Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K38/00—Medicinal preparations containing peptides
  • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • A61K38/55—Protease inhibitors
  • A61K38/57—Protease inhibitors from animals; from humans
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K38/00—Medicinal preparations containing peptides
  • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • A61K38/55—Protease inhibitors
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P19/00—Drugs for skeletal disorders
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P41/00—Drugs used in surgical methods, e.g. surgery adjuvants for preventing adhesion or for vitreum substitution
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
  • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
  • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
  • C12N9/14—Hydrolases (3)
  • C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
  • C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
  • C12N9/64—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
  • C12N9/6421—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
  • C12N9/6424—Serine endopeptidases (3.4.21)
  • C12N9/6445—Kallikreins (3.4.21.34; 3.4.21.35)

Definitions

• Proteases are involved in a broad range of biological pathways.
• serine proteases such as kallikrein, plasmin, elastase, urokinase plasminogen activator, thrombin, human lipoprotein-associated coagulation inhibitor, and coagulation factors such as factors Vila, LXa, Xa, XIa, and XUa have been implicated in pathways affecting blood flow, e.g., general and focal ischemia, tumor invasion, fibrinolysis, perioperative blood loss, and inflammation. Inhibitors of specific serine proteases, therefore, have received attention as potential drug targets for various ischemic maladies.
• aprotinin also called bovine pancreatic trypsin inhibitor or BPTI
• BPTI bovine pancreatic trypsin inhibitor
• CAS contact activation system
• Kallikrein a serine protease
• CAS is initially activated when whole blood contacts the surface of foreign substrates ⁇ e.g., kaolin, glass, dextran sulfate, or damaged bone surfaces.
• Kallikrein a serine protease
• Kallikrein is a plasma enzyme that initiates the CAS cascade leading to activation of neutrophils, plasmin, coagulation, and various kinins.
• Kallikrein is secreted as a zymogen (pre-kallikrein) that circulates as an inactive molecule until activated by a proteolytic event early in the contact activation cascade.
• pre-kallikrein pre-kallikrein
• specific inhibition of kallikrein would be a very attractive approach to control blood loss associated with CPB and the onset of systemic inflammatory response (SIR) as would be encountered during, for example, various invasive surgical procedures.
• aprotinin is not as widely used as would be expected.
• Aprotinin is not specific for kallikrein, but interacts with additional enzymes (e.g., plasmin) in multiple pathways.
• additional enzymes e.g., plasmin
• thrombosis due to aprotinin' s actions upon the fibrino lyric pathway.
• aprotinin' s actions upon the fibrino lyric pathway There is concern not only over such hyperacute events as major vessel thrombosis in the perioperative period, but also over graft patency after the CABG procedure.
• administration of aprotinin in humans can elicit severe hypersensitivity or anaphylactic or aiiaphylactoid reactions after the first and, more often, after repeat administration to patients.
• This invention is based on the discovery of peptides that inhibit serine proteases.
• Serine proteases such as, for example, kallikrein
• Preferred kallikrein peptide inhibitors include those described in United States Patent Nos. 6,333,402 and 6,057,287 to Markland et al, the contents of which are incorporated herein by reference in their entirety.
• the invention is directed in part to the use of the peptides in therapeutic methods and compositions suitable for use in eliminating or reducing various ischemias, including but not limited to perioperative blood loss, and the onset of systemic inflammatory response.
• Perioperative blood loss results from invasive surgical procedures that lead to contact activation of complement components and the coagulation/fibrinolysis systems. More specifically, the invention provides methods of using kallikrein inhibitors to reduce or prevent perioperative blood loss and a systemic inflammatory response in patients subjected to invasive surgical procedures, especially cardiothoracic surgeries.
• the invention is directed to a method for preventing or reducing ischemia in a patient comprising administering to the patient a composition comprising a polypeptide comprising the amino acid sequence: Xaal Xaa2 Xaa3 Xaa4 Cys Xaa6 Xaa7 Xaa8 Xaa9 XaalO Xaall Gly Xaal3 Cys Xaal5 Xaal6 Xaal7 Xaal 8 Xaal9 Xaa20 Xaa21 Xaa22 Xaa23 Xaa24 Xaa25 Xaa26 Xaa27 Xaa28 Xaa29 Cys Xaa31 Xaa32 Phe Xaa34 Xaa35 Gly Gly Cys Xaa39 Xaa40 Xaa41 Xaa42 Xaa43 Xaa44 Xaa45 Xaa46 X
• individual amino acid positions of SEQ ID ⁇ O:l can be one or more of the following: XaalO is Asp, Xaal 1 is Asp, Xaal3 is Pro, Xaal 5 is Arg, Xaal 6 is Ala, Xaal 7 is Ala, Xaal 8 is His, Xaal 9 is Pro, Xaa21 is Trp, Xaa31 is Glu, Xaa32 is Glu, Xaa34 is lie, Xaa35 is Tyr, Xaa39 is Glu.
• the invention is directed to a method for preventing or reducing the onset of systemic inflammatory response associated with a surgical procedure in a patient comprising administering to the patient a composition comprising a polypeptide comprising the amino acid sequence: Xaal Xaa2 Xaa3 Xaa4 Cys Xaa6 Xaa7 Xaa8 Xaa9 XaalO Xaall Gly Xaal3 Cys Xaal5 Xaal6 Xaal7 Xaal8 Xaal9 Xaa20 Xaa21 Xaa22 Xaa23 Xaa24 Xaa25 Xaa26 Xaa27 Xaa28 Xaa29 Cys Xaa31 Xaa32 Phe Xaa34 Xaa35 Gly Gly Cys Xaa39 Xaa40 Xaa41 Xaa42 Xaa43 Xaa44
• Xaa21 is an amino acid selected from the group consisting of: Trp, Phe, Tyr, His and He;
• Xaall is an amino acid selected from the group consisting of: Tyr and Phe;
• Xaa23 is an amino acid selected from the group consisting of: Tyr and Phe;
• Xaa31 is an amino acid selected from the group consisting of: Glu, Asp, Gin, Asn, Ser, Ala, Nal, Leu, He and Thr;
• Xaa32 is an amino acid selected from the group consisting of: Glu, Gin, Asp Asn, Pro, Thr, Leu, Ser, Ala, Gly and Nal;
• Xaa34 is an amino acid selected from the group consisting of: Thr, He, Ser, Val, Ala, Asn, Gly and Leu;
• Xaa35 is an amino acid selected from the group consisting of: Tyr, Trp and Phe;
• Xaa39 is an amino acid selected from the group consisting
• the surgical procedure can be a cardiothoracic surgery, such as, for example, cardiopulmonary bypass or coronary artery bypass grafting.
• individual amino acid positions of SEQ ID ⁇ O:l can be one or more of the following: XaalO is Asp, Xaal 1 is Asp, Xaal3 is Pro, Xaal5 is Arg, Xaal 6 is Ala, Xaal 7 is Ala, Xaal 8 is His, Xaal 9 is Pro, Xaa21 is Trp, Xaa31 is Glu, Xaa32 is Glu, Xaa34 is He, Xaa35 is Tyr, Xaa39 is Glu.
• the invention is directed to a method for preventing or reducing the onset of systemic inflammatory response associated with a surgical procedure in a patient comprising administering to the patient a composition comprising a polypeptide consisting of the amino acid sequence: Met His Ser Phe Cys Ala Phe Lys Ala Asp Asp Gly Pro Cys Arg Ala Ala His Pro Arg Trp Phe Phe Asn He Phe Thr Arg Gin Cys Glu Glu Phe He Tyr Gly Gly Cys Glu Gly Asn Gin Asn Arg Phe Glu Ser Leu Glu Glu Cys Lys Lys Met Cys Thr Arg Asp
• the surgical procedure is a cardiothoracic surgery, such as, for example, cardiopulmonary bypass or coronary artery bypass grafting.
• the invention is directed to a method for preventing or reducing ischemia in a patient comprising administering to the patient a composition comprising a polypeptide consisting of the amino acid sequence: Met His Ser Phe Cys Ala Phe Lys Ala Asp Asp Gly Pro Cys Arg Ala Ala His Pro Arg Trp Phe Phe Asn He Phe Thr Arg Gin Cys Glu Glu Phe He Tyr Gly Gly Cys Glu Gly Asn Gin Asn Arg Phe Glu Ser Leu Glu Glu Cys Lys Lys Met Cys Thr Arg Asp (SEQ HO NO:2), wherein the polypeptide inhibits kallikrein.
• the ischemia can be perioperative blood loss due to a surgical procedure performed on the patient, hi one embodiment, the surgical procedure is a cardiothoracic surgery, such as, for example, cardiopulmonary bypass or coronary artery bypass grafting.
• the invention is directed to a method for preventing or reducing the onset of systemic inflammatory response associated with a surgical procedure in a patient comprising administering to the patient a composition comprising a polypeptide consisting of the amino acid sequence: Ser Phe Cys Ala Phe Lys Ala Asp Asp Gly Pro Cys Arg Ala Ala His Pro Arg Trp Phe Phe Asn He Phe Thr Arg Ghi Cys Glu Glu Phe He Tyr Gly Gly Cys Glu Gly Asn Gin Asn Arg Phe Glu Ser Leu Glu Glu Cys Lys Lys Met Cys Thr Arg Asp (amino acids 3-60 of SEQ ID NO:2), wherein the polypeptide hibits kallikrein.
• the surgical procedure is a cardiothoracic surgery, such as, for example, cardiopulmonary bypass or coronary artery bypass grafting.
• the invention is directed to a method for preventing or reducing ischemia in a patient comprising administering to the patient a composition comprising a polypeptide consisting of the amino acid sequence: Ser Phe Cys Ala Phe Lys Ala Asp Asp Gly Pro Cys Arg Ala Ala His Pro Arg Trp Phe Phe Asn He Phe Thr Arg Gin Cys Glu Glu Phe He Tyr Gly Gly Cys Glu Gly Asn Gin Asn Arg Phe Glu Ser Leu Glu Glu Cys Lys Lys Met Cys Thr Arg Asp (amino acids 3-60 of SEQ ID NO:2), wherein the polypeptide inhibits kallikrein.
• the ischemia can be perioperative blood loss due to a surgical procedure performed on the patient, h one embodiment, the surgical procedure is a cardiothoracic surgery, such as, for example, cardiopulmonary bypass or coronary artery bypass grafting.
• a cardiothoracic surgery such as, for example, cardiopulmonary bypass or coronary artery bypass grafting.
• FIG. 1 is a simplified diagram of major multiple pathways and related events involved in the contact activation system and systemic inflammatory response (SIR) that can arise in a patient subjected to soft and bone tissue trauma such as that associated with a coronary artery bypass grafting (CABG) procedure, especially when the CABG procedure involves extra-corporeal blood circulation, such as cardiopulmonary bypass (Bypass Apparatus).
• SIR contact activation system and systemic inflammatory response
• FIG. 1 is a simplified diagram of major multiple pathways and related events involved in the contact activation system and systemic inflammatory response (SIR) that can arise in a patient subjected to soft and bone tissue trauma such as that associated with a coronary artery bypass grafting (CABG) procedure, especially when the CABG procedure involves extra-corporeal blood circulation, such as cardiopulmonary bypass (Bypass Apparatus).
• Arrows indicate activation from one component or event to another component or event in the cascade.
• Arrows in both directions indicate activating effects of components or events in both directions.
• FIG. 2 shows a portion of a DNA and corresponding deduced amino acid for a KI polypeptide of the invention in plasmid pPIC-K503.
• the inserted DNA encodes the mat ⁇ prepro signal peptide of Saccharomyces cerevisiae (underlined) fused in frame to the amino terminus of the PEP-1 KI polypeptide having the amino acid sequence enclosed by the boxed area.
• the amino acid sequence of the PEP-1 KI polypeptide shown in the boxed region is SEQ ID NO:2
• the corresponding nucleotide coding sequence of the KI polypeptide is SEQ ID NO:3.
• the dashed arrows indicate the location and direction of two PCR primer sequences in AOX regions that were used to produce sequencing templates.
• DNA sequence for the entire nucleotide sequence of the figure comprises the structural coding sequence for the fusion protein and is designated SEQ ID NO:27.
• FIGS. 3 A and 3B show an alignment of amino acid sequences of the preferred embodiments of the invention, the native LACI sequence from which these variants were derived (S ⁇ Q ID NO:32), and other known Kunitz domains (S ⁇ Q ID NOS:29-31 and 33-53). Cysteine residues are highlighted.
• the invention is based on the discovery of a group of kallikrein inhibitor (KI) polypeptides that inhibit plasma kallikrein with a specificity that permits their use in improved methods of preventing or reducing ischemia such as, for example, perioperative blood loss and/or a systemic inflammatory response (SIR) induced by kallikrein, especially, for example, in patients undergoing surgical procedures and particularly surgical procedures involving cardiothoracic surgery, e.g., cardiopulmonary bypass (CPB), such as a coronary artery bypass graft (CABG) procedures.
• KI kallikrein inhibitor
• KIs can be used specifically for, e.g., pediatric cardiac surgery, lung transplantation, total hip replacement and orthotopic liver transplantation, and to reduce or prevent perioperative stroke during CABG, extracorporeal membrane oxygenation (ECMO) and cerebrovascular accidents (CVA) during these procedures.
• Cardiothoracic surgery is surgery of the chest area, most commonly the heart and lungs.
• Typical diseases treated by cardiothoracic surgery include coronary artery disease, tumors and cancers of the lung, esophagus and chest wall, heart vessel and valve abnormalities, and birth defects involving the chest or heart.
• KI polypeptides useful in the invention comprise Kunitz domain polypeptides.
• these Kunitz domains are variant forms of the looped structure comprising Kunitz domain 1 of human lipoprotein-associated coagulation inhibitor (LACI) protein.
• LACI contains three internal, well-defined, peptide loop structures that are paradigm Kunitz domains (Girard, T. et al, 1989. Nature, 338:518-520). The three Kunitz domains of LACI confer the ability to bind and inhibit kallikrein, although not with exceptional affinity.
• Variants of Kunitz domain 1 of LACI described herein have been screened, isolated and bind kallikrein with enhanced affinity and specificity (see, for example, U.S. Patent Nos. 5,795,865 and 6,057,287, incorporated herein by reference).
• An example of a preferred polypeptide useful in the invention has the amino acid sequence defined by amino acids 3-60 of SEQ ID NO:2.
• Every polypeptide useful in the invention binds kallikrein, and preferred polypeptides are also kallikrein inhibitors (KI) as determined using kallikrein binding and inhibition assays known in the art.
• KI kallikrein inhibitors
• the enhanced affinity and specificity for kallikrein of the variant Kunitz domain polypeptides described herein provides the basis for their use in cardiothoracic surgery, e.g., CPB and especially CABG surgical procedures, to prevent or reduce perioperative blood loss and/or the onset of SIR in patients undergoing such procedures.
• the KI polypeptides used in the invention have or comprise the amino acid sequence of a variant Kunitz domain polypeptide originally isolated by screening phage display libraries for the ability to bind kallikrein.
• KI polypeptides useful in the methods and compositions of the invention comprise a Kunitz domain polypeptide comprising the amino acid sequence:
• Xaa refers to a position in a peptide chain that can be any of a number of different amino acids.
• XaalO can be Asp or Glu
• Xaal 1 can be Asp, Gly, Ser, Val, Asn, He, Ala or Thr
• Xaal 3 can be Pro, Arg, His, Asn, Ser, Thr, Ala, Gly, Lys or Gin
• Xaal 5 can be Arg, Lys, Ala, Ser, Gly, Met, Asn or Gin
• Xaal 6 can be Ala, Gly, Ser, Asp or Asn
• Xaal 7 can be Ala, Asn, Ser, He, Gly, Val, Gin or Thr
• Xaal 8 can be His, Leu, Gin or Ala
• Xaal 9 can be Pro, Gin, Leu, Asn or He
• Xaa21 can be Trp, Phe, Tyr, His or He
• Xaaa21 can be
• Xaa29, Xaa41, Xaa42, Xaa44, Xaa46, Xaa47, Xaa48, Xaa49, Xaa50, Xaa52, Xaa53 and Xaa54 can be any amino acid. Additionally, each of the first four and at last three amino acids of SEQ ID NO: 1 can optionally be present or absent and can be any amino acid, if present.
• Peptides defined according to SEQ ID NO:l form a set of polypeptides that bind to kallikrein.
• a KI polypeptide useful in the methods and compositions of the invention has the following variable positions: Xaal 1 can be Asp, Gly, Ser or Val; Xaal 3 can be Pro, Arg, His or Asn; Xaal 5 can be Arg or Lys; Xaal 6 can be Ala or Gly; Xaal 7 can be Ala, Asn, Ser or He; Xaal 8 can be His, Leu or Gin; Xaal 9 can be Pro, Gin or Leu; Xaa21 can be Trp or Phe; Xaa31 is Glu; Xaa32 can be Glu or Gin; Xaa34 can be He, Thr or Ser; Xaa35 is Tyr; and Xaa39 can be Glu, Gly or Ala.
• a more specific embodiment of the claimed invention is defined by the following amino acids at variable positions: XaalO is Asp; Xaal 1 is Asp; Xaal3 can be Pro or Arg; Xaal 5 is Arg; Xaal 6 can be Ala or Gly; Xaal 7 is Ala; Xaal 8 is His; Xaal9 is Pro;Xaa21 is Trp; Xaa31 is Glu; Xaa32 is Glu; Xaa34 can be He or Ser; Xaa35 is Tyr; and Xaa39 is Gly.
• polypeptides that comprise portions of the polypeptides described herein.
• polypeptides could comprise binding domains for specific kallikrein epitopes.
• fragments of the polypeptides described herein would also be encompassed.
• KI polypeptides useful in the methods and compositions described herein comprise a Kunitz domain.
• a subset of the sequences encompassed by SEQ ID NO:l are described by the following (where not indicated, "Xaa” refers to the same set of amino acids that are allowed for SEQ ID NO:l):
• FIGS. 3 A and 3B provides an amino acid sequence alignment of these sequences, the native LACI sequence from which these variants were derived (SEQ ID NO:32), and other known Kunitz domains (SEQ ID NOS: 29-31 and 33-53).
• the KI polypeptides useful in the methods and compositions described herein can be made synthetically using any standard polypeptide synthesis protocol and equipment.
• the stepwise synthesis of a KI polypeptide described herein can be carried out by the removal of an amino (N) terminal-protecting group from an initial (i.e., carboxy-terminal) amino acid, and coupling thereto of the carboxyl end of the next amino acid in the sequence of the polypeptide. This amino acid is also suitably protected.
• the carboxyl group of the incoming amino acid can be activated to react with the N-terminus of the bound amino acid by formation into a reactive group such as formation into a carbodiimide, a symmetric acid anhydride, or an "active ester" group such as hydroxybeiizotriazole or pentafluorophenyl esters.
• Preferred solid-phase peptide synthesis methods include the BOC method, which utilizes tert-butyloxycarbonyl as the ⁇ -amino protecting group, and the FMOC method, which utilizes 9-fluorenylmethloxycarbonyl to protect the ⁇ -amino of the amino acid residues. Both methods are well known to those of skill in the art (Stewart, J.
• Kunitz domain polypeptides and KI polypeptides useful in the compositions and methods of the invention can be produced by recombinant methods using any of a number of cells and corresponding expression vectors, including but not limited to bacterial expression vectors, yeast expression vectors, baculovirus expression vectors, mammalian viral expression vectors, and the like.
• Kunitz domain polypeptides and KI polypeptides useful in the compositions and methods of the invention can also be produced transgenically using nucleic acid molecules comprising a coding sequence for a Kunitz domain or KI polypeptide described herein, wherein the nucleic acid molecule can be integrated into and expressed from the genome of a host animal using transgenic methods available in the art.
• a Kunitz domain polypeptide or a KI polypeptide comprising the Kunitz domain it could be necessary or advantageous to fuse the coding sequence for a Kunitz domain polypeptide or a KI polypeptide comprising the Kunitz domain to another coding sequence in an expression vector to form a fusion polypeptide that is readily expressed in a host cell.
• the host cell that expresses such a fusion polypeptide also processes the fusion polypeptide to yield a Kunitz domain or KI polypeptide useful in the invention that contains only the desired amino acid sequence.
• any other amino acid(s) remain attached to the expressed Kunitz domain or KI polypeptide, such additional amino acid(s) should not diminish the kallikrein binding and/or kallikrein inhibitory activity of the Kunitz domain or KI polypeptide so as to preclude use of the polypeptide in the methods or compositions of the invention.
• a preferred recombinant expression system for producing KI polypeptides useful in the methods and compositions described herein is a yeast expression vector, which permits a nucleic acid sequence encoding the amino acid sequence for a KI polypeptide or Kunitz domain polypeptide to be linked in the same reading frame with a nucleotide sequence encoding the mat ⁇ prepro leader peptide sequence of Saccharomyces cerevisiae, which in turn is under the control of an operable yeast promoter.
• the resulting recombinant yeast expression plasmid can then be transfonned by standard methods into the cells of an appropriate, compatible yeast host, which cells are able to express the recombinant protein from the recombinant yeast expression vector.
• a host yeast cell transformed with such a recombinant expression vector is also able to process the fusion protein to provide an active KI polypeptide useful in the methods and compositions of the invention.
• a preferced yeast host for producing recombinant Kunitz domain polypeptides and KI polypeptides comprising such Kunitz domains is Pichia pastoris.
• KI polypeptides that are useful in the methods and compositions described herein can comprise a Kunitz domain polypeptide described herein.
• Some KI polypeptides can comprise an additional flanking sequence, preferably of one to six amino acids in length, at the amino and/or carboxy-terminal end, provided such additional amino acids do not significantly diminish kallikrein binding affinity or kallikrein inhibition activity so as to preclude use in the methods and compositions described herein.
• Such additional amino acids can be deliberately added to express a KI polypeptide in a particular recombinant host cell or can be added to provide an additional function, e.g., to provide a peptide to link the KI polypeptide to another molecule or to provide an affinity moiety that facilitates purification of the polypeptide.
• the additional amino acid(s) do not include cysteine, which could interfere with the disulfide bonds of the Kunitz domain.
• An example of a preferred Kunitz domain polypeptide useful in the methods and compositions of the invention has the amino acid sequence of residues 3-60 of SEQ ID NO:2.
• PEP-1 functional KI polypeptide having the amino acid sequence of SEQ ID NO:2 (see boxed region in FIG. 2).
• Particularly preferred KI polypeptides useful in the methods and compositions described herein have a binding affinity for kaHikrein that is on the order of 1000 times higher than that of aprotinin, which is currently approved for use in CABG procedures to reduce blood loss.
• the surprisingly high binding affinities of such KI polypeptides described herein indicate that such KI polypeptides exhibit a high degree of specificity for kallikrein to the exclusion of other molecular targets (see Table 1, below).
• use of such polypeptides according to the invention reduces much of the speculation as to the possible therapeutic targets in a patient.
• the lower degree of specificity exhibited by, for example, aprotinin leads to possible pleiotropic side effects and ambiguity as to its therapeutic mechanism.
• polypeptides defined by, for example, SEQ ID NO:l contain invariant positions, e.g., positions 5, 14, 30, 51 and 55 can be Cys only. Other positions such as, for example, positions 6, 7, 8, 9, 20, 24, 25, 26, 27, 28, 29, 41, 42, 44, 46, 47, 48, 49, 50, 52, 53 and 54 can be any amino acid (including non-naturally occurring amino acids).
• one or more amino acids correspond to that of a native sequence (e.g., SEQ ID NO:32, see FIG. 3).
• at least one variable position is different from that of the native sequence, hi yet another preferred embodiment, the amino acids can each be individually or collectively substituted by a conservative or non-conservative amino acid substitution.
• amino acid substitutions replace an amino acid with another amino acid of similar chemical structure and may have no affect on protein function.
• Non-conservative amino acid substitutions replace an amino acid with another ammo acid of dissimilar chemical structure.
• conserved amino acid substitutions include, for example, Asn->Asp, Arg->Lys and Ser->Thr.
• 1, 1, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20 and/or 21 of these amino acids can be independently or collectively, in any combination, selected to correspond to the corresponding position of SEQ JD NO:2.
• Other positions for example, positions 10, 11, 13, 15, 16, 17, 18, 19, 21, 22,
• SEQ ID NO:l defines a set of possible sequences. Each member of this set contains, for example, a cysteine at positions 5, 14, 30, 51 and 55, and any one of a specific set of amino acids at positions 10, 11, 13, 15, 16, 17, 18, 19, 221, 22, 23, 31, 32, 34, 35, 39, 40, 43 and 45.
• 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18 and/or 19 of these amino acids can be independently or collectively, in any combination, selected to correspond to the corresponding position of SEQ ID NO:2.
• the peptide preferably has at least 80 %, at least 85 %, at least 90 % or at least 95 % identity to SEQ ID NO:2.
• the present invention is also directed to methods for preventing or reducing ischemia.
• Preferred in the invention are methods for preventing or reducing perioperative blood loss and/or a systemic inflammatory response (SIR) in a patient, especially associated with cardiothoracic surgery.
• a method for treatment involves the administration of a KI polypeptide comprising a Kunitz domain.
• One embodiment of the method involves using a peptide containing an amino acid sequence of SEQ ID NO:l that has an affinity for kallikrein that is approximately 1000-fold or more higher than that of a broad range serine protease, e.g., aprotinin, which is isolated from bovine lung and currently approved for use in CABG procedures (TRASYLOL ® , Bayer Corporation Pharmaceutical Division, West Haven, Connecticut).
• a broad range serine protease e.g., aprotinin
• a number of surgical procedures especially those involving extra-corporeal circulation, e.g., cardiothoracic surgery, such as, for example, CPB, and/or bone trauma, such as sternal split or hip replacement, are at risk for perioperative blood loss and inflammation.
• a contact activation system CAS
• SIR systemic inflammatory response
• the blood loss that occurs associated with cardiothoracic surgery e.g., CPB, as in a CABG procedure, probably results from extensive capillary leakage, which can result in significant loss of blood that must be replaced by immediate blood transfusion.
• the methods described herein are useful for preventing or reducing various ischemias including, for example, perioperative blood loss and SIR in a patient subjected to a surgical procedure, and especially wherein the surgical procedure requires extra-corporeal circulation, e.g., cardiothoracic surgery, such as, for example, CPB.
• the methods of the invention are particularly useful for preventing or reducing perioperative blood loss and/or SIR in a patient subjected to a CABG procedure requiring CPB or other cardiac surgery.
• compositions for medical use comprise a KI polypeptide described herein.
• Such compositions useful can further comprise one or more pharmaceutically acceptable buffers, carriers, and excipients, which can provide a desirable feature to the composition including, but not limited to, enhanced administration of the composition to a patient, enhanced circulating half-life of the KI polypeptide of the composition, enhanced compatibility of the composition with patient blood chemistry, enhanced storage of the composition, and/or enhanced efficacy of the composition upon administration to a patient, hi addition to a KI polypeptide described herein, compositions can further comprise one or more other pharmaceutically active compounds that provide an additional prophylactic or therapeutic benefit to a patient of an invasive surgical procedure.
• compositions useful in the methods of the invention comprise any of the Kunitz domain polypeptides or KI polypeptides comprising such Kunitz domain polypeptides described herein.
• Particularly preferred are KI polypeptides comprising a Kunitz domain polypeptide having a 58-amino acid sequence of amino acids 3-60 of SEQ ID NO:2.
• An example of such a particularly preferred KI polypeptide useful in the methods and compositions of the invention is the PEP-1 KI polypeptide having the 60-amino acid sequence of SEQ ID NO:2.
• a nucleotide sequence encoding the amino acid sequence of SEQ ID NO:2 is provided in SEQ ID NO:3 (see, e.g. , nucleotides 309-488 in FIG. 2).
• the invention also provides degenerate forms of the nucleotide sequence of SEQ ID NO:3 by simply substituting one or more of the known degenerate codons for each amino acid encoded by the nucleotide sequence.
• nucleic acid molecules can comprise the nucleotide sequence of nucleotides 7-180 of SEQ ID NO:3, degenerate fonns, and portions thereof, including but not limited to, recombinant phage genomes, recombinant mammalian viral vectors, recombinant insect viral vectors, yeast mini chromosomes, and various plasmids.
• plasmids include those used to clone and/or express such nucleotide coding sequences.
• Expression vectors provide a promoter, which can be operably linked to a particular nucleotide sequence and an appropriate host cell, which is able to transcribe the particular nucleotide coding sequence into a functional messenger RNA (rnRNA) and also translate the mRNA into the corresponding polypeptide. A polypeptide so produced can then be isolated from the host cell.
• Nucleic acid molecules comprising a nucleic acid sequence encoding a Kunitz domain or KI polypeptide described herein can be made by standard nucleic acid synthesis methods, recombinant DNA methodologies, polymerase chain reaction (PCR) methods, and any combination thereof.
• Surgical procedures that involve blood loss include those involving extra-corporeal circulation methods such as cardiothoracic surgery, e.g., CPB. hi such methods, a patient's heart is stopped and the circulation, oxygenation, and maintenance of blood volume are carried out artificially using an extra-corporeal circuit and a synthetic membrane oxygenator. These techniques are commonly used during cardiac surgery. Additionally, it is apparent that surgery involving extensive trauma to bone, such as the sternal split necessary in CABG or hip replacement procedures, is also associated with activation of the CAS, which can result in a variety of disruptions in the blood and vasculature.
• Atherosclerotic coronary artery disease causes a narrowing of the lumen of one or several of the coronary arteries; this limits the flow of blood to the myocardium (t.e., the heart muscle) and can cause angina, heart failure, and myocardial infarcts.
• the coronary circulation can be almost completely occluded, causing life threatening angina or heart failure, with a very high mortality.
• CABG procedures may be required to bridge the occluded blood vessel and restore blood to the heart; these are potentially life saving.
• CABG procedures are among the most invasive of surgeries in which one or more healthy veins or arteries are implanted to provide a "bypass" around the occluded area of the diseased vessel.
• CABG procedures carry with them a small but important perioperative risk, but they are very successful in providing patients with immediate relief from the mortality and morbidity of atherosclerotic cardiovascular disease.
• repeat CABG procedures are frequently necessary, as indicated by a clear increase in the number of patients who eventually undergo second and even third procedures; the perioperative mortality and morbidity seen in primary CABG procedures is increased in these re-do procedures.
• the heart is stopped using a cardioplegic solution, the patient cooled to help prevent brain damage, and the peripheral circulating volume increased by an extracorporeal circuit, i.e., the CPB circuit, which requires "priming" with donor blood and saline mixtures are used to fill the extracorporeal circuit.
• CPB has been extensively used in a variety of procedures performed for nearly half a century with successful outcomes.
• the interaction between artificial surfaces, blood cells, blood proteins, damaged vascular endothelium, and extravascular tissues, such as bone disturbs hemostasis and frequently activates the CAS, which, as noted above, can result in a variety of disruptions in the blood and vasculature. Such disruption leads to excess perioperative bleeding, which then requires immediate blood transfusion.
• a consequence of circulating whole blood through an extracorporeal circuit in CPB can also include the systemic inflammatory response (SHI), which is initiated by contact activation of the coagulation and complement systems.
• SHI systemic inflammatory response
• ARDS adult respiratory distress syndrome
• impairment of kidney and splanchnic circulation and induction of a general coagulopathy leading to blood loss and the need for transfusions
• additional pathologies associated with SIR include neurocognitive deficits, stroke, renal failure, acute myocardial infarct, and cardiac tissue damage.
• Blood transfusions also present a significant risk of infection and elevate the cost of CABG or other similar procedures that require CPB. h the absence of any pharmacological intervention, three to seven units of blood must typically be expended on a patient, even with excellent surgical techniques. Accordingly, there is considerable incentive for the development of new and improved pharmacologically effective compounds to reduce or prevent perioperative bleeding and SIR in patients subjected to CPB and CABG procedures.
• KI polypeptides described herein can be administered to a patient before, " during, and/or after a surgical procedure in a pharmaceutically acceptable composition.
• pharmaceutically acceptable composition refers to a non- toxic carrier or excipient that may be administered to a patient, together with a compound of this invention, and wherein the carrier or excipient not destroy the biological or pharmacological activity of the composition.
• KI polypeptides described herein can be administered locally or systemically by any suitable means for delivery of a kallikrein inhibitory amount of the KI polypeptides to a patient including but not limited to systemic administrations such as, for example, intravenous and inhalation. Parenteral administration is particularly preferred.
• compositions for intravenous administration are solutions in sterile isotonic aqueous buffer.
• Other pharmaceutically acceptable carriers include, but are not limited to, sterile water, saline solution, and buffered saline (including buffers like phosphate or acetate), alcohol, vegetable oils, polyethylene glycols, gelatin, lactose, amylose, magnesium stearate, talc, silicic acid, paraffin, etc.
• the composition can also include a solubilizing agent and a local anaesthetic such as lidocaine to ease pain at the site of the injection, preservatives, stabihzers, wetting agents, emulsifiers, salts, lubricants, etc. as long as they do not react deleteriously with the active compounds.
• a solubilizing agent such as lidocaine to ease pain at the site of the injection, preservatives, stabihzers, wetting agents, emulsifiers, salts, lubricants, etc. as long as they do not react deleteriously with the active compounds.
• the composition can comprise conventional excipients, e.g., pharmaceutically acceptable organic or inorganic carrier substances suitable for parenteral, enteral or intranasal application which do not deleteriously react with the active compounds.
• the ingredients will be supplied either separately or mixed together in unit dosage form, for example, as a dry lyophilized powder or water free concentrate in a hermetically sealed container such as an ampoule or sachette indicating the quantity of active agent in activity units.
• a hermetically sealed container such as an ampoule or sachette indicating the quantity of active agent in activity units.
• the composition is to be administered by infusion, it can be dispensed with an infusion bottle containing sterile pharmaceutical grade "water for injection" or saline.
• an ampoule of sterile water for injection or saline can be provided so that the ingredients can be mixed prior to administration.
• the methods of the invention comprise administering a KI polypeptide to a patient as an intravenous infusion according to any approved procedure.
• a KI polypeptide described herein can be administered to a patient subjected to a CABG procedure at the times similar to those currently used in approved protocols for administering aprotinin and in an amount necessary to provide a patient with a required number or concentration of kallikrein inhibitory units (KIU).
• KIU kallikrein inhibitory units
• a KI polypeptide described herein can also be administered to a patient in the immediate postoperative period, when bleeding abnormalities can occur as a consequence of downstream effects of SIR.
• a KI polypeptide described herein can be administered to a patient as an initial loading dose, e.g., an effective amount over the course of a convenient time, such as 10 minutes, prior to induction of anesthesia. Then, at induction of anesthesia, a second dose of KI polypeptide can be inj ected into the CPB priming fluid ("pump prime volume"). The patient can then be placed on a continuous and controlled intravenous infusion dose for the duration of the surgical procedure, and after the procedure if indicated.
• an initial loading dose e.g., an effective amount over the course of a convenient time, such as 10 minutes
• a second dose of KI polypeptide can be inj ected into the CPB priming fluid ("pump prime volume").
• the patient can then be placed on a continuous and controlled intravenous infusion dose for the duration of the surgical procedure, and after the procedure if indicated.
• compositions and methods of the invention are likely to require fewer milligrams (mg) per patient to provide a patient with the required number or concentration of KIU.
• Table 1 below, provides a comparison of the affinity (K; ]app ) of the PEP-1 KI polypeptide for kallikrein and eleven other known plasma proteases.
• the PEP-1 KI polypeptide is highly specific for human plasma kallikrein.
• the affinity (K j ⁇ app ) of PEP-1 for kallikrein is 1000 times higher than the affinity of aprotinin for kallikrein: the K j>app of PEP-1 for kallikrein is about 44 pM (Table 1), whereas the K j app of aprotinin for kallikrein is 30,000 pM.
• a dose of PEP-1 could be approximately 1000 times lower than that used for aprotinin on a per mole basis.
• consideration of several other factors may provide a more accurate estimation of the dose of PEP-1 required in practice.
• Such factors include the amount of kallikrein activated during CPB in a particular patient, the concentration of kallikrein required to elicit an SIR, and the bioavailability and pharmacological distribution of PEP-1 in a patient. Nevertheless, use of a KI polypeptide in methods according to the invention and provided in doses currently approved for the use of aprotinin is still expected to provide significant improvements over the current use of the less specific, lower affinity, bovine aprotinin. For example, the total amount of circulating prekallikrein in plasma is estimated at approximately 500 nM (Silverberg, M. et al, "The Contact System and Its Disorders," in Blood: Principles and Practice ofHematology, Handin, R.
• PEP-1 offers a significant advantage over aprotinin in the amount of protein that would be required to inliibit SIR.
• a concentration of PEP-1 of lnM would inhibit 99.6% of kallikrein present at 1 nM (i.e., only 0.4 pM free kallikrein remaining in the blood), whereas, an aprotinin concentration of 1 nM would only inliibit 24.5% of the kallikrein present at 1 nM.
• an aprotinin concentration in the plasma of at least 3 ⁇ M is required (i.e., 3000 times higher concentration than for PEP-1).
• an initial clinical dose of PEP-1 can be estimated from a recommended dose regimen of aprotinin (1 x 10 6 KIU) mentioned above.
• 140 mg corresponds to approximately 4.3 ⁇ M aprotimn (molecular weight of aprotinin is 6512 Daltons).
• the specific activity of aprotinin in the standard inhibitory assay used for PEP-1 is 0.4 KlU/mg of polypeptide.
• the specific activity of the PEP-1 KI polypeptide is 10 KlU/mg in the standard inhibition assay, a dose of only 5.6 mg of PEP-1 would be required to provide the number of KIUs equivalent to 140 mg of aprotinin.
• the KI polypeptides can be non-naturally occurring, and they can be produced synthetically or recombinantly, as noted above, thereby avoiding potential contamination of transmissible diseases that can arise during isolation of a protein from a natural animal source, such as in the case of aprotinin, which is isolated from bovine lung.
• aprotinin which is isolated from bovine lung.
• Increasingly important to administrative and public acceptance of a treatment or pharmaceutical composition comprising a polypeptide is the avoidance of possible contamination with and transmission to human patients of various pathological agents.
• Of particular interest for the safety of proteins isolated from a bovine tissue is the elimination of the possible risk of exposure to viral mediated diseases, bacterial mediated diseases, and, especially, transmissible bovine spongiform encephalopathies.
• aprotinin which is a bovine protein that is documented to cause anaphylactic and anaphylactoid responses in patients, especially in repeat administrations, such as second time CABG procedures. Additionally, the highly specific binding of the KI polypeptides described herein to kallikrein will effectively limit or eliminate the thrombotic tendencies observed with aprotinin, and reduce the problems observed with graft patency following CABG procedures.
• PEP-1 A non-naturally occurring, KI polypeptide (PEP-1) useful in the compositions and methods of the invention was identified as a kallikrein binding polypeptide displayed on a recombinant phage from a phage display library.
• PEP-1 has the following amino acid sequence: Glu Ala Met His Ser Phe Cys Ala Phe Lys Ala Asp Asp Gly Pro Cys Arg Ala Ala His Pro Arg Trp Phe Phe Asn He Phe Thr Arg Gin Cys Glu Glu Phe He Tyr Gly Gly Cys Glu Gly Asn Gin Asn Arg Phe Glu Ser Leu Glu Glu Cys Lys Lys Met Cys Thr Arg Asp (SEQ ID NO:2).
• the molecular weight of PEP- 1 is 7,054 Daltons.
• the nucleotide sequence (SEQ ID NO: 3) of the recombinant phage DNA encoding the PEP-1 amino acid sequence was isolated and sequenced by standard methods determined from the recombinant phage DNA.
• PEP-1 was produced in amounts useful for further characterization as a recombinant protein in His4 ' phenotype host cells of yeast strain Pichia pastoris.
• Example 2 Construction of a recombinant plasmid to express KI polypeptides.
• the initial plasmid, pHLL-D2 is ampicillin resistant and contains a wild-type allele of His4 from P. pastoris.
• the final DNA sequence comprising the coding sequence for the mat ⁇ Prepro-PEP-1 fusion protein in the recombinant expression plasmid pPIC-K503 is shown in FIG. 2.
• the DNA sequence of pfflL-D2 was modified to produce pPIC-K503, as follows:
• the AatH site bearing the bla gene located downstream of His4 was removed by restriction digestion, fill-in, and ligation modifying the sequence from GACGTC (SEQ ID NO:25) to GACGTACGTC (SEQ ID NO:26). This modification was made to facilitate the cloning of expression cassettes having AatH sites into the plasmid.
• the DNA encoding PEP-1 was synthesized based on the nucleotide sequence from the original kallikrein- binding display phage and consisted of 450 base pairs (bp).
• the final DNA sequence of the insert in the pHIL-D2 plasmid is flanked by a 5' AOX1 sequence and a 3' AOX1 sequence (portions of which are shown in FIG. 2) and encode a fusion protein comprising the mat ⁇ prepro signal peptide of S. cerevisiae fused to the structural coding sequence for the PEP-1 KI polypeptide.
• the signal peptide was added to facilitate the secretion of PEP-1 from the yeast host cells.
• the oligonucleotides to forni the insert were synthesized and obtained commercially (Genesis Labs, The Woodlands, TX), and the insert was generated by polymerase chain reaction (PCR).
• PCR polymerase chain reaction
• the linked synthetic DNA encoding the mat ⁇ prepro/PEP-1 fusion protein was then incorporated by ligation into the modified pHIL-D2 plasmid between the BstBI andEcoRI sites.
• the ligation products were used to transform Escherichia coli strain XL1 Blue.
• a PCR assay was used to screen E. coli transformants for the desired plasmid construct.
• DNA from cell extracts was amplified by PCR using primers containing the 5' AOX1 and 3' AOX1 sequences (see above and FIG. 2).
• PCR products of the correct number of base pairs were sequenced.
• approximately 20-50 bp on either side of the cloning sites were sequenced, and the predicted sequence was obtained.
• the final DNA sequence of the insert in the pHIL-D2 plasmid (to yield plasmid pPIC-K503) is shown in FIG.
• Example 3 Manufacture of PEP-1 from recombinant yeast cell line.
• Spheroplasts of P. pastoris GS115 having the His4 ⁇ phenotype were transfonned with the expression plasmid pPIC-K503 (above) following linearization of the plasmid at the Sacl site and homologous recombination of the plasmid DNA into the host 5' AOX1 locus.
• the phenotype of the production strain is His4 + .
• the entire plasmid was inserted into the 5' AOX1 genomic sequence of the yeast.
• Isolates from the transformation were screened for growth in the absence of exogenous histidine with methanol as the sole carbon source. Greater than 95% of the transformants retained the wild-type ability to grow with methanol as the sole carbon source, thereby demonstrating that the plasmid had been inserted into the host genome by homologous recombination rather than transplacement. These transformants did not require exogenous histidine for growth, thereby demonstrating that the plasmid had integrated into the host genome. Selected colonies were cloned. Small culture expression studies were performed to identify clones secreting the highest levels of active PEP-1 into the culture medium.
• PEP-1 secretion levels in clarified culture supernatant solutions were quantified for PEP-1 levels by sodium dodecyl sulfate pofyacrylamide gel electrophoresis (SDS-PAGE) and evaluated for kallil ⁇ ein inhibition.
• SDS-PAGE sodium dodecyl sulfate pofyacrylamide gel electrophoresis
• a yeast clone was selected for PEP-1 production based on its high level of PEP-1 expression among cultures sampled.
• P. pastoris producing PEP-1 were prepared commercially (MDS Pharma Services, Bothell, Washington).
• a standard production of PEP-1 in yeast comprised three steps as follows: (1) preparation of the seed culture, (2) fermentation, and (3) recovery of the culture.
• Flasks were inoculated in an orbital shaker (300 rpm) for approximately 13 hours at 30°
• a mixed feed phase which lasted approximately 83 hours, was then initiated by the addition of a glycerol and methanol feed. At the end of this time, the fermentation was terminated, and the fermenter contents were diluted with purified water.
• the purification and processing of PEP-1 consisted of five steps as follows: (1) expanded bed chromatography, (2) cation exchange chromatography, (3) hydrophobic interaction chromatography (HIC), (4) ultrafiltration and diafiltration, and (5) final filtration and packaging.
• the initial purification step consisted of expanded bed chromatography.
• the diluted fermenter culture was applied to the equilibrated column packed with Streamline SP resin (Amersham Pharmacia Streamline 200 chromatography column, Amersham Pharmacia, Piscataway, New Jersey).
• the top adaptor was raised above the expanded bed enhance washing. The flow was stopped and the bed was allowed to settle. The adaptor was moved down so that it was slightly above the settled bed. The direction of the flow was reversed.
• the effluent was collected. Washing was continued in a downward mode using 50 mM sodium acetate, pH 4.0.
• PEP-1 was eluted from the column using 50 mM sodium acetate, pH 6.0.
• the eluate was collected in a 50 liter container.
• the eluate was then filtered through a 0.22 ⁇ filter into a clean container located in the purification site. Additional samples were collected for the determination of PEP-1 concentration.
• a cation exchange chromatography step was then performed using the filtered eluate from the expanded bed column.
• PEP-1 was eluted from the column using 15 mM trisodium citrate, pH 6.2. Additional proteins were removed from the PEP-1 preparation by hydrophobic interaction chromatography (HIC). Prior to HIC, the eluate from the cation exchange column was diluted with ammonium sulfate.
• HIC hydrophobic interaction chromatography
• the eluate was applied to the column, and the PEP-1 was eluted using ammonium sulfate (0.572 M) in potassium phosphate (100 mM), pH 7.0.
• the eluate was collected in fractions based on A280 values. All fractions were collected into sterile, pre-weighed PETG bottles.
• a final filtration step was performed prior to packaging in order to minimize the bioburden in the bulk PEP-1.
• the bulk solution was filtered through a 0.22 ⁇ filter and collected into a sterile, pre-weighed PETG bottle. A sample was removed for lot release testing. The remainder of the bulk was dispensed aseptically into sterile PETG bottles and stored at -20°C.
• a ldnetic test was used to measure inhibitory activity of KI polypeptides, such as PEP-1.
• the kinetic assay measures fluorescence following kallikrein-mediated cleavage of a substrate, prolylphenylalanylarginyl amino methyl coumarin.
• a known amount of kallikrein was incubated with a serially diluted KI polypeptide reference standard or serially diluted KI polypeptide test samples, in a suitable reaction buffer on a microtiter plate. Each sample was run in triplicate. The substrate solution was added, and the plate read immediately using an excitation wavelength of 360 nm and an emission wavelength of 460 run. At least two each of the reference standard and sample curves were required to have an R-squared value of 0.95 to be considered valid.

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