AU2004202448B2 - OB Fusion Protein Compositions and Methods - Google Patents

Description

P/00/011 28/5/91 Regulation 3.2

AUSTRALIA

Patents Act 1990

ORIGINAL

COMPLETE SPECIFICATION STANDARD PATENT Name of Applicant: Actual Inventors Address for service Amgen Inc.

Benjamin Mann and Randy Ira Hecht is: WRAY ASSOCIATES Level 4, The Quadrant 1 William Street Perth, WA 6000 Attorney code: WR Invention Title: OB Fusion Protein Compositions and Methods This application is a Divisional Application by virtue of Section 39 of Australian Patent Application 54305/01.

The following statement is a full description of this invention, including the best method of performing it known to me:- -1/2- OB FUSION PROTEIN COMPOSITIONS AND METHODS Field of the Invention The present invention relates to Fc-OB fusion protein compositions and methods for preparation and use thereof.

Background Although the molecular basis for obesity is largely unknown, the identification of the "OB gene" and protein encoded ("OB protein" or "leptin") has shed some light on mechanisms the body uses to regulate body fat deposition. See, PCT publication, WO 96/05309 (12/22/96), Friedman et al.; Zhang et al., Nature 372: 425-432 (1994); see also, the Correction at Nature 374: 479 (1995). The OB protein is active in vivo in both ob/ob mutant mice (mice obese due to a defect in the production of the OB gene product) as well as in normal, wild type mice. The biological activity manifests itself in, among other things, weight loss. See Qenerally, Barrinaga, "Obese" Protein Slims Mice, Science 269: 475-4-6 (1995). The OB protein, derivatives and use thereof as modulators for the control of weight and adiposity of animals, including mammals and humans, has been disclosed in greater detail in PCT publication WO 96/05309 (12/22/96), hereby incorporated by reference, including figures.

The other biological effects of OB protein are not well characterized. It is known, for instance, that in ob/ob mutant mice, administration of OB protein results in a decrease in serum insulin levels, and serum glucose levels. It is also known that administration of OB protein results in a decrease in body fat. This was observed in both ob/ob mutant mice, as well as non-obese normal mice. Pelleymounter et al., Science 269 540-543 (1995); Halaas et al., Science 269: 543-546 (1995). See also, Campfield et al., Science 269: 546-549 (1995)(Peripheral and central administration of microgram doses of OB protein reduced food intake and body weight of ob/ob and diet-induced obese mice but not in db/db obese mice.) In none of these reports have toxicity's been observed, even at the highest doses.

Despite the promise of clinical application of the OB protein, the mode of action of the OB protein in vivo is not clearly elucidated. Information on the OB receptor, shows high affinity binding of the OB protein detected in the rat hypothalamus, which indicates

OB

receptor location. Stephens et al., Nature 377: 530- 532. The db/db mouse displays the identical phenotype as the ob/ob mouse, extreme obesity and Type II diabetes; this phenotype is thought to be due to a defective OB receptor, particularly since db/db mice fail to respond to OB protein administration. See Stephens et al., supra.

With the advances in recombinant

DNA

technologies, the availability of recombinant proteins for therapeutic use has engendered advances in protein formulation and chemical modification. One goal of such modification is protein protection and decreased degradation. Fusion proteins and chemical attachment may effectively block a proteolytic enzyme from physical contact with the protein backbone itself, and thus prevent degradation. Additional advantages include, under certain circumstances, increasing the stability, circulation time, and the biological activity of the therapeutic protein. A review article describing protein modification and fusion proteins is Francis, Focus on Growth Factors 3:4-10 (May 1992) (published by Mediscript, Mountview Court, Friern Barnet Lane, London OLD, UK).

One such modification is the use of the Fc region of immunoglobulins. Antibodies comprise two functionally independent parts, a variable domain known as "Fab", which binds antigen, and a constant domain, known as "Fc" which provides the link to effector functions such as complement or phagocytic cells. The Fc portion of an immunoglobulin has a long plasma halflife, whereas the Fab is short-lived. Capon, et al., Nature 337: 525-531 (1989).

Therapeutic protein products have been constructed using the Fc domain to provide longer halflife'or to incorporate functions such as Fc receptor binding, protein A binding, complement fixation and placental transfer which all reside in the Fc proteins of immunoglobulins. Id. For example, the Fc region of an IgGl antibody has been fused to the N-terminal end of CD30-L, a molecule which binds CD30 receptors expressed on Hodgkin's Disease tumor cells, anaplastic lymphoma cells, T-cell leukemia cells and other malignant cell types. See, U.S. Patent No. 5,480,981. IL-10, an antiinflammatory and antirejection agent has been fused to murine Fc72a in order to increase the cytokine's short circulating half-life. Zheng, X. et al., The Journal of Immunology, 154: 5590-5600 (1995). Studies have also evaluated the use of tumor necrosis factor receptor linked with the Fc protein of human IgGl to treat patients with septic shock. Fisher, C. et al., N. Engl.

J. Med., 334: 1697-1702 (1996); Van Zee, K. et al., The Journal of Immunology, 156: 2221-2230 (1996). Fc has also been fused with CD4 receptor to produce a therapeutic protein for treatment of AIDS. See, Capon et al., Nature, 337:525-531 (1989). In addition, the N-terminus of interleukin 2 has also been fused to the Fc portion of IgGl or IgG3 to overcome the short half life of interleukin 2 and its systemic toxicity. See, Harvill et al., Immunotechnology, 1: 95-105 (1995).

Due to the identification of the OB protein as a promising therapeutic protein, there exists a need to develop OB analog compositions for clinical application in conjunction with or in place of OB protein administration. Such development would include OB analog compositions where protein formulations and chemical modifications achieve decreased protein degradation, increased stability and circulation time.

The present invention provides such compositions.

Summary of the Invention The present invention relates to Fc-OB fusion protein compositions, methods of preparation of such compositions and uses thereof. In particular, the present invention relates to a genetic fusion protein comprising the Fc region or analogs of immunoglobulins fused to the N-terminal portion of the OB protein or analogs. The Fc-OB fusion protein is capable of dimerizing via the cysteine residues of the Fc region.

Unexpectedly, genetic fusion modification with Fc at the N-terminus of the OB protein demonstrates advantages in stability, clearance rate and decreased degradation which are not seen in OB protein or with fusion of Fc to the C-terminus of the OB protein. Surprisingly and importantly, the N-terminus modification provides unexpected protein protection from degradation, increases circulation time and stability, when compared to the OB protein or Fc modification to the OB protein C-terminus. Such unexpected advantages from the Fc modification to OB protein would be advantageous to OB protein consumers, in that these changes contribute to lower doses required or less frequent dosing. Thus, as described below in more detail, the present invention -5/1has a number of aspects relating to the genetic modification of proteins via fusion of the Fc region to the OB protein (or analogs thereof), as well as, specific modifications, preparations and methods of use thereof.

According to a first aspect the present invention provides a protein having a formula selected from the group consisting of: R, R 2 and R, L R 2 wherein R, is a Fc protein or analog thereof,

R

2 is an OB protein or analog thereof, and L is a linker.

According to a second aspect the present invention provides a fusion protein comprising an Fc protein, analog or derivative thereof, fused to the N-terminus of an OB protein, analog or derivative thereof.

According to a third aspect the present invention provides a nucleic acid sequence encoding for a protein having the formula selected from the group consisting of: R, R2 and RI L R 2 wherein RI is a Fc protein or analog thereof,

R

2 is an OB protein or analog thereof, and L is a linker.

According to a fourth aspect the present invention provides a nucleic acid sequence encoding for a fusion protein having a Fc protein, analog or derivative thereof, fused to the N-terminus of an OB protein, analog or derivative thereof.

According to a fifth aspect the present invention provides a vector containing a nucleic acid sequence according to the third or fourth aspect.

According to a sixth aspect the present invention provides a prokaryotic or eukaryotic host cell containing the vector of the fifth aspect.

According to a seventh aspect the present invention provides z process for producing a protein of the first or second aspect comprising the steps of culturing, under suitable conditions, the host cell of the sixth aspect, and isolating the protein produced.

-5/2- According to an eighth aspect the present invention provides a pharmaceutical composition comprising an effective amount of a protein according to the first or second aspect, in a pharmaceutically acceptable diluent, adjuvant or carrier.

According to a ninth aspect the present invention provides a method of treatment of a disorder selected from the group consisting of excess weight, diabetes, high blood lipid level, arterial sclerosis, arterial plaque, the reduction or prevention of gall stones formation, insufficient lean tissue mass, insufficient sensitivity to insulin, and stroke, wherein the method consists of administering a therapeutically effective amount of the protein according to the first or second aspect.

Unless the context clearly requires otherwise, throughout the description and the claims4 the words 'comprise', 'comprising', and the like are to be ccnstrued in an inclusive sense as opposed to an exclusive or exhaustive sense; that is to say, in the sense of "including, but not limited to".

Accordingly, in a preferred embodiment, the present invention provides a Fc-OB fusion protein wherein Fc is genetically fused to the N-terminus of the OB protein (or analogs thereof). In addition, the Fc portion may also be linked to the N-terminus of the OB protein (or analogs thereof) via peptide or chemical linkers as known in the art. As noted above and described in more detail below, the Fc-OB fusion protein has unexpected protections from degradation and increased circulation time and stability when compared to the OB protein or C-terminus OB-Fc fusion proteins. Additional aspects of the present invention, therefore, include not only Fc-OB fusion protein compositions, but also DNA sequences encoding such proteins, related vectors and host -6/1cells containing such vectors, both useful for producing fusion proteins of the present invention.

In another embodiment, the present invention provides for preparing the Fc-OB fusion protein. Such methods include recombinant DNA techniques for preparation of recombinant proteins. Furthermore, such aspects include methods of fermentation and purification as well.

In yet another embodiment, the present invention provides methods for treating excess weight in an individual or animals, including modulation of and/or fat deposition by the administration of Fc-OB fusion proteins. Due to the Fc-OB fusion protein characteristics, methods are contemplated which reduce the amount .and/or frequency of dosageof OB protein by using Fc-OB weight reducing agent.

In a further embodiment, the present invention provides for therapies for the treatment of co-morbidities associated with excess fat, such as diabetes, dys- or hyperlipidemias, arterial sclerosis, arterial plaque, the reduction or prevention of gall stones formation, stroke, and also an increase in insulin sensitivity and/or an increase in lean tissue mass.

In yet another embodiment, the present invention also provides for elated pharmaceutical compositions of the Fc-OB proteins, analogs and derivatives thereof, for use in the above therapies.

Brief Description of the Drawings FIGURE 1 Recombinant murine metOB (double stranded) DNA (SEQ ID NOS.: 1 and 2) and amino acid sequence (SEQ ID NO: 3).

-6/2- FIGURE 2 Recombinant human metOB analog (double stranded) DNA (SEQ ID NOS: 4 and 5) and amino acid sequence (SEQ ID NO: 6).

FIGURE 3 Recombinant human metFc-OB (double stranded) DNA (SEQ ID NOS: 7 and 8) and amino acid sequence (SEQ ID NO: 9).

FIGURE 4 Recombinant human metFc-OB variant (double stranded) DNA (SEQ ID NOS: 10 and 11) and amino acid sequence (SEQ ID NO: 12).

FIGURE 5 Recombinant human metFc-OB variant (double stranded) DNA (SEQ ID NOS: 13 and 14) and amino acid sequence (SEQ ID NO: FIGURE 6 Recombinant human metFc-OB variant (double stranded) DNA (SEQ ID NOS: 16 and 17) and amino acid sequence (SEQ ID NO: 18).

Detailed Description The present invention relates to Fc-OB fusion protein compositions, methods of preparation of such compositions and uses thereof. In particular, the present invention relates to the genetic or chemical fusion of the Fc region of immunoglobulins to the N-terminal portion of the OB protein. Unexpectedly, fusion of Fc at the N-terminus of the OB protein demonstrates advantages which are not seen in OB protein or with fusion of Fc at the C-terminus of the OB protein. Surprisingly, the N-terminally modified Fc-OB protein provides unexpected protein protection from degradation, increased circulation time and increased stability. Accordingly, the Fc-OB fusion protein, and analogs or derivatives thereof, as well as, related methods of use and preparation, are described in more detail below.

Compositions The Fc sequence of the recombinant human Fc-OB sequence set forth in SEQ. ID. NO. 9 (See Figure 3) may be selected from the human immunoglobulin IgG-1 heavy chain, see Ellison, J.W. et al., Nucleic Acids Res. 4071-4079 (1982), or any other Fc sequence known in the art other IgG classes including but not limited to IgG-2, IgG-3 and IgG-4, or other immunoglobulins).

Variant, analogs or derivatives of the Fc portion may be constructed by, for example, making various substitutions of residues or sequences.

Cysteine residues can be deleted or replaced with other amino acids to prevent formation of disulfide crosslinks of the Fc sequences. In particular amino acid at position 5 of SEQ. ID. NO. 9 is a cysteine residue. The recombinant Fc-OB sequence of SEQ. ID.

NO. 9 is a 378 amino acid Fc-OB protein (not counting the methionine residue). The first amino acid sequence for the recombinant Fc-OB protein of Figure 3 is referred to as +1 with the methionine at the -1 position.

One may remove the cysteine residue at position 5 or substitute it with one or more amino acids. An alanine residue may be substituted for the cysteine residue at position 6 giving the variant amino acid sequence of Figure 4 (SEQ. ID. NO. 12). The recombinant Fc-OB protein of Figure 4 is a 378 amino acid Fc-OB protein (not counting the methionine residue). The first amino acid sequence for the recombinant Fc-OB protein of Figure 4 is referred to as +1 with the methionine at the -1 position.

Likewise, the cysteine at position 5 of SEQ.

ID. NO. 9 could be substituted with a serine or other amino acid residue or deleted. A variant or analog may also be prepared by deletion of amino acids at positions 1, 3, 4 and 5 as with the variant in SEQ. ID. NO. (See Figure Substitutions at these positions can also be made and are with in the scope of this invention. The recombinant Fc-OB protein of Figure 5 is a 373 amino acid Fc-OB protein (not counting the methionine residue). The first amino acid sequence for the recombinant Fc-OB protein of Figure 5 is referred to as +1 with the methionine at the -1 position.

Modifications may also be made to introduce four amino acid substitutions to ablate the Fc receptor binding site and the complement (Clq) binding site.

These variant modifications from SEQ. ID. NO. 15 would include leucine at position 15 substituted with glutamate, glutamate at position 98 substituted with alanine, and lysines at positions 100 and 102 substituted with alanines (see Figure 6 and SEQ. ID. NO.

18). The recombinant Fc-OB protein of Figure 6 is a 373 amino acid Fc-OB protein (not counting the methionine residue). The first amino acid sequence for the recombinant Fc-OB protein of Figure 6 is referred to as +1 with the methionine at the -1 position.

-9- Likewise, one or more tyrosine residues can be replaced by phenyalanine residues as well. In addition, other variant amino acid insertions, deletions and/or substitutions are also contemplated and are within the scope of the present invention. Furthermore, alterations may be in the form of altered amino acids, such as peptidomimetics or D-amino acids. The Fc protein may be also linked to the OB proteins of the Fc-OB protein by "linker" moieties whether chemical or amino acids of varying lengths. Such chemical linkers are well known in the art. Amino acid linker sequences can include but are not limited to: ala, ala, ala; ala, ala, ala, ala; ala, ala, ala, ala, ala; gly, gly; gly, gly, gly; gly, gly, gly, gly, gly; gly, gly, gly, gly, gly, gly, gly; gly-pro-gly; gly, gly, pro, gly, gly; and any combination of subparts (a) through The OB portion of the Fc-OB fusion protein may be selected from the recombinant murine set forth in SEQ. ID. NO. 3 (See Figure or the recombinant human protein as set forth in Zhang et al., Nature, supra, (herein incorporated by reference) or those lacking a glutaminyl residue at position 28. (See Zhang et al, Nature, supra, at page 428.) One may also use the recombinant human OB protein analog as set forth in SEQ.

ID. NO. 6 (See Figure which contains: an arginine in place of lysine at position 35; and a leucine in place of isoleucine at position 74. (A shorthand abbreviation for this analog is the recombinant human R->L 35

I->L

74 The amino acid sequences for the recombinant human and recombinant murine proteins or analogs with or without the fused Fc portion at the N-terminus of the OB protein are set forth below with a methionyl residue at the -l position; however, as with any of the present OB proteins and analogs, the methionyl residue may be absent.

The murine protein is substantially homologous to the human protein, particularly as a mature protein, and, further, particularly at the N-ter-minus. One may prepare an analog of the recombinant human protein by altering (such as substituting amino acid residues), in the recombinant human sequence, the amino acids which diverge from the murine sequence. Because the recombinant human protein has biological activity in mice,, such an analog would likely be active in humans.

For example, using a human protein having a lysine at residue 35 and an isoleucine at residue 74 according to the numbering of SEQ. ID. NO. 6, wherein the first amino acid is valine, and the amino acid at position 146 is cysteine, one may substitute with another amino acid one or more of the amino acids at positions 32, 35, 50, 64, 68, 71, 74, 77, 89, 97, 100, 105, 106, 107, 108, 111, 118, 136, 138, 142, and 145. One may select the amino acid at the corresponding position of the murine protein, (SEQ. ID. NO. or another amino acid.

One may further prepare "consensus" molecules based on the rat OB protein sequence. Murakami et al., Biochem. Biophys. Res. Comm. 209: 944-9521 (1995) herein incorporated by reference. Rat OB protein differs from human OB protein at the following positions (using the numbering of SEQ. ID. NO. 4, 32, 33, 35, 50, 68, 21, L74, 78, 89, 97, 100, 101, 102, 105, 106j, 107, 108, 1I11, 1li, 136, 138 and 145. One may substitute with another amino acid one or more of the amino acids at these divergent positions. The positions in bold print are those in which the murine OB protein as well as the -11rat CE protein are divergent from the human CE protein, and thus, are particularly suitable for alteration. At one or more of a positions, one may substitute an amino acid from the corresponding rat CE protein, or another aci.d.

The positions from both rat and murine CE protein which diverge from the mature human CE protein are: 4, 32, 33, 35, 50, 64, 68, 71, 74, 77, 78, 89, 97, 100, 102, 105, 106, 107, 108, 111, 118, 136, 138, 142, and 145. An CE protein according to SEQ. ID. NO. 6 having one or more of the above amino acids replaced with another amino acid, such as the amino acid found in the corresponding rat or murine sequence, may also be effective.

1 in addition, the amino acids found in rhesus monkey CE protein which diverge from the mature human CE protein are (with identities noted in parentheses in one letter amino acid abbreviation): 8 35 48(V, 53(Q), 60(1), 66(I), 67(N), 89(L), 100(l), 108 112 and 118 Since the recombinant human CE protein is active in cynomolgus monkeys, a human CE protein accordinar to SEQ. ID. NC. 6 (with lysine at position 35 and isoleucine at position 74) having one or more of the rhesus monkey divergent amino acids replaced with another amino acid, such as the amino acids in parentheses, may be effective. It should be noted that certain rhesus divergent amino acids are also those found in the above murine species (positions 68, 89, 100 and 112) Thus, one may prepare a murine/rhesus/human consensus molecule having (using the numbering of SEQ. ID. NC. 6 having a lysine at position and an isoleucine at position 74) having one or more of the amino acids at positions replaced by another amino acid: 4, 8, 32, 33, 35, 48, 50, 53, 60, 64, 66, 67, 68, 71, 74, 77, 78, 89, 97, 100Q, 102, 105, 106, 107, 108, 111, 112, 118, 136, 138, 142, and 145.

-12- Other analogs may be prepared by deleting a part of the protein amino acid sequence. For example, the mature protein lacks a leader sequence (-22 to One may prepare the following truncated forms of human OB protein molecules (using the numbering of SEQ. ID.

NO. 6): amino acids 98-146 amino acids 1-32 amino acids 40-116 amino acids 1-99 and (connected to) 112-146 amino acids 1-99 and (connected to) 112-146 having one or more of amino acids 100-111 placed between amino acids 99 and 112.

In addition, the truncated forms may also have altered one or more of the amino acids which are divergent (in the rat, murine, or rhesus OB protein) from human OB protein. Furthermore, any alterations may be in the form of altered amino acids, such as peptidomimetics or D-amino acids.

Therefore, the present invention encompasses a Fc-OB fusion protein wherein the OB protein is selected from: the amino acid sequence 1-146 as set forth in SEQ. ID. NO. 3 (below) or SEQ. ID. NO. 6; the amino acid sequence 1-146 as set forth in SEQ. ID. NO. 6 having a lysine residue at position 35 and an isoleucine residue at position 74; the amino acid sequence of subpart (b) having a different amino acid substituted in one or more of the following positions (using the numbering according to SEQ. ID. NO. 6 and retaining the same numbering even in the absence of a glutaminyl residue at position 28): 4, 32, 33, 35, 50, 64, 68, 71, 74, 77, 78, 89, 97, 100, 102, 105, 106, 107, 108, 111, .118, 136, 138, 142, and 145; -13the amino acid sequence of subparts or optionally lacking a glutaminyl residue at position 28; the amino acid sequence of subparts or having a methionyl residue at the N-terminus; a truncated OB protein analog selected from among: (using the numbering of SEQ. ID. NO. 6): amino acids 98-146 (ii) amino acids 1-32 (iii) amino acids 40-116 (iv) amino acids 1-99 and 112-146 amino acids 1-99 and 112-146 having one or more of amino acids 100-111 placed between amino acids 99 and 112; and, (vi) the truncated OB analog of subpart having one or more of amino acids 100, 102, 105, 106, 107, 108, 111, 118, 136, 138, 142, and 145 substituted with another amino acid; (vii) the truncated analog of subpart (ii) having one or more of amino acids 4, 8 and 32 substituted with another amino acid; (viii) the truncated analog of subpart (iii) having one or more of amino acids 50, 53, 64, 66, 67, 68, 71, 74, 77, 78, 89, 97, 100, 102, 105, 106, 107, 108, 111 and 112 replaced with another amino acid; (vix) the truncated analog of subpart (iv) having one or more of amino acids 4, 8, 32, 33, 35, 48, 50, 53, 60, 64, 66, 67, 68, 71, 74, 77, 78, 89, 97, 112, 118, 136, 138, 142, and 145 replaced with another amino acid; and the truncated analog of subpart (v) having one or more of amino acids 4, 32, 33, -14- 64, 68, 71, 74, 77, 78, 89, 97, 100, 102, 105, 106, 107, 108, 111, 118, 136, 138, 142, and 145 replaced with another amino acid; (xi) the truncated analog of any of subparts having an N-terminal methionyl residue; and the OB protein or analog derivative of any of subparts through comprised of a chemical moiety connected to the protein moiety; a derivative of subpart wherein said chemical moiety is a water soluble polymer moiety; a derivative of subpart wherein said water soluble polymer moiety is polyethylene glycol; a derivative of subpart wherein said water soluble polymer moiety is a polyaminoacid moiety; a derivative of subpart through (j) wherein said moiety is attached at solely the N-terminus of said protein moiety; and an OB protein, analog or derivative of any of subparts through in a pharmaceutically acceptable carrier.

Derivatives The present Fc-OB fusion proteins (herein the term "protein" is used to include "peptide," Fc, OB or analogs, such as those recited infra, unless otherwise indicated) are derivatized by the attachment of one or more chemical moieties to the Fc-OB fusion protein moiety. These chemically modified derivatives may be further formulated for intraarterial, intraperitoneal, intramuscular subcutaneous, intravenous, oral, nasal, pulmonary, topical or other routes of administration as discussed below. Chemical modification of biologically active proteins has been found to provide additional advantages under certain circumstances, such as increasing the stability and circulation time of the therapeutic protein and decreasing immunogenicity. See, U.S. Patent No. 4,179,337, Davis et al., issued December 18, 1979. For a review, see Abuchowski et al., in Enzymes as Drugs. S. Holcerberg and J. Roberts, eds. pp. 367-383 (1981)); Francis et al., supra.

The chemical moieties suitable for such derivatization may be selected from among various water soluble polymers. The polymer selected should be water soluble so that the protein to which it is attached does not precipitate in an aqueous environment, such as a physiological environment. Preferably, for therapeutic use of the end-product preparation, the polymer will be pharmaceutically acceptable. One skilled in the art will be able to select the desired polymer based on such considerations as whether the polymer/protein conjugate will'be used therapeutically, and if so, the desired dosage, circulation time, resistance to proteolysis, and other considerations. For the present proteins and peptides, the effectiveness of the derivatization may be ascertained by administering the derivative, in the desired form by osmotic pump, or, more preferably, by injection or infusion, or, further formulated for oral, pulmonary or nasal delivery, for example), and observing biological effects as described herein.

The water soluble polymer may be selected from the group consisting of, for example, polyethylene glycol, copolymers of ethylene glycol/propylene glycol, carboxymethylcellulose, dextran, polyvinyl alcohol, polyvinyl pyrolidone, poly-1, 3-dioxolane, poly-1,3,6-trioxane, ethylene/maleic anhydride copolymer, polyaminoacids (either homopolymers or random copolymers), and dextran or poly(n-vinyl pyrolidone)polyethylene glycol, propylene glycol homopolymers, polypropylene oxide/ethylene oxide co-polymers, polyoxyethylated polyols and polyvinyl alcohol. Polyethylene glycol propionaldenhyde may have advantages in manufacturing due to its stability in water. Also, succinate and styrene may also be used.

The OB or Fc proteins used to formulate the Fc-OB fusion protein, may be prepared by attaching polyaminoacids or branch point amino acids to the Fc or OB protein (or analogs) moiety. For example, the polyaminoacid may be an additional carrier protein which, like the Fc fused to the OB protein or OB analog of the present invention, serves to also increase the circulation half life of the protein in addition to the advantages achieved via the Fc-OB fusion protein above.

For the present therapeutic or cosmetic purpose of the present invention, such polyaminoacids should be those which have or do not create neutralizing antigenic response, or other adverse responses. Such polyaminoacids may be selected from the group consisting of serum album (such as human serum albumin), an additional antibody or portion thereof the Fc region), or other polyaminoacids, e.g. lysines. As indicated below, the location of attachment of the polyaminoacid may be at the N-terminus of the Fc-OB protein moiety, or C-terminus, or other places in between, and also may be connected by a chemical "linker" moiety to the Fc-OB protein.

The polymer may be of any molecular weight, and may be branched or unbranched. For polyethylene glycol, the preferred molecular weight is between about 2 kDa and about 100 kDa (the term "about" indicating that in preparations of polyethylene glycol, some molecules will weigh more, some less, than the stated molecular weight) for ease in handling and manufacturing. Other sizes may be used, depending on the desired therapeutic profile the duration of sustained release desired, the effects, if any on biological activity, the ease in handling, the degree or 1 -17lack of antigenicity and other known effects of the polyethylene glycol to a therapeutic protein or analog).

The number of polymer molecules so attached may vary, and one skilled in the art will be able to ascertain the effect on function. One may mono-derivatize, or may provide for a di-, tri-, tetraor some combination of derivatization, with the same or different chemical moieties polymers, such as different weights of polyethylene glycols). The proportion of polymer molecules to protein (or peptide) molecules will vary, as will their concentrations in the reaction mixture. In general, the optimum ratio (in terms of efficiency of reaction in that there is no excess unreacted protein or polymer) will be determined by factors such as the desired degree of derivatization mono, di-, tri-, etc.), the molecular weight of the polymer selected, whether the polymer is branched or unbranched, and the reaction conditions.

The chemical moieties should be attached to the protein with consideration of effects on functional or antigenic domains of the protein. There are a number of attachment methods available to those skilled in the art. EP 0 401 384 herein incorporated by reference (coupling PEG to G-CSF), see also Malik et al., Exp.

Hematol. 20: 1028-1035 (1992) (reporting pegylation of GM-CSF using tresyl chloride). For example, polyethylene glycol may be covalently bound through amino acid residues via a reactive group, such as, a free amino or carboxyl group. Reactive groups are those to which an activated polyethylene glycol molecule may be bound. The amino acid residues having a free amino group may include lysine residues and the N-terminal amino acid residue. Those having a free carboxyl group may include aspartic acid residues, glutamic acid residues, and the C-terminal amino acid residue.

Sulfhydryl groups may also be used as a reactive group -18for attaching the polyethylene glycol molecule(s).

Preferred for therapeutic purposes is attachment at an amino group, such as attachment at the N-terminus or lysine group. Attachment at residues important for receptor binding should be avoided if receptor binding is desired.

One may specifically desire N-terminally chemically modified Fc-OB fusion protein. Using polyethylene glycol as an illustration of the present compositions, one may select from a variety of polyethylene glycol molecules (by molecular weight, branching, etc.), the proportion of polyethylene glycol molecules to protein (or peptide) molecules in the reaction mix, the type of pegylation reaction to be performed, and the method of obtaining the selected N-terminally pegylated protein. The method of obtaining the N-terminally pegylated preparation separating this moiety from other monopegylated moieties if necessary) may be by purification of the N-terminally pegylated material from a population of pegylated protein molecules. Selective N-terminal chemical modification may be accomplished by reductive alkylation which exploits differential reactivity of different types of primary amino groups (lysine versus the N-terminal) available for derivatization in a particular protein. Under the appropriate reaction conditions, substantially selective derivatization of the protein at the N-terminus with a carbonyl group containing polymer is achieved. For example, one may selectively N-terminally pegylate the protein by performing the reaction at a pH which allows one to take advantage of the pKa differences between the E-amino group of the lysine residues and that of the a-amino group of the N-terminal residue of the protein. By such selective derivatization, attachment of a water soluble polymer to a protein is controlled: the conjugation with the -19polymer takes place predominantly at the N-terminus of the protein and no significant modification of other reactive groups, such as the lysine side chain amino groups, occurs. Using reductive alkylation, the water soluble polymer may be of the type described above, and should have a single reactive aldehyde for coupling to the protein. Polyethylene glycol propionaldehyde, containing a single reactive aldehyde, may be used.

An N-terminally monopegylated derivative is preferred for ease in production of a therapeutic.

N-terminal pegylation ensures a homogenous product as characterization of the product is simplified relative to di-, tri- or other multi-pegylated products. The use of the above reductive alkylation process for preparation of an N-terminal product is preferred for ease in commercial manufacturing.

ComDlexes The Fc-OB fusion protein, analog or derivative thereof may be administered complexed to a binding composition. Such binding composition may have the effect of prolonging the circulation time even further than that achieved with the Fc-OB fusion protein, analog or derivative. Such composition may be a protein (or synonymously, peptide). An example of a binding protein is OB protein receptor or portion thereof, such as a soluble portion thereof. Other binding proteins may be ascertained by examining OB protein or Fc-OB protein in serum, or by empirically screening for the presence of binding. Binding proteins used will typically not interfere with the ability of OB protein, Fc-OB fusion proteins, or analogs or derivatives thereof, to bind to endogenous OB protein receptor and/or effect signal transduction.

Pharmaceutical Compositions The present invention also provides methods of using pharmaceutical compositions of the Fc-OB fusion proteins and derivatives. Such pharmaceutical compositions may be for administration for injection, or for oral, pulmonary, nasal, transdermal or other forms of administration. In general, comprehended by the invention are pharmaceutical compositions comprising effective amounts of protein or derivative products of the invention together with pharmaceutically acceptable diluents, preservatives, solubilizers, emulsifiers, adjuvants and/or carriers. Such compositions include diluents of various buffer content Tris-HCl, acetate, phosphate), pH and ionic strength; additives such ,as detergents and solubilizing agents Tween Polysorbate 80), anti-oxidants ascorbic acid, sodium metabisulfite), preservatives Thimersol, benzyl alcohol) and bulking substances lactose, mannitol); incorporation of the material into particulate preparations of polymeric compounds such as polylactic acid, polyglycolic acid, etc. or into liposomes. Hylauronic acid may also be used, and this may have the effect of promoting sustained duration in the circulation. Such compositions may influence the physical state, stability, rate of in vivo release, and rate of in vivo clearance of the present proteins and derivatives. See, Remington's Pharmaceutical Sciences, 18th Ed. (1990, Mack Publishing Co., Easton, PA 18042) pages 1435-1712 which are herein incorporated by reference. The compositions may be prepared in liquid form, or may be in dried powder, such as lyophilized form. Implantable sustained release formulations are also contemplated, as are transdermal formulations.

Contemplated for use herein are oral solid dosage forms, which are described generally in Remington's Pharmaceutical Sciences, 18th Ed. 1990 (Mack -21- Publishing Co. Easton PA 18042) at Chapter 89, which is herein incorporated by reference. Solid dosage forms include tablets, capsules, pills, troches or lozenges, cachets or pellets. Also, liposomal or proteinoid encapsulation may be used to formulate the present compositions (as, for example, proteinoid microspheres reported in U.S. Patent No. 4,925,673). Liposomal encapsulation may be used and the liposomes may be derivatized with various polymers U.S. Patent No.

5,013,556). A description of possible solid dosage forms for the therapeutic is given by Marshall, K. In: Modern Pharmaceutics Edited by G. S. Banker and C. T.

Rhodes Chapter 10, 1979, herein incorporated by reference. In general, the formulation will include the Fc-OB fusion protein (or analog or derivative), and inert ingredients which allow for protection against the stomach environment, and release of the biologically active material in the intestine.

Also specifically contemplated are oral dosage forms of the above derivatized proteins. Fc-OB fusion protein may be chemically modified so that oral delivery of the derivative is efficacious. Generally, the chemical modification contemplated is the attachment of at least one moiety to the protein (or peptide) molecule itself, where said moiety permits inhibition of proteolysis; and uptake into the blood stream from the stomach or intestine. Also desired is the increase in overall stability of the protein and increase in circulation time in the body. Examples of such moieties include: Polyethylene glycol, copolymers of ethylene glycol and propylene glycol, carboxymethyl cellulose, dextran, polyvinyl alcohol, polyvinyl pyrrolidone and polyproline. Abuchowski and Davis, Soluble Polymer-Enzyme Adducts. In: "Enzymes as Drugs", Hocenberg and Roberts, eds., Wiley-Interscience, New York, NY, (1981), pp. 367-383; Newmark, et al., J. Appl.

-22- Biochem. 4: 185-189 (1982). Other polymers that could be used are poly-1,3-dioxolane and poly-l,3,6-tioxocane.

Preferred for pharmaceutical usage, as indicated above, are polyethylene glycol moieties.

For the Fc-OB fusion protein, analog or derivative, the location of release may be the stomach, the small intestine the duodenum, jejunum, or ileum), or the large intestine. One skilled in the art has available formulations which will not dissolve in the stomach, yet will release the material in the duodenum or elsewhere in the intestine. Preferably, the release will avoid the deleterious effects of the stomach environment, either by protection of the Fc-OB fusion protein, analog or derivative, or by release of the biologically active material beyond the stomach environment, such as in the intestine.

To ensure full gastric resistance a coating impermeable to at least pH 5.0 is essential. Examples of the more common inert ingredients that are used as enteric coatings are cellulose acetate trimellitate (CAT), hydroxypropylmethylcellulose phthalate (HPMCP), HPMCP 50, HPMCP 55, polyvinyl acetate phthalate (PVAP), Eudragit L30D, Aquateric, cellulose acetate phthalate (CAP), Eudragit L, Eudragit S, and Shellac. These coatings may be used as mixed films.

A coating or mixture of coatings can also be used on tablets, which are not intended for protection against the stomach. This can include sugar coatings, or coatings which make the tablet easier to swallow.

Capsules may consist of a hard shell (such as gelatin) for delivery of dry therapeutic i.e. powder; for liquid forms, a soft gelatin shell may be used. The shell material of cachets could be thick starch or other edible paper. For pills, lozenges, molded tablets or tablet triturates, moist massing techniques can be used.

-23- The therapeutic can be included in the formulation as fine multiparticulates in the form of granules or pellets of particle size about 1 mm. The formulation of the material for capsule administration could also be as a powder, lightly compressed plugs or even as tablets. The therapeutic could be prepared by compression.

Colorants and flavoring agents may all be included. For example, the protein (or derivative) may be formulated (such as by liposome or microsphere encapsulation) and then further contained within an edible product, such as a refrigerated beverage containing colorants and flavoring agents.

One may dilute or increase the volume of the therapeutic with an inert material. These diluents could include carbohydrates, especially mannitol, a-lactose, anhydrous lactose, cellulose, sucrose, modified dextrans and starch. Certain inorganic salts may be also be used as fillers including calcium triphosphate, magnesium carbonate and sodium chloride.

Some commercially available diluents are Fast-Flo, Emdex, STA-Rx 1500, Emcompress and Avicell.

Disintegrants may be included in the formulation of the therapeutic into a solid dosage form.

Materials used as disintegrates include but are not limited to starch including the commercial disintegrant based on starch, Explotab. Sodium starch glycolate, Amberlite, sodium carboxymethylcellulose, ultramylopectin, sodium alginate, gelatin, orange peel, acid carboxymethyl cellulose, natural sponge and bentonite may all be used. Another form of the disintegrants are the insoluble cationic exchange resins. Powdered gums may be used as disintegrants and as binders and these can include powdered gums such as agar, Karaya or tragacanth. Alginic acid and its sodium salt are also useful as disintegrants.

-24- Binders may be used to hold the therapeutic agent together to form a hard tablet and include materials from natural products such as acacia, tragacanth, starch and gelatin. Others include methyl cellulose ethyl cellulose (EC) and carboxymethyl cellulose (CMC). Polyvinyl pyrrolidone (PVP) and hydroxypropylmethyl cellulose (HPMC) could both be used in alcoholic solutions to granulate the therapeutic.

An antifrictional agent may be included in the formulation of the therapeutic to prevent sticking during the formulation process. Lubricants may be used as a layer between the therapeutic and the die wall, and these can include but are not limited to; stearic acid including its magnesium and calcium salts, polytetrafluoroethylene (PTFE), liquid paraffin, vegetable oils and waxes. Soluble lubricants may also be used such as sodium lauryl sulfate, magnesium lauryl sulfate, polyethylene glycol of.various molecular weights, Carbowax 4000 and 6000.

Glidants that might improve the flow properties of the drug during formulation and to aid rearrangement during compression might be added. The glidants may include starch, talc, pyrogenic silica and hydrated silicoaluminate.

To aid dissolution of the therapeutic into the aqueous environment a surfactant might be added as a wetting agent. Surfactants may include anionic detergents such as sodium lauryl sulfate, dioctyl sodium sulfosuccinate and dioctyl sodium sulfonate. Cationic detergents might be used and could include benzalkonium chloride or benzethomium chloride. The list of potential nonionic detergents that could be included in the formulation as surfactants are lauromacrogol 400, polyoxyl 40 stearate, polyoxyethylene hydrogenated castor oil 10, 50 and 60, glycerol monostearate, polysorbate 40, 60, 65 and 80, sucrose fatty-acid ester, methyl cellulose and carboxymethyl cellulose. These surfactants could be present in the formulation of the protein or derivative either alone or as a mixture in different ratios.

Additives which potentially enhance uptake of the protein (or derivative) are for instance the fatty acids oleic acid, linoleic acid and linolenic acid.

Controlled release formulation may be desirable. The drug could be incorporated into an inert matrix which permits release by either diffusion or leaching mechanisms gums. Slowly degenerating matrices may also be incorporated into the formulation, alginates, polysaccahrides. Another form of a controlled release of this therapeutic is by a method based on the Oros therapeutic system (Alza Corp.), i.e., the drug is enclosed in a semipermeable membrane which allows water to enter and push drug out through a single small opening due to osmotic effects. Some enteric coatings also have a delayed release effect.

Other coatings may be used for the formulation. These include a variety of sugars which could be applied in a coating pan. The therapeutic agent could also be given in a film coated tablet and the materials used in this instance are divided into 2 groups. The first are the nonenteric materials and include methyl cellulose, ethyl cellulose, hydroxyethyl cellulose, methylhydroxy-ethyl cellulose, hydroxypropyl cellulose, hydroxypropyl-methyl cellulose, sodium carboxy-methyl cellulose, providone and the polyethylene glycols. The second group consists of the enteric materials that are commonly esters of phthalic acid.

A mix of materials might be used to provide the optimum film coating. Film coating may be carried out in a pan coater or in a fluidized bed or by compression coating.

-26- Also contemplated herein is pulmonary delivery of the present protein (or derivatives thereof). The protein (or derivative) is delivered to the lungs of a mammal while inhaling and traverses across the lung epithelial lining to the blood stream. (Other reports of this include Adjei et al., Pharmaceutical Research 7: 565-569 (1990); Adjei et al., International Journal of Pharmaceutics 63: 135-144 (1990) (leuprolide acetate); Braquet et al., Journal of Cardiovascular Pharmacology 13 (suppl. s.143-146 (1989) (endothelin-l);Hubbard et al., Annals of Internal Medicine 3: 206-212 (1989)(al-antitrypsin); Smith et al., J. Clin. Invest. 84: 1145-1146 (1989)(a-l-proteinase); Oswein et al., "Aerosolization of Proteins", Proceedings of Symposium on Respiratory Drug Delivery II, Keystone, Colorado, March, 1990 (recombinant human growth hormone); Debs et al., The Journal of Immunology 140: 3482-3488 (1988) (interferon-y and tumor necrosis factor a) and Platz et al., U.S.

Patent No. 5,284,656 (granulocyte colony stimulating factor).

Contemplated for use in the practice of this invention are a wide range of mechanical devices designed for pulmonary delivery of therapeutic products, including but not limited to nebulizers, metered dose inhalers, and powder inhalers, all of which are familiar to those skilled in the art.

Some specific examples of commercially available devices suitable for the practice of this invention are the Ultravent nebulizer, manufactured by Mallinckrodt, Inc., St. Louis, Missouri; the Acorn II nebulizer, manufactured by Marquest Medical Products, Englewood, Colorado; the Ventolin metered dose inhaler, manufactured by Glaxo Inc., Research Triangle Park, North Carolina; and the Spinhaler powder inhaler, manufactured by Fisons Corp., Bedford, Massachusetts.

-27- All such devices require the use of formulations suitable for the dispensing of protein (or analog or derivative). Typically, each formulation is specific to the type of device employed and may involve the use of an appropriate propellant material, in addition to diluents, adjuvants and/or carriers useful in therapy.

The protein (or derivative) should most advantageously be prepared in particulate form with an average particle size of less than 10 pm (or microns), most preferably 0.5 to 5 pm, for most effective delivery to the distal lung.

Carriers include carbohydrates such as trehalose, mannitol, xylitol, sucrose, lactose, and sorbitol. Other ingredients for use in formulations may include DPPC, DOPE, DSPC and DOPC. Natural or synthetic surfactants may be used. Polyethylene glycol may be used (even apart from its use in derivatizing the protein or analog). Dextrans, such as cyclodextran, may be used. Bile salts and other related enhancers may be used. Cellulose and cellulose derivatives may be used. Amino acids may be used, such as use in a buffer formulation.

Also, the use of liposomes, microcapsules or microspheres, inclusion complexes, or other types of carriers is contemplated.

Formulations suitable for use with a nebulizer, either jet or ultrasonic, will typically comprise Fc-OB protein, analogs or derivatives thereof, dissolved in water at a concentration of about 0.1 to mg of biologically active protein per mL of solution.

The formulation may also include a buffer and a simple sugar for protein stabilization and regulation of osmotic pressure). The nebulizer formulation may also contain a surfactant, to reduce or prevent surface -28induced aggregation of the protein caused by atomization of the solution in forming the aerosol.

Formulations for use with a metered-dose inhaler device will generally comprise a finely divided powder containing the protein (or derivative) suspended in a propellant with the aid of a surfactant. The propellant may be any conventional material employed for this purpose, such as a chlorofluorocarbon, a hydrochlorofluorocarbon, a hydrofluorocarbon, or a hydrocarbon, including trichlorofluoromethane, dichlorodifluoromethane, dichlorotetrafluoroethanol, and 1,1,1, 2 -tetrafluoroethane, or combinations thereof.

Suitable surfactants include sorbitan trioieate and soya lecithin. Oleic acid may also be useful as a surfactant.

Formulations for dispensing from a powder inhaler device will comprise a finely divided dry powder containing protein (or derivative) and may also include a bulking agent, such as lactose, sorbitol, sucrose, mannitol, trehalose, or xylitol in amounts which facilitate dispersal of the powder from the device, 50 to 90% by weight of the formulation.

Nasal delivery of the protein (or analog or derivative) is also contemplated. Nasal delivery allows the passage of the protein to the blood stream directly after administering the therapeutic product to the nose, without the necessity for deposition of the product in the lung. Formulations for nasal delivery include those with dextran or cyclodextran. Delivery via transport across other mucus membranes is also contemplated.

Dosage One skilled in the art will be able to ascertain effective dosages by administration and observing the desired therapeutic effect. Due to the N-terminus modification of the OB protein, the present -29invention provides unexpected protein protection from degradation, and increases circulation time and stability, when compared to OB protein or C-terminus modification of the OB protein. One skilled in the art, therefore, will be able to ascertain from these changes that an effective dosage may require lower doses or less frequent dosing.

Preferably, the formulation of the molecule will be such that between about .10 gg/kg/day and 10 mg/kg/day will yield the desired therapeutic effect.

The effective dosages may be determined using diagnostic tools over time. For example, a diagnostic for measuring the amount of OB protein or Fc-OB fusion protein in the blood (or plasma or serum) may first be used,to determine endogenous levels of protein. Such diagnostic tools may be in the form of an antibody assay, such as an antibody sandwich assay. The amount of endogenous OB protein is quantified initially, and a baseline is determined. The therapeutic dosages are determined as the quantification of endogenous and exogenous OB protein or Fc-OB fusion protein (that is, protein, analog or derivative found within the body, either self-produced or administered) is continued over the course of therapy. The dosages may therefore vary over the course of therapy, with a relatively high dosage being used initially, until therapeutic benefit is seen, and lower dosages used to maintain the therapeutic benefits.

Ideally, in situations where solely reduction in blood lipid levels is desired, where maintenance of reduction of blood lipid levels is desired, or an increase in lean body mass is desired, the dosage will be insufficient to result in weight loss. Thus, during an initial course of therapy of an obese person, dosages may be administered whereby weight loss and concomitant blood lipid level lowering or concomitant fat tissue decrease/lean mass increase is achieved. Once sufficient weight loss is achieved, a dosage sufficient to prevent re-gaining weight, yet sufficient to maintain desired blood lipid levels or lean mass increase (or, prevention of lean mass depletion) may be administered. These dosages can be determined empirically, as the effects of OB or Fc-OB protein are reversible, Campfield et al., Science 269: 546-549 (1995) at 547). Thus, if a dosage resulting in weight loss is observed when weight loss is not desired, one would administer a lower dose in order to achieve the desired blood lipid levels or increase in lean tissue mass, yet maintain the desired weight.

For increasing an individual's sensitivity to insulin, similar dosage considerations may be taken into account. Lean mass increase without weight loss may be achieved sufficient to decrease the amount of insulin (or, potentially, amylin, thiazolidinediones, or other potential diabetes treating drugs) an individual would be administered for the treatment of diabetes.

For increasing overall strength, there may be similar dosage considerations. Lean mass increase with concomitant increase in overall strength may be achieved with doses insufficient to result in weight loss. Other benefits, such as an increase in red blood cells (and oxygenation in the blood) and a decrease in bone resorption or osteoporosis may also be achieved in the absence of weight loss.

Combinations The present methods may be used in conjunction with other medicaments, such as those useful for the treatment of diabetes insulin, possibly, thiazolidinediones, amylin, or antagonists thereof), cholesterol and blood pressure lowering medicaments (such as those which reduce blood lipid levels br other -31cardiovascular medicaments), and activity increasing medicaments amphetamines). Appetite suppressants may also be used (such as those affecting the levels of serotonin or neuropeptide Such administration may be simultaneous or may be in seriatim.

In addition, the present methods may be used in conjunction with surgical procedures, such as cosmetic surgeries designed to alter the overall appearance of a body liposuction or laser surgeries designed to reduce body mass). The health benefits of cardiac surgeries, such as bypass surgeries or other surgeries designed to relieve a deleterious condition caused by blockage of blood vessels by fatty deposits, such as arterial plaque, may be increased with concomitant use of the present compositions and methods.

Methods to eliminate gall stones, such as ultrasonic or laser methods, may also be used either prior to, during or after a course of the present therapeutic methods.

Furthermore, the present methods may be used as an adjunct to surgeries or therapies for broken bones, damaged muscle, or other therapies which would be improved by an increase in lean tissue mass.

The following examples are offered to more fully illustrate the invention, but are not to be construed as limiting the scope thereof.

EXAMPLE 1: Use of Murine FC-OB Protein Via Subcutaneous Injection This example demonstrates that injection subcutaneously of murine Fc-OB protein results in weight loss in normal mice. Normal (non-obese) CD1 mice were administered murine Fc-OB protein via subcutaneous injections over a 22 day time period. A dosage of 10 mg protein/kg body weight/day resulted in a 14% 1.1%) loss from baseline weight by the 22nd day of injections.

A dosage of PBS resulted in a 3.9% loss from -32baseline weight by the 22nd day of injections. The weight loss with the use of 10 mg protein/kg body weight/day of Fc-OB protein in obese CD1 mice resulted in a 10% loss from baseline weight and a dosage of PBS resulted in a 8.7% loss from baseline weight, both by the 22nd day of injections Presented below are the percent differences from baseline weight in CD1 mice (8 weeks old): Table 1 Weight Loss Upon Subcutaneous Injection Time Vehicle (PBS) Lean/Recombinant Obese/Recombinant (days) Fc-OB Fusion Fc-OB Fusion Protein Protein 1-2 44 -3.6 .41 -1.03 1.36 3-4 -1.07 .13 -6.8 1.5 -2.7 1.1 5-6 13 1.1 -9.5 1.2 -4.9 7-8 92 .29 -12.5 1.6 -7.7 2.9 9-10 1.6 1.3 -12.6 1.9 -8.2 2.9 11-12 -1.98 1 -13.6 1.96 -8.6 2.9 13-14 -5.2 1.3 -14.6 3.6 15-16 -8.6 0.1 -14.5 2 -9.4 2.2 17-18 -8.5 .64 -16.1 1.8 -9.6 2.99 19-20 -4.1 .99 -16 1.5 -10.4 3.3 21-22 -3.9 3.3 -14.1 1.1 -10 4.3 As can be seen, at the end of a 22 day subcutaneous regime, animals receiving the FC-OB protein lost over 14.1% of their body weight in lean and 10% of body weight in obese, as compared to animals only receiving the PBS vehicle and as compared to baseline.

Surprisingly, animals receiving Fc-OB protein up to 22 days continued to loose weight up until 28 -33days, 4 days after the last injection. Normal (nonobese) CD1 mice administered 10 mg protein/kg body weight/day of murine Fc-OB protein via subcutaneous injections stopped at day 22 resulted in a 21% loss from baseline weight at day 28 as compared to 14% loss at day 22. Likewise, obese CD1 mice administered 10 mg protein/kg body weight/day of murine Fc-OB protein stopped at day 22 resulted in a 13% loss from baseline weight at day 28 compared to 10% loss at day 22. At day 34 weight loss was maintained at 10% loss in obese mice where lean mice recovered to 5% loss. Controls in each system from day 22 through day 34 averaged from 4% in obese mice and 7% gain in lean mice.

EXAMPLE 2: Use of Human FC-OB Protein Via Subcutaneous Injection in C57 Mice This example demonstrates that injection subcutaneously of human Fc-OB protein results in weight loss in normal mice. Normal (non-obese) C57 mice were administered human Fc-OB protein via subcutaneous injections over a 7 day time period. A dosage of 10 mg protein/kg body weight/day resulted in a 12% 1.3%) loss from baseline weight by the 7th day of injections.

A dosage of 1 mg protein/kg body weight/day resulted in a 8.9% loss from baseline weight by the 7th day of injections. The weight loss with the use of mg protein/kg body weight/day of human OB protein in obese C57 mice resulted in a 1.1% loss from baseline weight and a dosage of 1 mg protein/kg body weight/day resulted in a 2.5% loss from baseline weight, both by the 7th day of injections.

Results Presented below are the percent differences from baseline weight in C57 mice (8 weeks old): -34- Table 2 Weight Loss Upon Subcutaneous Injection Time Vehicle (PBS) Recombinant Recombinant OB (days) Fc-OB Fusion Protein Protein 1-2 .258 1.3 -6.4 1.6 -2.1 .91 3-4 2.2 1.1 -12.1 1.5 78 .36 5-6 4.5 2 -11.5 1.5 -1.7 .6 7-8 7.0 2.1 -11.9 1.6 0.1 1.2 9-10 9.0 -11.5 1.3 7.2 2.7 11-12 10 3.8 -9 10.9 2.9 13-14 12.5 4.4 -9.5 1.6 12.3 6.4 15-16 11.1 1.0 -3.0 1.5 10.3 3.3 17-18 17.2 3.6 8.0 1.3 13.3 3.4 As can be seen, at the end of a day 17 after a 7 day subcutaneous regime at 10 mg/kg/day, animals receiving the FC-OB protein recovered to 8% of their body weight. Animals receiving dosages of 1 mg/kg/day after a 7 day subcutaneous regime returned to 6.4% of body weight after 12 days.

These studies also show that during recovery periods from day 7 to day 22, after the last injection at day 7, body weight recovery is slower in the Fc-OB treated C57 mice that with the OB treated mice. This suggests that the Fc-OB protein is not cleared as quickly as OB protein thereby causing the extended weight loss effect.

EXAMPLE 3: Dose Response of CF7 Mice Treated with Fc-OB Fusion Protein An additional study demonstrated that there was a dose response to continuous administration of Fc-OB protein. In this study, obese CF7 mice, weighing 35-40 g were administered recombinant human Fc-OB protein using methods similar to the above example. The results are set forth in Table 3, below, (with body weight lost as compared to baseline, measured as above): Table 3 Dose Response With Continuous Administration Dose Time Reduction in Body Weight 0.25 mg/kg/day Day 5 4 mg/kg/day Day 5 12 1 mg/kg/day Day 5 16 As can be seen, increasing the dose from 0.25 mg/kg/day to 1 mg/kg/day increased the weight lost from 4% to 16%. It is also noteworthy that at day 5, the 1 mg/kg/day dosage resulted in a 16% reduction in body weight. These studies also showed slow weight recovery rates to 0% suggesting that the Fc-OB protein is not quickly cleared thereby causing the extended weight loss effect.

EXAMPLE 4: Pharmacokinetics of recombinant human Fc-OB in CD-1 Mice and Dogs This study demonstrated the pharmacokinetic properties of recombinant human met Fc-OB protein in CD-1 mice and dogs. Following intravenous or subcutaneous dosing at 1 mg/kg/day, serum concentrations of recombinant human met Fc-OB protein and human met OB protein were determined by an enzyme-linked immunosorbent assay (ELISA).

In both species, an increase in exposure, as quantified by higher peak serum concentrations and larger areas under-the-serum-concentration-curve (AUC), was observed when compared to recombinant met-human OB -36protein. Fc-OB has lower systemic clearance than recombinant met-human OB protein. This is seen in the lower clearance and longer half-life of Fc-OB over OB protein. The increase in size causes not only an increase in protein stability, but also a decrease in the efficiency of renal clearance. As a result, Fc-OB is cleared slower from the systemic circulation. The increases in peak time, peak serum concentrations and AUC for Fc-OB protein are consistent with lower clearance. Fc-OB protein will yield substantially higher systemic exposure when compared to OB protein.

Results are shown in Table 4 below: Table 4 Pharmacokinetic Properties Species CD-1 Mice CD-1 Mice Beagle Dogs Route of Intravenous Subcutaneous Subcutaneous Administration OB Fc-OB OB Fc-OB OB Fc-OB protein protein protein p n rotein orotein protein Dose Level 1 1 1 1 0.5 (mg/kg) Peak Time 0.14 6 2.8 8 Peak Serum 1520 7550 300 1120 Concentration (ng/mL) AUC (ngqh/rL) 1470 366000 1230 132000 2200' 52500 Half-life 0.491 21.4 0.388 2.13 22.9 Clearance 681 2.73 (mL/h/kg) EXAMPLE This example demonstrates that in normal mice which are not obese and do not have elevated blood lipid levels, administration of human recombinant Fc-OB -37protein results in a lowering of cholesterol, glucose and triglyceride levels. In addition, this example demonstrates that these levels remain low over a three day recovery period.

Normal CD1 mice were administered recombinant human Fc-OB protein via subcutaneous injections. Blood samples were taken 24 hours after day 23, the last day of injection. As discussed above, the animals lost weight at the dosages administered. As shown in Table 5, the mice had substantial reduction of serum cholesterol, glucose and triglycerides in a dosedependent fashion when compared to controls: Table Dose Glucose Cholesterol Triglycerides PBS 232.6 15.1 67.8 3.6 52.6 3.7 1 mg/kg/day 225.8 29.1 54 5.6 43 8.7 mg/kg/day 193.2 21.4 53.4 5.7 38 11 1 mg/kg every 2 days 242.0 9.3 52.6 4.4 40.8 7.2 mg/kg every 2 197.4 27.9 51.4 5.9 29.8 6.3 days 1 mg/kg every 3 days 244.8 19.5 60.8 7.3 54 7.1 mg/kg every 3 188 31.2 52.2 6.9 26.2 10.7 days These data demonstrate that the Fc-OB protein, or analogs or derivatives thereof, are effective blood lipid lowering agents.

EXAMPLE 6: A obese human patient is administered human Fc-OB protein, or analog or derivative for the purpose of weight reduction. The obese patient also has elevated -38levels of blood lipids, including elevated levels of cholesterol, above 200 mg/100 ml. The patient attains a satisfactory weight reduction over the course of Fc-OB therapy. A maintenance dose of Fc-OB protein or analog or derivative is administered to the non-obese patient to maintain lowered blood lipid levels, including lowered cholesterol levels, below 200 mg/100 ml. The dose administered is insufficient to result in further weight loss. Administration is chronic. Levels of circulating Fc-OB protein or analog or derivative may be monitored using a diagnostic kit, such as an antibody assay against the OB protein (or other antigenic source if applicable).

EXAMPLE 7: A non-obese human patient undergoes coronary bypass surgery or other invasive treatment to alleviate advanced stages arterial plaque .formation. After the surgery, the patient is administered a maintenance dose of Fc-OB protein or analog or derivative in order to prevent the re-formation of arterial plaque. The dose administered is insufficient to result in weight loss.

Administration is chronic. Levels of circulating Fc-OB protein or analog or derivative may be monitored using a diagnostic kit, such as an antibody assay against the OB protein (or other antigenic source if applicable).

EXAMPLE 8: A non-obese human patient experiences hypertension due to restricted blood flow from clogged arteries. The patient is administered a dose of Fc-OB protein, or analog or derivative thereof sufficient to reduce arterial plaque resulting in clogged arteries.

Thereafter, the patient is monitored for further arterial plaque formation, and hypertension. If the condition re-appears, the patient is re-administered an -39effective amount of Fc-OB protein, analog or derivative sufficient to restore blood flow, yet insufficient to result in weight loss. Levels of circulating Fc-OB protein or analog or derivative may be monitored using a diagnostic kit, such as an antibody assay against the Fc-OB protein (or other antigenic source if applicable).

EXAMPLE 9: A human patient experiences gall stones.

Either the gall stones are not removed and the formation of additional gall stones is sought to be avoided, or the gall stones are removed but the gall bladder remains (as, for example, using laser or ultrasonic surgery) and the formation of additional gall stones is sought to be avoided. The patient is administered an effective amount of Fc-OB protein, analog or derivative thereof to result in prevention of accumulation of additional gall stones or re-accumulation of gall stones. Levels of circulating Fc-OB protein or analog or derivative may be monitored using a diagnostic kit, such as an antibody assay against the Fc-OB protein (or other antigenic source if applicable) EXAMPLE A diabetic human patient desires to use decreased dosages of insulin for treatment of diabetes.

The patient is administered an effective amount of Fc-OB protein, analog or derivative thereof to result in an increase in lean tissue mass. The patient's sensitivity to insulin increases, and the dosage of insulin necessary to alleviate symptoms of diabetes is decreased, either in terms of a decrease in the units of insulin needed, or in terms of a decrease in the number of injections of insulin needed per day. Levels of circulating Fc-OB protein or analog or derivative may be monitored using a diagnostic kit, such as an antibody assay against the OB protein (or other antigenic source if applicable) EXAMPLE 11: A non-obese human patient desires an increase in lean tissue mass for therapeutic purposes, such as recovery from illness which depleted lean tissue mass.

The patient is administered an effective amount of Fc-OB protein, analog or derivative thereof to result in the desired increase in lean tissue mass. Increase in lean tissue mass is monitored using DEXA scanning. Levels of circulating Fc-OB protein or analog or derivative may be monitored using a diagnostic kit, such as an antibody assay against the OB protein (or other antigenic source if applicable).

MATERIALS AND METHODS Animals. Wild type CDl mice and C57B16 mice were used for the above examples. The age of the mice at the initial time point was 8 weeks, and the animals were weight stabilized.

Feeding and Weight Measurement. Mice were given ground rodent chow (PMI Feeds, Inc.) in powdered food feeders (Allentown Caging and Equipment) which allowed a more accurate and sensitive measurement than use of regular block chow. Weight was measured at the same time each day (2:00 for the desired period.

Body weight on the day prior to the injection was defined as baseline weight. The mice used weighed 18-22 grams.

Housing. Mice were single-housed, and maintained under humane conditions.

-41- Administration of Protein or Vehicle. Protein (as described below) or vehicle (phosphate buffered saline, pH 7.4) were administered by subcutaneous injections or intravenously.

Controls. Control animals were those who were injected with the vehicle alone without either Fc-OB fusion protein or OB protein added to the vehicle.

Protein. Sequence ID. Nos. 1, 2 and 3 set forth murine recombinant OB DNA and protein (Figure 1), and Sequence ID. Nos. 4, 5 and 6 set forth an analog recombinant human OB DNA and protein (Figure As noted above recombinant human OB protein as in SEQ. ID.. NO. 6 has a lysine residue at position 35 and an isoleucine residue at position 74. Furthermore, the recombinant human protein set forth in Zhang et al., Nature, supra, and PCT publication WO 96/05309 (12/22/96) (both incorporated by reference including figures), and the murine and human analog recombinant proteins of Figures 1 and 2 are illustrative of the OB protein which may be used in forming the Fc-OB fusion protein of the present methods of treatment and manufacture of a medicament. Other OB or Fc proteins or analogs or derivatives thereof may also be used to form the Fc-OB fusion protein.

Herein, the first amino acid of the amino acid sequence for recombinant OB protein is referred to as and is valine, and the amino acid at position -1 is methionine. The C-terminal amino acid is number 146 (cysteine) (see Figures 1 and The first amino acid sequence for recombinant human Fc-OB protein of Figure 3 is referred to as and is glutamate, and the amino acid at position -1 is methionine. The C-terminal amino acid is number 378 (cysteine). The first amino acid sequence for the recombinant human Fc-OB protein variant -42of Figure 4 is referred to as and is glutamate, and the amino acid at position -1 is methionine. The C-terminal amino acid is number 378 (cysteine). The first amino acid sequence for the recombinant human Fc-OB protein variant of Figure 5 is referred to as +1, and is aspartic acid, and the amino acid at position -1 is methionine. The C-terminal amino acid is number 373 (cysteine). The first amino acid sequence for the recombinant human Fc-OB protein variant of Figure 6 is referred to as and is aspartic acid, and the amino acid at position -1 is methionine. The C-terminal amino acid is number is 373 (cysteine).

Expression Vector and Host Strain The plasmid expression vector used is pAMG21 (ATCC accession number 98113), which is a derivative of pCFM1656 (ATCC accession number 69576) and contains appropriate restriction sites for insertion of genes downstream from the lux PR promoter (see US Patent No.

5,169,318 for a description of the lux expression system). The Fc-OB DNA, described below and shown in Figures 3-6, was created and ligated into the expression vector pAMG21 linearized with restriction endonucleases NdeI and BamHI and transformed into the E. coli host strain, FM5. E. coli FM5 cells were derived at Amgen Inc., Thousand Oaks, CA from Z. coli K-12 strain (Bachmann, et al., Bacterial. Rev. 40: 116-167 (1976)) and contain the integrated lambda phage repressor gene, ci857 (Sussman et al., C. R. Acad. Sci. 254: 1517-1579 (1962)). Vector production, cell transformation, and colony selection were performed by standard methods, Sambrook, et al., Molecular Cloning: A Laboratory Manual, 2d Edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.) Host cells were grown in LB media.

~I

-43- Fc-OB DNA Construction The plasmid pFc-A3 (described below) served as the source of sequence for human immunoglobulin IgGheavy chain from amino acid number 99 (Glu) to the natural carboxyl terminus. The human IgG-1 sequence can be obtained from Genebank (P01857).

The human OB sequence is disclosed above as well as Zhang et al., Nature, supra, and PCT publication WO 96/05309 both incorporated by reference including drawings. The OB DNA was ligated into the expression vector pCFM1656 linearized with restriction endonucleases XbaI and BamHI using standard cloning procedures, Sambrook, et al., Molecular Cloning: A Laboratory Manual, 2d Edition, Cold Spring Harbor Laboratory Press, Cold Spting Harbor, The plasmid pCFMi656 carrying the OB DNA sequence served as the source of sequence for the recombinant human OB gene.

The genetic fusing of these two sequences was carried out by the method of PCR overlap extension (Ho, et al., Site Directed Mutagenesis By Overlap Extension Using The Polymerase Chain Reaction, Gene 77:51-59(1989)). The product of the PCR was cleaved with restriction endonuclease NdeI to create a end and with restriction endonuclease BamHI to create a 3'-cohesive terminus. The vector, pAMG21, was similarly cleaved. A ligation was performed with the fusion fragment and the linearized vector. Ligated DNA was transformed by electroporation into the E. coli host strain. Clones surviving on kanamycin selection agar plates were checked for expression of Fc-OB-sized protein. Plasmid from individual clones was isolated and the sequence of the gene coding region verified.

When additional modifications of the Fc-OB gene were desired, the PCR technique was used again to engineer the changes. Two sets of changes were- -44performed at the N-terminus of the Fc portion of the fusion protein (SEQ. ID. No. 9) to create the variants SEQ. ID. NOS. 12 and 15. Another variant was constructed to introduce four amino acid substitutions to ablate the Fc-receptor binding site (leucine at position 15 substituted with glutamate), and the complement (Clq) binding site (glutamate at position 98 substituted with alanine, lysine at position 100 substituted with alanine, and lysine at position 102 substituted with alanine (See, Xin Xiao Zheng et. al, J.

Immunol. 154: 5 5 9 0 5 6 0 0 (1995)). The template for this construct was Seq. ID. No. 15 and the resulting variant was SEQ. ID. Nos. 18.

DFC-A3 Vector Construction A plasmid, pFc-A3, containing the region encoding the Fc portion of human immunoglobulin IgG-1 heavy chain (See Ellison, J. W. et. al, Nucleic Acids Res. 10:4071-4079 (1982)), from the first amino acid Glu-99 of the hinge domain to the carboxyl terminus plus a 5'-NotI fusion site and 3'-SalI and XbaI sites, was made by PCR amplification of the human spleen cDNA library. PCR reactions were in a final volume of 100 ml and employed 2 units of Vent DNA polymerase in 20 mM Tris-HCl (pH 10 mM KC1, 10 mM (NH4)2SO 4 2 mM MgSO4, 0.1% Triton X-100 with 400 mM each dNTP and 1 ng of the cDNA library to be amplified together with 1 uM of each primer. Reactions were initiated by denaturation at 95 OC for 2 min, followed by 30 cycles of 95 OC for 30 s, 55 Oc for 30 s, and 73 OC for 2 min. The primer incorporated a NotI site immediately 5' to the first residue (Glu-99) of the hinge domain of IgG-l.

The 3'-primer incorporated SalI and Xbal sites. The 717 base pair PCR product was digested with NotI and Sail, the resulting DNA fragment was isolated by electrophoresis through 1% agarose and purified'and cloned into NotI, Sall-digested pBluescript II KS vector (Stratagene). The insert in the resulting plasmid, pFc-A3, was sequenced to confirm the fidelity of the PCR reaction.

Methods for Production The methods below for production have been used to produce biologically active recombinant methionyl murine or human analog OB protein and Fc-OB fusion proteins. Similar methods may be used to prepare biologically active methionyl human OB protein.

Fermentation Process A batch fermentation process was used. Media compositions are set forth below.

A portion of the media consisting of primarily nitrogen sources was sterilized (by raising temperature to 120-123 0 C for 25-35 minutes) in the fermentation vessel. Upon cooling, carbon, magnesium, phosphate, and trace metal sources were added aseptically. An overnight culture of the above recombinant murine protein-producing bacteria of 500 mL (grown in LB broth) was added to the fermentor. When the culture optical density (measured at 600 nm as an indicator for cell density) reached 15-25 absorption units, an autoinducer solution (0.5 mg/mL homoserine lactone) was added (1 mL/L) to the culture to induce the recombinant gene expression. The fermentation process was allowed to continue for additional 10 to 16 hours, followed by harvesting the broth by centrifugation.

-46- Media Composition: Batch: 34 g/L Yeast extract 78 g/L Soy peptone 0.9 g/L Potassium chloride 5.0 g/L Hexaphos 1.7 g/L Citric acid 120 g/L Glycerol g/L MgSO4-7H20 0.2 mL/L Trace Metal Solution 0.5 mL/L P2000 Antifoam Trace Metal Solution: Ferric Chloride (FeC13-6H20): 27 g/L Zinc Chloride (ZnC12-4H20): 2 g/L Cobalt Chloride (CoC12-6H20): 2 g/L Sodium Molybdate (NaMo04-2H20): 2 g/L Calcium Chloride (CaCl2-2H20): 1 g/L Cupric Sulfate (CuSO4-5H20): 1.9 g/L Boric Acid (H3B03): 0.5 g/L Manganese Chloride (MnC12-4H20): 1.6 g/L Sodium Citrate dihydrate: 73.5 g/L Purification Process for Human Fc-OB Fusion Protein Purification for human Fc-OB fusion protein was accomplished by the steps below (unless otherwise noted, the following steps were performed at 4'C).

Purification for murine and human OB protein is disclosed in PCT publication WO 96/05309, supra, herein incorporated by reference.

1. Cell paste. E. coli cell paste was suspended in 5 times volumes of distilled water. The cells in the water were further broken by two passes -47through a microfluidizer. The broken cells were centrifuged at 4.2k rpm for 1 hour in a Beckman JB-6 centrifuge with a J5-4.2 rotor.

2. Inclusion body wash. The supernatant from above was removed and the pellet was resuspended with five volumes of distilled water. The mixture was centrifuged as in step 1.

3. Solubilization. The pellet was solubilized with 10 volumes of 50 mM tris, pH 8.5, 8 M guanidine hydrochloride, 10 mM dithiothreitol and stirred for one hour at room temperature. The solution is made 40 mM cystamine dihydrochloride and stirred for one hour.

4. The solution from step 3 is added to 20 to volumes of the following refold solution: 50 mM tris, pH 8.5, 0.8 M arginine, 2 M urea, and 4 mM cysteine. The refold is stirred for 16 hours at 8°C.

Buffer exchange. The solution from step 4 is concentrated and diafiltered into 10 mM tris, pH 6. Acid precipitation. The solution from step 5 is adjusted to pH 4.75 with 50% glacial acid and incubated for 30 minutes at room temperature. The solution is filtered.

7. Cation exchange chromatography. The solution from step 6 is adjusted to pH 7.0 and loaded onto a CM Sepharose Fast Flow column at 10'C. A twenty column volume gradient is done at 10 mM phosphate, pH 0 to 0.1 M NaCl.

8. Anion exchange chromatography. The CM elution pool from step 7 is diluted 5 fold with 5 mM tris, pH 7.5 and loaded onto a Q Sepharose Fast Flow at A 20 column volume gradient is done at 10 mM tris, pH 7.5, 0 to 0.2M NaCl.

9. Hydrophobic interaction chromatography. The Q sepharose pool is made 0.75M ammonium sulfate and loaded on a methyl Macroprep hydrophobic interaction 00 Column at room temperature. At 20 column volume gradient is done at mM Phosphate, pH 7.0, 0.75M to OM ammonium sulphate.

Buffer exchange. The pool from step 9 is concentrated as necessary and dialyzed against PBS buffer.

00oo While the present invention has been described in terms of ,I preferred embodiments, it is understood that variations and modifications will occur to those skilled in the art. Therefore, it is intended that the appended claims cover all such equivalent variations which come within the scope of the invention as claimed.

Throughout this specification, unless the context requires otherwise, the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers.

The discussion of the background art is included exclusively for the purpose of providing a context for the present invention. It should be appreciated that the discussion is not an acknowledgement or admission that any of the material referred to was common general knowledge in the field relevant to the present invention in Australia or elsewhere before the priority date.

49 SEQUENCE LISTING GENERAL

INFORMATION:

APPLICANT: Mann, Michael

B.

Hecht, Randy I.

(ii) TITLE OF INVENTION: OB FUSION PROTEIN COMPOSITIONS

AND

METHODS

(iii) NUMBER OF SEQUENCES: 18 (iv) CORRESPONDENCE

ADDRESS:

ADDRESSEE: Amgen Inc.

STREET: 1840 DeHavilland Drive CITY: Thousand Oaks STATE: CA COUNTRY: USA ZIP: 91320-1789 COMPUTER READABLE

FORM:

MEDIUM TYPE: Floppy disk COMPUTER: IBM PC compatible OPERATING SYSTEM:

PC-DOS/MS-DOS

SOFTWARE: PatentIn Release Version #1.30 (vi) CURRENT APPLICATION

DATA:

APPLICATION NUMBER: US 08/770,973 FILING DATE: 20-DEC-1996

CLASSIFICATION:

(viii) ATTORNEY/AGENT

INFORMATION:

NAME: Knight, Matthew

W.

REGISTRATION NUMBER: 36,846 REFERENCE/DOCKET NUMBER: A-416 INFORMATION FOR SEQ ID NO:l: SEQUENCE

CHARACTERISTICS:

LENGTH: 491 base pairs TYPE: nucleic acid STRANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (ix) FEATURE: NAME/KEY: misc_feature LOCATION: 41 OTHER INFORMATION: /note= "Met ATG" 50 (xi) SEQUENCE DESCRIPTION: SEQ IID NO:1: TCTAGATTTO AGTTTTA.ACT TTTAGA-AGGA GGAATAACAT TCAGGACGAC ACCAAAACCT TAATTAAAAC OATCOTTACG CACCCAGTCG GTCTCCGCTA AACAGCGTGT TACCGGTCTG CCCGATCCTA AC-CTTGTCCA AAATGGACCA GACCCTGGCT CTCCCTGCCG TCCCAGAACG TTCTTCAGAT CGCTA.ACGAC GCTGCACCTG CTGGCATTCT CCAAATCCTO CTCCCTGCCG ACCGGAATCC CTGGACGGCG TCCTGGAAGC ATCCCTC-TAC GTCCCGTCTG CAGGGTTCCC TTCAGGACA? CCTTCAGCAG TTAATGGATC C INFORMATION FOR SEQ ID NO:2: SEQUENCE CHARACTERISTICS: LENGTH: 491 base pairs TYPE: nuclei-c acid STRANDEDNESS: double TOPOLOGY: linear (ii) MO--ECULE TYPE: cDNA (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2: AGATCTIAAAC T-CAAAATTGA AAATCTTCCT CCTTATTGTA AGTCCTGCTG :GGTTTTGGA ATTAATTTTG CTAGCAATOC GTGGGTCAGC CAGAGOCOAT TTGTCGCACA ATOOCCAGAC GGGCTAGGAT :CGAACAGGT TTTACCTGGT CTGGGACCGA GAGGGACGGC AGGGTCTTGC AAGAAGTCTA OCCATTGCTO CGACGTGGAC GACCGTAAGA GGTTTAGGAC GAGGOACGOC TGGCCTTAGG GACCTGCCCC AGGACCTTCG TAGGOACATO CAGGGCAGAC GTCCCAGOG AAGTCCTGTA. OGAAOTCGTC AATTACCTAG G AT GGTAC CGA

CGTATCAACO

GACTTCATCC

CTATACCAGC

CTCGAGAACC

CAGACCTCAG

AGCACCGAA-

C TGGAC-T T

TACCATGGCT

CCATAGTTOC

CTGAAGTAGG

C AT ATGGTC C

GA-CTCTTGG

GTCTGGAGTC

TCGTGGCTTC

GACCTGCAA

TCCAGAAAGT

ACATCAGTCA

CGGGTCTGCA

AGGTGTTA.AC

TTCOCGACCT

GTCTTCAGA.A

TTGTTGCTCT

CTCCGGAATG

AGGTCTTTCA

TOTAGTCAGT

GCCCAGACGT

TCCACAATTG

AAGCGCTGGA

CAGAAGTCTT

AACAACGAGA

GAGGCCTTAC

120 180 240 300 360 420 480 491 120 180 240 300 360 420 480 491 51 INFORMATION FOR SEQ ID NO: 3 SEQUENCE CHARACTERISTICS: LENGTH: 1147 amino acids TYPE: amino acid STRANDEIDNESS: unknown TOPOLOGY: unknown (ii) MOLECULE TYPE: protein (ix) FEATURE: NAME/KEY: Protein LOCATION: 2.

OTHER INFORMATION: /note= "Met (xi) SEQUENCE DESCRIPTION: SEQ ID NO:>: Met Val Pro le Gin Lys Val Gin Asp Asp (ATO) starts at -11" 1 Th r Ala Ile Val L-,eu Cys Gly Ile Lys Leu Leu Oiu Ser Val2 Arg Val Ser Leu Arg Gin Ala Asn G'-y Met 55 Ser Zeu Ser Lau Asp Leu Asp Gin Leu Giy T yr 120 lie Asp G 1 r Asn his Leu 105 Ser Lys Thnr Pro Ala Gin A I a Pro Val

CGI

G lv Val ?he Val2 125 L'vs Ser Pro Gin Asp Ser Asp Ser Arg Leu Gin Giy Ser Leu Gin Asp Ile Leu Gin Gin Leu Asp Vai Ser 2.30 135 140 Pro Giu Cys 1.45 52 INFORMATION FOR SEQ ID NO:4: Ci) SEQUENCE CHARACTERISTICS: LENGTH: 454 base pairs TYPE: nucleic acid STRANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (ix) FEATURE: NAME/KEY: miscfeature LOCATION: 4 OTHER INFORMATION: /note= "Met ATG" Cxi) SEQUENCE DESCRIPTION: SEQ ID NO:4: CATATGGTAC CGATCCAGAA AGTTCAGGAC GACACCAAAA ACGCGTATCA ACGACATCAG TCACACCCAG TCGGTGAGCT CTGGACTTCA TCCCGGGTCT GCACCCGATC CTGACCTTT GCTGTATACC AGCAGATCTT AACCTCCATG CCGTCCCGTA GACCTCGAGA ACCTTCGCGA CCTGCTGCAC GTGCTGGCAT CCATGGGCTT CAGGTCTTGA GACTCTGGAC TCTCTGGGCG TACACCACCG AAGTTGTTGC TCTOTCCCGT CTGCAGGGTT CAGCTGGACC TGTCTCCGGG TTGTTAATGG ATCC INFORMATION FOR SEQ ID i) SEQUENCE CHARACTERISTICS: CA) LENGTH: 454 base pairs TYPE: nucleic acid STRANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA CCTTAATTAA AACGATCGTT CCAAACAGCG TGTTACAGGC CCAAAATGGA CCAGACCCTG ACGTTCTTCA GATCTCTAAC TCTCCAAA7C CGCCACCTG GGGTCCTGGA AGCATCCGGT CCCTTCAGGA CATGCTTTGG (xi) SEQUENCE DESCRIPTION: SEQ ID OTATACCATG OCTAGGTCTT TCAAGTCCTC CTGTGGTTTT OGAATTAATT T'GCTAGCAA TGCGCATAGT TGCTGTAGTC AGTGTGGGTC AGCCACTCGA GATTTGTCGC ACAATGTCCG 53J GACCTGAAGT AGGGCCCAGA CGTGGGCTAG CGACATATGG TCGTCTAGAA TTGGAGGTAC CTGGAGCTCT TGGAAGCGCT GGACGACGTG GGTACCCGAA GTCCAGAACT CTGAGACCTG ATGTCGTGGC TTCAACAACG AGACAGGOCA GTCGACCTGG ACAGAGGCCC AACAATTACC INFORMATION FOR SEQ ID NO:6: SEQUENCE CHARACTERISTICS LENGTH: 147 amino a TYPE: amino acid STRANDEDNESS: ur.knc TOPOLOGY: unknown (ii) MOLECULE TYPE: protein GACTGGAACA GGTTTTACCT GGTCTGGGAC GOCAGGOCAT TGCAAGAAGT CTAGAGATTG CACGACCGTA AGAGGTTTAG GACGGTGGAC AGAGACCCGC CCCAGGACCT TCGTAGGCCA GACGTCCCA.A GGGAAGTCCT GTACGAAACC

TAGG

180 240 300 360 420 454 (ix) FEATURE: NAME/KEY: Protein LOCATION: 1 OTHER INFOPJ'LATION: /note= "Met (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6: (ATG) starts at -1"1 Met Val Pro Ilie Gin Lys Val Gin Asp Asp Thr Lys Thr Leu 1.

Thr S er lie Lys Ile Val Thr Lys CGin Arg 7!e Asn Asp 71 e 25 Asp His Thr Gin Val Thr Gly Phe Ile Pro Ser Vai Ser Leu His Pro Tyr Gin Gin Ile Leu Thr Leu Ser Lys Gin Thr Leu Ile Leu Aia Gin Thar Ser Met Leu Pro Asp Arg Asn Val Ile Ser Asn Giu Asn Leu Leu Leu His Ala Phe Ser Lys Cys His Leu Pro 1.00 Trp Ala Ser Giy Leu 105 Giu Thr Leu Asp Ser Leu Gly 110 54 Gly Val Leu Glu Ala Ser Gly Tyr Ser Thr Glu Val Val Ala Leu Ser 115 120 125 Arg Leu Gin Gly Ser Leu Gin Asp Met Leu Trip G1r, Leu Asp Leu Ser 130 135 140 Pro Gly Cys 145 INFORMATION FOR SEQ 1D NO:7: SEQUENCE CHARACTERISTICS: LENGTH: 1150 base pairs TYPE: nucleic acid STRANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (ix) FEATURE: NAME/KEY: misc-Feature LOCATION: 4 OTHER INFORMATION: /note= 'Met =ATG" (xi) SEQUENCE DESCRIPTION: SEQ ID NO:'> CATATGGAAC CCAAATCTTG TGACAAAACT CACACATGCC

CTCCTGGGGG

TCCCGGACCC

AAGTTCAACT

GAGCAGTACA

CTGAATGGCA

AAAACCATCT

TCCCGGGATG

CCCAGCGACA

ACGCCTCCCG

A.AGAGCAGGT

AACCACTACA

GACCGTCAGT

CTGAGGTCAC

GGTACGTGGA

ACAGCACGTA

AGGAGTACAA

CCAAAGCCAA

AGCTGACCAA

TCGCCGTGGA

TGCTGGACTC

GGCAGCAGGG

C GCAGAAGAG

CTTCCTCTTC

ATGCGTGGTG

CGGCGTGGAG

CCGTGTGGTC

GTGCAAGGTC

AGGGCAGCCC

GAACCAGGTC

GTGGGAGAGC

CGACGGCTCC

GAACGTCTTC

CCTCTCCCTG

CCCCCAAAAC

GTGGACGTGA

GTGCATAATZG

AGCGTCCTCA

TCCAACA-AAG

CGAGAACCAC

AGCCTGACCT

ALATGGGCAGC

TTCTTCCTCT

TCATGC TOC C

TCTCCGGGTA

C AC CGT0CCC C CAAGGAC AC

GCCACGA.AGA

CCA.AGAC?-A

CCGTCC:GCA

CCCTCCCAGC

AGGTOTACAC

CCTGGTCA.A

CGGAGAACA-2

ACAGCAAGCT

TGATGCATCA

AAGTACCGAT

AGCACCTCA.A

CCTCATGATC

CCCTCAGGTC

GCCCCGGCAG

CCAGGACTGG

CCCCATCGAG

CCTGCCCCCA

AGGCTTCTAT

CTACAAGACC

CACCGTGGAC

GGCTCTGCAC

CCAGAAAGTT

55 CAGGACCACA CCAAAACCTT AATTAAAACC ATOOTTACOC ACCCAGTCGG TGAGCTCTAA ACAGAAACTT ACAGCCCTGG CCGATCCTGA CCTTCTCCA.A A.ATGCACCAC- ACCCTGGCTC TCCATGCCCT CCCGTAACGT TATCCACATC TCTA-ACGACC CTGCACGTGC TGGCATTCTC CAAATCC:C-C CACCTGCCAT CTGGACTCTC TGGGCGGGGT CCTGGAAGCA TCCGGTTACA TCCCGTCTGC AGGGTTCCCT TCAGGACATC CTTTGGCAGC

TAATGGATCC

INFORM-ATION FOR SEQ ID NO: Ci) SEQUENCE CHARACTERISTICS: LENGTH: 1150 base pairs TYPE: nucleic acid STRLANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA

GT'ATCAACGA

AC TTC ATCC C

TATACCACCA

TCGAGAACCT

CCCCTTCACC

GCAC CGA-ACT TGGAC CTCT C

CATCACTCAC

GGCTCTCCAC

GATCTTA.ACC

TCC ACC TO

TTCACACT

TC-TTCCTCTC

TCCCGGTT-T

780 840 S900 960 1020 1080 1140 1150 (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8: GTATACCTTG GGTTTAGAAC ACTGTTTTCA CTCTGTACGG

GAGGACCCCC

AGGGCCTGGG

TTCA.AGTTGA

CT CGTC AT CT

CACTTACCGT

TTTTGGTAGA,

AGGGCCCTAC

GGGTCGCTCT

TGCGGAGGGC

TTCTCGTCCA

TTGGTGATCT

CT-GGCAGTCA

GACTCCACTC

CCATGCACCT

TGTCGTGCAT

TCCTCATCTT

GG-ITTCGCTT

TCGACTGGTT

AGCGGCACCT

ACGACCTGAC

CC CT CGTCC C

GCTCTTCTC

GAAGGAGAAG

TACGCACCAC

GCCGCAC CTC

GOCACACCAG

C AC GTTCC AG

TCCCGTCGCC

CTTGGTCCAG

CACCCTCTCC

GCTGCCGAGC

CTTGCAGAAG

OGACAGGGAC

GGGGCTTTTC

C ACC TCACT

CACOTATTAC

TCCCAGGAGT

ACGTTGTTTC

GCTCTTGGTG

TCGGACTGGA

TTACCCGTCG

AAGAAGGAGA

AGTACGAGCC

AGAGGCCCAT

GTGOCACCOC

GGCTTCCTCTG

CC CTGCTTCT-

GCTTCTGTT±

COCAGGACGOT

GGGAGGGTCC

TCCACATCTG

CCGACCACTT

GCCTCTTGTT

TCTCCTTCCA

AC TAOOTACT

TTCATGCCTA

TCCTCCACTT

GGACTACTAG

COCACTCCAC

CGCCCCCTC

CCTCCTCACC

CCCGTACCTC

CCACCGCCGT

TC CGAACATA

CATOTTOTOG

CTCCCACCTG

CCACACGTO

CCT C TTTC AA 120 180 240 300 360 420 480 540 600 660 720 56 GTCCTGCTGT GGTTTTGGAA TTAATTTT-C TAGCAATGCG TGGGTCAGCC ACTCGAGATT TGTCTTTCAA TGTCCGOACC GGCTAGGACT OGA.ACAGGTT TTACCTGGTC TGACCOAC AGGTACGGCA GGGCATTGCA ATAGGTCTA- AGATTGCTGG GACGTGCACG ACCGTA.AGAG GT--AGC-ACO GTGGACGGTA GACCTGAGAG ACCCGCCCCA GGACCTTCGT AGGCCAATGT AGGGCAGACO TCCCAAGGGA AGTCCTGTAC GAAACCGTCG

ATTACCTAGG

INFOPR4ATTON FOR SEQ -D NO:9: SEQUENCE CHARAC:ERIS?:CS: LENGTH: 379 amino acids TYPE: amino acic4 STRANDEDNESS: unknown TOPOLOGY: unknown (ii) MOLECULE TYPE: protein

CATAGTTOCT

TGAAGTAGCGG

ATATGGTCOT

AGCTCTTGGA

CCCGAAGTCC

CC-TOCCTTCA

AC CTGGAC AG

C-TAGTCAGTG

CCCAGACGTG

CTAGAATTGG

AGCGCTGGAC

AGAACTC'-GA

ACAACGAGAC

AGGCCCALACA

780 840 900 960 102C 1080 1140 1150 (ix) FEATURE: NAME/KEY: Protein LOCATION: I OTHER INFOPY!,ATION: /note= I'met (ATO) starts at (xi) SEQUENCE DESCR-::IO:J.: SEQ 1D NO:9: Met 0Th Pro Lys Ser Cvs Aso Lys Thr Hi's 1 510 Ala Pro Glu Leu Leu Gly Gly Pro Ser Val 25 Pro Lys Asp Thr Leu Met Ilie Ser Arg Thr 40 Val Val AspD Val Ser '-is Glu Asp Pro Glu 55 Val Asp Gly Val Giu Val His Asr Ala Lys 70 Thr Cys Pro Pro Cys Pro Phe Leu Phe Pro Pro Lys pro Glu Val Thr Cys Val Val Lys Phe Asn Trp Tyr Thr Lys Pro Arg Glu GTh 75 57 Gin Tyr Asn Ser Thr Tyr Arg Gin Ala Pro Thr 145 Ser Tyr Tyr Phe Lys 225 Asp Ile Asp Gin Asn 305 His Leu Ser Aso Trp Leu Pro 115 Arg Glu 130 Lys Asn Asp Ile Lys Thr Ser Lys 195 Ser Cys 210 Ser Leu Asp Thr Set :-is Phe Ile 275 Thr Leu 290 Val Ie Val Leu Gliu Thr Thr Glu 355 Leu 100 Ala Pro Gin Ala Thr 180 Leu Ser Ser Lys Thr 260 Pro Ala Gin Ala Leu 340 Va1 Asn Pro Gin Va1 Val 165 Pro Va1 Leu Thr 245 G-In Gly Va I lie Phe 325 Asp Val Gly ILe Va1 Set 150 Glu Pro Val Met Ser 230 Leu Ser Leu Tyr Ser 310 Set Ser Ala Ls Glu Tyr 135 Leu Trp Val Asp His 215 Pro Ile Val Gin 295 Asn Lvs Leu Leu Val Glu Lys 120 Thr Thr Glu eu Lys 200 Glu Gly Lys Set Pro 280 Gin Asp Set Gly Ser 360 Val Ser 90 Tyr Lys 105 Thr Ile Leu Pro Cys Leu Set Asn 170 Asp Ser 185 Ser Arg Ala Leu Lys Val Thr Ile 250 Ser Lys 265 Ile Leu Ile Leu Leu G1u Cys His 330 Gly Val 345 Arg Leu Val Leu Thr Val Leu His Cys Ser Pro Val 155 Glv Aso Tro His Pro 235 Val Thr Asn 315 Leu Leu Gin Lys Lys Set 140 Lys Gin Gly Gin Asn 220 Ile Thr Lys Leu Set 300 Leu Pro Giu Gly Val Ala 125 Arg Gly Pro Ser Gin 205 His G in Arg Va1 Ser 285 Met Arg Trp Ala Set 365 Set 110 Lys Asp Phe Glu Phe 190 Gly Tyr Lys Lie Thr 270 Lys Pro Asp Ala Ser 350 Leu Asn Gly G~lu Tyr Asn 175 Phe Asn Thr Val Asn 255 Gly Met Ser Leu Set 335 Gly Gin Lvs Gin Leu Pro 160 Asn Leu Val Gin Gin 240 Asp Leu Asp Arg Leu 320 Gly Tyr Asp 58 Met Leu Trp Gin Leu Asp Leu Ser Pro Gly Cys 370 375 INFORM4ATION FOR SEQ ID NO:lO: SEQUENCE CHARACTERISTICS: LENGTH: 1150 base pairs TYPE: nucleic acid STRANIDEDNESS:- double TOPOLOGY: linear (ii) MOLECULE TYPE: cONA (ix) FEATURE: NAME/KEY: misc-feature LOCATION: 4 OTHER INFORMATION: /note= "Met: ATG" (xiJ) SEQUENCE IDESCRIP-1TIO: SEQ ID CATATGGAAC CAAkTCTGC TCACAAAACT CACACATGTC CACCTTCTCC AGCTCCGGAA

CTCCTGGGCG

TCCCGGACCC

AAGTTCAACT

GAGCACTACA

CTGAATGGCCA

AAAACCATCT

TCCCGGGATG

CCCAGCGACA

ACGCCTCCCG

AAGAGCAGGT

AACCACTACA

CAGGACOACA

ACCCAGTCGG

CCGATCCTGA

GTCCTTCAGT

CTCAGGTCAC

CGTACGTGGA

ACACCACGTA

AGGAGTACA.A

C CAAAGCCAA

AGCTGACCAA

TCGCCGTGGA

TGCTGGACTC

GGCAGCAGGG

CGCAGA.AGAC

C CAAAAC CTT

TGAGCTCTA.A

CCTTGTCCA-A

CTTCCTCTTC

ATCCGTGGTG

CG CCGTCCAC

CCGTCTGGTC

CTGCAAGCTC

ACGGCAGCCC

GA.ACCAGGTC

GTGGGAGAGC

CGACGGCTCC

CA.ACGTCTTC

CC TCTC C C T

AATTA.AAACG

ACAGAAAGTT

X-ATGGACCAG

C CC CCAAAA C

GTGGACGTGA

GTGCATA.ATC

AGCGTCCTCA

TCCAACA-AAG

CCACAACCAC

AGCCTGACCT

AATGGGCAGC

TTCTTCCTCT

TCATGCTCCC

TCTCCGGCTA

AT CCTTACC

ACAGCCCTGC

ACCCTGGCTC

CCAAGGACAC

GCCACCAAGA

CCA.ACACAAA

C C TC OTOC A C C C-CCCAGC AG CT-A C AC

CCTCCTCA-A

CGCAGAACAA

ACAGCAAGCT

TCATCCATOA

AAGTACC CAT

CTATCAACGA

ACTTCATCCC

TATACCAGCA

CCTCATGATC

CCCTGAGGTC

CCC OCAC

CCAGGACTCC

CCCCATCGAG

CTCCCC CA

ACGCTTCTAT

CTACAAGACC

CACCGTCGAC

GGCTCTOCAC

CCAGAAAGTT

CATCAGTCAC

GCGTCTGCAC

GATCTTAACC

120 180 240 300 360 420 480 540 600 660 720 780 840 900 59 TCCATGCCGT CCCGTAACGT TATCCAGATC CTGCACGTGC TGGCATTCTC CAAATCCTGC CTGGACTCTC TGGGCGGGGT CCTGGAAGCA TCCCGTCTGC AGGGTTCCCT TCAGGACATC-

TAATGGATCC

INFORMATION FOR SEQ ID NO:11: SEQUENCE CHARACTERISTICS LENGTH: 1150 base p TYPE: nucleic acid STRANDEDNESS: doubi TOPOLOGY: linear (ii) MOLEC UTE TYPE: cDNA TCTAACGACC TCOAGAACCT TCOCGACCTG CACCTOCCAT GOCCTTCAGG TCTTOAOACT TCCOOTTACA GCACCGAAGT TGTTGc--cTO CTTTGGCAGC TOGACCTGTC TCCOG:7TOT 960 1020 1080 1140 1150 (xi) SEQUENCE DESCRIPTION: SEQ ID NO:ll: OTATACCTTO OTTTTAOACO ACTGTTTTOA GTOTGTACAG GOAACAOG TCGAOGCCTT GAGGACC CCC

AGGGCCTGG

TTCALAGTTGA

CTCGTCATGT

GACTTACCGT

TTTTGGTAGA

AGGGCCCTAC

GGGTCGCTGT

TGCGGAGGGC

TTCTCGTCCA

TTGGTGATGT

GTCCTGCTGT

TGGGTCAGCC

CAGGAAGTCA

OACTCCAGTO

CCATGCACCT

TOTCGTGCAT

TCCTCATGTT

GGTTTCGGTT

TCGACTGGTT

AGCGGCACCT

ACGACCTGAG

CC GTC GTCC C

GCGTCTTCTC

GGTTTTGGA.A

ACTCGAGATT

GA.AGOAGAAG

TACGCACCAC

GCCGCACCTC

GGCACACCAG

CACOTTCCAG

TCCCGTCG

CTTOGTCCAG

CACCCTCTCG

GCTOCCGAGG

.CTTGCAGXAG

GGAGAGGGAC

TTAATTTTGC

TGTCTTTCAA

GGOTTTTG

CACCTOCACT

CACGTATTAC

TCGCAOC-AGT

AGGTTOTTTC

GCTCTTOGTO

TCOGACTGGA

TTACCCGTCG

A.AGAAG GAG A

AGTACGAGGC

AGAGGCCCAT

TAGCA.ATGCG

TGTCCGGACC

GGTTCCTGTG

CGGTGCTTCT

GGTTC-TGTTT

GGCAGGACOT

GGGAGGGTCG

TCCACATGTO

CGGACCAGTT

GCCTCTTGTT

TGTCGTTCGA

ACTACGTACT

TTCATGGCTA

CATAGTTGCT

TGAAGTAGGG

GGAG-%C TAG

GOAC:-CCAG

CGGCOCCCTC

GGTCCT'CACC

GGGGTAGCTC

GGACGGGGGT

TCCGA.AGATA

GATGTTCTGG,

GTGGCACCTG

CCGAGACGTG

GGTCTTTCALA

GTAGTCAGTG

CCCAGACGTG

60 GGCTAGGACT OOAACAGOTT TTACCTOGTC AGGTACGGCA OGGCATTGCA ATAGGTCTAG GACGTGCACG ACCGTX.AGAG GTTTAOGACG GACCTGAGAG ACCCGCCCCA GGACCTTCGT AGGGCAGACG TCCCAAGGGA AGTCCTOTAC

ATTACCTAG

INFORMATION FOR SEQ ID NO:12: SEQUENCE CHARACTERISTICS LENGTH: 379 amino a TYPE: amino acid STRANDEDNESS: unkno TOPOLOG*Y* flkown (ii) MOLECULE TYPE: protein TGOGACOGAC ATATOOTCOT CTAGAATTGG AGATTOCTOG AOCTCTTOOA ACOCTOGAC GTOGACGOTA CCCGAAGTCC AGAACTCTGA AGGCCAATGT CGTOOCTTCA ACAACGAGAC OAAACCGTCG ACCTGGACAO AGGCCCAACA 900 960 1020 1080 1140 1150 (ix) FEATURE: NAME/KEY: Protein LOCATION: I OTHER INF-PYMATION: /note= 'Met (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12: (ATO) starts at -1"1 Met Olu Pro Lys Ser Ala Aso Lys Thr His Thr Cys Pro Pro Cys Pro Pro Glu Leu iLeu Gly Gly Pro Ser 25 Arg ?r-e Leu ?)-ie Pro Pro Lys Thr Cys Val Pro Lys Asp Val Val Asp Th r Leu Met lie Ser 40 Asp Thr Pro Glu Val P ?ie Val Ser His Pro Glu Val Asn Trp Tyr Val Asp Oly Val Glu Gln Val 70 Tyr Asn Ala Lys Th r 75 Val1 Pro Arg Olu Glu Tyr Asn Ser Arg Val Val Leu Thr Val Leu His Asn Lys Gin Asp Tro Leu 100 Oly Lys Glu Cys Lys Val 61 Ala Leu Pro Ala Pro Ile Glu Lys Thr Ile Ser Lys Ala Lys Gly Gin 115 120 125 Pro Arg 0-lu Pro Gin Va 1 E

L

2

A

I

A

G

3(

H:

LE

Se 13 Thr Ly 145 Ser As ryr Ly ryr Se2 ?he Sei 21C ~ys Sez 25 .sp Asp le Ser sp Phe in Thr 290 sn Val 05 Ls Val u Glu r Thr 0 s Asn Gin p Tie Ala s Thr Thr 180 Lvs Leu 195 C:s Ser Leu Ser Thr Lys His Thr 260 7le Pro 275 Leu Ala Ile Gin 1 Leu Ala P 3 Thr Leu A 340 0lu Val V 355 1 Va Va 16 Pr Th Va Le Thr 245 Gin Zly /al :le >he 25 sp al 1 Ser 150 i Glu 5 Pro Val 1 Met Ser 230 Leu Ser Leu Tvr Ser 1 310 Ser L Ser L Ala L Tv 13 Le' Tr Va Asp His 215 Pro Ile Val -is 11 295 ~sn ~ys eu eu r Thr Leu Pro Pr 5 u Thr Cys Leu Va 15 p Glu Ser Asn Gl 170 1 Leu Asp Ser As 185 Lys Ser Arg Tr 200 Glu Ala Leu Hi.

Gly Lys Val Pr 23E Lys Thr Ile Val 250 Ser Ser Lys Gin 265 Pro Ile Leu Thr 280 Gin 7le Leu Thr Asp Leu Glu Asn 315 Ser Cys His Leu 330 Gly Gly Val Leu 345 Ser Arg Leu Gin 360 *0 s 1 5 y

/C

2

I

T

L

S

3'

PL

Pr Gl Ser Arg 140 Lys Gly Gin Pro Glv Ser 'In Gin 205 isn His le Gin hr Arg ys Val eu Ser I 285 er MeE 00 eu Arg A :o Trp A .u Ala S As- PhE GlL Phe 190 Glv Ty r Lys Ile Thr 270 ys )ro IsZ .1 a en Glu Tvr 1 Asn 175 Phe Asn Tb' r Va1 Asn 255 Gly Met Sen r Leu L 3 Ser C 335 Gly T Leu Pro 160 Asn Leu Val Gin Gin 240 Asp Leu ksp ~rg leu ly yr 350 Leu Gin Asp Gly Ser 365 Met Leu 370 Trp Gin Leu Asp Leu Ser Pro Gly Cys 375 62 INFORMATION FOR SEQ ID NO:13: SEQUENCE CHARACTERISTICS: LENGTH: 1135 base pairs TYPE: nucleic acid STRLANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (ix) FEATURE: NAME/KEY: misc-feature LOCATION: 4 OTHER INFORMATION: /note= "Met ATGO" (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13: CATATOCACA AAACTCACAC ATGTCCACC-T TCTCCAGCTC CCCA.ACTCCT GCCCGCTCCT

TCAGTCTTCC

CTCACATCCG

GTGGACGGCG

ACGTACCGTC

TACAAGTCCA

GCCAAAGGGC

AC CAAGA.AC C

GTGGAGTGGG

GACTCCGACC

CAGGGGAACG

AAGAGCCTCT

ACCTTAATTA

TCTAAACAGA

TCCAAAATOC

AACGTTATCC

TCTTCCCCCC

TCCTCGTGCA

TGCACCTCCA

TGCTCACCT

ACGTCTCCAA

AGCCCCGACA

ACCTCAGCCT

AGAGCAATOG

GCTCCTTCTT

TCTTCTCATC

CCCTCTCTCC

.AAAC OAT C T

AAGTTACAGG

ACCAGACCOT

AGATCTCTA-A

AAAACCCAAG

CGTGACCCAC

TAATCCCA-AC

CCTCACCGTC

CAAACCCCTC

ACCACAGGTC

CACCTGCCTC

GCACCCGGAG

CCTCTACAGC

CTCCGTGATG

GCCTAAAGTA

TACGCGTATC

CCTGGACTTC

GGCTCTATAC

CCACCTCGAG

GACACCCTCA

GAACACCCTC

ACAAAGC CC

CTGCACCAGC

C CAGC CCC CA

TACACCCTGC

GTCAAACGCT

AAC AAC TAC A

AAGCTCACCG

CATGAGGCTC

CCGATCCAGA

AACGACATCA

ATCCCGGGTC

CACCAGATOT

A.ACCTTCCG

TGATCTC CC C

AGCTCA.ATT

GGCAGCACCA

ACTCGCTGAA

TC CAGAAAAC CCCCATC CCC -TATC C CAG

ACACCACCCC

TGGACAAGAG

i GCACAACCA

AAGTTCAGGA

CTCACACCCA

TGCACCC CAT

TA.ACCTCCAT

ACCTGCTCA

CACCCCTCAC

CAkACTCCTAC

CTACAACAC

TCCCAACCAG

CATCTCCAAA

CCATGAGCTC

CGACATCCC

TCCCCTGCTC

CACOTGCCAC

CTACACGCAG

CCACACCAAA

GTCCCTCAC

CCTCACCTTG

OCCGTCCCGT

CGTGCTGGCA

120 180 240 300 360 420 480 540 600 660 720 780 840 900 960 1020 TTCTCCAAAT CCTCCCACCT OCCATOCOCT TCACCTCTTC ACACTCTGCA CTCTCTGCGC 63 GGGGTCCTGG AAGCATCCCO TTACAGCACC GAAGTTGTTG CTCTGTCC7CG TCTGCAGGGT TCCCTTCAGG ACATGCTTTG GCAGCTGGAC CTGTCTCCCG GTTGTTAATG GATCC INFORMATION FOR SEQ ID NO:14: SEQUENCE CHARACTERISTICS: LENGTH: 1135 base pairs TYPE: nucleic acid STRANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (xi) SEQUENCE DESCRIPTION: SEQ ID NO:14: GTATACCTGT TTTGAGTGTC TACAGGTGGA ACAGGTCGAG OCOTTOAGGA CCCCCCAGGA 1080 1135

AGTCAGAAGG

CAGTGTACGC

CACCTGCCGC

TGCATOOCAC

ATGTTCACGT

CGGTTTCCCG

TGGTTCTTGG

CACCTCACCC

CTGAGGCTGC

GTCCCCTTOC

TTCTCGGAGA

TGGAATTA.AT

AGATTTGTCT

AGGTTTTACC

TTGCAATAGG

AAGAGGTTTA

AGAAGGGGGG

ACCACCACCT

ACCTCCACGT

ACCAGTCGCA

TCCAGAGGTT

TCGGGGCTCT

TCCAGTCGGA

TCTCGTTACC

CGAGGAAGAA

AGAAGAGTAC

GOGACAGAGO

TTTGCTAGCA

TTCA.ATGTCC

TGGTCTGGGA

TCTAGAGATT

GOACGOTGGA

TTTTGGGTTC

GCACTCGGTG

ATTACGGTTC

GGAGTGGCAG

GTTTCGGGAG

TGGTGTCCAC

CTGGACGGAC

CGTCGGCCTC

GGAGATGTCG

GAGGCACTAC

CCCATTTCAT

ATGCGCATAG

GGACCTGAAG

CCGACATATG

GCTGGAGCTC

CGGTACCOGA

CTGTGGGAGT

CTTCTGGGAC

TGTTTCGGCG

GACGTGGTCC

GGTCGGGGGT

ATGTOGGACG

CAGTTTCCGA

TTGTTGATGT

TTCGAGTGOC

OTACTCCGAG

GGCTAGGTCT

TTGCTGTAGT

TAGGGCCCAG

GTCGTCTAGA

TTGGA.AGCGC

AGTCCAGAAC

ACTAGAGGGC

TCCAGTTCAA

CCC TC CTC CT

TGACCGACTT

AGCTCTTTTG

GGGGTAOGGC-

AGATAGGGTC

TCTGGTGCGG

ACCTGTTCTC

ACGTGTTGGT

TTCAAGTCCT

CAGTGTIGGGT

ACGTGOCTA

ATTGGAGGTA

TGGACGACGT

TCTGAGACCT

CTGGGGACTC

OTTGACCATO

CATGTTGTCG

ACCGTTCCTC

GTAGAGGTTT

CCTACTCGAC

GCTGTAGCGG

AGGOCACOAC

GTCCACCGTC

GATGTGCGTC

GCTGTGGTTT

CAGCCACTCG

GGACTGGAAC

CGGCAGGGCA

GCACGACCGT

GAGAGACCCG

120 180 240 300 360 420 480 540 600 660 720 780 840 900 960 1020 1080 CCCCAGGACC TTCGTAGGCC AATGTCGTGG CTTCAACAAC GAGACAGGGC AGACGTCCCA 64 AGGGAAGTCC TGTACGAAAC CGTCGACCTG GACAGAGGCC CAACAATTAC CTAGG INFORMATION FOR SEQ ID SEQUENCE CHARACTERISTICS: LENGTH: 374 amino acids TYPE: amino acid STRANDEDNESS: unknown TOPOLOGY: unknown (ii) MOLECULE TYPE: protein (ix) FEATURE: NAME/KEY: Protein LOCATION: 1 OTHER INFORMATION: /note= "Met (ATG) scares ac (xi) SEQUENCE DESCRIPTION: SEQ ID 1135 -1" Met Asp Lys Thr His Thr Cys Pro Pro Cys 1 Gly Met His Val Tyr Gly lie Val Gly Ile Glu His Arg Lys Glu Tyr 130 Pro Ser Asp Asn Val Glu Lys 115 Thr Ser Arg Pro Ala Val Tyr 100 Thr Leu 5 Val Thr Glu Lys Ser Lys Ile Pro Phe Pro Val Thr 70 Val Cys Ser Pro Leu Glu Lys 55 Lys Leu Lys Lys Ser 135 Phe Val 40 Phe Pro Thr Val Ala 120 Arg Pro 25 Thr Asn Arg Val Ser 105 Lys Asp 10 Pro Cys Trp Glu Leu 90 Asn Gly Glu Pro Ala Pro Glu Leu Lys Pro Lys Asp Thr Val Val Val Asp Val Tyr Val Asp Gly Val Glu Gin Tyr Asn Ser 75 His Gin Asp Trp Leu Lys Ala Leu Pro Ala 110 Gin Pro Arg Glu Pro 125 Leu Thr Lys Asn Gin 140 Leu Leu Ser Glu Thr Asn Pro Gin Val Ser Leu Thr Cys Leu Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val 150 155 65 Glu Trp Glu Ser Asn Gly Gin Pro Glu Asn Asn Tyr Lys Thr Thr Pro 165 170 175 Pro Val Leu Asp Ser Asp Gly Ser Phe Phe Leu Tyr Ser Lys Leu Thr 180 185 190 Val Asp Lys Ser Arg Trp Gin Gin Gly Asn Val Phe Ser Cys Ser Val 195 200 205 Met His Glu Ala Leu His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu 210 215 220 Ser Pro Gly Lys Val Pro Ile Gin Lys Val Gin Asp Asp Thr Lys Thr 225 230 235 240 Leu Ile Lys Thr lie Val Thr Arg Ile Asn Asp Ile Ser His Thr Gin 245 250 255 Ser Val Ser Ser Lys Gin Lys Val Thr Gly Leu Asp Phe Ile Pro Gly 260 265 270 Leu His Pro Ile Leu Thr Leu Ser Lys Met Asp Gin Thr Leu Ala Val 275 280 285 Tyr Gin Gin Ile Leu Thr Ser Met Pro Ser Arg Asn Val Ile Gin Ile 290 295 300 Ser Asn Asp Leu Glu Asn Leu Arg Asp Leu Leu His Val Leu Ala Phe 305 310 315 320 Ser Lys Ser Cys His Leu Pro Trp Ala Ser Gly Leu Glu Thr Leu Asp 325 330 335 Ser Leu Gly Gly Val Leu Glu Ala Ser Gly Tyr Ser Thr Glu Val Val 340 345 350 Ala Leu Ser Arg Leu Gin Gly Ser Leu Gin Asp Met Leu Trp Gin Leu 355 360 365 Asp Leu Ser Pro Gly Cys 370 INFORMATION FOR SEQ ID NO:16: SEQUENCE CHARACTERISTICS: LENGTH: 1135 base pairs TYPE: nucleic acid STRANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA 66 (ix) FEATURE: NAME/KEY: misc-feature LOCATION: 4 OTHER !NFORMATION: /note= "Met ATGO" (xi) SEQUENCE DESCRIPTION: SEQ ID NO:16: CATATGGACA AAACTCACAC ATOCCCACCG TOCCCAGCTC CGGAACTCGA AGGTGGTCCG

TCAGTCTTCC

CTCACATGCG

GTGGACGGCG

ACGTACCGTG

TACGCATGCG

GC CAAAGGOC

ACCAAGAACC

GTGGAGTGGG

GACTCCGACG

CAGGGGAACG

AAGAGCCTCT

ACCTTAATTA

TCTAA.ACAGA

TCCAAAATGG

AACGTTATCC

TTCTCCAAAkT

GGGGTCCTG

TCCCTTCAGG

TCTTCCCCCC

TGGTGGTOGA

TGGAGGTGCA

TGGTCAGCGT

CGGTCTCCAA

AGCCCCGAGA

AGGTCAGCCT

AGAGCAATOG

OCTCCTTCTT

TCTTCTCATO

CCC TGTCTCC

AAACGATCCT

AAGTTACAOG

ACCAGACCCT

AGATCTCTAA

CCTGCCACCT

AAGCATCCGG

ACATGCTTTG

AAAACCCAAO

CGTGAGCCAC

TAATGCCAAG

CC TCAC CGTC

CAAAGCCCTC

ACCACAOOTG

GACCTGCCTG

GCAGCCGGAO

CCTCTACAGC

CTCCGTGATG

COOT AAAG TA

TACGCGTATC

CCTC-GACTTC

GGCTGTATAC

CGACCTCGAG

CCCATGGGCT

TTACAGCACC

GCAGCTGGAC

GACACCCTCA

GAAGACCCTG

ACAAAGCCGC

CTGCACCAOG

CC AGCC C CCA

TACACCCTGC

GTCAAAGGCT

AAC AAC TA CA

AAGCTCACCG

CATGAGGCTC

CCGATCCAGA

AACGACATCA

ATCCCGGOTC

CAGCAGATCT

AACCTTCGCG

TCAGGTC7TO

C-AAGTTGTTG

C TGTC TC C G

TGATCTCCCG

AGGTCA.AGTT

GGOAGGAGCA

ACTGGCTGAA

TCGAGAAAAC

CCCCATCCCG

TC TAT CC CAG AGAC CAC 0CC

TOOGACA.AGAG

TGCACAACCA

AAGTTCAGGA

GTCACACCCA

T GC AC CC OAT

TAACCTCCAT

ACCTOCTGCA

AGACTCTOGA

C TCTGTC CC C

GTTGTTAATG

OACCCCTGAO

CAACTGGTAC

GTACAACAGC

TGGCAAAZGCT

CATCTCCAAA

GGATGAGCTG

CGACATCGCC

TCCCGTGCTG

CACOTOOCAG

CTACACGCAG

CGACACCAAA

GTCCOTGAGC

CCTGACCTTG

OCCGTCCCGT

CGTGCTGGCA

CTCTCTGGGC

TCTGCAGGGT

GATCC

120 180 240 300 360 420 480 540 600 660 720 780 840 900 960 1020 1080 1135 67 INFORMATION FOR SEQ ID NO:l7: SEQUENCE CHARACTERISTICS: LENGTH: 1135 base pairs TYPE: nucleic acid STRANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: cONA (xi) SEQUENCE DESCRIPTION: SEQ ID NJO:17: GTATACCTGT TTTGAGTGTG TACGGGTGGC ACGGGTCGAG GCCTTGAGCT TCCACCAGGC

AGTCAGAAGG

CAGTGTACGC

CACCTGCCGC

TGCATGGCAC

ATGCGTACGC

CGGTTTCCCG

TGGTTCTTGG,

CACCTCACCC

CTGAGGCTGC

GTCCCCTTGC

TTCTCGGAGA

TGGAATTAAT

AGATTTGTCT

AGGTTTTACC

TTGCAATAGG

AAGAGGTTTA

CCC CAGGACC

AGGGAAGTCC

AGAAGGGGGG

ACCACCACCT

ACCTCCACGT

ACCAGTCGCA

GCCAGAGGTT

TCGGGGCTCT

TCCAGTCGGA

TCTCGTTACC

CGAGGAAGAA

AGAAGAGTAC

GGGACAGAGG

TTTGCTAGCA

TTCA.ATGTCC

TGGTCTGGGA

TCTAGAGATT

GGACOOTGGA

TTCGTAGGCC

T GTACGAA AC

TTTTGGGTCC

GCACTCGGTG

ATTACGGTTC

GGAGTGGCAG

GTTTCGGGAG

TGGTGTCCAC

CTGGACGGAC

CGTCGGCCTC

GGAGATGTCG

GAGOCACTAC

CCCATTTCAT

ATGCGCATAG

GGACCTGAAG

CCGACATATG

GCTGGAGCTC

CGGTACCCGA

AAkTGTCGTGG

CGTCGACCTG

CTGTGGGAGT

CTTCTGGGAC

TGTTTCGGCG

GACGTGGTCC

GGTCGGGGGT

ATGTGGGACG

CAGTTTCCGA

TTGTTGATGT

TTCGAGTGGC

GTACTCCGAG

GGCTAGGTCT

TTGCTGTAGT

TAGGGCCCAG

GTCGTCTAGA

TTGGA.AGCGC

AGTCCAGAAC

CTTCAACAAC

GACAGAGGCC

ACTAGAGGGC

TCCAGTTCAA

CCCTCCTCGT

TGACCGACTT

AGCTCTTTTG

GGGGTAGGGC

AGATAGGGTC

TCTGGTGCGG

ACCTGTTCTC

ACGTGTTGGT

TTCAAGTCCT

CAGTGTGGGT

ACGTGGGCTA

ATTGGAGGTA

TGGACGACGT

TCTGAGACCT

GAGACAGGGC

CAACAATTAC

CZ'GGGC-ACTC

GTTGACCATG

CATGT-GTCG

AC CGTT-C GA

GTAGAGGTTT

CC-TACTCGAC

GCTGTAGCGG

AGGGCACGAC

GTCCACCGTC

GATGTC-CGTC

GCTGTGGTTT

CAGCCACTCG

GGACTGGAAC

CGGCAGGGCA

GCACGACCGT

GAGAGACCCG

AGACGTCCCA

CTAGG

120 180 240 300 360 420 480 540 600 660 720 780 840 900 960 1020 1080 1135 68 INFORMATION FOR SEQ ID NO:18: Wi SEQUENCE CHARACTERISTICS: LENGTH: 374 amino acids TYPE: amino acid STRLANDEDNESS: unknown TOPOLOGY: unknown (ii) MOLECULE TYPE: protein (ix) FEATURE: NAME/KEY: Protein LOCATION: 1 OTHER INFORMATION: /note= "Met (xi) SEQUENCE DESCRIPTION: SEQ ID NO:18: Met Asp Lys Thr His Thr Cys Pro Pro Cys (ATG) starts at -111 1 Gly Met His Val1 Tyr Gly Ile Val1 S er 145 Gly Ile Glu His Arg Lys Glu Tyr 130 Leu Pro Ser Asp Asn Val1 Ala Ly s 115 Thr Thr Ser Arg Pro Ala ValI Tvr 100 Thr Leu Cys Val1 T hr Glu Lys Ser Ala Ile Pro Leu Phe Pro Val Thr 70 Val1 Cys Ser Pro Val1 150 Leu Glu Lys 55 Lys Leu Ala Lys S er 135 Lys Phe Val1 40 Phe Pro Thr Val1 Ala 120 Arg Gly Pro 25 Thr Asn Arg Val1 Ser 105 Lys Asp iPhe Pro Cys Trp Glu Leu 90 As n Gly Glu Tyr Pro Lys Val Tvr Glu 75 FHis Ly s Gin Leu Pro 155 Ala Pro Val1 Val Gin Gin Al a Pro Thr 140 Ser Pro Lys Val1 Asp Tyr Asp Leu Arq 125 Lys Asp Glu Asp Aso Gly Asn Trp Pro 110 Glu Asn Ile Leu Thr Val1 Val1 Ser Leu Ala Pro G1 n Al a Giu I eu Ser Glu Thr Asn Pro Gln Val1 Val1 160 Glu Trp Giu Ser Asn Gly Gin Pro Glu Asn Asn Tyr Lys Thr Thr Pro 165 170 175 69 Pro Val Leu Val Asp Lys 195 Met His Glu 210 Ser Pro Gly 225 Leu Ile Lys Ser Val Ser Leu His Pro 1 275 Tyr Gin Gin I 290 Ser Asn Asp L 305 Ser Lys Ser C~ Ser Leu Gly Gl 34 Ala Leu Ser Ar 355 Asp Leu Ser Pr 370

A

Al Ly T11 i le le Is 0 SO Ser A~ 30 ~r Arg Tr a Leu Hi S Val Pr 23 r Ile Va~ 245 -Lys G l: Leu Thr Leu Thr Glu Asn 310 His Leu 325 ValI Leu Leu Gin Cly Cys sp Cly Ser Phe Phe Leu 185 ~p Gin Gin Gly Asni Val 200 s Asn His Tyr Thr Gin 215 o Ile Gin Lys Val Gin 0 235 1. Thr Arg Ile Asn Asp 250 Lys Val Thr Gly Leu 1 265 *Leu Ser Lys Met Asp G 280 Ser Met Pro Ser Arg A 295 3 Leu Arg Asp Leu Leu Ht 315 Pro Trp Ala Ser Gly LE 330 Giu Ala Ser Gly Tyr Se 345 Gly Ser Leu Gin Asp Me 360

T

P1 As sr 00 i S yr Ser he Ser 205 Ps Ser .0 p Asp e Ser p Phe i Thr 285 Val I Val L Glu T~ Thr G: 32 Leu Tz 365 Le Th

H;

nlE 270 ,eu eu hr lu s0 -p ~S SE U Se r Ly s Th.

Prc Ala Gin Al a Leu 335 Val1 Gin eu Thr ~r Val r Leu s Thr 240 r Gin D Cly Val Ile Ph e 320 Asp Val1 Leu

Claims (17)

1. A protein having a formula selected from the group consisting of: R 1 R2 00 t and R 1 L R 2 wherein the protein is complexed to a binding composition, R 1 is a Fc c protein, an Fc protein analog thereof, or an Fc protein derivative thereof, R 2 is an OB NC protein, an OB protein analog thereof, or an OB protein derivative thereof, and L is a 0 linker, and wherein said Fc protein, said Fc protein analog thereof, or said Fc protein cN derivative thereof is selected from the group consisting of: the Fc amino acid sequences as set forth in of SEQ ID Nos: 9, 12, 15, and 18; the amino acid sequence of subpart having a different amino acid substituted or deleted in one or more of the following positions (using the numbering according to SEQ ID NO:9): one or more cysteine residues replace by an alanine or serine residue; (ii) one or more tyrosine residues replaced by a phenylalanine residue; (iii) the amino acid at position 5 replaced with an alanine; (iv) the amino acid at position 20 replaced with glutamate; the amino acid at position 103 replaced with an alanine; (vi) the amino acid at position 105 replaced with an alanine; (vii) the amino acid at position 107 replaced with an alanine; (viii) the amino acids at positions 1, 2, 3, 4, or 5 deleted; (ix) one or more residues replaced or deleted to ablate the Fc receptor binding site; one or more residues replaced or deleted to ablate the complement (clq) binding site; and (ix) a combination of subparts i-x; the amino acid sequence of subparts or having a methionyl residue at the N-terminus; Mar. 2008 17:35 No. 4110 P. 21/65 00 -71- O the Fc protein, Fc protein analog, or Fc protein derivative of any of subparts through comprised of a water soluble polymer moiety connected to the 0o protein moiety; a derivative of subpart wherein said water soluble polymer moiety is Spolyethylene glycol; S(f) a derivative of subpart wherein said water soluble polymer moiety is a Spolyamino acid moiety; and c a derivative of subpart wherein said water soluble polymer moiety is attached at solely the N-terminus of said protein moiety.

2. The protein according to claim 1, wherein said OB protein, said OB protein analog thereof, or said OB protein derivative thereof is selected from the group consisting of: the amino acid sequence 1-146 as set forth in SEQ. ID. NO. 3 or SEQ. ID. NO. 6; the amino acid sequence 1-146 as set forth in SEQ. ID. NO. 6 having a lysine residue at position 35 and an isoleucine residue at position 74; the amino acid sequence of subpart having a different amino acid substituted in one or more of the following positions (using the numbering according to SEQ. ID. NO. 4, 8, 32, 33, 35, 48, 50, 53, 60, 64, 66, 67, 68, 71, 74, 77, 78, 89, 97, 100, 102, 105, 106, 107, 108, 111, 112, 118, 136, 138, 142, and 145; the amino acid sequence of subparts or optionally lacking a glutaminyl residue at position 28; the amino acid sequence of subparts or having a methionyl residue at the N-terminus; a truncated OB protein analog selected from among: (using the numbering of SEQ. ID. NO. 6 having a lysine residue at position 35, and an isoleucine residue at position 74): amino acids 98-146; 2008 17:36 ~.10 P 26 No.4110 P. 22/65 00 -72- (ii) amino acids 1-32; (iii) amino acids 40-116; 00 (iv) amino acids 1-99 and 112-146; amino acids 1-99 and 112-146 having one or more of amino acids N 100-111 sequentially placed between amino acids 99 and 112; and (vi) the truncated OB analog of subpart (fXi) having one or more of amino acidsl100, 102, 105, 106, 107, 108, 111, 112, 118, 136, 138, 142, andl145 substituted with another amino acid; (vii) the truncated analog of subpart having one or more of amino acids 4, 8, and 32 substituted with another amino acid; (viii) the truncated analog of subpart (fXiii) having one or more of amino acids 50, 53, 60, 64, 66, 67, 68, 71, 74, 77, 78, 89, 97, 100, 102, 105, 106, 107, 108, 111, and 112 replaced with another amino acid; (ix) the truncated analog of subpart having one or more of amino acids 4, 8, 32, 33, 35, 48, 50, 53, 60, 64, 66, 67, 68, 71, 74, 77, 78, 89, 97, 112, 118, 136, 138, 142, and 145 replaced with another amino acid; the truncated analog of subpart (fXv) having one or more of amino acids 4, 8, 32, 33, 35, 48, 50, 53, 60, 64, 66, 67, 68, 71, 74, 77, 78, 89, 97, 100, 102, 105, 106, 107, 108, 111, 112, 118, 136, 138, 142, and 145 replaced with another amino acid; (xi) the truncated analog of any of subparts having an N- terminal methionyt residue; the OB protein, OB protein analog, or OB protein derivative of any of subparts through comprised of a water soluble moiety connected to the protein moiety; a derivative of subpart wherein said water soluble moiety is polyethylene glycol; a derivative of subpart wherein said water soluble moiety is a polyamino acid moiety; and 1O.Mar. 2Q08 17:36 ~o.411C P. 23/6~ 2008 17:36 No. 4110 P. 23/65 00 O O -73- S(j) a derivative of subpart wherein said water soluble polymer moiety is attached at solely the N-terminus of said protein moiety. 00

3. The protein of daim I or claim 2 wherein the linker sequence is one or Smore amino acids selected from the group consisting of: Glycine, Asparagine, Serine, SThreonine and Alanine. c

4. The protein of any of claims 1, 2, or 3, wherein the linker is selected from the group consisting of: ala-ala-ala; ala-ala-ala-ala; ala-ala-ala-ala-ala; gly-gly; gly-gly-gly; gly-gly-gly-gly-gly; gly-gly-gly-gly-gly-gly-gly; gly-pro-gly; gly-gly-pro-gly-gly; and any combination of subparts through The protein according to any of claims 1, 2, 3, or 4, wherein the binding composition prolongs the circulation time of the protein in vivo.

6. The protein according to any of claims 1, 2, 3, 4 or 5, wherein the binding composition does not interfere with the ability of the protein to bind to an endogenous OB protein receptor or effect signal transduction.

7. The protein according to any of claims 1, 2, 3, 4, 5 or 6, wherein the binding composition is a protein or peptide. Mar. 2008 11:36 No. 4110 P. 24/65 2008 17:36 No- 4110 P. 24/65 -74-

8. The protein according to any of claims 1, 2, 3, 4, 5, 6 or 7, wherein the binding composition is an OB protein receptor or portion of an OB protein receptor.

9. A protein comprising a Fc protein, an Fc protein analog thereof, or an Fc protein derivative thereof, complexing to a binding composition, the protein selected from the group consisting of: the Fc amino acid sequences as set forth in of SEQ ID Nos: 9, 12,15, and 18; the amino acid sequence of subpart having a different amino acid substituted or deleted in one or more of the following positions (using the numbering according to SEQ ID NO:9): one or more cysteine residues replace by an alanine or serine residue; (ii) (iii) (iv) (v) (vi) (vii) (viii) (ix) one or more tyrosine residues replaced by a phenylalanine residue; the amino acid at position 5 replaced with an alanine; the amino acid at position 20 replaced with glutamate; the amino acid at position 103 replaced with an alanine; the amino acid at position 105 replaced with an alanine; the amino acid at position 107 replaced with an alanine; the amino acids at positions 1, 2, 3, 4, or 5 deleted; one or more residues replaced or deleted to ablate the Fc receptor binding site; one or more residues replaced or deleted to ablate the complement (clq) binding site; and (ix) a combination of subparts i-x; the amino acid sequence of subparts or having a methionyl residue at the N-terminus; Mar. 2008 17:36 No- 4110 P. 25/65 00 0 O the Fc protein, Fc protein analog, or Fc protein derivative of any of subparts through comprised of a water soluble polymer moiety connected to the 00 protein moiety; a derivative of subpart wherein said water soluble polymer moiety is polyethylene glycol; N a derivative of subpart wherein said water soluble polymer moiety is a Spolyamino acid moiety; and a derivative of subpart wherein said water soluble polymer moiety is attached at solely the N-terminus of said protein moiety; fused to the N-terminus of an OB protein, OB protein analog thereof, or OB protein derivative thereof. The protein according to claim 9, wherein the binding composition prolongs the circulation time of the protein in vivo.

11. The protein according to claim 9 or claim 10, wherein the binding composition does not interfere with the ability of the protein to bind to an endogenous OB protein receptor or effect signal transduction.

12. The protein according to any of claims 9, 10, or 11, wherein the binding composition is a protein or peptide.

13. The protein according to any of claims 9, 10, 11 or 12, wherein the binding composition is an OB protein receptor or portion of an OB protein receptor.

14. A nucleic acid sequence encoding for a protein complexed to a binding composition, the protein having the formula selected from the group consisting of: R 1 R 2 and R 1 L R 2 wherein R, is a Fc protein, an Fc protein analog thereof, or an Fc protein derivative thereof, selected from the group consisting of: Mar. 2008 17:36 No- 4110 P. 26/65 -76- the Fc amino acid sequences as set forth in of SEQ ID Nos: 9, 12, 15, and 18; the amino acid sequence of subpart having a different amino acid substituted or deleted in one or more of the following positions (using the numbering according to SEQ ID NO:9): one or more cysteine residues replace by an alanine or serine residue; (ii) (iii) (iv) (v) (vi) (vii) (viii) (ix) one or more tyrosine residues replaced by a phenylalanine residue; the amino acid at position 5 replaced with an alanine; the amino acid at position 20 replaced with glutamate; the amino acid at position 103 replaced with an alanine; the amino acid at position 105 replaced with an alanine; the amino acid at position 107 replaced with an alanine; the amino acids at positions 1, 2, 3, 4, or 5 deleted; one or more residues replaced or deleted to ablate the Fc receptor binding site; one or more residues replaced or deleted to ablate the complement (clq) binding site; and (ix) a combination of subparts i-x; the amino acid sequence of subparts or having a methionyl residue at the N-terminus; the Fc protein, Fc protein analog, or Fc protein derivative of any of subparts through comprised of a water soluble polymer moiety connected to the protein moiety; a derivative of subpart wherein said water soluble polymer moiety is polyethylene glycol; a derivative of subpart wherein said water soluble polymer moiety is a polyamino acid moiety; and Mar. 2008 17:36 No. 4110 P. 27/65 oo 00 -77- O a derivative of subpart wherein said water soluble polymer moiety is attached at solely the N-terminus of said protein moiety; 00 R 2 is an OB protein, OB protein analog thereof, or OB Protein derivative thereof; and g L is a linker. A nucleic acid sequence encoding a protein according to any of claims 1, c 2, 3, 4, 5, or 6, wherein the binding composition prolongs the circulation time of the protein in vivo.

16. A nucleic acid sequence encoding a protein according to any of claims 1, 2, 3, 4, 5, or 6, wherein the binding composition does not interfere with the ability of the protein to bind to an endogenous OB protein receptor or effect signal transduction.

17. A nucleic acid sequence encoding a protein according to any of claims 1, 2, 3, 4, 5, or 6, wherein the binding composition is a protein or peptide.

18. A nucleic acid sequence encoding a protein according to any of claims 1, 2, 3, 4, 5, or 6, wherein the binding composition is an OB protein receptor or portion of an OB protein receptor.

19. The nucleic acid sequence according to claim 14 encoding for a protein having an OB protein, an OB protein analog, or an OB protein derivative selected from the group consisting of: the amino acid sequence 1-146 as set forth in SEQ. ID. NO. 3 or SEQ. ID. NO. 6; the amino acid sequence 1-146 as set forth in SEQ. ID. NO. 6 having a lysine residue at position 35 and an isoleucine residue at position 74; Mar. 2008 17:36 4110 P. 28/65 2008 17:36 No.4110 P. 28/65 00 -78- the amino acid sequence of subpart having a different amino acid substituted in one or more of the following positions (using the numbering according to 00 SEQ. ID. NO. 4, 8, 32, 33, 35, 48, 50, 53, 60, 64, 66, 67, 68, 71, 74, 77, 78, 89, 97, 100, 102, 105, 106, 107, 108, 111, 112, 118, 136, 138, 142, and 145; the amino acid sequence of subparts or optionally lacking a glutaminy1 residue at position 28; the amino acid sequence of subparts or having a methionyl residue at the N-terminus; a truncated OB protein analog selected from among: (using the numbering of SEQ. ID. NO. 6 having a lysine residue at position 35, and an isoleucine residue at position 74): amino acids 98-146; (ii) amino acids 1-32; (iii) amino acids 40-116; (iv) ami1no acids 1-99 and 112-1 46; amino acids 1-99 and 112-146 having one or more of amino acids

100-111 sequentially placed between amino acids 99 and 112; and (vi) the truncated OR analog of subpart having one or more of amino acids 100, 102, 105, 106, 107, 108, 111, 112, 118, 136, 138, 142, and 145 substituted with another amino acid; (vii) the truncated analog of subpart having one or more of amino acids 4, 8, and 32 substituted with another amino acid; (viii) the truncated analog of subpart (fXiii) having one or more of amino acids 50, 53, 60, 64, 66, 67, 68, 71, 74, 77, 78, 89, 97, 100, 102, 105, 106, 107, 108, 111, and 112 replaced with another amino acid; (ix) the truncated analog of subpart having one or more of amino acids 4, 8, 32, 33, 35, 48, 50, 53, 60, 64, 66, 67, 68, 71, 74, 77, 78, 89, 97, 112, 118, 136, 138, 142, and 145 replaced with another amino acid; Mar, 2008 17:37 No. 4110 P. 29/65 00 -79- the truncated analog of subpart having one or more of amino acids 4, 8, 32, 33, 35, 48, 50, 53, 60, 64, 66, 67, 68, 71, 74, 77, 78, 89, 97, 100, 102, 0o 105, 106, 107, 108, 111,112, 118, 136,138,142, and 145 replaced with another amino acid; S(xi) the truncated analog of any of subparts (fXi)(x) having an N- c terminal methionyl residue; the OB protein, OB protein analog, or OB protein derivative of any of c subparts through comprised of a water soluble moiety connected to the protein moiety; a derivative of subpart wherein said water soluble moiety is polyethylene glycol; a derivative of subpart wherein said water soluble moiety is a polyamino acid moiety; and a derivative of subpart wherein said water soluble polymer moiety is attached at solely the N-terminus of said protein moiety. The nucleic acid sequence of any of claims 14, 15, 16, 17, 18, or 19 encoding for a protein with a linker sequence of one or more amino acids selected from the group consisting of: Gly, Asn, Ser, Thr and Ala. 21. The nucleic acid sequence of any of claims 14, 15, 16, 17, 18, 19, or encoding for a protein with a linker selected from the group consisting of: ala-ala-ala; ala-ala-ala-ala; ala-ala-ala-ala-ala; gly-gly; gly-gly-gly; gly-gly-gly-gly-gly; gly-gly-gly-gly-gly-gly-gly; Mar. 2008 17:37 No- 4110 P. 30/65 gly-pro-gly; gly-gly-pro-gly-gly; and any combination of subparts through 22. A nucleic acid sequence encoding for a protein complexed to a binding composition, the protein having a Fc protein, an Fc protein analog thereof, or an Fc protein derivative thereof, selected from the group consisting of: the Fc amino acid sequences as set forth in of SEQ ID Nos: 9, 12, 15, and 18; the amino acid sequence of subpart having a different amino acid substituted or deleted in one or more of the following positions (using the numbering according to SEQ ID NO:9): one or more cysteine residues replace by an alanine or serine residue; (ii) (iii) (iv) (v) (vi) (vii) (viii) (ix) one or more tyrosine residues replaced by a phenylalanine residue; the amino acid at position 5 replaced with an alanine; the amino acid at position 20 replaced with glutamate; the amino acid at position 103 replaced with an alanine; the amino acid at position 105 replaced with an alanine; the amino acid at position 107 replaced with an alanine; the amino acids at positions 1, 2, 3, 4, or 5 deleted; one or more residues replaced or deleted to ablate the Fc receptor binding site; one or more residues replaced or deleted to ablate the complement (clq) binding site; and (ix) a combination of subparts i-x; the amino acid sequence of subparts or having a methionyl residue at the N-terminus; Mar. 2008 17:37 No. 4110 P. 31/65 c -81 O the Fc protein, Fc protein analog, or Fc protein derivative of any of subparts through comprised of a water soluble polymer moiety connected to the O protein moiety; a derivative of subpart wherein said water soluble polymer moiety is polyethylene glycol; S(f) a derivative of subpart wherein said water soluble polymer moiety is a Spolyamino acid moiety; and a derivative of subpart wherein said water soluble polymer moiety is attached at solely the N-terminus of said protein moiety; fused to the N-terminus of an OB protein, analog or derivative thereof. 23. A nucleic acid sequence encoding a protein according to any of claims 14, 16, 17, 18, 19, 20, 21, or 22, wherein the binding composition prolongs the circulation time of the protein in vivo. 24. A nucleic add sequence encoding a protein according to any of claims 14, 16, 17, 18,19, 20, 21, 22, or 23, wherein the binding composition does not interfere with the ability of the protein to bind to an endogenous OB protein receptor or effect signal transduction. A nucleic acid sequence encoding a protein according to any of claims 14, 16, 17, 18, 19, 20, 21, 22, 23, or 24, wherein the binding composition is a protein or peptide. 26. A nucleic acid sequence encoding a protein according to any of claims 14, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25, wherein the binding composition is an OB protein receptor or portion of an OB protein receptor. lO.Mar. 2008 17:37 o 1C P 26 No.4110 P. 32/65 00 -82- 27. A vector containing a nucleic acid sequence according to any of claims 14, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, or 26. 00 28. The vector of claim 27 wherein the vector is pAMG21 and the nudleic acid N ~sequence is according to any of claims 14, 15,16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, or 27. 29. A prokaryotic or eukaryotic host cell containing the vector of dlaim 27 or claim 28. A process for producing a protein of any of claims 1, 2, 3, 4, 5, 6, 7, 8, 9, 11, 12, or 13, comprising the steps of culturing the host cell of claim 29, and isolating the protein produced. 31. The process of claim 30 further comprising the step of purifying the protein produced. 32. A pharmaceutical composition comprising an effective amount of a protein according to any of claims 1, 2, 3,4, 5, 6,7, 8,9,10, 11, 12, orl13, ina pharmaceutically acceptable diluent, adjuvant, or carrier. 33. A method of treatment of a disorder selected from the group consisting of excess weight, diabetes, high blood lipid level, arterial sclerosis, arterial plaque, the reduction or prevention of gall stones formation, insufficient lean tissue mass, insufficient sensitivity to insulin, and stroke, wherein the method consists of administering a therapeutically effectve amount of the protein according to any of claims 1, 2,3, 4,5, 6,7, 8, 9,10, 11, 12, or 13. Mar, 2008 17:37 No. 4110 P. 33/65 -83- 34. Use of a protein according any of claims 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,11,12, or 13, for the manufacture of a medicament for the treatment of a disorder selected from the group consisting of excess weight, diabetes, high blood lipid level, arterial sclerosis, arterial plaque, the reduction or prevention of gall stones formation, insufficient lean tissue mass, insufficient sensitivity to insulin, and stroke.