensitive primary hits in Example 28A were expressed in 14 ml culture tubes and their enzymatic activity was measured at 25 'C, 34 'C and 37 *C for 1 hour, 2 hours or 5 overnight in order to verify the desired phenotype of decreased activity at elevated temperatures. Protein was expressed and purified as in Example 27 with the exception that the expression was performed in 14 ml tubes rather than a 96-well plate. Four (4) pl of each hMMP-1 mutant supernatant was transferred to a 96-well 10 microplate. Supernatants were activated with APMA as described in Example 28A above, except that the solution was incubated at the reaction temperature of 25 1C, 34 *C, or 37 *C for 2 hours. As above, following activation, 100 pl of TCNB containing 10 pM Mca-K-P-L-G-L-Dpa-A-R-NH 2 fluorescent substrate was added to each tube at the indicated reaction temperature (25 *C, 34 *C or 37 *C) for one hour. Wild-type 15 hMMP-1 was used as a positive control and supernatant from cells transformed with the vector was used as a negative control. Fluorescence was detected by measuring fluorescence in a fluorescent plate reader at 320 nm exitation/405 nm emission. Relative fluorescence units (RFU) were determined. Duplicate reactions were performed for each sample, reaction temperature, and positive and negative control. 20 The data is shown in Table 24A (1 hour incubation); Table 24B (2 hour incubations) and Table 24C (overnight incubation), below. Mutants that were active at 25*C but demonstrated at least a 33% decreased activity at 34'C or 37"C (i.e. had a ratio of activity at 25"C and 34"C or a ratio of activity of 25*C and 37"C equal to or greater than 1.5 under any of the time point conditions tested were identified as 25 temperature sensitive Hits. Tables 24A-24C, below, list the hMMP-1 mutation, the RFU at 25 "C, 34 'C and 37 *C, and the ratio of the activities (at both 25"C/34*C and 25*C/37*C) of 64 hMMP-1 mutants whose decreased enzymatic activity at elevated temperatures were confirmed. Some of the hMMP-1 mutants, were noticeably more active at 25 "C than at an elevated temperature. For example, hMMP-1 mutant 30 D179N (SEQ ID NO:368) was 87.5% more active at 25 "C than 37 "C after an overnight incubation (see e.g. Table 24C). Additionally, although expression levels, and therefore overall RFU values, varied in different experiments, the ratios of the activities remained the same. For example, mutant D156T was tested twice (see WO 2009/111083 PCT/US2009/001486 - 249 Table 24C below) and although each test gave different data RFU values the ratio of the values were similar and consistently within the 1.5 ratio parameter. Table 24A. Temperature Sensitive hMMP-1 Mutants, 1 hour incubation hMMP-1 SEQ ID RFU RFU RFU Ratio Ratio mutation NO 25 *C 34 *C 37 *C 25 0 C/ 25 0 C/ 34 0 C 37 0 C L95K 328 2677.64 553.00 572.70 4.84 4.68 D105A 340 3496.48 697.79 1119.92 5.01 3.12 D105F 336 1749.85 554.69 685.49 3.15 2.55 D105G 335 7450.35 2196.32 3514.50 3.39 2.12 D105I 338 4720.96 638.42 943.44 7.39 5.00 D105L 339 2636.80 490.04 552.90 5.38 4.77 D105N 332 7487.95 776.33 1513.73 9.65 4.95 D105R 331 1732.70 641.23 736.92 2.70 2.35 D105S 334 8637.40 3782.36 6510.05 2.28 1.33 D105W 337 4263.51 1321.69 2422.77 3.23 1.76 D105T 333 2666.45 770.72 1685.33 3.46 1.58 R150P 345 7568.19 1678.59 2010.33 4.51 3.76 D151G 346 973.47 517.98 595.63 1.88 1.63 F155A 348 1800.92 592.07 596.31 3.04 3.02 D156K 350 8718.91 1733.90 1839.60 5.03 4.74 D156T 352 8034.06 2216.02 2255.25 3.63 3.56 D156L 356 1825.01 528.43 619.10 3.45 2.95 D156A 357 1495.21 450.17 496.04 3.32 3.01 D156W 354 1006.97 463.48 493.84 2.17 2.04 D156V 355 1140.60 484.30 504.38 2.36 2.26 D156T 352 2796.00 581.90 743.53 4.80 3.76 D156H 349 3489.60 578.59 711.59 6.03 4.90 D156R 351 4983.67 678.23 734.95 7.35 6.78 G159V 363 3416.77 705.80 739.87 4.84 4.62 G159T 359 4081.99 1732.63 1865.15 2.36 2.19 A176F 365 967.31 539.31 517.16 1.79 1.87 D179N 368 4105.85 492.00 513.37 8.35 8.00 E180Y 374 8803.90 3904.31 5268.18 2.25 1.67 E180T 373 5957.38 1155.89 1430.72 5.15 4.16 E180F 377 7484.41 2677.89 3141.69 2.79 2.38 D181L 382 1629.22 559.04 549.09 2.91 2.97 D181K 378 844.40 570.98 569.44 1.48 1.48 E182T 384 2244.96 653.93 668.01 3.43 3.36 E182Q 383 1066.68 583.87 582.84 1.83 1.83 T185R 390 1599.19 867.00 872.66 1.84 1.83 T185H 389 3616.30 1601.20 1842.01 2.26 1.96 T185Q 391 4365.21 1512.02 1899.46 2.89 2.30 T185A 395 1374.00 567.04 608.05 2.42 2.26 T185E 388 2145.28 1263.20 1399.76 1.70 1.53 N187R 398 1659.90 955.75 1054.91 1.74 1.57 WO 2009/111083 PCT/US2009/001486 -250 N187M 402 2842.50 1343.95 1464.36 2.12 1.94 N187F 401 1846.10 716.62 786.07 2.58 2.35 N187K 397 2428.31 1703.73 1914.84 1.43 1.27 N1871 404 2455.44 .717.51 773.59 3.42 3.17 R195V 411 3121.02 1947.80 2132.94 1.60 1.46 A198L 416 4547.61 1570.19 2061.87 2.90 2.21 A198M 415 1948.92 1101.86 1535.22 1.77 1.27 G206A 418 667.50 543.90 540.79 1.23 1.23 G206S 417 608.46 427.44 412.07 1.42 1.48 S210V 419 1952.12 961.54 1791.55 2.03 1.09 Y218S 421 1674.47 1531.03 1573.00 1.09 1.06 F223E 422 5837.16 2747.99 4955.08 2.12 1.18 V227C 433 1138.96 684.05 722.68 1.67 1.58 V227E 430 5892.76 653.81 803.12 9.01 7.34 V227W 437 716.50 607.92 646.75 1.18 1.11 Q228P 439 676.11 488.99 495.88 1.38 1.36 L229T 440 768.59 492.66 491.49 1.56 1.56 L2291 441 1470.04 753.87 1231.17 1.95 1.19 D233E 443 1195.07 959.25 1056.45 1.25 1.13 1234A 447 1402.15 1014.61 1127.63 1.38 1.24 1234T 446 857.79 644.52 712.49 1.33 1.20 1234E 444 2281.82 591.10 762.52 3.86 2.99 1240S 449 2678.36 776.88 1314.40 3.45 2.04 1240C 448 1540.91 474.82 666.63 3.25 2.31 Table 24B. Temperat re Sensitive hMMP-1 Mutants, 2 hours incubation hMMP-1 SEQ ID RFU RFU RFU Ratio Ratio mutation NO 25 *C 34 *C 37 *C 25 0 C/ 25 0 C/ 34 0 C 37 0 C L95K 328 4650.42 748.29 746.89 6.21 6.23 D105A 340 5669.31 824.07 1336.14 6.88 4.24 D105F 336 2980.00 623.89 818.63 4.78 3.64 D105G 335 8821.81 2759.24 4313.40 3.20 2.05 D1051 338 6832.34 780.32 1110.07 8.76 6.15 D105L 339 4206.38 534.24 607.46 7.87 6.92 D105N 332 8920.05 918.13 1727.44 9.72 5.16 D105R 331 2821.20 722.46 813.68 3.90 3.47 D105S 334 9355.63 4607.18 7274.97 2.03 1.29 D105W 337 6663.80 1690.93 3081.59 3.94 2.16 D105T 333 4457.16 974.63 2220.03 4.57 2.01 R150P 345 8750.30 2315.11 2497.86 3.78 3.50 D151G 346 1264.62 589.27 616.51 2.15 2.05 F155A 348 2824.01 779.72 746.59 3.62 3.78 D156K 350 8576.47 2210.63 2310.30 3.88 3.71 D156T 352 8727.27 2679.17 2752.35 3.26 3.17 D156L 356 2916.24 576.84 688.08 5.06 4.24 WO 2009/111083 PCT/US2009/001486 -251 D156A 357 2299.63 533.68 554.21 4.31 4.15 D156W 354 1502.86 539.74 575.12 2.78 2.61 D156V 355 1593.06 534.71 542.36 2.98 2.94 D156T 352 4469.68 690.87 848.14 6.47 5.27 D156H 349 5387.79 698.77 819.82 7.71 6.57 D156R 351 7020.81 793.83 872.40 8.84 8.05 G159V 363 4673.44 856.78 838.46 5.45 5.57 G159T 359 6704.95 2294.40 2347.74 2.92 2.86 A176F 365 1609.85 654.43 618.72 2.46 2.60 D179N 368 5660.69 644.51 656.31 8.78 8.63 E180Y 374 8557.09 4979.24 6079.36 1.72 1.41 E180T 373 7870.99 1532.35 1794.15 5.14 4.39 E180F 377 8508.13 3597.75 3975.22 2.36 2.14 D181L 382 2710.97 619.39 611.92 4.38 4.43 D181K 378 1130.63 625.01 608.68 1.81 1.86 E182T 384 3702.08 791.23 826.28 4.68 4.48 E182Q 383 1331.50 639.84 623.11 2.08 2.14 T185R 390 2637.31 1187.63 1183.37 2.22 2.23 T185H 389 5593.77 2278.26 2534.15 2.46 2.21 T185Q 391 7006.87 2250.58 2642.74 3.11 2.65 T185A 395 2474.96 663.82 707.09 3.73 3.50 T185E 388 3948.43 2088.15 2091.32 1.89 1.89 N187R 398 3006.08 1352.97 1421.87 2.22 2.11 N187M 402 4934.44 1811.35 1893.07 2.72 2.61 N187F 401 3227.96 877.21 931.04 3.68 3.47 N187K 397 4182.49 2425.34 2652.79 1.72 1.58 N1871 404 4218.55 849.11 887.80 4.97 4.75 R195V 411 4847.81 2724.92 2984.10 1.78 1.62 A198L 416 6756.76 2056.50 2642.76 3.29 2.56 A198M 415 3777.50 1708.61 2155.58 2.21 1.75 G206A 418 872.27 603.01 586.57 1.45 1.49 G206S 417 932.69 492.65 463.60 1.89 2.01 S210V 419 3349.95 1249.47 2314.86 2.68 1.45 Y218S 421 2878.50 2373.98 2350.27 1.21 1.22 F223E 422 8318.70 3685.68 6209.93 2.26 1.34 V227C 433 1998.67 950.01 992.19 2.10 2.01 V227E 430 7904.54 839.00 1015.12 9.42 7.79 V227W 437 996.55 729.20 787.87 1.37 1.26 Q228P 439 1082.56 607.78 586.63 1.78 1.85 L229T 440 1221.05 580.15 564.49 2.10 2.16 L2291 441 2790.27 1050.86 1803.44 2.66 1.55 D233E 443 2195.02 1393.95 1454.71 1.57 1.51 1234A 447 2375.42 1473.70 1594.08 1.61 1.49 1234T 446 1199.18 713.83 796.81 1.68 1.50 1234E 444 3920.02 705.86 923.57 5.55 4.24 1240S 449 3867.71 973.97 1575.05 3.97 2.46 1240C 448 2688.75 561.91 853.66 4.78 3.15 WO 2009/111083 PCT/US2009/001486 - 252 Table 24C. Temperature Sensitive hMMP-1 Mutants, Overnight incubation hMMP-1 SEQ ID RFU RFU RFU Ratio Ratio mutation NO 25 *C 34 *C 37 *C 25 0 C/ 25 0 C/ 34 0 C 37 0 C L95K 328 7744.34 1803.12 1677.96 4.29 4.62 D105A 340 8466.62 1302.84 1931.17 6.50 4.38 D105F 336 6725.59 938.60 1173.23 7.17 5.73 D105G 335 8940.06 3560.75 5390.32 2.51 1.66 D1051 338 8394.32 1614.57 1958.96 5.20 4.29 D105L 339 6546.78 957.95 1070.51 6.83 6.12 D105N 332 9119.04 1459.16 2347.74 6.25 3.88 D105R 331 5775.25 1407.06 1499.57 4.10 3.85 D105S 334 9300.85 5584.70 8234.95 1.67 1.13 D105W 337 8617.36 2851.22 4593.06 3.02 1.88 D105T 333 7910.47 1899.25 3292.01 4.17 2.40 R150P 345 9011.11 3533.16 3559.66 2.55 2.53 D151G 346 1956.65 959.80 1097.68 2.04 1.78 F155A 348 4891.89 2016.76 1843.31 2.43 2.65 D156K 350 8696.27 3968.92 3858.90 2.19 2.25 D156T 352 8972.20 3971.43 3854.84 2.26 2.33 D156L 356 5254.55 972.64 1232.94 5.40 4.26 D156A 357 3585.37 1098.25 1110.73 3.26 3.23 D156W 354 2570.24 1091.27 1206.22 2.36 2.13 D156V 355 2208.99 954.21 997.64 2.31 2.21 D156T 352 7229.28 1256.02 1540.11 5.76 4.69 D156H 349 7587.19 1451.49 1763.27 5.23 4.30 D156R 351 8622.23 1735.02 1846.71 4.97 4.67 G159V 363 6555.27 1821.53 1683.20 3.60 3.89 G159T 359 9105.95 3210.57 3160.07 2.84 2.88 A176F 365 4191.69 1414.21 1336.32 2.96 3.14 D179N 368 7317.57 1504.84 1485.28 4.86 4.93 E180Y 374 9281.77 6080.89 6894.61 1.53 1.35 E180T 373 8475.04 2585.89 2809.15 3.28 3.02 E180F 377 9360.74 5183.25 5335.15 1.81 1.75 D181L 382 4534.34 1078.98 1000.80 4.20 4.53 D181K 378 1869.47 946.27 928.55 1.98 2.01 E182T 384 6752.25 1483.52 1496.55 4.55 4.51 E182Q 383 2212.75 1065.07 1035.24 2.08 2.14 T185R 390 6281.97 2425.71 2300.61 2.59 2.73 T185H 389 8531.85 3164.69 3515.59 2.70 2.43 T185Q 391 9044.23 3639.00 4012.93 2.49 2.25 T185A 395 6156.97 1110.68 1059.61 5.54 5.81 T185E 388 8479.18 3868.06 3892.33 2.19 2.18 N187R 398 7593.11 2415.63 2370.01 3.14 3.20 WO 2009/111083 PCT/US2009/001486 - 253 N187M 402 8605.76 2769.52 2720.28 3.11 3.16 N187F 401 7352.85 1612.23 1704.23 4.56 4.31 N187K 397 8667.36 3458.94 3709.62 2.51 2.34 N1871 404 8306.40 1459.25 1465.77 5.69 5.67 R195V 411 8634.05 4648.03 4960.91 1.86 1.74 A198L 416 8795.36 3469.36 4181.78 2.54 2.10 A198M 415 8352.73 3215.69 3637.79 2.60 2.30 G206A 418 2492.53 1038.14 974.96 2.40 2.56 G206S 417 2845.84 908.82 808.42 3.13 3.52 S210V 419 7104.17 2441.96 3939.90 2.91 1.80 Y218S 421 7740.61 4057.37 4093.29 1.91 1.89 F223E 422 9650.44 4849.58 7645.34 1.99 1.26 V227C 433 5833.84 2207.20 2432.82 2.64 2.40 V227E 430 8630.90 2283.07 2152.81 3.78 4.01 V227W 437 3070.92 1370.13 1456.45 2.24 2.11 Q228P 439 3673.33 1162.95 1081.32 3.16 3.40 L229T 440 3543.75 1103.34 1030.05 3.21 3.44 L2291 441 7333.92 1832.18 3268.93 4.00 2.24 D233E 443 6694.93 2570.71 2661.43 2.60 2.52 1234A 447 6250.56 3890.90 4043.80 1.61 1.55 1234T 446 3507.08 1099.58 1228.23 3.19 2.86 1234E 444 7541.73 1365.08 1901.96 5.52 3.97 1240S 449 4376.99 2108.15 2592.19 2.08 1.69 1240C 448 6170.51 1174.96 2223.23 5.25 2.78 Table 25 below depicts the residual activity (the ratio of hMMP-1 mutant RFU/wt hMMP-1 RFU) of the hMMP-1 mutants following overnight incubation with the fluorescent peptide. The activity of mutants at 25 *C, 34 *C, or 37 *C were 5 compared to the activity of wild-type hMMP- 1 at the respective temperatures. At 25'C, five hMMP-1 mutants (E180F, El80Y, DI56T, D156K, R150P) were more active than wildtype hMMP-1 as indicated by a residual activity >1. At elevated temperatures, all of the hMMP- 1 mutants exhibited an overall decrease in activity when compared to wildtype hMMP-1 at the same temperature, thus confirming the 10 phenotype of the hMMP- 1 mutants as temperature sensitive mutants. Table 25. Residual Activity of hMMP-1 Temperature Sensitive Mutants, Overnight Incubation hMMP-1 SEQ ID Residual Residual Residual mutation NO Activity Activity Activity 25 *C 34 *C 37 *C L95K 328 0.80 0.20 0.20 D105A 340 0.93 0.15 0.22 D105F 336 0.74 0.11 0.13 WO 2009/111083 PCT/US2009/001486 - 254 D105G 335 0.99 0.42 0.60 D1051 338 0.93 0.19 0.22 D105L 339 0.72 0.11 0.12 D105N 332 1.01 0.17 0.26 D105R 331 0.64 0.16 0.17 D105S 334 1.03 0.65 0.92 D105W 337 0.95 0.33 0.51 D105T 333 0.87 0.22 0.37 R150P 345 0.99 0.41 0.44 D151G 346 0.22 0.11 0.12 F155A 348 0.51 0.22 0.22 D156K 350 0.97 0.46 0.46 D156T 352 1.00 0.46 0.46 D156L 356 0.58 0.11 0.14 D156A 357 0.40 0.13 0.12 D156W 354 0.28 0.13 0.14 D156V 355 0.24 0.11 0.11 D156T 352 0.80 0.15 0.17 D156H 349 0.84 0.17 0.20 D156R 351 0.95 0.20 0.21 G159V 363 0.73 0.21 0.20 G159T 359 1.00 0.37 0.39 A176F 365 0.43 0.16 0.16 D179N 368 0.81 0.17 0.18 E180Y 374 1.02 0.70 0.85 E180T 373 0.93 0.30 0.35 E180F 377 1.03 0.60 0.66 D181L 382 0.50 0.12 0.12 D181K 378 0.21 0.11 0.11 E182T 384 0.74 0.17 0.18 E182Q 383 0.24 0.12 0.13 T185R 390 0.69 0.28 0.28 T185H 389 0.94 0.37 0.43 T185Q 391 1.00 0.42 0.49 T185A 395 0.68 - 0.13 0.13 T185E 388 0.93 0.45 0.48 N187R 398 0.84 0.28 0.29 N187M 402 0.95 0.32 0.33 N187F 401 0.81 0.19 0.21 N187K 397 0.95 0.40 0.46 N1871 404 0.92 0.17 0.18 R195V 411 0.96 0.54 0.59 A198L 416 0.98 0.40 0.49 A198M 415 0.87 0.36 0.42 G206A 418 0.27 0.12 0.12 G206S 417 0.31 0.10 0.10 S210V 419 0.78 0.29 0.44 WO 2009/111083 PCT/US2009/001486 -255 Y218S 421 0.85 0.47 0.50 F223E 422 1.07 0.57 0.86 V227C 433 0.64 0.26 0.27 V227E 430 0.95 0.27 0.24 V227W 437 0.34 0.16 0.16 Q228P 439 0.38 0.13 0.13 L229T 440 0.37 0.12 0.12 L2291 441 0.76 0.20 0.38 D233E 443 0.69 0.28 0.31 1234A 447 0.69 0.45 0.45 1234T 446 0.39 0.13 0.14 1234E 444 0.83 0.16 0.21 1240S 449 0.48 0.25 0.29 1240C 448 0.68 0.14 0.25 C. hMMP-1 Top Mutant Hits Fourteen (14) positions were identified at top hit positions: 95, 105, 150, 156, 159, 179, 180, 182, 185, 187, 198, 227, 234 and 240. Twenty three (23) hMMP-1 5 mutants at 14 positions were selected as top hits based on two criteria, including: 1) the ratio of the activities (25 *C to 37 *C and 25 'C to 34 *C); and 2) the activity (in RFUs). All of the mutants listed in Table 26 below had an activity greater than 2000 and a ratio of 25 'C to 37 *C greater than 2. The eleven Hits identified with a ** are the Hits that ranked high for both the ratio or activities and the activity level, and were 10 used to develop a combinatorial library as described in Example 29. Table 26: Top Hits L95K** D105I D105N** D105L D105A D105G R150P** D156R D156H D156K** D156T** G159V** G159T D179N** E180T** E18OF E182T T185Q N1871 A198L** V227E** 1234E 1240S** Example 29 Combinatorial hMMP-1 Variant Library In this example, a combinatorial hMMP-1 variant library was generated from 15 the mutants selected in Example 28C and shown in Table 26 with a double asterix WO 2009/111083 PCT/US2009/001486 -256 (**). Mutants at positions 182, 185 and 187 were excluded in the generation of the combinatorial library because of the importance of these positions for hMMP- 1 catalytic activity. The library contained every possible combination of amino acid variants for each of the selected mutants. Table 27 depicts all mutant combinations 5 contained in the library. The positions indicated are with respect to positons corresponding to amino acid residues of hMMP-1 set forth in SEQ ID NO:327. Each row and column indicates one polypeptide containing the noted mutations. For example, 156K 179N 227E, refers to a polypeptide containing three amino acid replacements at positions corresponding to positions set forth in SEQ ID NO:327: D 10 by K at position 156, D by N at position 179 and V by E at position 227. The library was generated and expressed as described in Example 27. Table 27. Combinatorial Library Mutants 95K 150P 156T 156K 179N 227E 150P 156T 240S 105N 105N 240S 156K 179N 198L 150P 156T 227E 150P 105N 227E 156K 179N 180T 150P 156T 198L 156K 105N 198L 156K 159V 240S 150P 156T 180T 156T 105N 180T 156K 159V 227E 150P 156T 179N 159V 105N 179N 156K 159V 198L 150P 156T 159V 179N 105N 159V 156K 159V 180T 105N 227E 240S 180T 105N 156K 156K 159V 179N 105N 198L 240S 198L 105N 156T 156T 227E 240S 105N 198L 227E 227E 105N 150P 156T 198L 240S 105N 180T 240S 240S 95K 240S 156T 198L 227E 105N 180T 227E 227E 240S 95K 227E 156T 180T 240S 105N 180T 198L 198L 240S 95K 198L 156T 180T 227E 105N 179N 240S 198L 227E 95K 180T 156T 180T 198L 105N 179N 227E 180T 240S 95K 179N 156T 179N 240S 105N 179N 198L 180T 227E 95K 159V 156T 179N 227E 105N 179N 180T 180T 198L 95K 156T 156T 179N 198L 105N 159V 240S 179N 240S 95K 150P 156T 179N 180T 105N 159V 227E 179N 227E 95K 105N 156T 159V 240S 105N 159V 198L 179N 198L 95K 156K 156T 159V 227E 105N 159V 180T 179N 180T 180T 227E 240S 156T 159V 198L 105N 159V 179N 159V 240S 180T 198L 240S 156T 159V 180T 105N 156K 240S 159V 227E 180T 198L 227E 156T 159V 179N 105N 156K 227E 159V 198L 179N 227E 240S 150P 227E 240S 105N 156K 198L 159V 180T 179N 198L 240S 198L 227E 240S 105N 156K 180T 159V 179N 179N 198L 227E 150P 198L 240S 105N 156K 179N 156K 240S 179N 180T 240S 150P 198L 227E 105N 156K 159V 156K 227E 179N 180T 227E 150P 180T 240S 105N 156T 240S 156K 198L 179N 180T 198L 150P 180T 227E 105N 156T 227E WO 2009/111083 PCT/US2009/001486 - 257 156K 180T 159V 227E 240S 150P 180T 198L 105N 156T 198L 156K 179N 159V 198L 240S 150P 179N 240S 105N 156T 180T 156K 159V 159V 198L 227E 150P 179N 227E 105N 156T 179N 156T 240S 159V 180T 240S 150P 179N 198L 105N 156T 159V 156T 227E 159V 180T 227E 150P 179N 180T 105N 150P 240S 156T 198L 159V 180T 198L 150P 159V 240S 105N 150P 227E 156T 180T 159V 179N 240S 150P 159V 227E 105N 150P 198L 156T 179N 159V 179N 227E 150P 159V 198L 105N 150P 180T 156T 159V 159V 179N 198L 150P 159V 180T 105N 150P 179N 150P 240S 159V 179N 180T 150P 159V 179N 105N 150P 159V 150P 227E 156K 227E 240S 150P 156K 240S 105N 150P 156K 150P 198L 156K 198L 240S 150P 156K 227E 105N 150P 156T 150P 180T 156K 198L 227E 150P 156K 198L 95K 227E 240S 150P 179N 156K 180T 240S 150P 156K 180T 95K 198L 240S 150P 156K 156K 180T 227E 156K 180T 198L 150P 156K 179N 150P 159V 156K 179N 240S 150P 156K 159V 95K 180T 240S 95K 180T 227E 179N 180T 198L 240S 156T 159V 180T 198L 95K 180T 198L 179N 180T 198L 227E 156T 159V 179N 240S 95K 179N 240S 159V 198L 227E 240S 156T 159V 179N 227E 95K 179N 227E 159V 180T 227E 240S 156T 159V 179N 198L 95K 179N 198L 159V 180T 198L 240S 156T 159V 179N 180T 95K 179N 180T 159V 180T 198L 227E 150P 198L 227E 240S 95K 159V 240S 159V 179N 227E 240S 150P 180T 227E 240S 95K 159V 227E 159V 179N 198L 240S 150P 180T 198L 240S 95K 159V 198L 159V 179N 198L 227E 150P 180T 198L 227E 95K 159V 180T 159V 179N 180T 240S 150P 179N 227E 240S 95K 159V 179N 159V 179N 180T 227E 150P 179N 198L 240S 95K 156K 240S 159V 179N 180T 198L 150P 179N 198L 227E 95K 156K 227E 156K 198L 227E 240S 150P 179N 180T 240S 95K 156K 198L 156K 180T 227E 240S 150P 179N 180T 227E 95K 156K 180T 156K 180T 198L 240S 150P 179N 180T 198L 95K 156K 179N 156K 180T 198L 227E 150P 159V 227E 240S 95K 156K 159V 156K 179N 227E 240S 150P 159V 198L 240S 95K 198L 227E 156K 179N 198L 240S 150P 159V 198L 227E 95K 156T 240S 156K 179N 198L 227E 150P 159V 180T 240S 95K 156T 227E 156K 179N 180T 240S 150P 159V 180T 227E 95K 156T 198L 156K 179N 180T 227E 150P 159V 180T 198L 95K 156T 180T 156K 179N 180T 198L 150P 159V 179N 240S 95K 156T 179N 156K 159V 227E 240S 150P 159V 179N 227E 95K 156T 159V 156K 159V 198L 240S 150P 159V 179N 198L 95K 150P 240S 156K 159V 198L 227E 150P 159V 179N 180T 95K 150P 227E 156K 159V 180T 240S 150P 156K 227E 240S 95K 150P 198L 156K 159V 180T 227E 150P 156K 198L 240S 95K 150P 180T 156K 159V 180T 198L 150P 156K 198L 227E 95K 150P 179N 156K 159V 179N 240S 150P 156K 180T 240S 95K 150P 159V 156K 159V 179N 227E 150P 156K 180T 227E 95K 150P 156K 156K 159V 179N 198L 150P 156K 180T 198L WO 2009/111083 PCT/US2009/001486 -258 95K 150P 156T 156K 159V 179N 180T 150P 156K 179N 240S 95K 105N 240S 156T 198L 227E 240S 150P 156K 179N 227E 95K 105N 227E 156T 180T 227E 240S 150P 156K 179N 198L 95K 105N 198L 156T 180T 198L 240S 150P 156K 179N 180T 95K 105N 180T 156T 180T 198L 227E 150P 156K 159V 240S 95K 105N 179N 156T 179N 227E 240S 150P 156K 159V 227E 95K 105N 159V 156T 179N 198L 240S 156T 179N 180T 240S 95K 105N 156K 156T 179N 198L 227E 156T 179N 180T 227E 95K 105N 156T 156T 159V 227E 240S 156T 179N 180T 198L 95K 105N 150P 156T 159V 198L 240S 150P 156T 227E 240S 180T 198L 227E 240S 156T 159V 198L 227E 150P 156T 198L 240S 179N 198L 227E 240S 156T 159V 180T 240S 150P 156T 198L 227E 179N 180T 227E 240S 156T 159V 180T 227E 150P 156T 180T 240S 150P 156T 180T 227E 105N 156T 198L 240S 95K 180T 198L 227E 150P 156T 180T 198L 105N 156T 180T 227E 95K 179N 180T 227E 150P 156T 179N 240S 105N 156T 180T 198L 95K 179N 180T 198L 150P 156T 179N 227E 105N 156T 179N 240S 95K 159V 227E 240S 150P 156T 179N 198L 105N 156T 179N 227E 95K 159V 198L 240S 150P 156T 179N 180T 105N 156T 179N 198L 95K 159V 198L 227E 150P 156T 159V 240S 105N 156T 179N 180T 95K 159V 180T 240S 150P 156T 159V 227E 105N 156T 159V 240S 95K 159V 180T 227E 150P 156T 159V 198L 105N 156T 159V 227E 95K 159V 180T 198L 150P 156T 159V 180T 105N 156T 159V 198L 95K 159V 179N 240S 150P 156T 159V 179N 105N 156T 159V 180T 95K 159V 179N 227E 105N 198L 227E 240S 105N 156T 159V 179N 95K 159V 179N 198L 105N 180T 227E 240S 105N 150P 227E 240S 95K 159V 179N 180T 105N 180T 198L 240S 105N 150P 198L 240S 95K 156K 227E 240S 105N 180T 198L 227E 105N 150P 198L 227E 95K 156K 198L 240S 105N 179N 227E 240S 105N 150P 180T 240S 95K 156K 198L 227E 105N 179N 198L 240S 105N 150P 180T 227E 95K 156K 180T 240S 105N 179N 198L 227E 105N 150P 180T 198L 95K 156K 180T 227E 105N 179N 180T 240S 105N 150P 179N 240S 95K 156K 180T 198L 105N 179N 180T 227E 105N 150P 179N 227E 95K 156K 179N 240S 105N 179N 180T 198L 105N 150P 179N 198L 95K 156K 179N 227E 105N 159V 227E 240S 105N 150P 179N 180T 95K 156K 179N 198L 105N 159V 198L 240S 105N 150P 159V 240S 95K 156K 179N 180T 105N 159V 198L 227E 105N 150P 159V 227E 95K 156K 159V 240S 105N 159V 180T 240S 105N 150P 159V 198L 95K 156K 159V 227E 105N 159V 180T 227E 105N 150P 159V 180T 95K 156K 159V 198L 105N 159V 180T 198L 105N 150P 159V 179N 95K 156K 159V 180T 105N 159V 179N 240S 105N 150P 156K 240S 95K 156K 159V 179N 105N 159V 179N 227E 105N 150P 156K 227E 95K 156T 227E 240S 105N 159V 179N 198L 105N 150P 156K 198L 95K 156T 198L 240S 105N 159V 179N 180T 105N 150P 156K 180T 95K 156T 198L 227E 105N. 156K 227E 240S 105N 156K 180T 227E 95K 156T 180T 240S 105N 156K 198L 240S 105N 156K 180T 198L 105N 150P 156K 179N 105N 156K 198L 227E 105N 156K 179N 240S 105N 150P 156K 159V WO 2009/111083 PCT/US2009/001486 -259 105N 156K 180T 240S 105N 156K 179N 227E 105N 150P 156T 240S 150P 156K 159V 198L 105N 156K 179N 198L 105N 150P 156T 227E 150P 156K 159V 180T 105N 156K 179N 180T 105N 150P 156T 198L 150P 156K 159V 179N 105N 150P 156T 179N 105N 150P 156T 180T 105N 156K 159V 240S 105N 150P 156T 159V 95K 156T 179N 198L 105N 156K 159V 227E 95K 198L 227E 240S 95K 156T 179N 180T 105N 156K 159V 198L 95K 180T 227E 240S 95K 156T 159V 240S 105N 156K 159V 180T 95K 180T 198L 240S 95K 156T 159V 227E 105N 156K 159V 179N 95K 179N 227E 240S 95K 156T 159V 198L 105N 156T 227E 240S 95K 179N 198L 240S 95K 156T 159V 180T 105N 156T 198L 227E 95K 179N 198L 227E 95K 156T 159V 179N 105N 156T 180T 240S 95K 179N 180T 240S 95K 150P 227E 240S 95K 150P 198L 240S 95K 105N 156K 179N 95K 150P 198L 227E 95K 105N 156K 159V 95K 150P 180T 240S 95K 105N 156T 240S 95K 150P 180T 227E 95K 105N 156T 227E 95K 150P 180T 198L 95K 105N 156T 198L 95K 150P 179N 240S 95K 105N 156T 180T 95K 150P 179N 227E 95K 105N 156T 179N 95K 150P 179N 198L 95K 105N 156T 159V 95K 150P 179N 180T 95K 105N 150P 240S 95K 150P 159V 240S 95K 105N 150P 227E 95K 150P 159V 227E 95K 105N 150P 198L 95K 150P 159V 198L 95K 105N 150P 180T 95K 150P 159V 180T 95K 105N 150P 179N 95K 150P 159V 179N 95K 105N 150P 159V 95K 150P 156K 240S 95K 105N 150P 156K 95K 150P 156K 227E 95K 105N 150P 156T 95K 150P 156K 198L 95K - 105N 179N 227E 95K 150P 156K 180T 95K 105N 179N 198L 95K 150P 156K 179N 95K 105N 179N 180T 95K 150P 156K 159V 95K 105N 159V 240S 95K 150P 156T 240S 156K 159V 179N 198L 227E 95K 150P 156T 227E 179N 180T 198L 227E 240S 95K 150P 156T 198L 159V 180T 198L 227E 240S 95K 150P 156T 180T 159V 179N 198L 227E 240S 95K 150P 156T 179N 159V 179N 180T 227E 240S 95K 150P 156T 159V 159V 179N 180T 198L 240S 95K 105N 227E 240S 159V 179N 180T 198L 227E 95K 105N 198L 240S 156K 180T 198L 227E 240S 95K 105N 198L 227E 156K 179N 198L 227E 240S 95K 105N 180T 240S 156K 179N 180T 227E 240S 95K 105N 180T 227E 156K 179N 180T 198L 240S 95K 105N 180T 198L 156K 179N 180T 198L 227E 95K 105N 179N 240S 156K 159V 198L 227E 240S 95K 156T 180T 227E 156K 159V 180T 227E 240S 95K 156T 180T 198L 156K 159V 180T 198L 240S WO 2009/111083 PCT/US2009/001486 - 260 95K 156T 179N 240S 156K 159V 180T 198L 227E 95K 156T 179N 227E 156K 159V 179N 227E 240S 95K 105N 159V 227E 156K 159V 179N 198L 240S 95K 105N 159V 198L 150P 156K 159V 198L 227E 95K 105N 159V 180T 156K 159V 179N 180T 240S 95K 105N 159V 179N 156K 159V 179N 180T 227E 95K 105N 156K 240S 156K 159V 179N 180T 198L 95K 105N 156K 227E 156T 180T 198L 227E 240S 95K 105N 156K 198L 156T 179N 198L 227E 240S 95K 105N 156K 180T 156T 179N 180T 227E 240S 156T 179N 180T 198L 240S 150P 156K 159V 179N 180T 156T 179N 180T 198L 227E 150P 156T 198L 227E 240S 156T 159V 198L 227E 240S 150P 156T 180T 227E 240S 156T 159V 180T 227E 240S 150P 156T 180T 198L 240S 156T 159V 180T 198L 240S 150P 156T 180T 198L 227E 156T 159V 180T 198L 227E 150P 156T 179N 227E 240S 156T 159V 179N 227E 240S 150P 156T 179N 198L 240S 156T 159V 179N 198L 240S 150P 156T 179N 198L 227E 156T 159V 179N 198L 227E 150P 156T 179N 180T 240S 156T 159V 179N 180T 240S 150P 156T 179N 180T 227E 156T 159V 179N 180T 227E 150P 156T 179N 180T 198L 156T 159V 179N 180T 198L 150P 156T 159V 227E 240S 150P 180T 198L 227E 240S 150P 156T 159V 198L 240S 150P 179N 198L 227E 240S 150P 156T 159V 198L 227E 150P 179N 180T 227E 240S 150P 156T 159V 180T 240S 150P 179N 180T 198L 240S 150P 156T 159V 180T 227E 150P 179N 180T 198L 227E 150P 156T 159V 180T 198L 150P 159V 198L 227E 240S 150P 156T 159V 179N 240S 150P 159V 180T 227E 240S 150P 156T 159V 179N 227E 150P 159V 180T 198L 240S 150P 159V 180T 198L 227E 150P 159V 179N 227E 240S 150P 156T 159V 179N 180T 150P 159V 179N 198L 240S 105N 180T 198L 227E 240S 150P 159V 179N 198L 227E 105N 179N 198L 227E 240S 150P 159V 179N 180T 240S 105N 179N 180T 227E 240S 150P 159V 179N 180T 227E 105N 179N 180T 198L 240S 150P 159V 179N 180T 198L 105N 179N 180T 198L 227E 150P 156K 198L 227E 240S 105N 159V 198L 227E 240S 150P 156K 180T 227E 240S 105N 159V 180T 227E 240S 150P 156K 180T 198L 240S 105N 159V 180T 198L 240S 150P 156K 180T 198L 227E 105N 159V 180T 198L 227E 150P 156K 179N 227E 240S 105N 159V 179N 227E 240S 150P 156K 179N 198L 240S 105N 159V 179N 198L 240S 150P 156K 179N 198L 227E 105N 159V 179N 198L 227E 150P 156K 179N 180T 240S 105N 159V 179N 180T 240S 150P 156K 179N 180T 227E 105N 159V 179N 180T 227E 150P 156K 179N 180T 198L 105N 159V 179N 180T 198L 150P 156K 159V 227E 240S 105N 156K 198L 227E 240S WO 2009/111083 PCT/US2009/001486 - 261 150P 156K 159V 198L 240S 105N 156K 180T 227E 240S 105N 156K 180T 198L 240S 105N 150P 179N 180T 240S 150P 156K 159V 180T 240S 105N 156K 180T 198L 227E 150P 156K 159V 180T 227E 105N 156K 179N 227E 240S 150P 156K 159V 180T 198L 105N 156K 179N 198L 240S 150P 156K 159V 179N 240S 105N 156K 179N 198L 227E 150P 156K 159V 179N 227E 105N 156K 179N 180T 240S 150P 156K 159V 179N 198L 105N 156K 179N 180T 227E 105N 156K 179N 180T 198L 105N 150P 159V 180T 227E 105N 156K 159V 227E 240S 105N 150P 159V 180T 198L 105N 156K 159V 198L 240S 105N 150P 159V 179N 240S 105N 156K 159V 198L 227E 105N 150P 159V 179N 227E 105N 156K 159V 180T 240S 105N 150P 159V 179N 198L 105N 156K 159V 180T 227E 105N 150P 159V 179N 180T 105N 156K 159V 180T 198L 105N 150P 156K 227E 240S 105N 156K 159V 179N 240S 105N 150P 156K 198L 240S 105N 156K 159V 179N 227E 105N 150P 156K 198L 227E 105N 156K 159V 179N 198L 105N 150P 156K 180T 240S 105N 156K 159V 179N 180T 105N 150P 156K 180T 227E 105N 156T 198L 227E 240S 105N 150P 156K 180T 198L 105N 156T 180T 227E 240S 105N 150P 156K 179N 240S 105N 156T 180T 198L 240S 105N 150P 156K 179N 227E 105N 156T 180T 198L 227E 105N 150P 156K 179N 198L 105N 156T 179N 227E 240S 105N 150P 156K 179N 180T 105N 156T 179N 198L 240S 105N 150P 156K 159V 240S 105N 156T 179N 198L 227E 105N 150P 156K 159V 227E 105N 156T 179N 180T 240S 105N 150P 156K 159V 198L 150P 156T 159V 179N 198L 105N 156T 179N 180T 227E 105N 156T 179N 180T 198L 105N 150P 156K 159V 179N 105N 156T 159V 227E 240S 105N 150P 156T 227E 240S 105N 156T 159V 198L 240S 105N 150P 156T 198L 240S 105N 156T 159V 198L 227E 105N 150P 156T 198L 227E 105N 156T 159V 180T 240S 105N 150P 156T 180T 240S 105N 156T 159V 180T 227E 105N 150P 156T 180T 227E 105N 156T 159V 180T 198L 105N 150P 156T 180T 198L 105N 156T 159V 179N 240S 105N 150P 156T 179N 240S 105N 156T 159V 179N 227E 105N 150P 156T 179N 227E 105N 156T 159V 179N 198L 105N 150P 156T 179N 198L 105N 156T 159V 179N 180T 105N 150P 156T 179N 180T 105N 150P 198L 227E 240S 105N 150P 156T 159V 240S 105N 150P 180T 227E 240S 105N 150P 156T 159V 227E 105N 150P 180T 198L 240S 105N 150P 156T 159V 198L 105N 150P 180T 198L 227E 105N 150P 156T 159V 180T 105N 150P 179N 227E 240S 105N 150P 156T 159V 179N 105N 150P 179N 198L 240S 95K 180T 198L 227E 240S 105N 150P 179N 198L 227E 95K 179N 198L 227E 240S 95K 179N 180T 227E 240S 95K 156T 159V 198L 227E WO 2009/111083 PCT/US2009/001486 - 262 105N 150P 179N 180T 227E 95K 179N 180T 198L 240S 105N 150P 179N 180T 198L 95K 179N 180T 198L 227E 105N 150P 159V 227E 240S 95K 159V 198L 227E 240S 105N 150P 159V 198L 240S 95K 159V 180T 227E 240S 105N 150P 159V 198L 227E 95K 159V 180T 198L 240S 105N 150P 159V 180T 240S 95K 159V 180T 198L 227E 95K 159V 179N 227E 240S 95K 156T 159V 179N 180T 95K 159V 179N 198L 240S 95K 150P 198L 227E 240S 95K 159V 179N 198L 227E 95K 150P 180T 227E 240S 95K 159V 179N 180T 240S 95K 150P 180T 198L 240S 95K 159V 179N 180T 227E 95K 150P 180T 198L 227E 95K 159V 179N 180T 198L 95K 150P 179N 227E 240S 95K 156K 198L 227E 240S 95K 150P 179N 198L 240S 95K 156K 180T 227E 240S 95K 150P 179N 198L 227E 95K 156K 180T 198L 240S 95K 150P 179N 180T 240S 95K 156K 180T 198L 227E 95K 150P 179N 180T 227E 95K 156K 179N 227E 240S 95K 150P 179N 180T 198L 95K 156K 179N 198L 240S 95K 150P 159V 227E 240S 95K 156K 179N 198L 227E 95K 150P 159V 198L 240S 95K 156K 179N 180T 240S 95K 150P 159V 198L 227E 95K 156K 179N 180T 227E 95K 150P 159V 180T 240S 95K 156K 179N 180T 198L 95K 150P 159V 180T 227E 95K 156K 159V 227E 240S 95K 150P 159V 180T 198L 95K 156K 159V 198L 240S 95K 150P 159V 179N 240S 95K 156K 159V 198L 227E 95K 150P 159V 179N 227E 105N 150P 156K 159V 180T 95K 156K 159V 180T 240S 95K 156K 159V 180T 227E 95K 150P 159V 179N 180T 95K 156K 159V 180T 198L 95K 150P 156K 227E 240S 95K 156K 159V 179N 240S 95K 150P 156K 198L 240S 95K 156K 159V 179N 227E 95K 150P 156K 198L 227E 95K 156K 159V 179N 198L 95K 150P 156K 180T 240S 95K 156K 159V 179N 180T 95K 150P 156K 180T 227E 95K 156T 198L 227E 240S 95K 150P 156K 180T 198L 95K 156T 180T 227E 240S 95K 150P 156K 179N 240S 95K 156T 180T 198L 240S 95K 150P 156K 179N 227E 95K 156T 180T 198L 227E 95K 150P 156K 179N 198L 95K 156T 179N 227E 240S 95K 150P 156K 179N 180T 95K 156T 179N 198L 240S 95K 150P 156K 159V 240S 95K 156T 179N 198L 227E 95K 150P 156K 159V 227E 95K 156T 179N 180T 240S 95K 150P 156K 159V 198L 95K 156T 179N 180T 227E 95K 150P 156K 159V 180T 95K 156T 179N 180T 198L 95K 150P 156K 159V 179N 95K 156T 159V 227E 240S 95K 150P 156T 227E 240S 95K 156T 159V 198L 240S 95K 150P 156T 198L 240S 95K 150P 156T 198L 227E 95K 105N 156K 159V 198L 95K 156T 159V 180T 240S 95K 150P 156T 180T 240S 95K 156T 159V 180T 227E 95K 150P 156T 180T 227E WO 2009/111083 PCT/US2009/001486 - 263 95K 156T 159V 180T 198L 95K 150P 156T 180T 198L 95K 156T 159V 179N 240S 95K 150P 156T 179N 240S 95K 156T 159V 179N 227E 95K 150P 156T 179N 227E 95K 156T 159V 179N 198L 95K 150P 156T 179N 198L 95K 150P 156T 179N 180T 95K 105N 156T 180T 227E 95K 150P 156T 159V 240S 95K 105N 156T 180T 198L 95K 150P 156T 159V 227E 95K 105N 156T 179N 240S 95K 150P 156T 159V 198L 95K 105N 156T 179N 227E 95K 150P 156T 159V 180T 95K 105N 156T 179N 198L 95K 150P 156T 159V 179N 95K 105N 156T 179N 180T 95K 105N 198L 227E 240S 95K 105N 156T 159V 240S 95K 105N 180T 227E 240S 95K 105N 156T 159V 227E 95K 105N 180T 198L 240S 95K 105N 156T 159V 198L 95K 105N 180T 198L 227E 95K 105N 156T 159V 180T 95K 105N 179N 227E 240S 95K 105N 156T 159V 179N 95K 105N 179N 198L 240S 95K 105N 150P 227E 240S 95K 105N 179N 198L 227E 95K 105N 150P 198L 240S 95K 105N 179N 180T 240S 95K 105N 150P 198L 227E 95K 105N 179N 180T 227E 95K 105N 150P 180T 240S 95K 105N 179N 180T 198L 95K 105N 150P 180T 227E 95K 105N 159V 227E 240S 95K 105N 150P 180T 198L 95K 105N 159V 198L 240S 95K 105N 150P 179N 240S 95K 105N 159V 198L 227E 95K 105N 150P 179N 227E 95K 150P 159V 179N 198L 95K 105N 159V 180T 240S 95K 105N 159V 180T 227E 95K 105N 150P 179N 180T 95K 105N 159V 180T 198L 95K 105N 150P 159V 240S 95K 105N 159V 179N 240S 95K 105N 150P 159V 227E 95K 105N 159V 179N 227E 95K 105N 150P 159V 198L 95K 105N 159V 179N 198L 95K 105N 150P 159V 180T 95K 105N 159V 179N 180T 95K 105N 150P 159V 179N 95K 105N 156K 227E 240S 95K 105N 150P 156K 240S 95K 105N 156K 198L 240S 95K 105N 150P 156K 227E 95K 105N 156K 198L 227E 95K 105N 150P 156K 198L 95K 105N 156K 180T 240S 95K 105N 150P 156K 180T 95K 105N 156K 180T 227E 95K 105N 150P 156K 179N 95K 105N 156K 180T 198L 95K 105N 150P 156K 159V 95K 105N 156K 179N 240S 95K 105N 150P 156T 240S 95K 105N 156K 179N 227E 95K 105N 150P 156T 227E 95K 105N 156K 179N 198L 95K 105N 150P 156T 198L 95K 105N 156K 179N 180T 95K 105N 150P 156T 180T 95K 105N 156K 159V 240S 95K 105N 150P 156T 179N 95K 105N 156K 159V 227E 95K 105N 150P 156T 159V 95K 105N 150P 179N 198L 150P 156T 159V 179N 198L 240S 95K 105N 156K 159V 180T 159V 179N 180T 198L 227E 240S 95K 105N 156K 159V 179N 156K 179N 180T 198L 227E 240S 95K 105N 156T 227E 240S 156K 159V 180T 198L 227E 240S 95K 105N 156T 198L 240S 156K 159V 179N 198L 227E 240S WO 2009/111083 PCT/US2009/001486 - 264 95K 105N 156T 198L 227E 156K 159V 179N 180T 227E 240S 95K 105N 156T 180T 240S 156K 159V 179N 180T 198L 240S 150P 156T 159V 179N 198L 227E 105N 159V 179N 198L 227E 240S 150P 156T 159V 179N 180T 240S 105N 159V 179N 180T 227E 240S 150P 156T 159V 179N 180T 227E 105N 159V 179N 180T 198L 240S 150P 156T 159V 179N 180T 198L 105N 159V 179N 180T 198L 227E 105N 179N 180T 198L 227E 240S 105N 156K 180T 198L 227E 240S 105N 159V 180T 198L 227E 240S 105N 156K 179N 198L 227E 240S 156K 159V 179N 180T 198L 227E 105N 156K 179N 180T 227E 240S 156T 179N 180T 198L 227E 240S 105N 156K 179N 180T 198L 240S 156T 159V 180T 198L 227E 240S 105N 156K 179N 180T 198L 227E 156T 159V 179N 198L 227E 240S 105N 156K 159V 198L 227E 240S 156T 159V 179N 180T 227E 240S 105N 156K 159V 180T 227E 240S 156T 159V 179N 180T 198L 240S 105N 156K 159V 180T 198L 240S 156T 159V 179N 180T 198L 227E 105N 156K 159V 180T 198L 227E 150P 179N 180T 198L 227E 240S 105N 156K 159V 179N 227E 240S 150P 159V 180T 198L 227E 240S 105N 156K 159V 179N 198L 240S 150P 159V 179N 198L 227E 240S 105N 156K 159V 179N 198L 227E 150P 159V 179N 180T 227E 240S 105N 156K 159V 179N 180T 240S 150P 159V 179N 180T 198L 240S 105N 156K 159V 179N 180T 227E 150P 159V 179N 180T 198L 227E 105N 156K 159V 179N 180T 198L 150P 156K 180T 198L 227E 240S 105N 156T 180T 198L 227E 240S 150P 156K 179N 198L 227E 240S 105N 156T 179N 198L 227E 240S 150P 156K 179N 180T 227E 240S 105N 156T 179N 180T 227E 240S 150P 156K 179N 180T 198L 240S 105N 156T 179N 180T 198L 240S 150P 156K 179N 180T 198L 227E 105N 156T 179N 180T 198L 227E 150P 156K 159V 198L 227E 240S 105N 156T 159V 198L 227E 240S 150P 156K 159V 180T 227E 240S 105N 156T 159V 180T 227E 240S 150P 156K 159V 180T 198L 240S 105N 156T 159V 180T 198L 240S 150P 156K 159V 180T 198L 227E 105N 156T 159V 180T 198L 227E 150P 156K 159V 179N 227E 240S 105N 156T 159V 179N 227E 240S 150P 156K 159V 179N 198L 240S 105N 156T 159V 179N 198L 240S 150P 156K 159V 179N 198L 227E 105N 156T 159V 179N 198L 227E 150P 156K 159V 179N 180T 240S 105N 156T 159V 179N 180T 240S 150P 156K 159V 179N 180T 227E 105N 156T 159V 179N 180T 227E 150P 156K 159V 179N 180T 198L 105N 156T 159V 179N 180T 198L 150P 156T 180T 198L 227E 240S 105N 150P 180T 198L 227E 240S 150P 156T 179N 198L 227E 240S 105N 150P 179N 198L 227E 240S 150P 156T 179N 180T 227E 240S 105N 150P 179N 180T 227E 240S 150P 156T 179N 180T 198L 240S 105N 150P 179N 180T 198L 240S 150P 156T 179N 180T 198L 227E 105N 150P 156T 159V 180T 227E 150P 156T 159V 198L 227E 240S 105N 150P 159V 179N 227E 240S 150P 156T 159V 180T 227E 240S 105N 150P 159V 179N 198L 240S 150P 156T 159V 180T 198L 240S 105N 150P 159V 179N 198L 227E 150P 156T 159V 180T 198L 227E 105N 150P 159V 179N 180T 240S 150P 156T 159V 179N 227E 240S 105N 150P 159V 179N 180T 227E 105N 150P 179N 180T 198L 227E 105N 150P 159V 179N 180T 198L WO 2009/111083 PCT/US2009/001486 -265 105N 150P 156K 198L 227E 240S 95K 159V 180T 198L 227E 240S 105N 150P 156K 180T 227E 240S 95K 159V 179N 198L 227E 240S 105N 150P 156K 180T 198L 240S 95K 159V 179N 180T 227E 240S 105N 150P 156K 180T 198L 227E 95K 159V 179N 180T 198L 240S 105N 150P 156K 179N 227E 240S 95K 159V 179N 180T 198L 227E 105N 150P 156K 179N 198L 240S 95K 156K 180T 198L 227E 240S 105N 150P 156K 179N 198L 227E 95K 156K 179N 198L 227E 240S 105N 150P 156K 179N 180T 240S 95K 156K 179N 180T 227E 240S 105N 150P 156K 179N 180T 227E 95K 156K 179N 180T 198L 240S 105N 150P 156K 179N 180T 198L 95K 156K 179N 180T 198L 227E 105N 150P 156K 159V 227E 240S 95K 156K 159V 198L 227E 240S 105N 150P 156K 159V 198L 240S 95K 156K 159V 180T 227E 240S 105N 150P 156K 159V 198L 227E 95K 156K 159V 180T 198L 240S 105N 150P 156K 159V 180T 240S 95K 156K 159V 180T 198L 227E 105N 150P 156K 159V 180T 227E 95K 156K 159V 179N 227E 240S 105N 150P 156K 159V 180T 198L 95K 156K 159V 179N 198L 240S 105N 150P 156K 159V 179N 240S 95K 156K 159V 179N 198L 227E 105N 150P 156K 159V 179N 227E 95K 156K 159V 179N 180T 240S 105N 150P 156K 159V 179N 198L 95K 156K 159V 179N 180T 227E 105N 150P 156K 159V 179N 180T 95K 156K 159V 179N 180T 198L 105N 150P 159V 198L 227E 240S 95K 156T 180T 198L 227E 240S 105N 150P 159V 180T 227E 240S 95K 156T 179N 198L 227E 240S 105N 150P 159V 180T 198L 240S 95K 156T 179N 180T 227E 240S 105N 150P 159V 180T 198L 227E 95K 156T 179N 180T 198L 240S 105N 150P 156T 198L 227E 240S 95K 156T 179N 180T 198L 227E 105N 150P 156T 180T 227E 240S 95K 156T 159V 198L 227E 240S 105N 150P 156T 180T 198L 240S 95K 156T 159V 180T 227E 240S 105N 150P 156T 180T 198L 227E 95K 156T 159V 180T 198L 240S 105N 150P 156T 179N 227E 240S 95K 156T 159V 180T 198L 227E 105N 150P 156T 179N 198L 240S 95K 156T 159V 179N 227E 240S 105N 150P 156T 179N 198L 227E 95K 156T 159V 179N 198L 240S 105N 150P 156T 179N 180T 240S 95K 156T 159V 179N 198L 227E 105N 150P 156T 179N 180T 227E 95K 156T 159V 179N 180T 240S 105N 150P 156T 179N 180T 198L 95K 156T 159V 179N 180T 227E 105N 150P 156T 159V 227E 240S 95K 156T 159V 179N 180T 198L 105N 150P 156T 159V 198L 240S 95K 150P 180T 198L 227E 240S 105N 150P 156T 159V 198L 227E 95K 150P 179N 198L 227E 240S 105N 150P 156T 159V 180T 240S 95K 150P 179N 180T 227E 240S 95K 150P 179N 180T 198L 240S 95K 150P 156T 159V 180T 240S 105N 150P 156T 159V 180T 198L 95K 150P 179N 180T 198L 227E 105N 150P 156T 159V 179N 240S 95K 150P 159V 198L 227E 240S 105N 150P 156T 159V 179N 227E 95K 150P 159V 180T 227E 240S 105N 150P 156T 159V 179N 198L 95K 150P 159V 180T 198L 240S 105N 150P 156T 159V 179N 180T 95K 150P 159V 180T 198L 227E 95K 179N 180T 198L 227E 240S 95K 150P 159V 179N 227E 240S 95K 150P 159V 179N 198L 240S 95K 105N 179N 198L 227E 240S 95K 150P 159V 179N 198L 227E 95K 105N 179N 180T 227E 240S WO 2009/111083 PCT/US2009/001486 - 266 95K 150P 159V 179N 180T 240S 95K 105N 179N 180T 198L 240S 95K 150P 159V 179N 180T 227E 95K 105N 179N 180T 198L 227E 95K 150P 159V 179N 180T 198L 95K 105N 159V 198L 227E 240S 95K 150P 156K 198L 227E 240S 95K 105N 159V 180T 227E 240S 95K 150P 156K 180T 227E 240S 95K 105N 159V 180T 198L 240S 95K 150P 156K 180T 198L 240S 95K 105N 159V 180T 198L 227E 95K 150P 156K 180T 198L 227E 95K 105N 159V 179N 227E 240S 95K 150P 156K 179N 227E 240S 95K 105N 159V 179N 198L 240S 95K 150P 156K 179N 198L 240S 95K 105N 159V 179N 198L 227E 95K 150P 156K 179N 198L 227E 95K 105N 159V 179N 180T 240S 95K 150P 156K 179N 180T 240S 95K 105N 159V 179N 180T 227E 95K 150P 156K 179N 180T 227E 95K 105N 159V 179N 180T 198L 95K 150P 156K 179N 180T 198L 95K 105N 156K 198L 227E 240S 95K 150P 156K 159V 227E 240S 95K 105N 156K 180T 227E 240S 95K 150P 156K 159V 198L 240S 95K 105N 156K 180T 198L 240S 95K 150P 156K 159V 198L 227E 95K 105N 156K 180T 198L 227E 95K 150P 156K 159V 180T 240S 95K 105N 156K 179N 227E 240S 95K 150P 156K 159V 180T 227E 95K 105N 156K 179N 198L 240S 95K 150P 156K 159V 180T 198L 95K 105N 156K 179N 198L 227E 95K I5OP 156K 159V 179N 240S 95K 105N 156K 179N 180T 240S 95K 150P 156K 159V 179N 227E 95K 105N 156K 179N 180T 227E 95K 150P 156K 159V 179N 198L 95K 105N 156K 179N 180T 198L 95K 150P 156K 159V 179N 180T 95K 105N 156K 159V 227E 240S 95K 150P 156T 198L 227E 240S 95K 105N 156K 159V 198L 240S 95K 150P 156T 180T 227E 240S 95K 105N 156K 159V 198L 227E 95K 150P 156T 180T 198L 240S 95K 105N 156K 159V 180T 240S 95K 150P 156T 180T 198L 227E 95K 105N 156K 159V 180T 227E 95K 150P 156T 179N 227E 240S 95K 105N 156K 159V 180T 198L 95K 150P 156T 179N 198L 240S 95K 105N 156K 159V 179N 240S 95K 150P 156T 179N 198L 227E 95K 105N 156K 159V 179N 227E 95K 150P 156T 179N 180T 240S 95K 105N 156K 159V 179N 198L 95K 150P 156T 179N 180T 227E 95K 105N 156K 159V 179N 180T 95K 150P 156T 179N 180T 198L 95K 105N 156T 198L 227E 240S 95K 150P 156T 159V 227E 240S 95K 105N 156T 180T 227E 240S 95K 150P 156T 159V 198L 240S 95K 105N 156T 180T 198L 240S 95K 150P 156T 159V 198L 227E 95K 105N 156T 179N 227E 240S 95K 150P 156T 159V 180T 227E 95K 105N 156T 179N 198L 240S 95K 150P 156T 159V 180T 198L 95K 105N 156T 179N 198L 227E 95K 150P 156T 159V 179N 240S 95K 105N 156T 179N 180T 240S 95K 150P 156T 159V 179N 227E 95K 105N 156T 179N 180T 227E 95K 150P 156T 159V 179N 198L 95K 105N 156T 179N 180T 198L 95K 150P 156T 159V 179N 180T 95K 105N 156T 159V 227E 240S 95K 105N 180T 198L 227E 240S 95K 105N 156T 159V 198L 240S 95K 105N 156T 159V 198L 227E 95K 105N 156T 159V 180T 240S 95K 105N 156T 159V 180T 227E 95K 105N 156T 159V 180T 198L WO 2009/111083 PCT/US2009/001486 - 267 95K 105N 156T 159V 179N 240S 95K 105N 156T 159V 179N 227E 95K 105N 156T 159V 179N 198L 95K 105N 156T 159V 179N 180T 95K 105N 150P 198L 227E 240S 95K 105N 150P 180T 227E 240S 95K 105N 150P 180T 198L 240S 95K 105N 150P 180T 198L 227E 95K 105N 150P 179N 227E 240S 95K 105N 150P 179N 198L 240S 95K 105N 150P 179N 198L 227E 95K 105N 150P 179N 180T 240S 95K 105N 150P 179N 180T 227E 95K 105N 150P 179N 180T 198L 95K 105N 150P 159V 227E 240S 95K 105N 150P 159V 198L 240S 95K 105N 150P 159V 198L 227E 95K 105N 150P 159V 180T 240S 95K 105N 150P 159V 180T 227E 95K 105N 150P 159V 180T 198L 95K 105N 150P 159V 179N 240S 95K 105N 150P 159V 179N 227E 95K 105N 150P 156K 179N 198L 95K 105N 150P 156K 179N 180T 95K 105N 150P 156K 159V 240S 95K 105N 150P 156K 159V 227E 95K 105N 150P 156K 159V 198L 95K 105N 150P 156K 159V 180T 95K 105N 150P 156K 159V 179N 95K 105N 150P 159V 179N 198L 95K 105N 150P 159V 179N 180T 95K 105N 150P 156K 227E 240S 95K 105N 150P 156K 198L 240S 95K 105N 150P 156K 198L 227E 95K 105N 150P 156K 180T 240S 95K 105N 150P 156K 180T 227E 95K 105N 150P 156K 180T 198L 95K 105N 150P 156T 227E 240S 95K 105N 150P 156T 198L 240S 95K 105N 150P 156T 198L 227E 95K 105N 150P 156T 180T 240S 95K 105N 150P 156T 180T 227E 95K 105N 150P 156T 180T 198L 95K 105N 150P 156T 179N 240S 95K 105N 150P 156T 179N 227E 95K 105N 150P 156T 179N 198L 95K 105N 150P 156T 179N 180T WO 2009/111083 PCT/US2009/001486 - 268 95K 105N 150P 156T 159V 240S 95K 105N 150P 156T 159V 227E 95K 105N 150P 156T 159V 198L 95K 105N 150P 156T 159V 180T 95K 105N 150P 156T 159V 179N 95K 105N 150P 156K 179N 240S 95K 105N 150P 156K 179N 227E 95K 105N 156T 180T 198L 227E 156K 159V 179N 180T 198L 227E 240S 156T 159V 179N 180T 198L 227E 240S 150P 159V 179N 180T 198L 227E 240S 150P 156K 179N 180T 198L 227E 240S 150P 156K 159V 180T 198L 227E 240S 150P 156K 159V 179N 198L 227E 240S 150P 156K 159V 179N 180T 227E 240S 150P 156K 159V 179N 180T 198L 240S 150P 156K 159V 179N 180T 198L 227E 150P 156T 179N 180T 198L 227E 240S 150P 156T 159V 180T 198L 227E 240S 150P 156T 159V 179N 198L 227E 240S 150P 156T 159V 179N 180T 227E 240S 150P 156T 159V 179N 180T 198L 240S 150P 156T 159V 179N 180T 198L 227E 105N 156K 179N 180T 198L 227E 240S 105N 156K 159V 180T 198L 227E 240S 105N 156K 159V 179N 198L 227E 240S 105N 156K 159V 179N 180T 198L 240S 105N 156K 159V 179N 180T 198L 227E 105N 159V 179N 180T 198L 227E 240S 105N 156K 159V 179N 180T 227E 240S 105N 156T 159V 179N 180T 198L 227E 105N 156T 179N 180T 198L 227E 240S 105N 150P 179N 180T 198L 227E 240S 105N 150P 159V 180T 198L 227E 240S 105N 150P 159V 179N 198L 227E 240S 105N 150P 159V 179N 180T 227E 240S 105N 150P 159V 179N 180T 198L 240S 105N 150P 159V 179N 180T 198L 227E 105N 150P 156K 180T 198L 227E 240S 105N 150P 156K 179N 198L 227E 240S 105N 150P 156K 179N 180T 227E 240S 105N 150P 156K 179N 180T 198L 240S 105N 150P 156K 179N 180T 198L 227E 105N 150P 156K 159V 198L 227E 240S 105N 150P 156K 159V 180T 227E 240S 105N 150P 156K 159V 180T 198L 240S 105N 150P 156K 159V 180T 198L 227E WO 2009/111083 PCT/US2009/001486 - 269 105N 150P 156K 159V 179N 227E 240S 105N 150P 156K 159V 179N 198L 240S 105N 150P 156K 159V 179N 198L 227E 105N 150P 156K 159V 179N 180T 240S 105N 150P 156K 159V 179N 180T 227E 105N 150P 156K 159V 179N 180T 198L 105N 150P 156T 179N 198L 227E 240S 105N 150P 156T 179N 180T 227E 240S 105N 150P 156T 179N 180T 198L 240S 105N 150P 156T 179N 180T 198L 227E 105N 150P 156T 159V 198L 227E 240S 105N 150P 156T 159V 180T 227E 240S 105N 150P 156T 159V 180T 198L 240S 105N 150P 156T 159V 180T 198L 227E 105N 150P 156T 159V 179N 198L 240S 105N 150P 156T 159V 179N 198L 227E 105N 150P 156T 180T 198L 227E 240S 105N 156T 159V 179N 198L 227E 240S 105N 156T 159V 179N 180T 198L 240S 105N 156T 159V 179N 180T 227E 240S 105N 156T 159V 180T 198L 227E 240S 95K 156T 159V 179N 198L 227E 240S 95K 156T 159V 179N 180T 227E 240S 95K 156T 159V 179N 180T 198L 240S 95K 156T 159V 179N 180T 198L 227E 95K 150P 179N 180T 198L 227E 240S 95K 150P 159V 180T 198L 227E 240S 95K 150P 159V 179N 198L 227E 240S 95K 150P 159V 179N 180T 227E 240S 95K 150P 159V 179N 180T 198L 240S 95K 150P 159V 179N 180T 198L 227E 105N 150P 156T 159V 179N 227E 240S 105N 150P 156T 159V 179N 180T 240S 105N 150P 156T 159V 179N 180T 227E 105N 150P 156T 159V 179N 180T 198L 95K 159V 179N 180T 198L 227E 240S 95K 156K 179N 180T 198L 227E 240S 95K 156K 159V 180T 198L 227E 240S 95K 156K 159V 179N 198L 227E 240S 95K 156K 159V 179N 180T 227E 240S 95K 156K 159V 179N 180T 198L 240S 95K 156K 159V 179N 180T 198L 227E 95K 156T 179N 180T 198L 227E 240S 95K 156T 159V 180T 198L 227E 240S 95K 150P 156K 159V 179N 180T 227E 95K 150P 156K 159V 179N 180T 198L 95K 150P 156T 180T 198L 227E 240S WO 2009/111083 PCT/US2009/001486 - 270 95K 150P 156T 179N 198L 227E 240S 95K 150P 156T 179N 180T 227E 240S 95K 150P 156T 179N 180T 198L 240S 95K 150P 156T 179N 180T 198L 227E 95K 150P 156T 159V 198L 227E 240S 95K 150P 156T 159V 180T 227E 240S 95K 150P 156T 159V 180T 198L 240S 95K 150P 156T 159V 180T 198L 227E 95K 150P 156T 159V 179N 227E 240S 95K 150P 156T 159V 179N 198L 240S 95K 150P 156T 159V 179N 198L 227E 95K 150P 156T 159V 179N 180T 240S 95K 150P 156T 159V 179N 180T 227E 95K 150P 156K 180T 198L 227E 240S 95K 150P 156K 179N 198L 227E 240S 95K 150P 156K 179N 180T 227E 240S 95K 150P 156K 179N 180T 198L 240S 95K 150P 156K 179N 180T 198L 227E 95K 150P 156K 159V 198L 227E 240S 95K 150P 156K 159V 180T 227E 240S 95K 150P 156K 159V 180T 198L 240S 95K 150P 156K 159V 180T 198L 227E 95K 150P 156K 159V 179N 227E 240S 95K 150P 156K 159V 179N 198L 240S 95K 150P 156K 159V 179N 198L 227E 95K 150P 156K 159V 179N 180T 240S 95K 105N 156K 180T 198L 227E 240S 95K 105N 156K 179N 198L 227E 240S 95K 105N 156K 179N 180T 227E 240S 95K 105N 156K 179N 180T 198L 240S 95K 105N 156K 179N 180T 198L 227E 95K 105N 156K 159V 198L 227E 240S 95K 105N 156K 159V 180T 227E 240S 95K 105N 156K 159V 180T 198L 240S 95K 105N 156K 159V 180T 198L 227E 95K 105N 156K 159V 179N 227E 240S 95K 105N 156K 159V 179N 198L 240S 95K 105N 156K 159V 179N 198L 227E 95K 105N 156K 159V 179N 180T 240S 95K 105N 156K 159V 179N 180T 227E 95K 105N 156K 159V 179N 180T 198L 95K 105N 156T 180T 198L 227E 240S 95K 150P 156T 159V 179N 180T 198L 95K 105N 179N 180T 198L 227E 240S 95K 105N 159V 180T 198L 227E 240S 95K 105N 159V 179N 198L 227E 240S 95K 105N 159V 179N 180T 227E 240S WO 2009/111083 PCT/US2009/001486 - 271 95K 105N 159V 179N 180T 198L 240S 95K 105N 159V 179N 180T 198L 227E 95K 105N 156T 159V 180T 198L 227E 95K 105N 156T 159V 179N 227E 240S 95K 105N 156T 159V 179N 198L 240S 95K 105N 156T 159V 179N 198L 227E 95K 105N 156T 159V 179N 180T 240S 95K 105N 156T 159V 179N 180T 227E 95K 105N 156T 159V 179N 180T 198L 95K 105N 150P 180T 198L 227E 240S 95K 105N 150P 179N 198L 227E 240S 95K 105N 150P 179N 180T 227E 240S 95K 105N 150P 179N 180T 198L 240S 95K 105N 150P 179N 180T 198L 227E 95K 105N 150P 159V 198L 227E 240S 95K 105N 150P 159V 180T 227E 240S 95K 105N 150P 159V 180T 198L 240S 95K 105N 150P 159V 180T 198L 227E 95K 105N 150P 159V 179N 227E 240S 95K 105N 150P 159V 179N 198L 240S 95K 105N 150P 159V 179N 198L 227E 95K 105N 150P 159V 179N 180T 240S 95K 105N 150P 159V 179N 180T 227E 95K 105N 150P 159V 179N 180T 198L 95K 105N 150P 156K 198L 227E 240S 95K 105N 150P 156T 179N 227E 240S 95K 105N 150P 156T 179N 198L 240S 95K 105N 150P 156T 179N 198L 227E 95K 105N 150P 156T 179N 180T 240S 95K 105N 150P 156T 179N 180T 227E 95K 105N 150P 156T 179N 180T 198L 95K 105N 150P 156T 159V 227E 240S 95K 105N 150P 156T 159V 198L 240S 95K 105N 150P 156T 159V 198L 227E 95K 105N 150P 156T 159V 180T 240S 95K 105N 150P 156T 159V 180T 227E 95K 105N 150P 156T 159V 180T 198L 95K 105N 150P 156T 159V 179N 240S 95K 105N 150P 156T 159V 179N 227E 95K 105N 150P 156T 159V 179N 198L 95K 105N 150P 156T 159V 179N 180T 95K 105N 156T 179N 198L 227E 240S 95K 105N 156T 179N 180T 227E 240S 95K 105N 156T 179N 180T 198L 240S 95K 105N 156T 179N 180T 198L 227E 95K 105N 156T 159V 198L 227E 240S 95K 105N 156T 159V 180T 227E 240S WO 2009/111083 PCT/US2009/001486 - 272 95K 105N 156T 159V 180T 198L 240S 95K 105N 150P 156K 180T 227E 240S 95K 105N 150P 156K 180T 198L 240S 95K 105N 150P 156K 180T 198L 227E 95K 105N 150P 156K 179N 227E 240S 95K 105N 150P 156K 179N 198L 240S 95K 105N 150P 156K 179N 198L 227E 95K 105N 150P 156K 179N 180T 240S 95K 105N 150P 156K 179N 180T 227E 95K 105N 150P 156K 179N 180T 198L 95K 105N 150P 156K 159V 227E 240S 95K 105N 150P 156K 159V 198L 240S 95K 105N 150P 156K 159V 198L 227E 95K 105N 150P 156K 159V 180T 240S 95K 105N 150P 156K 159V 180T 227E 95K 105N 150P 156K 159V 180T 198L 95K 105N 150P 156K 159V 179N 240S 95K 105N 150P 156K 159V 179N 227E 95K 105N 150P 156K 159V 179N 198L 95K 105N 150P 156K 159V 179N 180T 95K 105N 150P 156T 198L 227E 240S 95K 105N 150P 156T 180T 227E 240S 95K 105N 150P 156T 180T 198L 240S 95K 105N 150P 156T 180T 198L 227E 105N 150P 156K 159V 179N 198L 227E 240S 105N 150P 156K 159V 179N 180T 227E 240S 105N 150P 156K 159V 179N 180T 198L 240S 105N 150P 156K 159V 179N 180T 198L 227E 105N 150P 156T 179N 180T 198L 227E 240S 105N 150P 156T 159V 180T 198L 227E 240S 105N 150P 156T 159V 179N 198L 227E 240S 105N 150P 156T 159V 179N 180T 227E 240S 105N 150P 156T 159V 179N 180T 198L 240S 105N 150P 156T 159V 179N 180T 198L 227E 95K 150P 156T 159V 179N 180T 198L 240S 95K 150P 156T 159V 179N 180T 198L 227E 95K 105N 159V 179N 180T 198L 227E 240S 95K 105N 156K 179N 180T 198L 227E 240S 95K 105N 156K 159V 180T 198L 227E 240S 95K 105N 156K 159V 179N 198L 227E 240S 95K 105N 156K 159V 179N 180T 227E 240S 95K 105N 156K 159V 179N 180T 198L 240S 95K 105N 156K 159V 179N 180T 198L 227E 95K 105N 156T 179N 180T 198L 227E 240S 95K 156K 159V 179N 180T 198L 227E 240S 95K 156T 159V 179N 180T 198L 227E 240S 95K 150P 159V 179N 180T 198L 227E 240S WO 2009/111083 PCT/US2009/001486 - 273 95K 150P 156K 179N 180T 198L 227E 240S 95K 150P 156K 159V 180T 198L 227E 240S 95K 150P 156K 159V 179N 198L 227E 240S 95K 105N 150P 159V 180T 198L 227E 240S 95K 105N 150P 156T 179N 180T 198L 227E 95K 105N 150P 156T 159V 198L 227E 240S 95K 105N 150P 156T 159V 180T 227E 240S 95K 105N 150P 156T 159V 180T 198L 240S 95K 105N 150P 156T 159V 180T 198L 227E 95K 105N 150P 156T 159V 179N 180T 227E 105N 150P 156K 159V 180T 198L 227E 240S 105N 150P 156K 179N 180T 198L 227E 240S 105N 150P 159V 179N 180T 198L 227E 240S 105N 156K 159V 179N 180T 198L 227E 240S 105N 156T 159V 179N 180T 198L 227E 240S 150P 156K 159V 179N 180T 198L 227E 240S 150P 156T 159V 179N 180T 198L 227E 240S 95K 105N 150P 156T 179N 180T 198L 240S 95K 105N 150P 179N 180T 198L 227E 240S 95K 105N 156T 159V 179N 180T 198L 240S 95K 105N 156T 159V 179N 180T 198L 227E 95K 105N 156T 159V 179N 180T 227E 240S 95K 105N 156T 159V 179N 198L 227E 240S 95K 105N 156T 159V 180T 198L 227E 240S 95K 150P 156K 159V 179N 180T 198L 240S 95K 150P 156K 159V 179N 180T 198L 227E 95K 150P 156K 159V 179N 180T 227E 240S 95K 150P 156T 159V 179N 180T 227E 240S 95K 150P 156T 159V 179N 198L 227E 240S 95K 150P 156T 159V 180T 198L 227E 240S 95K 150P 156T 179N 180T 198L 227E 240S 95K 105N 150P 156T 159V 179N 180T 198L 95K 105N 150P 159V 179N 198L 227E 240S 95K 105N 150P 159V 179N 180T 227E 240S 95K 105N 150P 159V 179N 180T 198L 240S 95K 105N 150P 159V 179N 180T 198L 227E 95K 105N 150P 156K 180T 198L 227E 240S 95K 105N 150P 156K 179N 198L 227E 240S 95K 105N 150P 156K 179N 180T 227E 240S 95K 105N 150P 156K 179N 180T 198L 240S 95K 105N 150P 156K 179N 180T 198L 227E 95K 105N 150P 156K 159V 198L 227E 240S 95K 105N 150P 156K 159V 180T 227E 240S 95K 105N 150P 156K 159V 180T 198L 240S 95K 105N 150P 156K 159V 180T 198L 227E 95K 105N 150P 156K 159V 179N 227E 240S 95K 105N 150P 156K 159V 179N 198L 240S WO 2009/111083 PCT/US2009/001486 -274 95K 105N 150P 156K 159V 179N 198L 227E 95K 105N 150P 156K 159V 179N 180T 240S 95K 105N 150P 156K 159V 179N 180T 227E 95K 105N 150P 156K 159V 179N 180T 198L 95K 105N 150P 156T 180T 198L 227E 240S 95K 105N 150P 156T 179N 198L 227E 240S 95K 105N 150P 156T 179N 180T 227E 240S 95K 105N 150P 156T 159V 179N 227E 240S 95K 105N 150P 156T 159V 179N 198L 240S 95K 105N 150P 156T 159V 179N 198L 227E 95K 105N 150P 156T 159V 179N 180T 240S 105N 150P 156K 159V 179N 180T 198L 227E 240S 105N 150P 156T 159V 179N 180T 198L 227E 240S 95K 150P 156K 159V 179N 180T 198L 227E 240S 95K 150P 156T 159V 179N 180T 198L 227E 240S 95K 105N 156K 159V 179N 180T 198L 227E 240S 95K 105N 156T 159V 179N 180T 198L 227E 240S 95K 105N 150P 159V 179N 180T 198L 227E 240S 95k 105N 150P 156K 179N 180T 198L 227E 240S 95K 105N 150P 156K 159V 180T 198L 227E 240S 95K 105N 150P 156K 159V 179N 198L 227E 240S 95K 105N 150P 156K 159V 179N 180T 227E 240S 95K 105N 150P 156K 159V 179N 180T 198L 240S 95K 105N 150P 156K 159V 179N 180T 198L 227E 95K 105N 150P 156T 179N180T 198L 227E 240S 95K 105N 150P 156T 159V 180T 198L 227E 240S 95K 105N 150P 156T 159V 179N 198L 227E 240S 95K 105N 150P 156T 159V 179N 180T 227E 240S 95K 105N 150P 156T 159V 179N 180T 198L 240S 95K 105N 150P 156T 159V 179N 180T 198L 227E 95K 105N 150P 156K 159V 179N 180T 198L 227E 240S 95K 105N 150P 156T 159V 179N 180T 198L 227E 240S Example 30 Reversibility of Enzymatic Activity Following Decrease in Temperature In this example, the temperature sensitive hMMP-1 mutants that were 5 confirmed in Example 28B were further assayed to determine whether enzymatic activity at 25 *C was reversible or irreversible following subsequent exposure to elevated temperatures followed by a return to 25 "C. The hMMP-1 mutants were expressed in 14 ml culture tubes, as described in Example 28B. The putative Hits were tested for their activities under five conditions: at 25"C, 34"C or 37 0 C, and at 10 34 0 C or 37"C and subsequent re-exposure to the requisite temperature of 25'C (see WO 2009/111083 PCT/US2009/001486 - 275 Table 16 for reaction conditions). Mutants that were active at 25 0 C, showed decreased activity when raised to 34"C or 37"C (i.e. the ratio of the activities at 25 0 C/34 0 C or 25 0 C/37"C is equal to or greater than 1.5), and exhibited a baseline activity when lowered again to 25*C were scored as "Reversible Hits." Mutants that 5 were active at 25*C, showed decreased activity when raised to 34"C or 37"C (i.e. the ratio of the activities at 25 0 C/34 0 C or 25"C/37*C is equal to or greater than 1.5), and exhibited the same amount of decreased activity when lowered again to 25*C were scored as "Irreversible Hits." A. Reaction Conditions 10 The reversibility of enzymatic activity of each hMMP- 1 mutant was. determined using the previously described fluorescence assay as modified below. In short, the 4 ul of the supernatant of each hMMP- 1 mutant was diluted in TCNB with I mM APMA and transferred to a 96-well plate. Five different wells were prepared for each hMMP- 1 mutant as set forth in Table 16. The solution was incubated at the 15 initial reaction temperature (25 *C, 34 'C, or 37 *C) for 2 hours. This activation step cleaves the pro-peptide and generates mature hMMP-1. Following activation, 100 pl of TCNB with 10 ptiM Mca-K-P-L-G-L-Dpa-A

R-NH

2 fluorescent substrate was added to each well and reaction conditions were as summarized in Table 28, below. Briefly, each hMMP-1 mutant was exposed to each 20 of the five reaction conditions by incubation of the hMMP- 1 mutant in the presence of the fluorogenic substrate for an hour at the initial temperature. For each mutant, baseline activity at 25 'C, 34 *C, or 37 *C was assessed by incubation with the substrate for an additional 1 hour (2 hour condition) or overnight (overnight condition), followed by fluorescence measurement. To assess the 25 reversibility/irreversibility of activity, samples incubated for an initial 1 hour at 34 'C, or 37 *C were lowered to 25 "C and allowed to incubate for either an hour (2 hour condition) or 16 hours (overnight condition), followed by fluorescence measurement. Wild-type hMMP-1 was used as a positive control and supernatant from cells transformed with only vector was used as a negative control. Fluorescence was 30 detected by measuring fluorescence in a fluorescent plate reader at 320 nm exitation/405 nm emission. Relative fluorescence units (RFU) were determined. Duplicate reactions were performed for each sample, reaction temperature, and positive and negative control.

WO 2009/111083 PCT/US2009/001486 - 276 Table 28. Reaction Conditions Condition Initial Incubation at 2 Hours Overnight Temperature 25 *C 25 *C 25 *C - 2 hours overnight 34 *C 34 *C - 2 hours' overnight 34 *C to 34 *C 25 C a) 34 *C for 1 a) 34 C for 1 25 *C hour hour b) 25 *C for 1 b) 25 *C for 16 hour hours 37 *C 37 C - 2 hours overnight 37 *C to 37 C 25 *C a) 37 C for I a) 37 *C for 1 25 *C hour hour b) 25 *C for 1 b) 25 *C for 16 hour hours B. Results: Partially reversible hMMP-1 mutants Twenty six hMMP-1 mutants were determined to be partially reversible. Although the activity (in RFU) did not return to baseline activity observed at 25 *C, 5 an overall increase in activity was observed when the temperature was returned to 25 0 C compared to activity at 34 *C or 37 0 C. The results are shown in Tables 29-32 below, which list the activities (in RFUs) and the ratios of the activities. Tables 29 and 30 summarize the results of reversibility at 34 *C or 37 *C, respectively, of the hMMP-1 partially reversible mutants under the 2 hour condition. Tables 31 and 32 10 summarize the results of reversibility at 34 *C or 37 *C, respectively, of the partially reversible hMMP-1 mutants under the overnight condition. The results are similar under all reaction conditions, temperature and time. The activity at 34 0 C or 37 *C overnight is lower than the activity when incubated at 34 0 C or 37 *C for one hour then 25 *C overnight. For example, the activity of E180Y at 34 *C is 6080 RFU but 15 its activity at 34 OC then overnight at 25 *C increased to 8570 RFU (see Table 31, below). Table 29. Partially Reversible hMMP-1 mutants (2 Hours, 34 *C) hMMP-1 SEQ ID RFU RFU RFU Ratio Ratio mutation NO 25 *C 34 *C 34 to 25 0 C/ 25 0 C/ 25 0 C 34 0 C 34 to 25 0 C D105A 340 5669.31 824.07 922.97 6.88 6.14 D105F 336 2980.00 623.89 725.03 4.78 4.11 D105G 335 8821.81 2759.24 2966.37 3.20 2.97 WO 2009/111083 PCT/US2009/001486 - 277 D105S 334 9355.63 4607.18 6681.63 2.03 1.40 D105T 333 4457.16 974.63 1534.71 4.57 2.90 R150P 345 8750.30 2315.11 2506.15 3.78 3.49 G159T 359 6704.95 2294.40 2344.57 2.92 2.86 E180Y 374 8557.09 4979.24 6224.87 1.72 1.37 E180T 373 7870.99 1532.35 1852.46 5.14 4.25 E180F 377 8508.13 3597.75 3915.71 2.36 2.17 T185H 389 5593.77 2278.26 2429.05 2.46 2.30 T185Q 391 7006.87 2250.58 2397.60 3.11 2.92 T185A 395 2474.96 663.82 822.83 3.73 3.01 T185E 388 3948.43 2088.15 1862.83 1.89 2.12 N187R 398 3006.08 1352.97 1343.94 2.22 2.24 N187M 402 4934.44 1811.35 1793.14 2.72 2.75 N187K 397 4182.49 2425.34 2415.57 1.72 1.73 R195V 411 4847.81 2724.92 2517.49 1.78 1.93 A198L 416 6756.76 2056.50 2046.15 3.29 3.30 A198M 415 3777.50 1708.61 1725.14 2.21 2.19 S210V 419 3349.95 1249.47 1622.57 2.68 2.06 Y218S 421 2878.50 2373.98 2187.48 1.21 1.32 F223E 422 8318.70 3685.68 5283.08 2.26 1.57 V227W 437 996.55 729.20 834.38 1.37 1.19 L2291 441 2790.27 1050.86 1738.46 2.66 1.61 1240C 448 2688.75 561.91 884.15 4.78 3.04 Table 30. Partially Reversible hMMP-1 mutants (2 Hours, 37 *C) hMMP-1 SEQ ID RFU RFU RFU Ratio Ratio mutation NO 25 *C 37 *C 37 to 25 0 C/ 25 0 C/ 25 0 C 37 0 C 37 to 25 0 C D105A 340 5669.31 1336.14 1509.52 4.24 3.76 D105F 336 2980.00 818.63 1004.23 3.64 2.97 D105G 335 8821.81 4313.40 4643.53 2.05 1.90 D105S 334 9355.63 7274.97 7453.42 1.29 1.26 D105T 333 4457.16 2220.03 2177.84 2.01 2.05 R150P 345 8750.30 2497.86 3115.73 3.50 2.81 G159T 359 6704.95 2347.74 2530.78 2.86 2.65 E180Y 374 8557.09 6079.36 6421.56 1.41 1.33 E180T 373 7870.99 1794.15 1824.99 4.39 4.31 E180F 377 8508.13 3975.22 3981.79 2.14 2.14 T185H 389 5593.77 2534.15 2693.25 2.21 2.08 T185Q 391 7006.87 2642.74 2589.77 2.65 2.71 T185A 395 2474.96 707.09 730.58 3.50 3.39 T185E 388 3948.43 2091.32 2106.55 1.89 1.87 N187R 398 3006.08 1421.87 1476.42 2.11 2.04 N187M 402 4934.44 1893.07 1998.97 2.61 2.47 N187K 397 4182.49 2652.79 2902.79 1.58 1.44 WO 2009/111083 PCT/US2009/001486 - 278 R195V 411 4847.81 2984.10 3555.03 1.62 1.36 A198L 416 6756.76 2642.76 2540.07 2.56 2.66 A198M 415 3777.50 2155.58 2802.78 1.75 1.35 S210V 419 3349.95 2314.86 2277.32 1.45 1.47 Y218S 421 2878.50 2350.27 2383.67 1.22 1.21 F223E 422 8318.70 6209.93 7415.02 1.34 1.12 V227W 437 996.55 787.87 850.67 1.26 1.17 L2291 441 2790.27 1803.44 2453.07 1.55 1.14 1240C 448 2688.75 853.66 872.62 3.15 3.08 Table 31. Partially Re versible hMMP-1 mutants (Ove night, 34 *C) hMMP-1 SEQ ID RFU RFU RFU Ratio Ratio mutation NO 25 *C 34 *C 34 to 25 0 C/ 25 0 C/ 25 0 C 34 0 C 34 to 25 0 C D105A 340 8466.62 1302.84 1532.38 6.50 5.53 D105F 336 6725.59 938.60 1172.86 7.17 5.73 D105G 335 8940.06 3560.75 5314.44 2.51 1.68 D105S 334 9300.85 5584.70 9413.56 1.67 0.99 D105T 333 7910.47 1899.25 3254.16 4.17 2.43 R150P 345 9011.11 3533.16 4443.96 2.55 2.03 G159T 359 9105.95 3210.57 4179.05 2.84 2.18 E180Y 374 9281.77 6080.89 8570.48 1.53 1.08 E180T 373 8475.04 2585.89 3901.87 3.28 2.17 E180F 377 9360.74 5183.25 7022.64 1.81 1.33 T185H 389 8531.85 3164.69 5520.76 2.70 1.55 T185Q 391 9044.23 3639.00 5467.27 2.49 1.65 T185A 395 6156.97 1110.68 1585.53 5.54 3.88 T185E 388 8479.18 3868.06 4836.97 2.19 1.75 N187R 398 7593.11 2415.63 3156.74 3.14 2.41 N187M 402 8605.76 2769.52 4008.68 3.11 2.15 N187K 397 8667.36 3458.94 5465.35 2.51 1.59 R195V 411 8634.05 4648.03 5966.81 1.86 1.45 A198L 416 8795.36 3469.36 5027.30 2.54 1.75 A198M 415 8352.73 3215.69 4220.51 2.60 1.98 S210V 419 7104.17 2441.96 3664.23 2.91 1.94 Y218S 421 7740.61 4057.37 5769.79 1.91 1.34 F223E 422 9650.44 4849.58 9311.40 1.99 1.04 V227W 437 3070.92 1370.13 1632.51 2.24 1.88 L2291 441 7333.92 1832.18 4427.24 4.00 1.66 1240C 448 6170.51 1174.96 2389.06 5.25 2.58 Table 32. Partially Reversible hMMP-1 mutants (Overnight, 37 *C) hMMP-1 I SEQ ID RFU RFU [ RFU Ratio Ratio mutation NO 25 *C 37 *C 37 to 25 0 C/ 25 0

C/

WO 2009/111083 PCT/US2009/001486 - 279 25 0 C 37 0 C 37 to 25 0 C D105A 340 8466.62 1931.17 2589.08 4.38 3.27 D105F 336 6725.59 1173.23 1759.31 5.73 3.82 D105G 335 8940.06 5390.32 7139.57 1.66 1.25 D105S 334 9300.85 8234.95 8615.33 1.13 1.08 D105T 333 7910.47 3292.01 4482.74 2.40 1.76 R150P 345 9011.11 3559.66 5181.30 2.53 1.74 G159T 359 9105.95 3160.07 4338.35 2.88 2.10 E180Y 374 9281.77 6894.61 8986.47 1.35 1.03 E180T 373 8475.04 2809.15 3649.72 3.02 2.32 E180F 377 9360.74 5335.15 7183.36 1.75 1.30 T185H 389 8531.85 3515.59 6101.91 2.43 1.40 T185Q 391 9044.23 4012.93 5623.60 2.25 1.61 T185A 395 6156.97 1059.61 1315.46 5.81 4.68 T185E 388 8479.18 3892.33 5330.81 2.18 1.59 N187R 398 7593.11 2370.01 3425.18 3.20 2.22 N187M 402 8605.76 2720.28 4400.27 3.16 1.96 N187K 397 8667.36 3709.62 6374.32 2.34 1.36 R195V 411 8634.05 4960.91 7212.05 1.74 1.20 A198L 416 8795.36 4181.78 5395.22 2.10 1.63 A198M 415 8352.73 3637.79 5914.49 2.30 1.41 S210V 419 7104.17 3939.90 4626.58 1.80 1.54 Y218S 421 7740.61 4093.29 6181.92 1.89 1.25 F223E 422 9650.44 7645.34 9149.09 1.26 1.05 V227W 437 3070.92 1456.45 1695.81 2.11 1.81 L2291 441 7333.92 3268.93 5729.00 2.24 1.28 1240C 448 6170.51 2223.23 2050.31 2.78 3.01 C. Results: Non reversible hMMP-1 mutants Thirty eight hMMP-1 mutants were determined to be non reversible. The activity of these mutants at 34*C or 37"C, which is decreased compared to the activity 5 at 25 0 C, remained decreased when lowered to 25 0 C. The results are shown in Tables 33-36 below, which list the activities (in RFUs) and the ratios of the activities. Tables 33 and 34 summarize the results or at 34 'C or 37 *C, respectively, of the hMMP-1 irreversible mutants under the two hour condition. Tables 35 and 36 summarize the results of reversibility at 34 'C or 37 *C, respectively, of the irreversible hMMP-1 10 mutants under the overnight condition. The results are similar under all reaction conditions, temperature and time. The activity at 34 *C or 37 *C overnight is the same or similar to the activity when incubated at 34 *C or 37 'C for one hour then 25 WO 2009/111083 PCT/US2009/001486 - 280 'C overnight. For example, the activity of D105R at 34 *C is 1407 RFU and its activity at 34 *C then overnight at 25 *C is 1424 RFU (see Table 35, below). Table 33. Non Reversible hMMP-1 mutants (2 Hours, 34 *C) hMMP-1 SEQ ID RFU RFU RFU Ratio Ratio mutation NO 25 *C 34 *C 34 to 25 0 C/ 25 0 C/ 25 0 C 34 0 C 34 to 25 0 C L95K 328 4650.42 748.29 833.29 6.21 5.58 D1051 338 6832.34 780.32 908.39 8.76 7.52 D105L 339 4206.38 534.24 630.66 7.87 6.67 D105N 332 8920.05 918.13 1128.03 9.72 7.91 D105R 331 2821.20 722.46 843.19 3.90 3.35 D105W 337 6663.80 1690.93 2266.26 3.94 2.94 D151G 346 1264.62 589.27 664.86 2.15 1.90 F155A 348 2824.01 779.72 735.02 3.62 3.84 D156K 350 8576.47 2210.63 2318.28 3.88 3.70 D156T 352 8727.27 2679.17 2770.95 3.26 3.15 D156L 356 2916.24 576.84 655.46 5.06 4.45 D156A 357 2299.63 533.68 635.67 4.31 3.62 D156W 354 1502.86 539.74 637.12 2.78 2.36 D156V 355 1593.06 534.71 634.83 2.98 2.51 D156H 349 5387.79 698.77 784.55 7.71 6.87 D156R 351 7020.81 793.83 881.39 8.84 7.97 G159V 363 4673.44 856.78 789.92 5.45 5.92 A176F 365 1609.85 654.43 633.13 2.46 2.54 D179N 368 5660.69 644.51 644.98 8.78 8.78 D181L 382 2710.97 619.39 645.65 4.38 4.20 D181K 378 1130.63 625.01 609.58 1.81 1.85 E182T 384 3702.08 791.23 805.48 4.68 4.60 E182Q 383 1331.50 639.84 623.88 2.08 2.13 T185R 390 2637.31 1187.63 1158.47 2.22 2.28 N187F 401 3227.96 877.21 823.16 3.68 3.92 N1871 404 4218.55 849.11 869.19 4.97 4.85 G206A 418 872.27 603.01 592.13 1.45 1.47 G206S 417 932.69 492.65 507.75 1.89 1.84 V227C 433 1998.67 950.01 1115.17 2.10 1.79 V227E 430 7904.54 839.00 906.06 9.42 8.72 Q228P 439 1082.56 607.78 617.33 1.78 1.75 L229T 440 1221.05 580.15 605.83 2.10 2.02 D233E 443 2195.02 1393.95 1332.07 1.57 1.65 1234A 447 2375.42 1473.70 1456.58 1.61 1.63 1234T 446 1199.18 713.83 775.40 1.68 1.55 1234E 444 3920.02 705.86 829.15 5.55 4.73 1240S 449 3867.71 973.97 1027.84 3.97 3.76 WO 2009/111083 PCT/US2009/001486 -281 Table 34. Non Reversible hMMP-1 mutants (2 Hours, 37 *C) hMMP-1 SEQ ID RFU RFU RFU Ratio Ratio mutation NO 25 *C 37 *C 37 to 25 0 C/ 25 0 C/ 25 0 C 37 0 C 37 to 25 0 C L95K 328 4650.42 746.89 1092.61 6.23 4.26 D1051 338 6832.34 1110.07 1104.96 6.15 6.18 D105L 339 4206.38 607.46 624.88 6.92 6.73 D105N 332 8920.05 1727.44 1820.97 5.16 4.90 D105R 331 2821.20 813.68 846.09 3.47 3.33 D105W 337 6663.80 3081.59 3123.49 2.16 2.13 D151G 346 1264.62 616.51 628.65 2.05 2.01 F155A 348 2824.01 746.59 867.76 3.78 3.25 D156K 350 8576.47 2310.30 2080.22 3.71 4.12 D156T 352 8727.27 2752.35 2251.21 3.17 3.88 D156L 356 2916.24 688.08 652.06 4.24 4.47 D156A 357 2299.63 554.21 606.45 4.15 3.79 D156W 354 1502.86 575.12 582.43 2.61 2.58 D156V 355 1593.06 542.36 544.49 2.94 2.93 D156H 349 5387.79 819.82 881.23 6.57 6.11 D156R 351 7020.81 872.40 944.17 8.05 7.44 G159V 363 4673.44 838.46 932.14 5.57 5.01 A176F 365 1609.85 618.72 741.21 2.60 2.17 D179N 368 5660.69 656.31 636.18 8.63 8.90 D181L 382 2710.97 611.92 668.31 4.43 4.06 D181K 378 1130.63 608.68 646.77 1.86 1.75 E182T 384 3702.08 826.28 746.25 4.48 4.96 E182Q 383 1331.50 623.11 629.01 2.14 2.12 T185R 390 2637.31 1183.37 1158.87 2.23 2.28 N187F 401 3227.96 931.04 856.03 3.47 3.77 N1871 404 4218.55 887.80 879.78 4.75 4.80 G206A 418 872.27 586.57 654.37 1.49 1.33 G206S 417 932.69 463.60 552.97 2.01 1.69 V227C 433 1998.67 992.19 1130.51 2.01 1.77 V227E 430 7904.54 1015.12 1127.74 7.79 7.01 Q228P 439 1082.56 586.63 777.28 1.85 1.39 L229T 440 1221.05 564.49 747.87 2.16 1.63 D233E 443 2195.02 1454.71 1976.42 1.51 1.11 1234A 447 2375.42 1594.08 1460.23 1.49 1.63 1234T 446 1199.18 796.81 833.55 1.50 1.44 1234E 444 3920.02 923.57 867.78 4.24 4.52 1240S 449 3867.71 1575.05 1594.10 2.46 2.43 Table 35. Non Reversible hMMP-1 mutants (Overnight, 34 *C) hMMP-1 SEQ ID RFU RFU RFU Ratio Ratio mutation NO 25 0 C 34 0 C 34 to [ 25 0 C/ 25*C/ WO 2009/111083 PCT/US2009/001486 - 282 25 0 C 34 0 C 34 to -_ 25 0 C L95K 328 7744.34 1803.12 1892.59 4.29 4.09 D1051 338 8394.32 1614.57 1736.52 5.20 4.83 D105L 339 6546.78 957.95 988.23 6.83 6.62 D105N 332 9119.04 1459.16 1822.40 6.25 5.00 D105R 331 5775.25 1407.06 1424.59 4.10 4.05 D105W 337 8617.36 2851.22 4709.94 3.02 1.83 D151G 346 1956.65 959.80 1013.03 2.04 1.93 F155A 348 4891.89 2016.76 1493.70 2.43 3.28 D156K 350 8696.27 3968.92 4371.25 2.19 1.99 D156T 352 8972.20 3971.43 4480.62 2.26 2.00 D156L 356 5254.55 972.64 1011.27 5.40 5.20 D156A 357 3585.37 1098.25 1057.84 3.26 3.39 D156W 354 2570.24 1091.27 1126.01 2.36 2.28 D156V 355 2208.99 954.21 954.54 2.31 2.31 D156H 349 7587.19 1451.49 1440.25 5.23 5.27 D156R 351 8622.23 1735.02 1760.60 4.97 4.90 G159V 363 6555.27 1821.53 1524.05 3.60 4.30 A176F 365 4191.69 1414.21 1181.99 2.96 3.55 D179N 368 7317.57 1504.84 1458.70 4.86 5.02 D181L 382 4534.34 1078.98 984.43 4.20 4.61 D181K 378 1869.47 946.27 841.77 1.98 2.22 E182T 384 6752.25 1483.52 1570.77 4.55 4.30 E182Q 383 2212.75 1065.07 929.49 2.08 2.38 T185R 390 6281.97 2425.71 2808.30 2.59 2.24 N187F 401 7352.85 1612.23 1533.32 4.56 4.80 N1871 404 8306.40 1459.25 1598.90 5.69 5.20 G206A 418 2492.53 1038.14 906.63 2.40 2.75 G206S 417 2845.84 908.82 816.00 3.13 3.49 V227C 433 5833.84 2207.20 2739.65 2.64 2.13 V227E 430 8630.90 2283.07 2096.30 3.78 4.12 Q228P 439 3673.33 1162.95 1213.48 3.16 3.03 L229T 440 3543.75 1103.34 1105.90 3.21 3.20 D233E 443 6694.93 2570.71 3171.20 2.60 2.11 1234A 447 6250.56 3890.90 3608.10 1.61 1.73 1234T 446 3507.08 1099.58 1194.99 3.19 2.93 1234E 444 7541.73 1365.08 1817.16 5.52 4.15 1240S 449 4376.99 2108.15 2290.56 2.08 1.91 Table 36. Non Reversible hMMP-1 mutants (Overnight, 37 *C) hMMP-1 SEQ ID RFU RFU RFU Ratio Ratio mutation NO 25 *C 37 *C 37 to 25 0 C/ 25 0 C/ 25 0 C 37 0 C 37 to 25 0 C L95K 328 7744.34 1677.96 2463.18 4.62 3.14 WO 2009/111083 PCT/US2009/001486 -283 D1051 338 8394.32 1958.96 1925.73 4.29 4.36 D105L 339 6546.78 1070.51 939.53 6.12 6.97 D105N 332 9119.04 2347.74 2813.87 3.88 3.24 D105R 331 5775.25 1499.57 1312.01 3.85 4.40 D105W 337 8617.36 4593.06 5698.08 1.88 1.51 D151G 346 1956.65 1097.68 900.59 1.78 2.17 F155A 348 4891.89 1843.31 1882.95 2.65 2.60 D156K 350 8696.27 3858.90 4126.13 2.25 2.11 D156T 352 8972.20 3854.84 3990.29 2.33 2.25 D156L 356 5254.55 1232.94 1008.08 4.26 5.21 D156A 357 3585.37 1110.73 940.62 3.23 3.81 D156W 354 2570.24 1206.22 997.15 2.13 2.58 D156V 355 2208.99 997.64 777.35 2.21 2.84 D156H 349 7587.19 1763.27 1536.01 4.30 4.94 D156R 351 8622.23 1846.71 1764.13 4.67 4.89 G159V 363 6555.27 1683.20 1842.91 3.89 3.56 A176F 365 4191.69 1336.32 1553.01 3.14 2.70 D179N 368 7317.57 1485.28 1378.59 4.93 5.31 D181L 382 4534.34 1000.80 1020.08 4.53 4.45 D181K 378 1869.47 928.55 895.45 2.01 2.09 E182T 384 6752.25 1496.55 1319.53 4.51 5.12 E182Q 383 2212.75 1035.24 916.32 2.14 2.41 T185R 390 6281.97 2300.61 2829.34 2.73 2.22 N187F 401 7352.85 1704.23 1533.08 4.31 4.80 N1871 404 8306.40 1465.77 1560.83 5.67 5.32 G206A 418 2492.53 974.96 1057.32 2.56 2.36 G206S 417 2845.84 808.42 908.44 3.52 3.13 V227C 433 5833.84 2432.82 2707.71 2.40 2.15 V227E 430 8630.90 2152.81 2615.26 4.01 3.30 Q228P 439 3673.33 1081.32 1681.57 3.40 2.18 L229T 440 3543.75 1030.05 1488.58 3.44 2.38 D233E 443 6694.93 2661.43 4531.45 2.52 1.48 1234A 447 6250.56 4043.80 3433.03 1.55 1.82 1234T 446 3507.08 1228.23 1397.18 2.86 2.51 1234E 444 7541.73 1901.96 1783.16 3.97 4.23 1240S 449 4376.99 2592.19 3417.53 1.69 1.28 Example 31 Proteolytic Activity of hMMP-1 on insoluble collagen In this example, the collagenase activity of hMMP-1 was assessed for the 5 protein substrate collagen using SDS-PAGE analysis. Wildtype hMMP-1 cleaves insoluble collagen (aI (I) and a2(I) chains) into three-quarter and one-quarter length digestion products. In this assay, a fluorescein isothiocyanate (FITC)-conjugated collagen was used as the substrate and the reaction was monitored by SDS-PAGE of WO 2009/111083 PCT/US2009/001486 - 284 the reaction products. Cleavage of al (I) and c2(I) collagen chains results in three quarter and one-quarter length digestion products which are distinguishable from full length collagen by separation on SDS polyacrylamide gels. Alternatively, cleavage was assessed by fluorometric analysis. A similar assay can be used to assess the 5 activity of mutant hMMPs for cleavage activity at 25 *C versus 34 'C or 37 *C. A. SDS-PAGE Analysis In short, 2 ptg of hMMP-1 (purchased from R&D Systems, #901-MP; or BAP006_2 and BAP006_10 purified as described in Example 27) was diluted in TCNB containing 1 mM AMPA and incubated at the reaction temperature (25 *C or 10 37 *C) for 2 hours. This activation step cleaves the pro-peptide and generates mature hMMP-1. Subsequently, 6 jig of insoluble collagen conjugated to fluorescein isothiocyanate (FITC) (Anaspec #85111 or Sigma Collagen #C4361) in 20 pl TCNB was added to each activated hMMP-1 aliquot and the mixture was incubated at 25 'C or 37 *C for 24 hours or 6 days. 15 Cleavage of the insoluble collagen was observed by SDS/PAGE. The reaction mixture was separated on a 7.5 % SDS polyacrylamide gel and visualized by staining with Coomassie Blue dye. SDS/PAGE results show that after 24 hours incubation at 25 *C or 37 'C, hMMP-l partially cleaved the al(I) and a2(I) collagen chains into % and % length digestion products for all hMMP-1 proteins tested. After 6 days at 25 20 'C, complete cleavage into 3/4 and % length digestion products was observed. After 6 days at 37 *C, the collagen was digested completely. The 3/4 and % length collagen digestion products are thermally unstable at body temperature. B. Fluorometic Analysis Alternatively, collagenase activity was measured using a fluorescence assay. 25 5 jig hMMP-1 (purchased from R&D Systems, #901-MP; or BAP006_2 and BAP006_1 0 purified as described in Example 27) was diluted in TCNB containing 1 mM AMPA to a final concentration and incubated at 37 *C for 2 hours. The activity of hMMP-1 for FITC-labled collagen (Sigma #C4361 or Elastin #CF308) was assessed using a protocol adapted from Baici A et al. (1980) Anal. Biochem., 108: 30 230-232). Briefly, hMMP-1 was incubated with the substrate for 144 hours at 37*C. As a negative control, the substrate was incubated with buffer only. Following incubation, the reaction mixture was first centrifuged to remove insoluble particles. Fluorescence of the supernatant was detected by measuring fluorescence in a WO 2009/111083 PCT/US2009/001486 -285 fluorescent plate reader at 495 nm excitation/ 520 nm emission. Relative fluorescence units (RFU) were determined. Duplicate reactions were performed for each sample. The results (see Tables 37 and 38 below) show that incubation of insoluble collagen with wildtype hMMP-l at 37 *C for 144 hours resulted in cleavage of 5 collagen as indicated by high RFU values compared to buffer only control. For example, for cleavage of collagen from Sigma, all hMMPs tested had an RFU between about 1000.00-1200.00 compared to buffer only with an RFU value of about 400.00. The activity of purified collagens from CHO-S (BAP006_2) and BL21 cells (BAP006_1 0) for cleavage of Sigma insoluble collagen was comparable to hMMP- 1 10 purchased from R&D systems. For cleavage of Elastin collagen, the activity of recombinant hMMP-1 purchased from R&D and BAP006_10 were about 3000.00 RFU, while the activity of BAP006_2 was about 2000.00 RFU. Buffer only exhibited a background fluorescence for cleavage of Elastin collagen of about 1500.00 RFU. Table 37. Cleavage of Collagen (Sigma Insoluble Substrate) hMMP-1 37 *C 37 *C Avg 37 *C St Dev R&D systems 1163.17 1137.81 1150.49 17.93 Buffer only 481.49 490.57 486.03 6.42 BAP006 2 (CHO) 1265.61 1275.17 1270.39 6.76 BAP006 10 (BL21) 1292.36 1335.14 1313.75 30.25 15 Table 38. Cleavage of Collagen (Elastin Insoluble Substrate) hMMP-1 37 *C 37 *C Avg 37 0 C St Dev R&D systems 3488.224 2981.417 3235.32 357.66 Buffer only 1312.511 . 1807.479 1560.00 350.00 BAP006 2 (CHO) 1729.757 2297.573 2013.67 401.51 BAP006 10 (BL21) 2669.758 3056.381 2863.07 273.38 Since modifications will be apparent to those of skill in this art, it is intended that this invention be limited only by the scope of the appended claims. 20

Claims (52)

1. A method for treating an a disease or condition of the extracellular matrix (ECM), comprising: a) sub-epidermally administering to the ECM of a subject an activatable matrix degrading enzyme (AMDE), wherein: the AMDE is a matrix-degrading enzyme that is inactive in the ECM following sub-epidermal administration in the absence of an activating condition; the activating condition is not present in the ECM; and the AMDE is active for a limited time in the ECM following sub-epidermal administration upon exposure to an activating condition; and b) providing to the ECM an activating condition for the enzyme, whereby the AMDE is active in the ECM for a limited time.

2. The method of claim 1, wherein the activating condition is provided sequentially, simultaneously or intermittently to administering the MADE.

3. The method of claim 1 or claim 2, wherein the activating condition is selected from among pH, ionic strength, temperature and metal ions.

4. The method of any of claims 1-3, wherein an activator provides the activating condition.

5. The method of claim 4, wherein the activator is sub-epidermally administered to the ECM and the AMDE and activator are administered sequentially, simultaneously or intermittently.

6. The method of claim 4 or claim 5, wherein the activator is provided in the same composition as the AMDE or in a separate composition.

7. The method of any of claims 1-6, wherein sub-epidermal administration is selected from among subcutaneous administration, intramuscular administration, intralesional administration and intradermal administration. 287

8. The method of any of claims 1-7, wherein the AMDE is selected from among a cathepsin, a calpain, and a heparanase.

9. The method of claim 8 , wherein the AMDE is a cathepsin and the cathepsin is a cysteine protease or aspartic protease.

10. The method of claim 9, wherein the cathepsin is selected from among cathepsin S, cathepsin K, cathepsin L, cathepsin B, cathepsin C, cathepsin H, cathepsin F, cathepsin 0, cathepsin R, cathepsin V, cathepsin W, cathepsin D, and cathepsin E.

11. The method of claim 9 or claim 10, wherein the cathepsin has the sequence of amino acids selected from any of SEQ ID NOS: 57, 60, 1,65, 180, 68,71,74, 77, 183, 186, 189, 80, 195, 90, 93 and 96, or is an allelic, or species variant or other variant of any of SEQ ID NOS: 57, 60, 1, 65, 180, 68,71,74,77, 183, 186, 189, 80, 195, 90, 93 and 96.

12. The method of any of claims 3-11, wherein the activating condition is pH.

13. The method of claim 12, wherein the activating condition is an acidic pH.

14. The method of claim 13, wherein the pH is an acidic pH that is or is about in a range of 3 to 6.5, or 3.5 to 6, or 3 to 5.5, or 3 to 4.5, or 4 to 6, or 4 to 5.5, or 4.5 to 5, or 5 to 6.

15. The method of claim 13 or claim 14, wherein: the AMDE is inactive at neutral pH; the activator provides an acidic pH activating condition to activate the enzyme; and the AMDE is active at pH 5.5.

16. The method of any of claims 4-15, wherein the activator provides the acidic pH activating condition as a buffered solution at the pH.

17. The method of claim 16, wherein the buffer contains an acid selected from among 2-(N-morpholino)ethanesulfonic acid (MES), acetic acid, citric acid, citric phosphate and histidine.

18. The method of claim 16 or claim 17, wherein the ionic strength of the buffer is selected such that the AMDE is active for a predetermined time at neutral pH. 288

19. The method of claim 18, wherein the predetermined time is or is about 1 minute, 2 minutes, 3 minutes, 4 minutes, 5 minutes, 6 minutes, 7 minutes, 8 minutes, 9 minutes, 10 minutes, 20 minutes, 30 minutes, 40 minutes, 50 minutes, 1 hour, 2 hours, 3 hours or 4 hours.

20. The method of any of claims 13-19 , wherein the AMDE is a lysosomal enzyme.

21. The method of claim 20, wherein the AMDE is a cathepsin or a heparanase.

22. The method of claim 21, wherein the AMDE is a cathepsin and the cathepsin is a cysteine protease or aspartic protease.

23. The method of claim 22 , wherein the cathepsin is selected from among cathepsin B, cathepsin F, cathepsin H, cathepsin IS, cathepsin L, cathepsin V and cathepsin D.

24. The method of claim 23, wherein the cathepsin has a sequence of amino acids selected from any of SEQ ID NOS: 65, 71, 183,68,60, 1, 189 and 90, or is an allelic, or species variant or other variant of any of SEQ ID NOS: 65,71, 183,68,60, 1, 189 and 90.

25. The method of claim 23, wherein the cathepsin is cathepsin L.

26. The method of claim 25, wherein the cathepsin L enzyme is a single chain form.

27. The method of claim 25, wherein the cathepsin L enzyme is a two chain form.

28. The method of any of claims 25-27, wherein the cathepsin L enzyme comprises: a heavy chain having the sequence of amino acids set forth as amino acids 1-175 of SEQ ID NO: 1 or a sequence that exhibits at least 90% sequence identity to the sequence of amino acids 1-175; and a light chain having the sequence of amino acids set forth as amino acids 179-220 of SEQ ID NO: 1 or a sequence that exhibits at least 90% sequence identity to the sequence of amino acids 179-220. 289

29. The method of any of claims 25-28, wherein the cathepsin L has the sequence of amino acids set forth in SEQ ID NO: 1 or is an allelic, species or other variant thereof.

30. The method of any of claims 3-11 , wherein: the AMDE is modified to be temperature sensitive, whereby the AMDE is active at a temperature less than 37'C; the activator provides an activating condition that is a temperature less than 37'C; the AMDE is inactive at 37 0 C.

31. The method of claim 30 , wherein the activating condition is temperature and the temperature is or is about 20 'C, 21 'C, 22 'C, 23 'C, 24 'C, 25 'C, 26 'C, 27 'C, 28 'C, 29 C or 3 0 'C.

32. The method of any of claims 30-31, wherein the AMDE is selected from among a pancreatic elastase, an elastase-2A, an elastase-2B, a neutrophil elastase, a proteinase-3, an endogenous vascular elastase, a cathepsin G, a mast cell chymase, a mast cell tryptase, a plasmin, a thrombin, a granzyme B, a cathepsin S, a cathepsin K, a cathepsin L, a cathepsin B, a cathepsin C, a cathepsin H, a cathepsin F, a cathepsin 0, a cathepsin R, a cathepsin V, a cathepsin W, a calpain 1, a calpain 2, a legumain, a cathepsin Z, a cathepsin D, a cathepsin E, an MMP-1, an MMP-8, an MMP-13, and MMP-18, an MMP-2, an MMP-9, an MMP-3, an MMP-10, an MMP-11, an MMP-7, an MMP-26, an MMP-12, an MMP-14, an MMP-15, an MMP-16, and MMP-17, an MMP-19, an MMP-20, an ADAMTS-1, an ADAMTS-2, an ADAMTS-3, an ADAMTS-4, an ADAMTS-5, an ADAMTS-14 and a heparanse or allelic or species variants or other variants thereof.

33. The method of any of claims 30-32, wherein the activator is a cold buffer.

34. The method of claim 33 , wherein the activator is provided in the same composition as the AMDE or in a separate composition.

35. The method of any of claims 3-11, wherein the activating condition is a metal ion and the metal ion is Ca2+.

36. The method of any of claims 1-35, wherein AMDE degrades a component of the ECM selected from among a collagen, an elastin, a fibronectin and a proteoglycan. 290

37. The method of claim 36 , wherein the ECM component is collagen and the collagen is selected from among type I, type II, type III or type IV collagen.

38. The method of claim 37, wherein the collagen is type I collagen.

39. The method of any of claims 1-38, wherein the disease or condition of the ECM is a collagen-mediated disease or condition.

40. The method of claim 39 , wherein the collagen-mediated disease or condition is selected from among cellulite, Dupuytren's disease, Peyronie's disease, Ledderhose fibrosis, stiff joints, existing scars, scleroderma, lymphedema and collagenous colitis.

41. The method of claim 40 , wherein the collagen-mediated disease or condition is stiff joints that is frozen shoulder.

42. The method of claim 40 , wherein the collagen-mediated disease or condition is existing scars that is selected from among surgical adhesions, keloids, hypertrophic scars and depressed scars.

43. Use of an activatable matrix-degrading enzyme (AMDE) for formulation of a medicament for sub-epidermal administration for temporally degrading a component of the extracellular matrix (ECM) for treating a disease or condition of the ECM, wherein: the AMDE is formulated in an amount sufficient, when exposed to an activator, to degrade a component of the ECM associated with the disease or condition; the AMDE is a matrix-degrading enzyme that is inactive in the ECM following sub epidermal administration in the absence of the activator; and the AMDE is active for a limited time in the ECM following sub-epidermal administration upon exposure to an activating condition provided by the activator.

44. Use of a pharmaceutical composition, comprising an activatable matrix degrading enzyme (AMDE) formulated for sub-epidermal administration for treating a disease or condition of the ECM by temporally degrading a component of the extracellular matrix (ECM), wherein: the AMDE is formulated in an amount sufficient, when exposed to an activator, to degrade a component of the ECM associated with the disease or condition; 291 the AMDE is a matrix-degrading enzyme that is inactive in the ECM following sub epidermal administration in the absence of the activator; and the AMDE is active for a limited time in the ECM following sub-epidermal administration upon exposure to an activating condition provided by the activator.

45. The use of claim 43 or claim 44, wherein the medicament is for single dosage administration, and contains an amount of AMDE that is or is about 10 pg to 100 mg, 50 pg to 75 mg, 100 pg to 50 mg, 250 pg to 25 mg, 500 pg to 10 mg, 1 mg to 5 mg or 2 mg to 4 mg.

46. The use of any of claims 43-45, wherein the activator is formulated in the same composition as the AMDE or in a separate composition.

47. The use of any of claims 43-46, wherein the AMDE is selected from among a cathepsin, a calpain, and a heparanase.

48. The use of claim 47, wherein the AMDE is a cathepsin and the cathepsin is a cysteine protease or aspartic protease.

49. The use of claim 48, wherein the cathepsin is selected from among cathepsin S, cathepsin K, cathepsin L, cathepsin B, cathepsin C, cathepsin H, cathepsin F, cathepsin 0, cathepsin R, cathepsin V, cathepsin W, cathepsin D, and cathepsin E.

50. The use of claim 49, wherein the cathepsin is cathepsin L.

51. The use of any of claims 43-50, wherein the activating condition is selected from among pH, ionic strength, temperature and metal ions.

52. The use of any of claims 43-51, wherein the disease or condition of the ECM is a collagen-mediated disease or condition.