G-CSF receptor agonists

FIELD OF THE INVENTION
The present invention relates to human G-CSF receptor agonists with activity on hematopoietic cell differentiation and expansion.
BACKGROUND OF THE INVENTION
The human blood-forming (hematopoietic) system replaces a variety of white blood cells (including neutrophils, macrophages, and basophils/mast cells), red blood cells (erythrocytes) and clot-forming cells (megakaryocytes/platelets). The hematopoietic systems of the average male has been estimated to produce on the order of 4.5.times.10.sup.11 granulocytes and erythrocytes every year, which is equivalent to an annual replacement of total body weight (Dexter et al., BioEssays, 2;154-158, 1985).
It is believed that small amounts of certain hematopoietic growth factors account for the differentiation of a small number of progenitor "stem cells" into the variety of blood cell lines, for the tremendous proliferation of those lines, and for the ultimate differentiation of mature blood cells from those lines. Because the hematopoietic growth factors are present in extremely small amounts, the detection and identification of these factors has relied upon an array of assays which as yet only distinguish among the different factors on the basis of stimulative effects on cultured cells under artificial conditions.
U.S. Pat. No. 4,999,291 discloses DNA and methods for making G-CSF the disclosure of which is incorporated herein by reference in it entirety.
U.S. Pat. No. 4,810,643 relates to DNA and methods of making G-CSF and Cys to Ser substitution variants of G-CSF.
Kuga et al. (Biochem. + Biophys. Res. Comm. 159:103-111, 1989) made a series of G-CSF variants to partially define the structure-function relationship. Kuga et al. found that internal and C-terminal deletions abolished activity, while N-terminal deletions of up to 11 amino acids and amino acid substitutions at positions 1, 2 and 3 were active.
Watanabe et al. (Anal. Biochem. 195:38-44, 1991) made a variant to study G-CSF receptor binding in which amino acids 1 and 3 were changed to Tyr for radioiodination of the protein. Watanabe et al. found this Tyr.sup.1, Tyr.sup.3 G-CSF variant to be active.
WO 95/27732 describes, but does not show that the molecule has biological activity, a circularly permuted G-CSF ligand with a breakpoint at positions 68/69 creating a circularly permuted G-CSF ligand with a new N-terminus at the original position 69 of G-CSF and a new C-terminus at the original position 68 of G-CSF. WO 95/27732 also discloses circularly permuted GM-CSF, IL-2 and IL-4.
Rearrangement of Protein Sequences
In evolution, rearrangements of DNA sequences serve an important role in generating a diversity of protein structure and function. Gene duplication and exon shuffling provide an important mechanism to rapidly generate diversity and thereby provide organisms with a competitive advantage, especially since the basal mutation rate is low (Doolittle, Protein Science 1:191-200, 1992).
The development of recombinant DNA methods has made it possible to study the effects of sequence transposition on protein folding, structure and function. The approach used in creating new sequences resembles that of naturally occurring pairs of proteins that are related by linear reorganization of their amino acid sequences (Cunningham, et al., Proc. Natl. Acad. Sci. U.S.A. 76:3218-3222, 1979; Teather & Erfle, J. Bacteriol. 172: 3837-3841, 1990; Schimming et al., Eur. J. Biochem. 204: 13-19, 1992; Yamiuchi and Minamikawa, FEBS Lett. 260:127-130, 1991: MacGregor et al., FEBS Lett. 378:263-266, 1996). The first in vitro application of this type of rearrangement to proteins was described by Goldenberg and Creighton (J. Mol. Biol. 165:407-413, 1983). A new N-terminus is selected at an internal site (breakpoint) of the original sequence, the new sequence having the same order of amino acids as the original from the breakpoint until it reaches an amino acid that is at or near the original C-terminus. At this point the new sequence is joined, either directly or through an additional portion of sequence (linker), to an amino acid that is at or near the original N-terminus, and the new sequence continues with the same sequence as the original until it reaches a point that is at or near the amino acid that was N-terminal to the breakpoint site of the original sequence, this residue forming the new C-terminus of the chain.
This approach has been applied to proteins which range in size from 58 to 462 amino acids (Goldenberg & Creighton, J. Mol. Biol. 165:407-413, 1983; Li & Coffino, Mol. Cell. Biol. 13:2377-2383, 1993). The proteins examined have represented a broad range of structural classes, including proteins that contain predominantly .alpha.-helix (interleukin-4; Kreitman et al., Cytokine 7:311-318, 1995), .beta.-sheet (interleukin-1; Horlick et al., Protein Eng. 5:427-431, 1992), or mixtures of the two (yeast phosphoribosyl anthranilate isomerase; Luger et al., Science 243:206-210, 1989). Broad categories of protein function are represented in these sequence reorganization studies:
______________________________________EnzymesT4 lysozyme Zhang et al., Biochemistry 32:12311-12318 (1993); Zhang et al., Nature Struct. Biol. 1:434-438 (1995)dihydrofolate Buchwalder et al., Biochemistry 31:1621-1630reductase (1994); Protasova et al., Prot. Eng. 7:1373-1377 (1995)ribonuclease T1 Mullins et al., J. Am. Chem. Soc. 116:5529-5533 (1994); Garrett et al., Protein Science 5:204-211 (1996)Bacillus .beta.-glucanse Hahn et al., Proc. Natl. Acad. Sci. U.S.A. 91: 10417-10421 (1994)aspartate Yang & Schachman, Proc. Natl. Acad. Sci. U.S.A.transcarbamoylase 90:11980-11984 (1993)phosphoribosyl Luger et al., Science 243:206-210 (1989); Luger etanthranilate al., Prot. Eng. 3:249-258 (1990)isomerasepepsin/pepsinogen Lin et al., Protein Science 4:159-166 (1995)glyceraldehyde-3- Vignais et al., Protein Science 4:994-1000 (1995)phosphate dehydro-genaseornithine Li & Coffino, Mol. Cell. Biol. 13:2377-2383 (1993)decarboxylaseyeast Ritco-Vonsovici et al., Biochemistry 34:16543-phosphoglycerate 16551 (1995)dehydrogenaseEnzyme Inhibitorbasic pancreatic Goldenberg & Creighton, J. Mol. Biol. 165:407-413trypsin inhibitor (1983)Cytokinesinterleukin-1.beta. Horlick et al., Protein Eng. 5:427-431 (1992)interleukin-4 Kreitman et al., Cytokine 7:311-318 (1995)Tyrosine KinaseRecognition Domain.alpha.-spectrin SH3 Viguera, et al., J. Mol. Biol. 247:670-681 (1995)domainTransmembraneProteinomp A Koebnik & Kramer, J. Mol. Biol. 250:617-626 (1995)Chimeric Proteininterleukin-4- Kreitman et al., Proc. Natl. Acad. Sci. U.S.A. 91:Pseudomonas 6889-6893 (1994).exotoxin fusionmolecule______________________________________
The results of these studies have been highly variable. In many cases substantially lower activity, solubility or thermodynamic stability were observed (E. coli dihydrofolate reductase, aspartate transcarbamoylase, phosphoribosyl anthranilate isomerase, glyceraldehyde-3-phosphate dehydrogenase, ornithine decarboxylase, omp A, yeast phosphoglycerate dehydrogenase). In other cases, the sequence rearranged protein appeared to have many nearly identical properties as its natural counterpart (basic pancreatic trypsin inhibitor, T4 lysozyme, ribonuclease Ti, Bacillus -.beta.glucanase, interleukin-1.beta. .alpha.-spectrin SH3 domain, pepsinogen, interleukin-4). In exceptional cases, an unexpected improvement over some properties of the natural sequence was observed, e.g., the solubility and refolding rate for rearranged .alpha.-spectrin SH3 domain sequences, and the receptor affinity and anti-tumor activity of transposed interleukin-4-Pseudomonas exotoxin fusion molecule (Kreitman et al., Proc. Natl. Acad. Sci. U.S.A. 91:6889-6893, 1994; Kreitman et al., Cancer Res. 55:3357-3363, 1995).
The primary motivation for these types of studies has been to study the role of short-range and long-range interactions in protein folding and stability. Sequence rearrangements of this type convert a subset of interactions that are long-range in the original sequence into short-range interactions in the new sequence, and vice versa. The fact that many of these sequence rearrangements are able to attain a conformation with at least some activity is persuasive evidence that protein folding occurs by multiple folding pathways (Viguera, et al., J. Mol. Biol. 247:670-681, 1995). In the case of the SH3 domain of .alpha.-spectrin, choosing new termini at locations that corresponded to .beta.-hairpin turns resulted in proteins with slightly less stability, but which were nevertheless able to fold.
The positions of the internal breakpoints used in the studies cited here are found exclusively on the surface of proteins, and are distributed throughout the linear sequence without any obvious bias towards the ends or the middle (the variation in the relative distance from the original N-terminus to the breakpoint is ca. 10 to 80% of the total sequence length). The linkers connecting the original N- and C-termini in these studies have ranged from 0 to 9 residues. In one case (Yang & Schachman, Proc. Natl. Acad. Sci. U.S.A. 90:11980-11984, 1993), a portion of sequence has been deleted from the original C-terminal segment, and the connection made from the truncated C-terminus to the original N-terminus. Flexible hydrophilic residues such as Gly and Ser are frequently used in the linkers. Viguera, et al. (J. Mol. Biol. 247:670-681, 1995) compared joining the original N- and C-termini with 3- or 4-residue linkers; the 3-residue linker was less thermodynamically stable. Protasova et al. (Protein Eng. 7:1373-1377, 1994) used 3- or 5-residue linkers in connecting the original N-termini of E. coli dihydrofolate reductase; only the 3-residue linker produced protein in good yield.
SUMMARY OF THE INVENTION
The modified human G-CSF receptor agonists of the present invention can be represented by the Formula:
X.sup.1 -(L).sub.a -X.sup.2
wherein;
a is 0 or 1;
X.sup.1 is a peptide comprising an amino acid sequence corresponding to the sequence of residues n+1 through J;
X.sup.2 is a peptide comprising an amino acid sequence corresponding to the sequence of residues 1 through n;
n is an integer ranging from 1 to J-1; and
L is a linker.
In the formula above the constituent amino acids residues of human G-CSF are numbered sequentially 1 through J from the amino to the carboxyl terminus. A pair of adjacent amino acids within this protein may be numbered n and n+1 respectively where n is an integer ranging from 1 to J-1. The residue n+1 becomes the new N-terminus of the new G-CSF receptor agonist and the residue n becomes the new C-terminus of the new G-CSF receptor agonist.
The present invention relates to novel G-CSF receptor agonists of the following formula:
__________________________________________________________________________1 10Xaa Xaa Xaa Gly Pro Ala Ser Ser Leu Pro Gln Ser Xaa 20Leu Leu Xaa Xaa Xaa Glu Gln Val Xaa Lys Xaa Gln Gly Xaa Gly 30 40Ala Xaa Leu Gln Glu Xaa Leu Xaa Ala Thr Tyr Lys Leu Xaa Xaa 50Xaa Glu Xaa Xaa Val Xaa Xaa Gly His Ser Xaa Gly Ile Pro Trp 60 70Ala Pro Leu Ser Ser Xaa Pro Ser Xaa Ala Leu Xaa Leu Ala Gly 80Xaa Leu Ser Gln Leu Gis Ser Gly Leu Phe Leu Tyr Gln Gly Leu 90 100Leu Gln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu 110Xaa Thr Leu Gln Xaa Asp Val Ala Asp Phe Ala Xaa Thr Ile Trp 120 130Gln Gln Met Glu Xaa Xaa Gly Met Ala Pro Ala Leu Gln Pro Thr 140Gln Gly Ala Met Pro Ala Phe Ala Ser Ala Xaa Gln Xaa Xaa Ala 150 160Gly Gly Val Leu Val Ala Ser Xaa Leu Gln Xaa Phe Leu Xaa Xaa 170Ser Tyr Arg Val Leu Xaa Xaa Leu Ala Gln Pro (SEQ ID NO:1)__________________________________________________________________________
wherein
Xaa at position 1 is Thr, Ser, Arg, Tyr or Gly;
Xaa at position 2 is Pro or Leu;
Xaa at position 3 is Leu, Arg, Tyr or Ser;
Xaa at position 13 is Phe, Ser, His, Thr or Pro;
Xaa at position 16 is Lys, Pro, Ser, Thr or His;
Xaa at position 17 is Cys, Ser, Gly, Ala, Ile, Tyr or Arg;
Xaa at position 18 is Leu, Thr, Pro, His, Ile or Cys;
Xaa at position 22 is Arg, Tyr, Ser, Thr or Ala;
Xaa at position 24 is Ile, Pro, Tyr or Leu;
Xaa at position 27 is Asp, or Gly;
Xaa at position 30 is Ala, Ile, Leu or Gly;
Xaa at position 34 is Lys or Ser;
Xaa at position 36 is Cys or Ser;
Xaa at position 42 is Cys or Ser;
Xaa at position 43 is His, Thr, Gly, Val, Lys, Trp, Ala, Arg, Cys, or Leu;
Xaa at position 44 is Pro, Gly, Arg, Asp, Val, Ala, His, Trp, Gin, or Thr;
Xaa at position 46 is Glu, Arg, Phe, Arg, Ile or Ala;
Xaa at position 47 is Leu or Thr;
Xaa at position 49 is Leu, Phe, Arg or Ser;
Xaa at position 50 is Leu, Ile, His, Pro or Tyr;
Xaa at position 54 is Leu or His;
Xaa at position 64 is Cys or Ser;
Xaa at position 67 is Gln, Lys, Leu or Cys;
Xaa at position 70 is Gin, Pro, Leu, Arg or Ser;
Xaa at position 74 is Cys or Ser;
Xaa at position 104 is Asp, Gly or Val;
Xaa at position 108 is Leu, Ala, Val, Arg, Trp, Gln or Gly;
Xaa at position 115 is Thr, His, Leu or Ala;
Xaa at position 120 is Gln, Gly, Arg, Lys or His
Xaa at position 123 is Glu, Arg, Phe or Thr
Xaa at position 144 is Phe, His, Arg, Pro, Leu, Gln or Glu;
Xaa at position 146 is Arg or Gln;
Xaa at position 147 is Arg or Gln;
Xaa at position 156 is His, Gly or Ser;
Xaa at position 159 is Ser, Arg, Thr, Tyr, Val or Gly;
Xaa at position 162 is Glu, Leu, Gly or Trp;
Xaa at position 163 is Val, Gly, Arg or Ala;
Xaa at position 169 is Arg, Ser, Leu, Arg or Cys;
Xaa at position 170 is His, Arg or Ser;
wherein optionally 1-11 amino acids from the N-terminus and 1-5 from the C-terminus can be deleted; and
wherein the N-terminus is joined to the C-terminus directly or through a linker capable of joining the N-terminus to the C-terminus and having new C- and N-termini at amino acids;
______________________________________38-39 62-63 123-12439-40 63-64 124-12540-41 64-65 125-12641-42 65-66 126-12742-43 66-67 127-12843-44 67-68 128-12945-46 68-69 129-13048-49 69-70 130-13149-50 70-71 131-13252-53 71-72 132-13353-54 91-92 133-13454-55 92-93 134-13555-56 93-94 135-13656-57 94-95 136-13757-58 95-96 137-13858-59 96-97 138-13959-60 97-98 139-14060-61 98-99 140-14161-62 99-100 141-142 or 142-143.______________________________________
The G-CSF receptor agonists of the present invention may contain amino acid substitutions, deletions and/or insertions and may also have amino acid deletions at either/or both the N- and C-termini.
The more preferred breakpoints at which new C-terminus and N-terminus can be made are; 38-39, 39-40, 40-41, 41-42, 48-49, 53-54, 54-55, 55-56, 56-57, 57-58, 58-59, 59-60, 60-61, 61-62, 62-63, 64-65, 65-66, 66-67, 67-68, 68-69, 69-70, 96-97, 125-126, 126-127, 127-128, 128-129, 129-130, 130-131, 131-132, 132-133, 133-134, 134-135, 135-136, 136-137, 137-138, 138-139, 139-140, 140-141 and 141-142.
The most preferred breakpoints at which new C-terminus and N-terminus can be made are; 38-39, 48-49, 96-97, 125-126, 132-133 and 141-142.
A preferred embodiment of the present invention the linker (L) joining the N-terminus to the C-terminus is a polypeptide selected from the group consisting of:
GlyGlyGlySer (SEQ ID NO:2);
GlyGlyGlySerGlyGlyGlySer (SEQ ID NO:61);
GlyGlyGlySerGlyGlyGlySerGlyGlyGlySer (SEQ ID NO:62);
SerGlyGlySerGlyGlySer (SEQ ID NO:63);
GluPheGlyAsnMet (SEQ ID NO:64);
GluPheGlyGlyAsnMet (SEQ ID NO:65);
GluPheGlyGlyAsnGlyGlyAsnMet (SEQ ID NO:66); and
GlyGlySerAspMetAlaGly (SEQ ID NO:67).
The present invention also includes a human G-CSF receptor agonist polypeptide, comprising a modified G-CSF amino acid sequence of the Formula:
__________________________________________________________________________1 10Xaa Xaa Xaa Gly Pro Ala Ser Ser Leu Pro Gln Ser Xaa 20Leu Leu Xaa Xaa Xaa Glu Gln Val Xaa Lys Xaa Gln Gly Xaa Gly 30 40Ala Xaa Leu Gln Glu Xaa Leu Xaa Ala Thr Tyr Lys Leu Xaa Xaa 50Xaa Glu Xaa Xaa Val Xaa Xaa Gly His Ser Xaa Gly Ile Pro Trp 60 70Ala Pro Leu Ser Ser Xaa Pro Ser Xaa Ala Leu Xaa Leu Ala Gly 80Xaa Leu Ser Gln Leu Gis Ser Gly Leu Phe Leu Tyr Gln Gly Leu 90 100Leu Gln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu 110Xaa Thr Leu Gln Xaa Asp Val Ala Asp Phe Ala Xaa Thr Ile Trp 120 130Gln Gln Met Glu Xaa Xaa Gly Met Ala Pro Ala Leu Gln Pro Thr 140Gln Gly Ala Met Pro Ala Phe Ala Ser Ala Xaa Gln Xaa Xaa Ala 150 160Gly Gly Val Leu Val Ala Ser Xaa Leu Gln Xaa Phe Leu Xaa Xaa 170Ser Tyr Arg Val Leu Xaa Xaa Leu Ala Gln Pro (SEQ ID NO:1)__________________________________________________________________________
wherein
Xaa at position 1 is Thr, Ser, Arg, Tyr or Gly;
Xaa at position 2 is Pro or Leu;
Xaa at position 3 is Leu, Arg, Tyr or Ser;
Xaa at position 13 is Phe, Ser, His, Thr or Pro;
Xaa at position 16 is Lys, Pro, Ser, Thr or His;
Xaa at position 17 is Cys, Ser, Gly, Ala, Ile, Tyr or Arg;
Xaa at position 18 is Leu, Thr, Pro, His, Ile or Cys;
Xaa at position 22 is Arg, Tyr, Ser, Thr or Ala;
Xaa at position 24 is Ile, Pro, Tyr or Leu;
Xaa at position 27 is Asp, or Gly;
Xaa at position 30 is Ala, Ile, Leu or Gly;
Xaa at position 34 is Lys or Ser;
Xaa at position 36 is Cys or Ser;
Xaa at position 42 is Cys or Ser;
Xaa at position 43 is His, Thr, Gly, Val, Lys, Trp, Ala, Arg, Cys, or Leu;
Xaa at position 44 is Pro, Gly, Arg, Asp, Val, Ala, His, Trp, Gln, or Thr;
Xaa at position 46 is Glu, Arg, Phe, Arg, Ile or Ala;
Xaa at position 47 is Leu or Thr;
Xaa at position 49 is Leu, Phe, Arg or Ser;
Xaa at position 50 is Leu, Ile, His, Pro or Tyr;
Xaa at position 54 is Leu or His;
Xaa at position 64 is Cys or Ser;
Xaa at position 67 is Gln, Lys, Leu or Cys;
Xaa at position 70 is Gln, Pro, Leu, Arg or Ser;
Xaa at position 74 is Cys or Ser;
Xaa at position 104 is Asp, Gly or Val;
Xaa at position 108 is Leu, Ala, Val, Arg, Trp, Gln or Gly;
Xaa at position 115 is Thr, His, Leu or Ala;
Xaa at position 120 is Gln, Gly, Arg, Lys or His
Xaa at position 123 is Glu, Arg, Phe or Thr
Xaa at position 144 is Phe, His, Arg, Pro, Leu, Gln or Glu;
Xaa at position 146 is Arg or Gln;
Xaa at position 147 is Arg or Gln;
Xaa at position 156 is His, Gly or Ser;
Xaa at position 159 is Ser, Arg, Thr, Tyr, Val or Gly;
Xaa at position 162 is Glu, Leu, Gly or Trp;
Xaa at position 163 is Val, Gly, Arg or Ala;
Xaa at position 169 is Arg, Ser, Leu, Arg or Cys;
Xaa at position 170 is His, Arg or Ser;
wherein optionally 1-11 amino acids from the N-terminus and 1-5 from the C-terminus can be deleted;
wherein the N-terminus is joined to the C-terminus directly or through a linker capable of joining the N-terminus to the C-terminus and having new C- and N-terminus at amino acids;
2-3
10-11
12-13
18-19
122-123
158-159
169-170.
The present invention also encompasses recombinant human G-CSF receptor agonists co-administered or sequentially with one or more additional colony stimulating factors (CSF) including, cytokines, lymphokines, interleukins, hematopoietic growth factors which include but are not limited to GM-CSF, c-mpl ligand (also known as TPO or MGDF), M-CSF, erythropoietin (EPO), IL-1, IL-4, IL-2, IL-3, IL-5, IL 6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, IL-13, IL-15, LIF, flt3/flk2 ligand, human growth hormone, B-cell growth factor, B-cell differentiation factor, eosinophil differentiation factor and stem cell factor (SCF) also known as steel factor or c-kit ligand (herein collectively referred to as "colony stimulating factors" or "CSF"). These co-administered mixtures may be characterized by having the usual activity of both of the peptides or the mixture may be further characterized by having a biological or physiological activity greater than simply the additive function of the presence of the G-CSF receptor agonists or the second colony stimulating factor alone. The co-administration may also provide an enhanced effect on the activity or an activity different from that expected by the presence of the G-CSF ligand or the second colony stimulating factor. The co-administration may also have an improved activity profile which may include reduction of undesirable biological activities associated with native human G-CSF. In addition to the list above, IL-3 variants taught in WO 94/12639 and WO 94/12638 can be co-administered with the polypeptides of the present invention.
In addition, it is envisioned that in vitro uses would include the ability to stimulate bone marrow and blood cell activation and growth before the expanded cells are infused into patients

BRIEF DESCRIPTION OF THE FIGURES
FIG. 1 schematically illustrates the sequence rearrangement of a protein. The N-terminus (N) and the C-terminus (C) of the native protein are joined through a linker, or joined directly. The protein is opened at a breakpoint creating a new N-terminus (new N) and a new C-terminus (new-C) resulting in a protein with a new linear amino acid sequence. A rearranged molecule may be synthesized de novo as linear molecule and not go through the steps of joining the original N-terminus and the C-terminus and opening of the protein at the breakpoint.
FIG. 2 shows a schematic of Method I, for creating new proteins in which the original N-terminus and C-terminus of the native protein are joined with a linker and different N-terminus and C-terminus of the protein are created. In the example shown the sequence rearrangement results in a new gene encoding a protein with a new N-terminus created at amino acid 97 of the original protein, the original C-terminus (a.a. 174) joined to the amino acid 11 (a.a. 1-10 are deleted) through a linker region and a new C-terminus created at amino acid 96 of the original sequence.
FIG. 3 shows a schematic of Method II, for creating new proteins in which the original N-terminus and C-terminus of the native protein are joined without a linker and different N-terminus and C-terminus of the protein are created. In the example shown the sequence rearrangement results in a new gene encoding a protein with a new N-terminus created at amino acid 97 of the original protein, the original C-terminus (a.a. 174) joined to the original N-terminus and a new C-terminus created at amino acid 96 of the original sequence.
FIG. 4 shows a schematic of Method III, for creating new proteins in which the original N-terminus and C-terminus of the native protein are joined with a linker and different N-terminus and C-terminus of the protein are created. In the example shown the sequence rearrangement results in a new gene encoding a protein with a new N-terminus created at amino acid 97 of the original protein, the original C-terminus (a.a. 174) joined to amino acid 1 through a linker region and a new C-terminus created at amino acid 96 of the original sequence.

DETAILED DESCRIPTION OF THE INVENTION
Receptor agonists of the present invention may be useful in the treatment of diseases characterized by decreased levels of granulocytes of the hematopoietic system.
A G-CSF receptor agonist may be useful in the treatment or prevention of neutropenia. Many drugs may cause bone marrow suppression or hematopoietic deficiencies. Examples of such drugs are AZT, DDI, alkylating agents and anti-metabolites used in chemotherapy, antibiotics such as chloramphenicol, penicillin, gancyclovir, daunomycin and sulfa drugs, phenothiazones, tranquilizers such as meprobamate, analgesics such as aminopyrine and dipyrone, anti-convulsants such as phenytoin or carbamazepine, antithyroids such as propylthiouracil and methimazole and diuretics. G-CSF receptor agonists may be useful in preventing or treating the bone marrow suppression or hematopoietic deficiencies which often occur in patients treated with these drugs.
Hematopoietic deficiencies may also occur as a result of viral, microbial or parasitic infections and as a result of treatment for renal disease or renal failure, e.g., dialysis. The present peptide may be useful in treating such hematopoietic deficiency.
Another aspect of the present invention provides plasmid DNA vectors for use in the method of expression of these novel G-CSF receptor agonists. These vectors contain the novel DNA sequences described above which code for the novel polypeptides of the invention. Appropriate vectors which can transform host cells capable of expressing the G-CSF receptor agonists include expression vectors comprising nucleotide sequences coding for the G-CSF receptor agonists joined to transcriptional and translational regulatory sequences which are selected according to the host cells used. Vectors incorporating modified sequences as described above are included in the present invention and are useful in the production of the modified G-CSF receptor agonist polypeptides. The vector employed in the method also contains selected regulatory sequences in operative association with the DNA coding sequences of the invention and capable of directing the replication and expression thereof in selected host cells.
As another aspect of the present invention, there is provided a novel method for producing the novel family of human G-CSF receptor agonists. The method of the present invention involves culturing suitable cells or cell line, which has been transformed with a vector containing a DNA sequence coding for expression of the novel G-CSF receptor agonist polypeptide. Suitable cells or cell lines may include various strains of bacteria such as E. coli, yeast, mammalian cells, or insect cells may be utilized as host cells in the method of the present invention.
Other aspects of the present invention are methods and therapeutic compositions for treating the conditions referred to above. Such compositions comprise a therapeutically effective amount of one or more of the G-CSF receptor agonists of the present invention in a mixture with a pharmaceutically acceptable carrier. This composition can be administered either parenterally, intravenously or subcutaneously. When administered, the therapeutic composition for use in this invention is preferably in the form of a pyrogen-free, parenterally acceptable aqueous solution. The preparation of such a parenterally acceptable protein solution, having due regard to pH, isotonicity, stability and the like, is within the skill of the art.
The dosage regimen involved in a method for treating the above-described conditions will be determined by the attending physician considering various factors which modify the action of drugs, e.g. the condition, body weight, sex and diet of the patient, the severity of any infection, time of administration and other clinical factors. Generally, a daily regimen may be in the range of 0.5-150 .mu.g/kg of non-glycosylated G-CSF receptor agonists protein per kilogram of body weight. Dosages would be adjusted relative to the activity of a given receptor agonist and it would not be unreasonable to note that dosage regimens may include doses as low as 0.1 microgram and as high as 1 milligram per kilogram of body weight per day. In addition, there may exist specific circumstances where dosages of G-CSF receptor agonist would be adjusted higher or lower than the range of 0.5-150 micrograms per kilogram of body weight. These include co-administration with other CSF or growth factors; co-administration with chemotherapeutic drugs and/or radiation; the use of glycosylated G-CSF receptor agonists; and various patient-related issues mentioned earlier in this section. As indicated above, the therapeutic method and compositions may also include co-administration with other human factors. A non-exclusive list of other appropriate hematopoietins, CSFs and interleukins for simultaneous or serial co-administration with the polypeptides of the present invention includes GM-CSF, c-mpl ligand (also known as TPO or MGDF), M-CSF, erythropoietin (EPO), IL-1, IL-4, IL-2, IL-3, IL-5, IL 6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, IL-13, IL-15, LIF, flt3/flk2 ligand, human growth hormone, B-cell growth factor, B-cell differentiation factor, eosinophil differentiation factor and stem cell factor (SCF) also known as steel factor or c-kit ligand (herein collectively referred to as "colony stimulating factors"), or combinations thereof. In addition to the list above, IL-3 variants taught in WO 94/12639 and WO 94/12638 can be co-administered with the polypeptides of the present invention.
The G-CSF receptor agonists of the present invention may be useful in the mobilization of hematopoietic progenitors and stem cells in peripheral blood. Peripheral blood derived progenitors have been shown to be effective in reconstituting patients in the setting of autologous marrow transplantation. Hematopoietic growth factors, including G-CSF and GM-CSF, have been shown to enhance the number of circulating progenitors and stem cells in the peripheral blood. This has simplified the procedure for peripheral stem cell collection and dramatically decreased the cost of the procedure by decreasing the number of pheresis required. The G-CSF receptor agonist of the present invention may be useful in mobilization of stem cells and further enhance the efficacy of peripheral stem cell transplantation.
The G-CSF receptor agonists of the present invention may also be useful in the ex vivo expansion of hematopoietic progenitors. Colony stimulating factors (CSFs), such as G-CSF, have been administered alone, co-administered with other CSFs, or in combination with bone marrow transplants subsequent to high dose chemotherapy to treat the neutropenia and which is often the result of such treatment. However the period of severe neutropenia may not be totally eliminated. The myeloid lineage, which is comprised of monocytes (macrophages), granulocytes (including neutrophils) and megakaryocytes, is critical in preventing infections and bleeding which can be life-threatening. Neutropenia may also be the result of disease, genetic disorders, drugs, toxins, radiation and many therapeutic treatments such as conventional oncology therapy.
Bone marrow transplants have been used to treat this patient population. However, several problems are associated with the use of bone marrow to reconstitute a compromised hematopoietic system including: 1) the number of stem cells in bone marrow or other tissues, such as spleen or peripheral blood, is limited, 2) Graft Versus Host Disease, 3) graft rejection and 4) possible contamination with tumor cells. Stem cells and progenitor cells make up a very small percentage of the nucleated cells in the bone marrow, spleen and peripheral blood. It is clear that a dose response exists such that a greater number of multipotential hematopoietic progenitors will enhance hematopoietic recovery. Therefore, the in vitro expansion of stem cells should enhance hematopoietic recovery and patient survival. Bone marrow from an allogeneic donor has been used to provide bone marrow for transplant. However, Graft Versus Host Disease and graft rejection limit bone marrow transplantation even in recipients with HLA-matched sibling donors. An alternative to allogeneic bone marrow transplants is autologous bone marrow transplants. In autologous bone marrow transplants, some of the patient's own marrow is harvested prior to myeloablative therapy, e.g. high dose chemotherapy, and is transplanted back into the patient afterwards. Autologous transplants eliminate the risk of Graft Versus Host Disease and graft rejection. However, autologous bone marrow transplants still present problems in terms of the limited number of stems cells in the marrow and possible contamination with tumor cells. The limited number of multipotential hematopoietic progenitors may be overcome by ex-vivo expansion of the multipotential hematopoietic progenitors. In addition, stem cells can be specifically isolated based on the presence of specific surface antigens such as CD34+ in order to decrease tumor cell contamination of the marrow graft.
The following patents contain further details on separating stem cells, CD34+ cells, culturing the cells with hematopoietic factors, the use of the cells for the treatment of patients with hematopoietic disorders and the use of hematopoietic factors for cell expansion and gene therapy.
U.S. Pat. No. 5,061,620 relates to compositions comprising human hematopoietic stem cells provided by separating the stem cells from dedicated cells.
U.S. Pat. No. 5,199,942 describes a method for autologous hematopoietic cell transplantation comprising: (1) obtaining hematopoietic progenitor cells from a patient; (2) ex-vivo expansion of cells with a growth factor selected from the group consisting of IL-3, flt3 ligand, c-kit ligand, GM CSF, IL-1, GM-CSF/IL-3 fusion protein and combinations thereof; (3) administering cellular preparation to a patient.
U.S. Pat. No. 5,240,856 relates to a cell separator that includes an apparatus for automatically controlling the cell separation process.
WO 91/16116 describes devices and methods for selectively isolating and separating target cells from a mixture of cells.
WO 91/18972 describes methods for in vitro culturing of bone marrow, by incubating suspension of bone marrow cells, using a hollow fiber bioreactor.
WO 92/18615 relates to a process for maintaining and expanding bone marrow cells, in a culture medium containing specific mixtures of cytokines, for use in transplants.
WO 93/08268 describes a method for selectively expanding stem cells, comprising the steps of (a) separating CD34+ stem cells from other cells and (b) incubating the separated cells in a selective medium, such that the stem cells are selectively expanded.
WO 93/18136 describes a process for in vitro support of mammalian cells derived from peripheral blood.
WO 93/18648 relates to a composition comprising human neutrophil precursor cells with a high content of myeloblasts and promyelocytes for treating genetic or acquired neutropenia.
WO 94/08039 describes a method of enrichment for human hematopoietic stem cells by selection for cells which express c-kit protein.
WO 94/11493 describes a stem cell population that are CD34+ and small in size, which are isolated using a counterflow elutriation method.
WO 94/27698 relates to a method combining immunoaffinity separation and continuous flow centrifugal separation for the selective separation of a nucleated heterogeneous cell population from a heterogeneous cell mixture.
WO 94/25848 describes a cell separation apparatus for collection and manipulation of target cells.
The long term culturing of highly enriched CD34+ precursors of hematopoietic progenitor cells from human bone marrow in cultures containing IL-1.alpha., IL-3, IL-6 or GM-CSF is discussed in Brandt et al. (J. Clin. Invest. 86:932-941, 1990).
One aspect of the present invention provides a method for selective ex-vivo expansion of stem cells. The term "stem cell" refers to the multipotential hematopoietic cells as well as early myeloid progenitor and precursors cells which can be isolated from bone marrow, spleen or peripheral blood. The term "expansion" refers to the proliferation and differentiation of the cells. The present invention provides a method for selective ex-vivo expansion of stem cells, comprising the steps of; (a) separating stem cells from other cells, (b) culturing the separated stem cells with a selective medium which contains a G-CSF receptor agonist and optionally a second colony stimulating factor, and (c) harvesting the cultured stems cells. Stem cells, as well as committed progenitor cells destined to become neutrophils, erythrocytes, platelets, etc., may be distinguished from most other cells by the presence or absence of particular progenitor marker antigens, such as CD34, that are present on the surface of these cells and/or by morphological characteristics. The phenotype for a highly enriched human stem cell fraction is reported as CD34+, Thy-1+ and lin-, but it is to be understood that the present invention is not limited to the expansion of this stem cell population. The CD34+ enriched human stem cell fraction can be separated by a number of reported methods, including affinity columns or beads, magnetic beads or flow cytometry using antibodies directed to surface antigens such as the CD34+. Further, physical separation methods such as counterflow elutriation may be used to enrich hematopoietic progenitors. The CD34+ progenitors are heterogeneous, and may be divided into several sub-populations characterized by the presence or absence of co-expression of different lineage associated cell surface associated molecules. The most immature progenitor cells do not express any known lineage associated markers, such as HLA-DR or CD38, but they may express CD90(thy-1). Other surface antigens such as CD33, CD38, CD41, CD71, HLA-DR or c-kit can also be used to selectively isolate hematopoietic progenitors. The separated cells can be incubated in selected medium in a culture flask, sterile bag or in hollow fibers. Various colony stimulating factors may be utilized in order to selectively expand cells. Representative factors that have been utilized for ex-vivo expansion of bone marrow include, c-kit ligand, IL-3, G-CSF, GM-CSF, IL-1, IL-6, IL-11, flt-3 ligand or combinations thereof. The proliferation of the stem cells can be monitored by enumerating the number of stem cells and other cells, by standard techniques (e.g. hemacytometer, CFU, LTCIC) or by flow cytometry prior and subsequent to incubation.
Several methods for ex-vivo expansion of stem cells have been reported utilizing a number of selection methods and expansion using various colony stimulating factors including c-kit ligand (Brandt et al., Blood 83:1507-1514, 1994; McKenna et al., Blood 86:3413-3420, 1995), IL-3 (Brandt et al., Blood 83:1507-1514, 1994; Sato et al., Blood 82:3600-3609, 1993), G-CSF (Sato et al., Blood 82:3600-3609, 1993), GM-CSF (Sato et al., Blood 82:3600-3609, 1993), IL-1 (Muench et al., Blood 81:3463-3473, 1993), IL-6 (Sato et al., Blood 82:3600-3609, 1993), IL-11 (Lemoli et al., Exp. Hem. 21:1668-1672, 1993; Sato et al., Blood 82:3600-3609, 1993), flt-3 ligand (McKenna et al., Blood 86:3413 3420, 1995) and/or combinations thereof (Brandt et al., Blood 83:1507 1514, 1994; Haylock et al., Blood 80:1405-1412, 1992, Koller et al., Biotechnology 11:358-363, 1993; Lemoli et al., Exp. Hem. 21:1668-1672, 1993), McKenna et al., Blood 86:3413-3420, 1995; Muench et al., Blood 81:3463-3473, 1993; Patchen et al., Biotherapy 7:13-26, 1994; Sato et al., Blood 82:3600-3609, 1993; Smith et al., Exp. Hem. 21:870-877, 1993; Steen et al., Stem Cells 12:214-224, 1994; Tsujino et al., Exp. Hem. 21:1379-1386, 1993). Among the individual colony stimulating factors, hIL-3 has been shown to be one of the most potent in expanding peripheral blood CD34+ cells (Sato et al., Blood 82:3600-3609, 1993; Kobayashi et al., Blood 73:1836-1841, 1989). However, no single factor has been shown to be as effective as the combination of multiple factors. The present invention provides methods for ex vivo expansion that utilize novel G-CSF receptor agonists.
Another aspect of the invention provides methods of sustaining and/or expanding hematopoietic precursor cells which includes inoculating the cells into a culture vessel which contains a culture medium that has been conditioned by exposure to a stromal cell line such as HS-5 (WO 96/02662, Roecklein and Torok-Strob, Blood 85:997-1105, 1995) that has been supplemented with a G-CSF receptor agonist of the present invention.
Another projected clinical use of growth factors has been in the in vitro activation of hematopoietic progenitors and stem cells for gene therapy. Due to the long life-span of hematopoietic progenitor cells and the distribution of their daughter cells throughout the entire body, hematopoietic progenitor cells are good candidates for ex vivo gene transfection. In order to have the gene of interest incorporated into the genome of the hematopoietic progenitor or stem cell one needs to stimulate cell division and DNA replication. Hematopoietic stem cells cycle at a very low frequency which means that growth factors may be useful to promote gene transduction and thereby enhance the clinical prospects for gene therapy. Potential applications of gene therapy (review Crystal, Science 270:404-410, 1995) include; 1) the treatment of many congenital metabolic disorders and immunodeficiencies (Kay and Woo, Trends Genet. 10:253-257, 1994), 2) neurological disorders (Friedmann, Trends Genet. 10:210-214, 1994), 3) cancer (Culver and Blaese, Trends Genet. 10:174-178, 1994) and 4) infectious diseases (Gilboa and Smith, Trends Genet. 10:139-144, 1994).
There are a variety of methods, known to those with skill in the art, for introducing genetic material into a host cell. A number of vectors, both viral and non-viral have been developed for transferring therapeutic genes into primary cells. Viral based vectors include; 1) replication deficient recombinant retrovirus (Boris-Lawrie and Temin, Curr. Opin. Genet. Dev. 3:102-109, 1993; Boris-Lawrie and Temin, Annal. New York Acad. Sci. 716:59-71, 1994; Miller, Current Top. Microbiol. Immunol. 158:1-24, 1992) and replication-deficient recombinant adenovirus (Berkner, BioTechniques 6:616-629, 1988; Berkner, Current Top. Microbiol. Immunol. 158:39-66, 1992; Brody and Crystal, Annal. New York Acad. Sci. 716:90-103, 1994). Non-viral based vectors include protein/DNA complexes (Cristiano et al., PNAS USA. 90:2122-2126, 1993; Curiel et al., PNAS USA 88:8850-8854, 1991; Curiel, Annal. New York Acad. Sci. 716:36-58, 1994), electroporation and liposome mediated delivery such as cationic liposomes (Farhood et al., Annal. New York Acad. Sci. 716:23-35, 1994).
The present invention provides an improvement to the existing methods of expanding hematopoietic cells, into which new genetic material has been introduced, in that it provides methods utilizing G-CSF receptor agonists that may have improved biological activity and/or physical properties.
Determination of the Linker
The length of the amino acid sequence of the linker can be selected empirically or with guidance from structural information, or by using a combination of the two approaches.
When no structural information is available, a small series of linkers can be prepared for testing using a design whose length is varied in order to span a range from 0 to 50 .ANG. and whose sequence is chosen in order to be consistent with surface exposure (hydrophilicity, Hopp & Woods, Mol. Immunol. 20: 483-489, 1983; Kyte & Doolittle, J. Mol. Biol. 157:105-132, 1982; solvent exposed surface area, Lee & Richards, J. Mol. Biol. 55:379-400, 1971) and the ability to adopt the necessary conformation without deranging the configuration of the c-mpl receptor agonist (conformationally flexible; Karplus & Schulz, Naturwissenschaften 72:212-213, (1985).
Assuming an average of translation of 2.0 to 3.8 .ANG. per residue, this would mean the length to test would be between 0 to 30 residues, with 0 to 15 residues being the preferred range. Exemplary of such an empirical series would be to construct linkers using a cassette sequence such as Gly-Gly-Gly-Ser (SEQ ID NO:2) repeated n times, where n is 1, 2, 3 or 4. Those skilled in the art will recognize that there are many such sequences that vary in length or composition that can serve as linkers with the primary consideration being that they be neither excessively long nor short (cf., Sandhu, Critical Rev. Biotech. 12: 437-462, 1992); if they are too long, entropy effects will likely destabilize the three-dimensional fold, and may also make folding kinetically impractical, and if they are too short, they will likely destabilize the molecule because of torsional or steric strain.
Those skilled in the analysis of protein structural information will recognize that using the distance between the chain ends, defined as the distance between the c-alpha carbons, can be used to define the length of the sequence to be used, or at least to limit the number of possibilities that must be tested in an empirical selection of linkers. They will also recognize that it is sometimes the case that the positions of the ends of the polypeptide chain are ill-defined in structural models derived from x-ray diffraction or nuclear magnetic resonance spectroscopy data, and that when true, this situation will therefore need to be taken into account in order to properly estimate the length of the linker required. From those residues whose positions are well defined are selected two residues that are close in sequence to the chain ends, and the distance between their c-alpha carbons is used to calculate an approximate length for a linker between them. Using the calculated length as a guide, linkers with a range of number of residues (calculated using 2 to 3.8 .ANG. per residue) are then selected. These linkers may be composed of the original sequence, shortened or lengthened as necessary, and when lengthened the additional residues may be chosen to be flexible and hydrophilic as described above; or optionally the original sequence may be substituted for using a series of linkers, one example being the Gly-Gly-Gly-Ser (SEQ ID NO:2) cassette approach mentioned above; or optionally a combination of the original sequence and new sequence having the appropriate total length may be used.
Determination of the Amino and Carboxyl Termini of G-CSF Receptor Agonists
Sequences of G-CSF receptor agonists capable of folding to biologically active states can be prepared by appropriate selection of the beginning (amino terminus) and ending (carboxyl terminus) positions from within the original polypeptide chain while using the linker sequence as described above. Amino and carboxyl termini are selected from within a common stretch of sequence, referred to as a breakpoint region, using the guidelines described below. A novel amino acid sequence is thus generated by selecting amino and carboxyl termini from within the same breakpoint region. In many cases the selection of the new termini will be such that the original position of the carboxyl terminus immediately preceded that of the amino terminus. However, those skilled in the art will recognize that selections of termini anywhere within the region may function, and that these will effectively lead to either deletions or additions to the amino or carboxyl portions of the new sequence.
It is a central tenet of molecular biology that the primary amino acid sequence of a protein dictates folding to the three-dimensional structure necessary for expression of its biological function. Methods are known to those skilled in the art to obtain and interpret three-dimensional structural information using x-ray diffraction of single protein crystals or nuclear magnetic resonance spectroscopy of protein solutions. Examples of structural information that are relevant to the identification of breakpoint regions include the location and type of protein secondary structure (alpha and 3-10 helices, parallel and anti-parallel beta sheets, chain reversals and turns, and loops; Kabsch & Sander, Biopolymers 22: 2577-2637, 1983; the degree of solvent exposure of amino acid residues, the extent and type of interactions of residues with one another (Chothia, Ann. Rev. Biochem. 53:537-572; 1984) and the static and dynamic distribution of conformations along the polypeptide chain (Alber & Mathews, Methods Enzymol. 154: 511-533, 1987). In some cases additional information is known about solvent exposure of residues; one example is a site of post-translational attachment of carbohydrate which is necessarily on the surface of the protein. When experimental structural information is not available, or is not feasible to obtain, methods are also available to analyze the primary amino acid sequence in order to make predictions of protein tertiary and secondary structure, solvent accessibility and the occurrence of turns and loops. Biochemical methods are also sometimes applicable for empirically determining surface exposure when direct structural methods are not feasible; for example, using the identification of sites of chain scission following limited proteolysis in order to infer surface exposure (Gentile & Salvatore, Eur. J. Biochem. 218:603-621, 1993) Thus using either the experimentally derived structural information or predictive methods (e.g., Srinivisan & Rose Proteins: Struct., Funct. & Genetics, 22: 81-99, 1995) the parental amino acid sequence is inspected to classify regions according to whether or not they are integral to the maintenance of secondary and tertiary structure. The occurrence of sequences within regions that are known to be involved in periodic secondary structure (alpha and 3-10 helices, parallel and anti-parallel beta sheets) are regions that should be avoided. Similarly, regions of amino acid sequence that are observed or predicted to have a low degree of solvent exposure are more likely to be part of the so-called hydrophobic core of the protein and should also be avoided for selection of amino and carboxyl termini. In contrast, those regions that are known or predicted to be in surface turns or loops, and especially those regions that are known not to be required for biological activity, are the preferred sites for location of the extremes of the polypeptide chain. Continuous stretches of amino acid sequence that are preferred based on the above criteria are referred to as a breakpoint region.
TABLE 1______________________________________OLIGONUCLEOTIDES______________________________________L-11start.seq GCTCTGAGAG CCGCCAGAGC CGCCAGAGGG CTGCGCAAGG TGGCGTAGAA CGCG (SEQ ID NO:3)L-11stop.seq CAGCCCTCTG GCGGCTCTGG CGGCTCTCAG AGCTTCCTGC TCAAGTCTTT AGAG (SEQ ID NO:4)B1startP.seq GGGCTGCGCA AGGTGGCG (SEQ ID NO:5)b1stopP.seq ACACCATTGG GCCCTGCCAG G (SEQ ID NO:6)39start.seq GATCGACCAT GGCTTACAAG CTGTGCCACC CC (SEQ ID NO:7)38stop.Seq CGATCGAAGC TTATTAGGTG GCACACAGCTTCTCCT (SEQ ID NO:8)97start.seq GATCGACCAT GGCTCCCGAG TTGGGTCCCA CC (SEQ ID NO:9)96stop.Seq CGATCGAAGC TTATTAGGAT ATCCCTTCCAGGGCCT (SEQ ID NO:10)126start.seq GATCGACCAT GGCTATGGCC CCTGCCCTGC AG (SEQ ID NO:11)125stop.Seq CGATCGAAGC TTATTATCCC AGTTCTTCCA TCTGCT (SEQ ID NO:12)133start.seq GATCGACCAT GGCTACCCAG GGTGCCATGC CG (SEQ ID NO:13)132stop.seq CGATCGAAGC TTATTAGGGC TGCAGGGCAG GGGCCA (SEQ ID NO:14)142start.seq GATCGACCAT GGCTTCTGCT TTCCAGCGCC GG (SEQ ID NO:15)141stop.Seq CGATCGAAGC TTATTAGGCG AAGGCCGGCA TGGCAC (SEQ ID NO:16)96for.Seq ATATCCATGG CTCCGGAACT GGGTCCAACT CTG (SEQ ID NO:17)96rev.Seq ACCTCCAGGA AGCTCTGCAG ATGG (SEQ ID NO:18)125for.seq TATATCCATG GCTATGGCTC CAGCTCTGCA ACCAACTCAA GGTGCAATGC CAGCATTTGC ATCTG (SEQ ID NO:19)125rev.seq GATGGCTAGC AACCAGAACA CCACCTGCAC GACGTTGAAA AGCAGATGCA AATGCTGGCA TTG (SEQ ID NO:20)132for.seq TATATCCATG GCTACTCAAG GTGCTATGCC AGCTTTTGCT TCTGCTTTTC AACGTCG (SEQ ID NO:21)132rev.seq GCAGATGGCT AGCAACCAGA ACACCACCTG CACGACGTTG AAAAGCAGAA GCAAAAGC (SEQ ID NO:22)141for.seq CATGGCTTCT GCTTTTCAAC GTCGTGCAGG TGGTGTTCTG GTTG (SEQ ID NO:23)141rev.seq CTAGCAACCA GAACACCACC TGCACGACGT TGAAAAGCAG AAGC (SEQ ID NO:24)49start.seq GATCGACCAT GGCTCTGCTC GGACACTCTC TG (SEQ ID NO:68)48stop.seq CGATCGAAGC TTATTACACC AGCTCCTCGG GGTGGC (SEQ ID NO:69)77start.seq GATCGACCAT GGCTCAACTC CATAGCGGCC TT (SEQ ID NO:70)76stop.seq CGATCGAAGC TTATTAGCTC AAGCAGCCTG CCAGCT (SEQ ID NO:71)82start.seq GATCGACCAT GGCTCTTTTC CTCTACCAGG GG (SEQ ID NO:72)81stop.seq CGATCGAAGC TTATTAGCCG CTATGGAGTT GGCTCA (SEQ ID NO:73)84start.seq GATCGACCAT GGCTCTCTAC CAGGGGCTCC TG (SEQ ID NO:74)83stop.seq CGATCGAAGC TTATTAGAAA AGGCCGCTAT GGAGTT (SEQ ID NO:75)91start.seq GATCGACCAT GGCTGCCCTG GAAGGGATAT CC (SEQ ID NO:76)90stop.seq CGATCGAAGC TTATTACTGC AGGAGCCCCT GGTAGA (SEQ ID NO:77)112start.seq GATCGACCAT GGCTGACTTT GCCACCACCA TC (SEQ ID NO:78)111stop.seq CGATCGAAGC TTATTAGGCG ACGTCCAGCT GCAGTG (SEQ ID NO:79)117start.seq GATCGACCAT GGCTATCTGG CAGCAGATGG AA (SEQ ID NO:80)116stop.seq CGATCGAAGC TTATTAGGTG GTGGCAAAGT CGGCGA (SEQ ID NO:81)119start.seq GATCGACCAT GGCTCAGCAG ATGGAAGAAC TG (SEQ ID NO:82)118stop.seq CGATCGAAGC TTATTACCAG ATGGTGGTGG CAAAGT (SEQ ID NO:83)Z4849at.for CATGGCTTTG TTAGGACATT CTTTAGGTAT TCCATGGGCT CCTCTGAGCT (SEQ ID NO:84)Z4849at.rev CAGAGGAGCC CATGGAATAC CTAAAGAATG TCCTAACAAA GC (SEQ ID NO:85)______________________________________
TABLE 2__________________________________________________________________________DNA sequences__________________________________________________________________________pMON3485.Seq 1 ATGGCTTACA AGCTGTGCCA CCCCGAGGAG CTGGTGCTGC TCGGACACTC 51 TCTGGGCATC CCCTGGGCTC CCCTGAGCTC CTGCCCCAGC CAGGCCCTGC101 AGCTGGCAGG CTGCTTGAGC CAACTCCATA GCGGCCTTTT CCTCTACCAG151 GGGCTCCTGC AGGCCCTGGA AGGGATATCC CCCGAGTTGG GTCCCACCTT201 GGACACACTG CAGCTGGACG TCGCCGACTT TGCCACCACC ATCTGGCAGC251 AGATGGAAGA ACTGGGAATG GCCCCTGCCC TGCAGCCCAC CCAGGGTGCC301 ATGCCGGCCT TCGCCTCTGC TTTCCAGCGC CGGGCAGGAG GGGTCCTGGT351 TGCTAGCCAT CTGCAGAGCT TCCTGGAGGT GTCGTACCGC GTTCTACGCC401 ACCTTGCGCA GCCCTCTGGC GGCTCTGGCG GCTCTCAGAG CTTCCTGCTC451 AAGTCTTTAG AGCAAGTGAG GAAGATCCAG GGCGATGGCG CAGCGCTCCA501 GGAGAAGCTG TGTGCCACCT AATAA (SEQ ID NO:25)pMON3486.Seq 1 ATGGCTCCCG AGTTGGGTCC CACCTTGGAC ACACTGCAGC TGGACGTCGC 51 CGACTTTGCC ACCACCATCT GGCAGCAGAT GGAAGAACTG GGAATGGCCC101 CTGCCCTGCA GCCCACCCAG GGTGCCATGC CGGCCTTCGC CTCTGCTTTC151 CAGCGCCGGG CAGGAGGGGT CCTGGTTGCT AGCCATCTGC AGAGCTTCCT201 GGAGGTGTCG TACCGCGTTC TACGCCACCT TGCGCAGCCC TCTGGCGGCT251 CTGGCGGCTC TCAGAGCTTC CTGCTCAAGT CTTTAGAGCA AGTGAGGAAG301 ATCCAGGGCG ATGGCGCAGC GCTCCAGGAG AAGCTGTGTG CCACCTACAA351 GCTGTGCCAC CCCGAGGAGC TGGTGCTGCT CGGACACTCT CTGGGCATCC401 CCTGGGCTCC CCTGAGCTCC TGCCCCAGCC AGGCCCTGCA GCTGGCAGGC451 TGCTTGAGCC AACTCCATAG CGGCCTTTTC CTCTACCAGG GGCTCCTGCA501 GGCCCTGGAA GGGATATCCT AATAA (SEQ ID NO:26)pMON3487.Seq 1 ATGGCTATGG CCCCTGCCCT GCAGCCCACC CAGGGTGCCA TGCCGGCCTT 51 CGCCTCTGCT TTCCAGCGCC GGGCAGGAGG GGTCCTGGTT GCTAGCCATC101 TGCAGAGCTT CCTGGAGGTG TCGTACCGCG TTCTACGCCA CCTTGCGCAG151 CCCTCTGGCG GCTCTGGCGG CTCTCAGAGC TTCCTGCTCA AGTCTTTAGA201 GCAAGTGAGG AAGATCCAGG GCGATGGCGC AGCGCTCCAG GAGAAGCTGT251 GTGCCACCTA CAAGCTGTGC CACCCCGAGG AGCTGGTGCT GCTCGGACAC301 TCTCTGGGCA TCCCCTGGGC TCCCCTGAGC TCCTGCCCCA GCCAGGCCCT351 GCAGCTGGCA GGCTGCTTGA GCCAACTCCA TAGCGGCCTT TTCCTCTACC401 AGGGGCTCCT GCAGGCCCTG GAAGGGATAT CCCCCGAGTT GGGTCCCACC451 TTGGACACAC TGCAGCTGGA CGTCGCCGAC TTTGCCACCA CCATCTGGCA501 GCAGATGGAA GAACTGGGAT AATAA (SEQ ID NO:27)pMON3488.Seq 1 ATGGCTACCC AGGGTGCCAT GCCGGCCTTC GCCTCTGCTT TCCAGCGCCG 51 GGCAGGAGGG GTCCTGGTTG CTAGCCATCT GCAGAGCTTC CTGGAGGTGT101 CGTACCGCGT TCTACGCCAC CTTGCGCAGC CCTCTGGCGG CTCTGGCGGC151 TCTCAGAGCT TCCTGCTCAA GTCTTTAGAG CAAGTGAGGA AGATCCAGGG201 CGATGGCGCA GCGCTCCAGG AGAAGCTGTG TGCCACCTAC AAGCTGTGCC251 ACCCCGAGGA GCTGGTGCTG CTCGGACACT CTCTGGGCAT CCCCTGGGCT301 CCCCTGAGCT CCTGCCCCAG CCAGGCCCTG CAGCTGGCAG GCTGCTTGAG351 CCAACTCCAT AGCGGCCTTT TCCTCTACCA GGGGCTCCTG CAGGCCCTGG401 AAGGGATATC CCCCGAGTTG GGTCCCACCT TGGACACACT GCAGCTGGAC451 GTCGCCGACT TTGCCACCAC CATCTGGCAG CAGATGGAAG AACTGGGAAT501 GGCCCCTGCC CTGCAGCCCT AATAA (SEQ ID NO:28)pMON3489.Seq 1 ATGGCTTCTG CTTTCCAGCG CCGGGCAGGA GGGGTCCTGG TTGCTAGCCA 51 TCTGCAGAGC TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC101 AGCCCTCTGG CGGCTCTGGC GGCTCTCAGA GCTTCCTGCT CAAGTCTTTA151 GAGCAAGTGA GGAAGATCCA GGGCGATGGC GCAGCGCTCC AGGAGAAGCT201 GTGTGCCACC TACAAGCTGT GCCACCCCGA GGAGCTGGTG CTGCTCGGAC251 ACTCTCTGGG CATCCCCTGG GCTCCCCTGA GCTCCTGCCC CAGCCAGGCC301 CTGCAGCTGG CAGGCTGCTT GAGCCAACTC CATAGCGGCC TTTTCCTCTA351 CCAGGGGCTC CTGCAGGCCC TGGAAGGGAT ATCCCCCGAG TTGGGTCCCA401 CCTTGGACAC ACTGCAGCTG GACGTCGCCG ACTTTGCCAC CACCATCTGG451 CAGCAGATGG AAGAACTGGG AATGGCCCCT GCCCTGCAGC CCACCCAGGG501 TGCCATGCCG GCCTTCGCCT AATAA (SEQ ID NO:29)pMON3490.seq 1 ATGGCTTACA AGCTGTGCCA CCCCGAGGAG CTGGTGCTGC TCGGACACTC 51 TCTGGGCATC CCCTGGGCTC CCCTGAGCTC CTGCCCCAGC CAGGCCCTGC101 AGCTGGCAGG CTGCTTGAGC CAACTCCATA GCGGCCTTTT CCTCTACCAG151 GGGCTCCTGC AGGCCCTGGA AGGGATATCC CCCGAGTTGG GTCCCACCTT201 GGACACACTG CAGCTGGACG TCGCCGACTT TGCCACCACC ATCTGGCAGC251 AGATGGAAGA ACTGGGAATG GCCCCTGCCC TGCAGCCCAC CCAGGGTGCC301 ATGCCGGCCT TCGCCTCTGC TTTCCAGCGC CGGGCAGGAG GGGTCCTGGT351 TGCTAGCCAT CTGCAGAGCT TCCTGGAGGT GTCGTACCGC GTTCTACGCC401 ACCTTGCGCA GCCCACACCA TTGGGCCCTG CCAGCTCCCT GCCCCAGAGC451 TTCCTGCTCA AGTCTTTAGA GCAAGTGAGA AAGATCCAGG GCGATGGCGC501 AGCGCTCCAG GAGAAGCTGT GTGCCACCTA ATAA (SEQ ID NO:30)pMON3491.seq 1 ATGGCTCCCG AGTTGGGTCC CACCTTGGAC ACACTGCAGC TGGACGTCGC 51 CGACTTTGCC ACCACCATCT GGCAGCAGAT GGAAGAACTG GGAATGGCCC101 CTGCCCTGCA GCCCACCCAG GGTGCCATGC CGGCCTTCGC CTCTGCTTTC151 CAGCGCCGGG CAGGAGGGGT CCTGGTTGCT AGCCATCTGC AGAGCTTCCT201 GGAGGTGTCG TACCGCGTTC TACGCCACCT TGCGCAGCCC ACACCATTGG251 GCCCTGCCAG CTCCCTGCCC CAGAGCTTCC TGCTCAAGTC TTTAGAGCAA301 GTGAGAAAGA TCCAGGGCGA TGGCGCAGCG CTCCAGGAGA AGCTGTGTGC351 CACCTACAAG CTGTGCCACC CCGAGGAGCT GGTGCTGCTC GGACACTCTC401 TGGGCATCCC CTGGGCTCCC CTGAGCTCCT GCCCCAGCCA GGCCCTGCAG451 CTGGCAGGCT GCTTGAGCCA ACTCCATAGC GGCCTTTTCC TCTACCAGGG501 GCTCCTGCAG GCCCTGGAAG GGATATCCTA ATAA (SEQ ID NO:31)pMON3492.seq 1 ATGGCTATGG CCCCTGCCCT GCAGCCCACC CAGGGTGCCA TGCCGGCCTT 51 CGCCTCTGCT TTCCAGCGCC GGGCAGGAGG GGTCCTGGTT GCTAGCCATC101 TGCAGAGCTT CCTGGAGGTG TCGTACCGCG TTCTACGCCA CCTTGCGCAG151 CCCACACCAT TGGGCCCTGC CAGCTCCCTG CCCCAGAGCT TCCTGCTCAA201 GTCTTTAGAG CAAGTGAGAA AGATCCAGGG CGATGGCGCA GCGCTCCAGG251 AGAAGCTGTG TGCCACCTAC AAGCTGTGCC ACCCCGAGGA GCTGGTGCTG301 CTCGGACACT CTCTGGGCAT CCCCTGGGCT CCCCTGAGCT CCTGCCCCAG351 CCAGGCCCTG CAGCTGGCAG GCTGCTTGAG CCAACTCCAT AGCGGCCTTT401 TCCTCTACCA GGGGCTCCTG CAGGCCCTGG AAGGGATATC CCCCGAGTTG451 GGTCCCACCT TGGACACACT GCAGCTGGAC GTCGCCGACT TTGCCACCAC501 CATCTGGCAG CAGATGGAAG AACTGGGATA ATAA (SEQ ID NO:32)pMON3493.seq 1 ATGGCTACCC AGGGTGCCAT GCCGGCCTTC GCCTCTGCTT TCCAGCGCCG 51 GGCAGGAGGG GTCCTGGTTG CTAGCCATCT GCAGAGCTTC CTGGAGGTGT101 CGTACCGCGT TCTACGCCAC CTTGCGCAGC CCACACCATT GGGCCCTGCC151 AGCTCCCTGC CCCAGAGCTT CCTGCTCAAG TCTTTAGAGC AAGTGAGAAA201 GATCCAGGGC GATGGCGCAG CGCTCCAGGA GAAGCTGTGT GCCACCTACA251 AGCTGTGCCA CCCCGAGGAG CTGGTGCTGC TCGGACACTC TCTGGGCATC301 CCCTGGGCTC CCCTGAGCTC CTGCCCCAGC CAGGCCCTGC AGCTGGCAGG351 CTGCTTGAGC CAACTCCATA GCGGCCTTTT CCTCTACCAG GGGCTCCTGC401 AGGCCCTGGA AGGGATATCC CCCGAGTTGG GTCCCACCTT GGACACACTG451 CAGCTGGACG TCGCCGACTT TGCCACCACC ATCTGGCAGC AGATGGAAGA501 ACTGGGAATG GCCCCTGCCC TGCAGCCCTA ATAA (SEQ ID NO:33)pMON3494.seq 1 ATGGCTTCTG CTTTCCAGCG CCGGGCAGGA GGGGTCCTGG TTGCTAGCCA 51 TCTGCAGAGC TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC101 AGCCCACACC ATTGGGCCCT GCCAGCTCCC TGCCCCAGAG CTTCCTGCTC151 AAGTCTTTAG AGCAAGTGAG AAAGATCCAG GGCGATGGCG CAGCGCTCCA201 GGAGAAGCTG TGTGCCACCT ACAAGCTGTG CCACCCCGAG GAGCTGGTGC251 TGCTCGGACA CTCTCTGGGC ATCCCCTGGG CTCCCCTGAG CTCCTGCCCC301 AGCCAGGCCC TGCAGCTGGC AGGCTGCTTG AGCCAACTCC ATAGCGGCCT351 TTTCCTCTAC CAGGGGCTCC TGCAGGCCCT GGAAGGGATA TCCCCCGAGT401 TGGGTCCCAC CTTGGACACA CTGCAGCTGG ACGTCGCCGA CTTTGCCACC451 ACCATCTGGC AGCAGATGGA AGAACTGGGA ATGGCCCCTG CCCTGCAGCC501 CACCCAGGGT GCCATGCCGG CCTTCGCCTA ATAA (SEQ ID NO:34)pMON25181.seq 1 ATGGCTCCGG AACTGGGTCC AACTCTGGAC ACACTGCAGC TGGACGTCGC 51 CGACTTTGCC ACCACCATCT GGCAGCAGAT GGAAGAACTG GGAATGGCCC101 CTGCCCTGCA GCCCACCCAG GGTGCCATGC CGGCCTTCGC CTCTGCTTTC151 CAGCGCCGGG CAGGAGGGGT CCTGGTTGCT AGCCATCTGC AGAGCTTCCT201 GGAGGTGTCG TACCGCGTTC TACGCCACCT TGCGCAGCCC ACACCATTGG251 GCCCTGCCAG CTCCCTGCCC CAGAGCTTCC TGCTCAAGTC TTTAGAGCAA301 GTGAGAAAGA TCCAGGGCGA TGGCGCAGCG CTCCAGGAGA AGCTGTGTGC351 CACCTACAAG CTGTGCCACC CCGAGGAGCT GGTGCTGCTC GGACACTCTC401 TGGGCATCCC CTGGGCTCCC CTGAGCTCCT GCCCCAGCCA GGCCCTGCAG451 CTGGCAGGCT GCTTGAGCCA ACTCCATAGC GGCCTTTTCC TCTACCAGGG501 GCTCCTGCAG GCCCTGGAAG GGATATCCTA A (SEQ ID NO:35)pMON25182.seq 1 ATGGCTATGG CTCCAGCTCT GCAACCAACT CAAGGTGCAA TGCCAGCATT 51 TGCATCTGCT TTTCAACGTC GTGCAGGTGG TGTTCTGGTT GCTAGCCATC101 TGCAGAGCTT CCTGGAGGTG TCGTACCGCG TTCTACGCCA CCTTGCGCAG151 CCCACACCAT TGGGCCCTGC CAGCTCCCTG CCCCAGAGCT TCCTGCTCAA201 GTCTTTAGAG CAAGTGAGAA AGATCCAGGG CGATGGCGCA GCGCTCCAGG251 AGAAGCTGTG TGCCACCTAC AAGCTGTGCC ACCCCGAGGA GCTGGTGCTG301 CTCGGACACT CTCTGGGCAT CCCCTGGGCT CCCCTGAGCT CCTGCCCCAG351 CCAGGCCCTG CAGCTGGCAG GCTGCTTGAG CCAACTCCAT AGCGGCCTTT401 TCCTCTACCA GGGGCTCCTG CAGGCCCTGG AAGGGATATC CCCCGAGTTG451 GGTCCCACCT TGGACACACT GCAGCTGGAC GTCGCCGACT TTGCCACCAC501 CATCTGGCAG CAGATGGAAG AACTGGGATA A (SEQ ID NO:36)pMON25183.seq 1 ATGGCTACTC AAGGTGCTAT GCCAGCTTTT GCTTCTGCTT TTCAACGTCG 51 TGCAGGTGGT GTTCTGGTTG CTAGCCATCT GCAGAGCTTC CTGGAGGTGT101 CGTACCGCGT TCTACGCCAC CTTGCGCAGC CCACACCATT GGGCCCTGCC151 AGCTCCCTGC CCCAGAGCTT CCTGCTCAAG TCTTTAGAGC AAGTGAGAAA201 GATCCAGGGC GATGGCGCAG CGCTCCAGGA GAAGCTGTGT GCCACCTACA251 AGCTGTGCCA CCCCGAGGAG CTGGTGCTGC TCGGACACTC TCTGGGCATC301 CCCTGGGCTC CCCTGAGCTC CTGCCCCAGC CAGGCCCTGC AGCTGGCAGG351 CTGCTTGAGC CAACTCCATA GCGGCCTTTT CCTCTACCAG GGGCTCCTGC401 AGGCCCTGGA AGGGATATCC CCCGAGTTGG GTCCCACCTT GGACACACTG451 CAGCTGGACG TCGCCGACTT TGCCACCACC ATCTGGCAGC AGATGGAAGA501 ACTGGGAATG GCCCCTGCCC TGCAGCCCTA A (SEQ ID NO:37)pMON25184.seq 1 ATGGCTTCTG CTTTTCAACG TCGTGCAGGT GGTGTTCTGG TTGCTAGCCA 51 TCTGCAGAGC TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC101 AGCCCACACC ATTGGGCCCT GCCAGCTCCC TGCCCCAGAG CTTCCTGCTC151 AAGTCTTTAG AGCAAGTGAG AAAGATCCAG GGCGATGGCG CAGCGCTCCA201 GGAGAAGCTG TGTGCCACCT ACAAGCTGTG CCACCCCGAG GAGCTGGTGC251 TGCTCGGACA CTCTCTGGGC ATCCCCTGGG CTCCCCTGAG CTCCTGCCCC301 AGCCAGGCCC TGCAGCTGGC AGGCTGCTTG AGCCAACTCC ATAGCGGCCT351 TTTCCTCTAC CAGGGGCTCC TGCAGGCCCT GGAAGGGATA TCCCCCGAGT401 TGGGTCCCAC CTTGGACACA CTGCAGCTGG ACGTCGCCGA CTTTGCCACC451 ACCATCTGGC AGCAGATGGA AGAACTGGGA ATGGCCCCTG CCCTGCAGCC501 CACCCAGGGT GCCATGCCGG CCTTCGCCTA A (SEQ ID NO:38)pMON25185.seq 1 ATGGCTCCGG AACTGGGTCC AACTCTGGAC ACACTGCAGC TGGACGTCGC 51 CGACTTTGCC ACCACCATCT GGCAGCAGAT GGAAGAACTG GGAATGGCCC101 CTGCCCTGCA GCCCACCCAG GGTGCCATGC CGGCCTTCGC CTCTGCTTTC151 CAGCGCCGGG CAGGAGGGGT CCTGGTTGCT AGCCATCTGC AGAGCTTCCT201 GGAGGTGTCG TACCGCGTTC TACGCCACCT TGCGCAGCCC TCTGGCGGCT251 CTGGCGGCTC TCAGAGCTTC CTGCTCAAGT CTTTAGAGCA AGTGAGAAAG301 ATCCAGGGCG ATGGCGCAGC GCTCCAGGAG AAGCTGTGTG CCACCTACAA351 GCTGTGCCAC CCCGAGGAGC TGGTGCTGCT CGGACACTCT CTGGGCATCC401 CCTGGGCTCC CCTGAGCTCC TGCCCCAGCC AGGCCCTGCA GCTGGCAGGC451 TGCTTGAGCC AACTCCATAG CGGCCTTTTC CTCTACCAGG GGCTCCTGCA501 GGCCCTGGAA GGGATATCCT AA (SEQ ID NO:39)pMON25186.seq 1 ATGGCTATGG CTCCAGCTCT GCAACCAACT CAAGGTGCAA TGCCAGCATT 51 TGCATCTGCT TTTCAACGTC GTGCAGGTGG TGTTCTGGTT GCTAGCCATC101 TGCAGAGCTT CCTGGAGGTG TCGTACCGCG TTCTACGCCA CCTTGCGCAG151 CCCTCTGGCG GCTCTGGCGG CTCTCAGAGC TTCCTGCTCA AGTCTTTAGA201 GCAAGTGAGA AAGATCCAGG GCGATGGCGC AGCGCTCCAG GAGAAGCTGT251 GTGCCACCTA CAAGCTGTGC CACCCCGAGG AGCTGGTGCT GCTCGGACAC301 TCTCTGGGCA TCCCCTGGGC TCCCCTGAGC TCCTGCCCCA GCCAGGCCCT351 GCAGCTGGCA GGCTGCTTGA GCCAACTCCA TAGCGGCCTT TTCCTCTACC401 AGGGGCTCCT GCAGGCCCTG GAAGGGATAT CCCCCGAGTT GGGTCCCACC451 TTGGACACAC TGCAGCTGGA CGTCGCCGAC TTTGCCACCA CCATCTGGCA501 GCAGATGGAA GAACTGGGAT AA (SEQ ID NO:40)pMON25187.seq 1 ATGGCTACTC AAGGTGCTAT GCCAGCTTTT GCTTCTGCTT TTCAACGTCG 51 TGCAGGTGGT GTTCTGGTTG CTAGCCATCT GCAGAGCTTC CTGGAGGTGT101 CGTACCGCGT TCTACGCCAC CTTGCGCAGC CCTCTGGCGG CTCTGGCGGC151 TCTCAGAGCT TCCTGCTCAA GTCTTTAGAG CAAGTGAGAA AGATCCAGGG201 CGATGGCGCA GCGCTCCAGG AGAAGCTGTG TGCCACCTAC AAGCTGTGCC251 ACCCCGAGGA GCTGGTGCTG CTCGGACACT CTCTGGGCAT CCCCTGGGCT301 CCCCTGAGCT CCTGCCCCAG CCAGGCCCTG CAGCTGGCAG GCTGCTTGAG351 CCAACTCCAT AGCGGCCTTT TCCTCTACCA GGGGCTCCTG CAGGCCCTGG401 AAGGGATATC CCCCGAGTTG GGTCCCACCT TGGACACACT GCAGCTGGAC451 GTCGCCGACT TTGCCACCAC CATCTGGCAG CAGATGGAAG AACTGGGAAT501 GGCCCCTGCC CTGCAGCCCT AA (SEQ ID NO:41)pMON25188.seq 1 ATGGCTTCTG CTTTTCAACG TCGTGCAGGT GGTGTTCTGG TTGCTAGCCA 51 TCTGCAGAGC TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC101 AGCCCTCTGG CGGCTCTGGC GGCTCTCAGA GCTTCCTGCT CAAGTCTTTA151 GAGCAAGTGA GAAAGATCCA GGGCGATGGC GCAGCGCTCC AGGAGAAGCT201 GTGTGCCACC TACAAGCTGT GCCACCCCGA GGAGCTGGTG CTGCTCGGAC251 ACTCTCTGGG CATCCCCTGG GCTCCCCTGA GCTCCTGCCC CAGCCAGGCC301 CTGCAGCTGG CAGGCTGCTT GAGCCAACTC CATAGCGGCC TTTTCCTCTA351 CCAGGGGCTC CTGCAGGCCC TGGAAGGGAT ATCCCCCGAG TTGGGTCCCA401 CCTTGGACAC ACTGCAGCTG GACGTCGCCG ACTTTGCCAC CACCATCTGG451 CAGCAGATGG AAGAACTGGG AATGGCCCCT GCCCTGCAGC CCACCCAGGG501 TGCCATGCCG GCCTTCGCCT AA (SEQ ID NO:42)pMON3460.seq 1 ATGGCTCTGC TCGGACACTC TCTGGGCATC CCCTGGGCTC CCCTGAGCTC 51 CTGCCCCAGC CAGGCCCTGC AGCTGGCAGG CTGCTTGAGC CAACTCCATA101 GCGGCCTTTT CCTCTACCAG GGGCTCCTGC AGGCCCTGGA AGGGATATCC151 CCCGAGTTGG GTCCCACCTT GGACACACTG CAGCTGGACG TCGCCGACTT201 TGCCACCACC ATCTGGCAGC AGATGGAAGA ACTGGGAATG GCCCCTGCCC251 TGCAGCCCAC CCAGGGTGCC ATGCCGGCCT TCGCCTCTGC TTTCCAGCGC301 CGGGCAGGAG GGGTCCTGGT TGCTAGCCAT CTGCAGAGCT TCCTGGAGGT351 GTCGTACCGC GTTCTACGCC ACCTTGCGCA GCCCACACCA TTGGGCCCTG401 CCAGCTCCCT GCCCCAGAGC TTCCTGCTCA AGTCTTTAGA GCAAGTGAGA451 AAGATCCAGG GCGATGGCGC AGCGCTCCAG GAGAAGCTGT GTGCCACCTA501 CAAGCTGTGC CACCCCGAGG AGCTGGTGTA ATAA (SEQ ID NO:86)pMON3461.seq 1 ATGGCTCAAC TCCATAGCGG CCTTTTCCTC TACCAGGGGC TCCTGCAGGC 51 CCTGGAAGGG ATATCCCCCG AGTTGGGTCC CACCTTGGAC ACACTGCAGC101 TGGACGTCGC CGACTTTGCC ACCACCATCT GGCAGCAGAT GGAAGAACTG151 GGAATGGCCC CTGCCCTGCA GCCCACCCAG GGTGCCATGC CGGCCTTCGC201 CTCTGCTTTC CAGCGCCGGG CAGGAGGGGT CCTGGTTGCT AGCCATCTGC251 AGAGCTTCCT GGAGGTGTCG TACCGCGTTC TACGCCACCT TGCGCAGCCC301 ACACCATTGG GCCCTGCCAG CTCCCTGCCC CAGAGCTTCC TGCTCAAGTC351 TTTAGAGCAA GTGAGAAAGA TCCAGGGCGA TGGCGCAGCG CTCCAGGAGA401 AGCTGTGTGC CACCTACAAG CTGTGCCACC CCGAGGAGCT GGTGCTGCTC451 GGACACTCTC TGGGCATCCC CTGGGCTCCC CTGAGCTCCT GCCCCAGCCA501 GGCCCTGCAG CTGGCAGGCT GCTTGAGCTA ATAA (SEQ ID NO:87)pMON3462.seq 1 ATGGCTCTTT TCCTCTACCA GGGGCTCCTG CAGGCCCTGG AAGGGATATC 51 CCCCGAGTTG GGTCCCACCT TGGACACACT GCAGCTGGAC GTCGCCGACT101 TTGCCACCAC CATCTGGCAG CAGATGGAAG AACTGGGAAT GGCCCCTGCC151 CTGCAGCCCA CCCAGGGTGC CATGCCGGCC TTCGCCTCTG CTTTCCAGCG201 CCGGGCAGGA GGGGTCCTGG TTGCTAGCCA TCTGCAGAGC TTCCTGGAGG251 TGTCGTACCG CGTTCTACGC CACCTTGCGC AGCCCACACC ATTGGGCCCT301 GCCAGCTCCC TGCCCCAGAG CTTCCTGCTC AAGTCTTTAG AGCAAGTGAG351 AAAGATCCAG GGCGATGGCG CAGCGCTCCA GGAGAAGCTG TGTGCCACCT401 ACAAGCTGTG CCACCCCGAG GAGCTGGTGC TGCTCGGACA CTCTCTGGGC451 ATCCCCTGGG CTCCCCTGAG CTCCTGCCCC AGCCAGGCCC TGCAGCTGGC501 AGGCTGCTTG AGCCAACTCC ATAGCGGCTA ATAA (SEQ ID NO:88)pMON3463.seq 1 ATGGCTCTCT ACCAGGGGCT CCTGCAGGCC CTGGAAGGGA TATCCCCCGA 51 GTTGGGTCCC ACCTTGGACA CACTGCAGCT GGACGTCGCC GACTTTGCCA101 CCACCATCTG GCAGCAGATG GAAGAACTGG GAATGGCCCC TGCCCTGCAG151 CCCACCCAGG GTGCCATGCC GGCCTTCGCC TCTGCTTTCC AGCGCCGGGC201 AGGAGGGGTC CTGGTTGCTA GCCATCTGCA GAGCTTCCTG GAGGTGTCGT251 ACCGCGTTCT ACGCCACCTT GCGCAGCCCA CACCATTGGG CCCTGCCAGC301 TCCCTGCCCC AGAGCTTCCT GCTCAAGTCT TTAGAGCAAG TGAGAAAGAT351 CCAGGGCGAT GGCGCAGCGC TCCAGGAGAA GCTGTGTGCC ACCTACAAGC401 TGTGCCACCC CGAGGAGCTG GTGCTGCTCG GACACTCTCT GGGCATCCCC451 TGGGCTCCCC TGAGCTCCTG CCCCAGCCAG GCCCTGCAGC TGGCAGGCTG501 CTTGAGCCAA CTCCATAGCG GCCTTTTCTA ATAA (SEQ ID NO:89)pMON3464.seq 1 ATGGCTGCCC TGGAAGGGAT ATCCCCCGAG TTGGGTCCCA CCTTGGACAC 51 ACTGCAGCTG GACGTCGCCG ACTTTGCCAC CACCATCTGG CAGCAGATGG101 AAGAACTGGG AATGGCCCCT GCCCTGCAGC CCACCCAGGG TGCCATGCCG151 GCCTTCGCCT CTGCTTTCCA GCGCCGGGCA GGAGGGGTCC TGGTTGCTAG201 CCATCTGCAG AGCTTCCTGG AGGTGTCGTA CCGCGTTCTA CGCCACCTTG251 CGCAGCCCAC ACCATTGGGC CCTGCCAGCT CCCTGCCCCA GAGCTTCCTG301 CTCAAGTCTT TAGAGCAAGT GAGAAAGATC CAGGGCGATG GCGCAGCGCT351 CCAGGAGAAG CTGTGTGCCA CCTACAAGCT GTGCCACCCC GAGGAGCTGG401 TGCTGCTCGG ACACTCTCTG GGCATCCCCT GGGCTCCCCT GAGCTCCTGC451 CCCAGCCAGG CCCTGCAGCT GGCAGGCTGC TTGAGCCAAC TCCATAGCGG501 CCTTTTCCTC TACCAGGGGC TCCTGCAGTA ATAA (SEQ ID NO:90)pMON3465.seq 1 ATGGCTGACT TTGCCACCAC CATCTGGCAG CAGATGGAAG AACTGGGAAT 51 GGCCCCTGCC CTGCAGCCCA CCCAGGGTGC CATGCCGGCC TTCGCCTCTG101 CTTTCCAGCG CCGGGCAGGA GGGGTCCTGG TTGCTAGCCA TCTGCAGAGC151 TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC AGCCCACACC201 ATTGGGCCCT GCCAGCTCCC TGCCCCAGAG CTTCCTGCTC AAGTCTTTAG251 AGCAAGTGAG AAAGATCCAG GGCGATGGCG CAGCGCTCCA GGAGAAGCTG301 TGTGCCACCT ACAAGCTGTG CCACCCCGAG GAGCTGGTGC TGCTCGGACA351 CTCTCTGGGC ATCCCCTGGG CTCCCCTGAG CTCCTGCCCC AGCCAGGCCC401 TGCAGCTGGC AGGCTGCTTG AGCCAACTCC ATAGCGGCCT TTTCCTCTAC451 CAGGGGCTCC TGCAGGCCCT GGAAGGGATA TCCCCCGAGT TGGGTCCCAC501 CTTGGACACA CTGCAGCTGG ACGTCGCCTA ATAA (SEQ ID NO:91)pMON 3466.seq 1 ATGGCTATCT GGCAGCAGAT GGAAGAACTG GGAATGGCCC CTGCCCTGCA 51 GCCCACCCAG GGTGCCATGC CGGCCTTCGC CTCTGCTTTC CAGCGCCGGG101 CAGGAGGGGT CCTGGTTGCT AGCCATCTGC AGAGCTTCCT GGAGGTGTCG151 TACCGCGTTC TACGCCACCT TGCGCAGCCC ACACCATTGG GCCCTGCCAG201 CTCCCTGCCC CAGAGCTTCC TGCTCAAGTC TTTAGAGCAA GTGAGAAAGA251 TCCAGGGCGA TGGCGCAGCG CTCCAGGAGA AGCTGTGTGC CACCTACAAG301 CTGTGCCACC CCGAGGAGCT GGTGCTGCTC GGACACTCTC TGGGCATCCC351 CTGGGCTCCC CTGAGCTCCT GCCCCAGCCA GGCCCTGCAG CTGGCAGGCT401 GCTTGAGCCA ACTCCATAGC GGCCTTTTCC TCTACCAGGG GCTCCTGCAG451 GCCCTGGAAG GGATATCCCC CGAGTTGGGT CCCACCTTGG ACACACTGCA501 GCTGGACGTC GCCGACTTTG CCACCACCTA ATAA (SEQ ID NO:92)pMON3467.seq 1 ATGGCTCAGC AGATGGAAGA ACTGGGAATG GCCCCTGCCC TGCAGCCCAC 51 CCAGGGTGCC ATGCCGGCCT TCGCCTCTGC TTTCCAGCGC CGGGCAGGAG101 GGGTCCTGGT TGCTAGCCAT CTGCAGAGCT TCCTGGAGGT GTCGTACCGC151 GTTCTACGCC ACCTTGCGCA GCCCACACCA TTGGGCCCTG CCAGCTCCCT201 GCCCCAGAGC TTCCTGCTCA AGTCTTTAGA GCAAGTGAGA AAGATCCAGG251 GCGATGGCGC AGCGCTCCAG GAGAAGCTGT GTGCCACCTA CAAGCTGTGC301 CACCCCGAGG AGCTGGTGCT GCTCGGACAC TCTCTGGGCA TCCCCTGGGC351 TCCCCTGAGC TCCTGCCCCA GCCAGGCCCT GCAGCTGGCA GGCTGCTTGA401 GCCAACTCCA TAGCGGCCTT TTCCTCTACC AGGGGCTCCT GCAGGCCCTG451 GAAGGGATAT CCCCCGAGTT GGGTCCCACC TTGGACACAC TGCAGCTGGA501 CGTCGCCGAC TTTGCCACCA CCATCTGGTA ATAA (SEQ ID NO:93)pMON3499.seq 1 ATGGCTTTGT TAGGACATTC TTTAGGTATT CCATGGGCTC CTCTGAGCTC 51 CTGCCCCAGC CAGGCCCTGC AGCTGGCAGG CTGCTTGAGC CAACTCCATA101 GCGGCCTTTT CCTCTACCAG GGGCTCCTGC AGGCCCTGGA AGGGATATCC151 CCCGAGTTGG GTCCCACCTT GGACACACTG CAGCTGGACG TCGCCGACTT201 TGCCACCACC ATCTGGCAGC AGATGGAAGA ACTGGGAATG GCCCCTGCCC251 TGCAGCCCAC CCAGGGTGCC ATGCCGGCCT TCGCCTCTGC TTTCCAGCGC301 CGGGCAGGAG GGGTCCTGGT TGCTAGCCAT CTGCAGAGCT TCCTGGAGGT351 GTCGTACCGC GTTCTACGCC ACCTTGCGCA GCCCACACCA TTGGGCCCTG401 CCAGCTCCCT GCCCCAGAGC TTCCTGCTCA AGTCTTTAGA GCAAGTGAGA451 AAGATCCAGG GCGATGGCGC AGCGCTCCAG GAGAAGCTGT GTGCCACCTA501 CAAGCTGTGC CACCCCGAGG AGCTGGTGTA ATAA (SEQ ID NO:94)pG1110.Seq 1 CAGAGCTTCC TGCTCAAGTC TTTAGAGCAA GTGAGGAAGA TCCAGGGCGA 51 TGGCGCAGCG CTCCAGGAGA AGCTGTGTGC CACCTACAAG CTGTGCCACC101 CCGAGGAGCT GGTGCTGCTC GGACACTCTC TGGGCATCCC CTGGGCTCCC151 CTGAGCTCCT GCCCCAGCCA GGCCCTGCAG CTGGCAGGCT GCTTGAGCCA201 ACTCCATAGC GGCCTTTTCC TCTACCAGGG GCTCCTGCAG GCCCTGGAAG251 GGATATCCCC CGAGTTGGGT CCCACCTTGG ACACACTGCA GCTGGACGTC301 GCCGACTTTG CCACCACCAT CTGGCAGCAG ATGGAAGAAC TGGGAATGGC351 CCCTGCCCTG CAGCCCACCC AGGGTGCCAT GCCGGCCTTC GCCTCTGCTT401 TCCAGCGCCG GGCAGGAGGG GTCCTGGTTG CTAGCCATCT GCAGAGCTTC451 CTGGAGGTGT CGTACCGCGT TCTACGCCAC CTTGCGCAGC CCGACATGGC501 TACACCATTA GGCCCTGCCA GCTCCCTGCC C (SEQ ID NO:116)pG123122.Seq 1 GAACTGGGAA TGGCCCCTGC CCTGCAGCCC ACCCAGGGTG CCATGCCGGC 51 CTTCGCCTCT GCTTTCCAGC GCCGGGCAGG AGGGGTCCTG GTTGCTAGCC101 ATCTGCAGAG CTTCCTGGAG GTGTCGTACC GCGTTCTACG CCACCTTGCG151 CAGCCCGACA TGGCTACACC ATTAGGCCCT GCCAGCTCCC TGCCCCAGAG201 CTTCCTGCTC AAGTCTTTAG AGCAAGTGAG GAAGATCCAG GGCGATGGCG251 CAGCGCTCCA GGAGAAGCTG TGTGCCACCT ACAAGCTGTG CCACCCCGAG301 GAGCTGGTGC TGCTCGGACA CTCTCTGGGC ATCCCCTGGG CTCCCCTGAG351 CTCCTGCCCC AGCCAGGCCC TGCAGCTGGC AGGCTGCTTG AGCCAACTCC401 ATAGCGGCCT TTTCCTCTAC CAGGGGCTCC TGCAGGCCCT GGAAGGGATA451 TCCCCCGAGT TGGGTCCCAC CTTGGACACA CTGCAGCTGG ACGTCGCCGA501 CTTTGCCACC ACCATCTGGC AGCAGATGGA A (SEQ ID NO:117)pG125124.Seq 1 GGAATGGCCC CTGCCCTGCA GCCCACCCAG GGTGCCATGC CGGCCTTCGC 51 CTCTGCTTTC CAGCGCCGGG CAGGAGGGGT CCTGGTTGCT AGCCATCTGC101 AGAGCTTCCT GGAGGTGTCG TACCGCGTTC TACGCCACCT TGCGCAGCCC151 GACATGGCTA CACCATTAGG CCCTGCCAGC TCCCTGCCCC AGAGCTTCCT201 GCTCAAGTCT TTAGAGCAAG TGAGGAAGAT CCAGGGCGAT GGCGCAGCGC251 TCCAGGAGAA GCTGTGTGCC ACCTACAAGC TGTGCCACCC CGAGGAGCTG301 GTGCTGCTCG GACACTCTCT GGGCATCCCC TGGGCTCCCC TGAGCTCCTG351 CCCCAGCCAG GCCCTGCAGC TGGCAGGCTG CTTGAGCCAA CTCCATAGCG401 GCCTTTTCCT CTACCAGGGG CTCCTGCAGG CCCTGGAAGG GATATCCCCC451 GAGTTGGGTC CCACCTTGGA CACACTGCAG CTGGACGTCG CCGACTTTGC501 CACCACCATC TGGCAGCAGA TGGAAGAACT G (SEQ ID NO:118)pG1312.Seq 1 TTCCTGCTCA AGTCTTTAGA GCAAGTGAGG AAGATCCAGG GCGATGGCGC 51 AGCGCTCCAG GAGAAGCTGT GTGCCACCTA CAAGCTGTGC CACCCCGAGG101 AGCTGGTGCT GCTCGGACAC TCTCTGGGCA TCCCCTGGGC TCCCCTGAGC151 TCCTGCCCCA GCCAGGCCCT GCAGCTGGCA GGCTGCTTGA GCCAACTCCA201 TAGCGGCCTT TTCCTCTACC AGGGGCTCCT GCAGGCCCTG GAAGGGATAT251 CCCCCGAGTT GGGTCCCACC TTGGACACAC TGCAGCTGGA CGTCGCCGAC301 TTTGCCACCA CCATCTGGCA GCAGATGGAA GAACTGGGAA TGGCCCCTGC351 CCTGCAGCCC ACCCAGGGTG CCATGCCGGC CTTCGCCTCT GCTTTCCAGC401 GCCGGGCAGG AGGGGTCCTG GTTGCTAGCC ATCTGCAGAG CTTCCTGGAG451 GTGTCGTACC GCGTTCTACG CCACCTTGCG CAGCCCGACA TGGCTACACC501 ATTAGGCCCT GCCAGCTCCC TGCCCCAGAG C (SEQ ID NO:119)pG159158.Seq 1 AGCTTCCTGG AGGTGTCGTA CCGCGTTCTA CGCCACCTTG CGCAGCCCGA 51 CATGGCTACA CCATTAGGCC CTGCCAGCTC CCTGCCCCAG AGCTTCCTGC101 TCAAGTCTTT AGAGCAAGTG AGGAAGATCC AGGGCGATGG CGCAGCGCTC151 CAGGAGAAGC TGTGTGCCAC CTACAAGCTG TGCCACCCCG AGGAGCTGGT201 GCTGCTCGGA CACTCTCTGG GCATCCCCTG GGCTCCCCTG AGCTCCTGCC251 CCAGCCAGGC CCTGCAGCTG GCAGGCTGCT TGAGCCAACT CCATAGCGGC301 CTTTTCCTCT ACCAGGGGCT CCTGCAGGCC CTGGAAGGGA TATCCCCCGA351 GTTGGGTCCC ACCTTGGACA CACTGCAGCT GGACGTCGCC GACTTTGCCA401 CCACCATCTG GCAGCAGATG GAAGAACTGG GAATGGCCCC TGCCCTGCAG451 CCCACCCAGG GTGCCATGCC GGCCTTCGCC TCTGCTTTCC AGCGCCGGGC501 AGGAGGGGTC CTGGTTGCTA GCCATCTGCA G (SEQ ID NO:120)pG1918.Seq 1 GAGCAAGTGA GGAAGATCCA GGGCGATGGC GCAGCGCTCC AGGAGAAGCT 51 GTGTGCCACC TACAAGCTGT GCCACCCCGA GGAGCTGGTG CTGCTCGGAC101 ACTCTCTGGG CATCCCCTGG GCTCCCCTGA GCTCCTGCCC CAGCCAGGCC151 CTGCAGCTGG CAGGCTGCTT GAGCCAACTC CATAGCGGCC TTTTCCTCTA201 CCAGGGGCTC CTGCAGGCCC TGGAAGGGAT ATCCCCCGAG TTGGGTCCCA251 CCTTGGACAC ACTGCAGCTG GACGTCGCCG ACTTTGCCAC CACCATCTGG301 CAGCAGATGG AAGAACTGGG AATGGCCCCT GCCCTGCAGC CCACCCAGGG351 TGCCATGCCG GCCTTCGCCT CTGCTTTCCA GCGCCGGGCA GGAGGGGTCC401 TGGTTGCTAG CCATCTGCAG AGCTTCCTGG AGGTGTCGTA CCGCGTTCTA451 CGCCACCTTG CGCAGCCCGA CATGGCTACA CCATTAGGCC CTGCCAGCTC501 CCTGCCCCAG AGCTTCCTGC TCAAGTCTTT A (SEQ ID NO:121)pG32.Seq 1 TTAGGCCCTG CCAGCTCCCT GCCCCAGAGC TTCCTGCTCA AGTCTTTAGA 51 GCAAGTGAGG AAGATCCAGG GCGATGGCGC AGCGCTCCAG GAGAAGCTGT101 GTGCCACCTA CAAGCTGTGC CACCCCGAGG AGCTGGTGCT GCTCGGACAC151 TCTCTGGGCA TCCCCTGGGC TCCCCTGAGC TCCTGCCCCA GCCAGGCCCT201 GCAGCTGGCA GGCTGCTTGA GCCAACTCCA TAGCGGCCTT TTCCTCTACC251 AGGGGCTCCT GCAGGCCCTG GAAGGGATAT CCCCCGAGTT GGGTCCCACC301 TTGGACACAC TGCAGCTGGA CGTCGCCGAC TTTGCCACCA CCATCTGGCA351 GCAGATGGAA GAACTGGGAA TGGCCCCTGC CCTGCAGCCC ACCCAGGGTG401 CCATGCCGGC CTTCGCCTCT GCTTTCCAGC GCCGGGCAGG AGGGGTCCTG451 GTTGCTAGCC ATCTGCAGAG CTTCCTGGAG GTGTCGTACC GCGTTCTACG501 CCACCTTGCG CAGCCCGACA TGGCTACACC A (SEQ ID NO:122)pG4948.Seq 1 CTGCTCGGAC ACTCTCTGGG CATCCCCTGG GCTCCCCTGA GCTCCTGCCC 51 CAGCCAGGCC CTGCAGCTGG CAGGCTGCTT GAGCCAACTC CATAGCGGCC101 TTTTCCTCTA CCAGGGGCTC CTGCAGGCCC TGGAAGGGAT ATCCCCCGAG151 TTGGGTCCCA CCTTGGACAC ACTGCAGCTG GACGTCGCCG ACTTTGCCAC201 CACCATCTGG CAGCAGATGG AAGAACTGGG AATGGCCCCT GCCCTGCAGC251 CCACCCAGGG TGCCATGCCG GCCTTCGCCT CTGCTTTCCA GCGCCGGGCA301 GGAGGGGTCC TGGTTGCTAG CCATCTGCAG AGCTTCCTGG AGGTGTCGTA351 CCGCGTTCTA CGCCACCTTG CGCAGCCCGA CATGGCTACA CCATTAGGCC401 CTGCCAGCTC CCTGCCCCAG AGCTTCCTGC TCAAGTCTTT AGAGCAAGTG451 AGGAAGATCC AGGGCGATGG CGCAGCGCTC CAGGAGAAGC TGTGTGCCAC501 CTACAAGCTG TGCCACCCCG AGGAGCTGGT G (SEQ ID NO:123)pG6059.Seq 1 CCCCTGAGCT CCTGCCCCAG CCAGGCCCTG CAGCTGGCAG GCTGCTTGAG 51 CCAACTCCAT AGCGGCCTTT TCCTCTACCA GGGGCTCCTG CAGGCCCTGG101 AAGGGATATC CCCCGAGTTG GGTCCCACCT TGGACACACT GCAGCTGGAC151 GTCGCCGACT TTGCCACCAC CATCTGGCAG CAGATGGAAG AACTGGGAAT201 GGCCCCTGCC CTGCAGCCCA CCCAGGGTGC CATGCCGGCC TTCGCCTCTG251 CTTTCCAGCG CCGGGCAGGA GGGGTCCTGG TTGCTAGCCA TCTGCAGAGC301 TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC AGCCCGACAT351 GGCTACACCA TTAGGCCCTG CCAGCTCCCT GCCCCAGAGC TTCCTGCTCA401 AGTCTTTAGA GCAAGTGAGG AAGATCCAGG GCGATGGCGC AGCGCTCCAG451 GAGAAGCTGT GTGCCACCTA CAAGCTGTGC CACCCCGAGG AGCTGGTGCT501 GCTCGGACAC TCTCTGGGCA TCCCCTGGGC T (SEQ ID NO:124)pG6766.Seq 1 CAGGCCCTGC AGCTGGCAGG CTGCTTGAGC CAACTCCATA GCGGCCTTTT 51 CCTCTACCAG GGGCTCCTGC AGGCCCTGGA AGGGATATCC CCCGAGTTGG101 GTCCCACCTT GGACACACTG CAGCTGGACG TCGCCGACTT TGCCACCACC151 ATCTGGCAGC AGATGGAAGA ACTGGGAATG GCCCCTGCCC TGCAGCCCAC201 CCAGGGTGCC ATGCCGGCCT TCGCCTCTGC TTTCCAGCGC CGGGCAGGAG251 GGGTCCTGGT TGCTAGCCAT CTGCAGAGCT TCCTGGAGGT GTCGTACCGC301 GTTCTACGCC ACCTTGCGCA GCCCGACATG GCTACACCAT TAGGCCCTGC351 CAGCTCCCTG CCCCAGAGCT TCCTGCTCAA GTCTTTAGAG CAAGTGAGGA401 AGATCCAGGG CGATGGCGCA GCGCTCCAGG AGAAGCTGTG TGCCACCTAC451 AAGCTGTGCC ACCCCGAGGA GCTGGTGCTG CTCGGACACT CTCTGGGCAT501 CCCCTGGGCT CCCCTGAGCT CCTGCCCCAG C (SEQ ID NO:125)pG6968.Seq 1 CTGCAGCTGG CAGGCTGCTT GAGCCAACTC CATAGCGGCC TTTTCCTCTA 51 CCAGGGGCTC CTGCAGGCCC TGGAAGGGAT ATCCCCCGAG TTGGGTCCCA101 CCTTGGACAC ACTGCAGCTG GACGTCGCCG ACTTTGCCAC CACCATCTGG151 CAGCAGATGG AAGAACTGGG AATGGCCCCT GCCCTGCAGC CCACCCAGGG201 TGCCATGCCG GCCTTCGCCT CTGCTTTCCA GCGCCGGGCA GGAGGGGTCC251 TGGTTGCTAG CCATCTGCAG AGCTTCCTGG AGGTGTCGTA CCGCGTTCTA301 CGCCACCTTG CGCAGCCCGA CATGGCTACA CCATTAGGCC CTGCCAGCTC351 CCTGCCCCAG AGCTTCCTGC TCAAGTCTTT AGAGCAAGTG AGGAAGATCC401 AGGGCGATGG CGCAGCGCTC CAGGAGAAGC TGTGTGCCAC CTACAAGCTG451 TGCCACCCCG AGGAGCTGGT GCTGCTCGGA CACTCTCTGG GCATCCCCTG501 GGCTCCCCTG AGCTCCTGCC CCAGCCAGGC C (SEQ ID NO:126)pG7170.Seq 1 CTGGCAGGCT GCTTGAGCCA ACTCCATAGC GGCCTTTTCC TCTACCAGGG 51 GCTCCTGCAG GCCCTGGAAG GGATATCCCC CGAGTTGGGT CCCACCTTGG101 ACACACTGCA GCTGGACGTC GCCGACTTTG CCACCACCAT CTGGCAGCAG151 ATGGAAGAAC TGGGAATGGC CCCTGCCCTG CAGCCCACCC AGGGTGCCAT201 GCCGGCCTTC GCCTCTGCTT TCCAGCGCCG GGCAGGAGGG GTCCTGGTTG251 CTAGCCATCT GCAGAGCTTC CTGGAGGTGT CGTACCGCGT TCTACGCCAC301 CTTGCGCAGC CCGACATGGC TACACCATTA GGCCCTGCCA GCTCCCTGCC351 CCAGAGCTTC CTGCTCAAGT CTTTAGAGCA AGTGAGGAAG ATCCAGGGCG401 ATGGCGCAGC GCTCCAGGAG AAGCTGTGTG CCACCTACAA GCTGTGCCAC451 CCCGAGGAGC TGGTGCTGCT CGGACACTCT CTGGGCATCC CCTGGGCTCC501 CCTGAGCTCC TGCCCCAGCC AGGCCCTGCA G (SEQ ID NO:127)pG170169_seq 1 CACCTTGCGC AGCCCGACAT GGCTACACCA TTAGGCCCTG CCAGCTCCCT 51 GCCCCAGAGC TTCCTGCTCA AGTCTTTAGA GCAAGTGAGG AAGATCCAGG101 GCGATGGCGC AGCGCTCCAG GAGAAGCTGT GTGCCACCTA CAAGCTGTGC151 CACCCCGAGG AGCTGGTGCT GCTCGGACAC TCTCTGGGCA TCCCCTGGGC201 TCCCCTGAGC TCCTGCCCCA GCCAGGCCCT GCAGCTGGCA GGCTGCTTGA251 GCCAACTCCA TAGCGGCCTT TTCCTCTACC AGGGGCTCCT GCAGGCCCTG301 GAAGGGATAT CCCCCGAGTT GGGTCCCACC TTGGACACAC TGCAGCTGGA351 CGTCGCCGAC TTTGCCACCA CCATCTGGCA GCAGATGGAA GAACTGGGAA401 TGGCCCCTGC CCTGCAGCCC ACCCAGGGTG CCATGCCGGC CTTCGCCTCT451 GCTTTCCAGC GCCGGGCAGG AGGGGTCCTG GTTGCTAGCC ATCTGCAGAG501 CTTCCTGGAG GTGTCGTACC GCGTTCTACG C (SEQ ID NO:129)__________________________________________________________________________
TABLE 3__________________________________________________________________________PROTEIN SEQUENCES__________________________________________________________________________pMON3485.PepTyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu Gly His SerLeu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln AlaLeu Gln Leu Ala Gly Cys Leu Ser Gln Leu His Ser Gly Leu PheLeu Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pro GluLeu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val Ala Asp PheAla Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly Met Ala ProAla Leu Gln Pro Thr Gln Gly Ala Met Pro Ala Phe Ala Ser AlaPhe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser His Leu GlnSer Phe Leu Glu Val Ser Tyr Arg Val Leu Arg His Leu Ala GlnPro Ser Gly Gly Ser Gly Gly Ser Gln Ser Phe Leu Leu Lys SerLeu Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu GlnGlu Lys Leu Cys Ala Thr (SEQ ID NO:43)pMON3486.PepPro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val AlaAsp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly MetAla Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Ala Phe AlaSer Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser HisLeu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Leu Arg His LeuAla Gln Pro Ser Gly Gly Ser Gly Gly Ser Gln Ser Phe Leu LeuLys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Ala AlaLeu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cys His Pro GluGlu Leu Val Leu Leu Gly His Ser Leu Gly Ile Pro Trp Ala ProLeu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys LeuSer Gln Leu His Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu GlnAla Leu Glu Gly Ile Ser (SEQ ID NO:44)pMON3487.PepMet Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Ala PheAla Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala SerHis Leu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Leu Arg HisLeu Ala Gln Pro Ser Gly Gly Ser Gly Gly Ser Gln Ser Phe LeuLeu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly Asp Gly AlaAla Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cys His ProGlu Glu Leu Val Leu Leu Gly His Ser Leu Gly Ile Pro Trp AlaPro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly CysLeu Ser Gln Leu His Ser Gly Leu Phe Leu Tyr Gln Gly Leu LeuGln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu AspGln Met Glu Glu Leu Gly (SEQ ID NO:45)pMON3488.PepThr Gln Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gln Arg ArgAla Gly Gly Val Leu Val Ala Ser His Leu Gln Ser Phe Leu GluVal Ser Tyr Arg Val Leu Arg His Leu Ala Gln Pro Ser Gly GlySer Gly Gly Ser Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln ValArg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu CysAla Thr Tyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu GlyHis Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro SerGln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu His Ser GlyLeu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gly Ile SerPro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val AlaAsp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly MetAla Pro Ala Leu Gln Pro (SEQ ID NO:46)pMON3489.PepSer Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser HisLeu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Leu Arg His LeuAla Gln Pro Ser Gly Gly Ser Gly Gly Ser Gln Ser Phe Leu LeuLys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Ala AlaLeu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cys His Pro GluGlu Leu Val Leu Leu Gly His Ser Leu Gly Ile Pro Trp Ala ProLeu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys LeuSer Gln Leu His Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu GlnAla Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu Asp ThrLeu Gln Leu Asp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln GlnMet Glu Glu Leu Gly Met Ala Pro Ala Leu Gln Pro Thr Gln GlyAla Met Pro Ala Phe Ala (SEQ ID NO:47)pMON3490.PepTyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu Gly His SerLeu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln AlaLeu Gln Leu Ala Gly Cys Leu Ser Gln Leu His Ser Gly Leu PheLeu Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gly ILe Ser Pro GluLeu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val Ala Asp PheAla Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly Met Ala ProAla Leu Gln Pro Thr Gln Gly Ala Met Pro Ala Phe Ala Ser AlaPhe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser His Leu GlnSer Phe Leu Glu Val Ser Tyr Arg Val Leu Arg His Leu Ala GlnPro Thr Pro Leu Gly Pro Ala Ser Ser Leu Pro Gln Ser Phe LeuLeu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly Asp Gly AlaAla Leu Gln Glu Lys Leu Cys Ala Thr (SEQ ID NO:48)pMON3491.PepPro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val AlaAsp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly MetAla Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Ala Phe AlaSer Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser HisLeu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Leu Arg His LeuAla Gln Pro Thr Pro Leu Gly Pro Ala Ser Ser Leu Pro Gln SerPhe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly AspGly Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu CysHis Pro Glu Glu Leu Val Leu Leu Gly His Ser Leu Gly Ile ProTrp Ala Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu AlaGly Cys Leu Ser Gln Leu His Ser Gly Leu Phe Leu Tyr Gln GlyLeu Leu Gln Ala Leu Glu Gly Ile Ser (SEQ ID NO:49)pMON3492.PepMet Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Ala PheAla Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala SerHis Leu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Leu Arg HisLeu Ala Gln Pro Thr Pro Leu Gly Pro Ala Ser Ser Leu Pro GlnSer Phe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln GlyAsp Gly Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys LeuCys His Pro Glu Glu Leu Val Leu Leu Gly His Ser Leu Gly IlePro Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln LeuAla Gly Cys Leu Ser Gln Leu His Ser Gly Leu Phe Leu Tyr GlnGly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly ProThr Leu Asp Thr Leu Gln Leu Asp Val Ala Asp Phe Ala Thr ThrIle Trp Gln Gln Met Glu Glu Leu Gly (SEQ ID NO:50)pMON3493.PepThr Gln Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gln Arg ArgAla Gly Gly Val Leu Val Ala Ser His Leu Gln Ser Phe Leu GluVal Ser Tyr Arg Val Leu Arg His Leu Ala Gln Pro Thr Pro LeuGly Pro Ala Ser Ser Leu Pro Gln Ser Phe Leu Leu Lys Ser LeuGlu Gln Val Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln GluLys Leu Cys Ala Thr Tyr Lys Leu Cys His Pro Glu Glu Leu ValLeu Leu Gly His Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser SerCys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln LeuHis Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu GluGly Ile Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln LeuAsp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu GluLeu Gly Met Ala Pro Ala Leu Gln Pro (SEQ ID NO:51)pMON3494.PepSer Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser HisLeu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Leu Arg His LeuAla Gln Pro Thr Pro Leu Gly Pro Ala Ser Ser Leu Pro Gln SerPhe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly AspGly Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu CysHis Pro Glu Glu Leu Val Leu Leu Gly His Ser Leu Gly Ile ProTrp Ala Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu AlaGly Cys Leu Ser Gln Leu His Ser Gly Leu Phe Leu Tyr Gln GlyLeu Leu Gln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro ThrLeu Asp Thr Leu Gln Leu Asp Val Ala Asp Phe Ala Thr Thr IleTrp Gln Gln Met Glu Glu Leu Gly Met Ala Pro Ala Leu Gln ProThr Gln Gly Ala Met Pro Ala Phe Ala (SEQ ID NO:52)pMON25181.pepPro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val Ala Asp PheAla Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly Met Ala Pro Ala LeuGln Pro Thr Gln Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gln Arg ArgAla Gly Gly Val Leu Val Ala Ser His Leu Gln Ser Phe Leu Glu Val SerTyr Arg Val Leu Arg His Leu Ala Gln Pro Thr Pro Leu Gly Pro Ala SerSer Leu Pro Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys IleGln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys LeuCys His Pro Glu Glu Leu Val Leu Leu Gly His Ser Leu Gly Ile Pro TrpAla Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys LeuSer Gln Leu His Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala LeuGlu Gly Ile Ser (SEQ ID NO:53)pMON25182.pepMet Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Ala Phe Ala SerAla Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser His Leu Gln SerPhe Leu Glu Val Ser Tyr Arg Val Leu Arg His Leu Ala Gln Pro Thr ProLeu Gly Pro Ala Ser Ser Leu Pro Gln Ser Phe Leu Leu Lys Ser Leu GluGln Val Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu CysAla Thr Tyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu Gly His SerLeu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu GlnLeu Ala Gly Cys Leu Ser Gln Leu His Ser Gly Leu Phe Leu Tyr Gln GlyLeu Leu Gln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu AspThr Leu Gln Leu Asp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln Gln MetGlu Glu Leu Gly (SEQ ID NO:54)pMON25183.pepThr Gln Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gln Arg Arg Ala GlyGly Val Leu Val Ala Ser His Leu Gln Ser Phe Leu Glu Val Ser Tyr ArgVal Leu Arg His Leu Ala Gln Pro Thr Pro Leu Gly Pro Ala Ser Ser LeuPro Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln GlyAsp Gly Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cys HisPro Glu Glu Leu Val Leu Leu Gly His Ser Leu Gly Ile Pro Trp Ala ProLeu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser GlnLeu His Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu GlyIle Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val AlaAsp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly Met Ala ProAla Leu Gln Pro (SEQ ID NO:55)pMON25184.pepSer Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser His Leu GlnSer Phe Leu Glu Val Ser Tyr Arg Val Leu Arg His Leu Ala Gln Pro ThrPro Leu Gly Pro Ala Ser Ser Leu Pro Gln Ser Phe Leu Leu Lys Ser LeuGlu Gln Val Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys LeuCys Ala Thr Tyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu Gly HisSer Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln Ala LeuGln Leu Ala Gly Cys Leu Ser Gln Leu His Ser Gly Leu Phe Leu Tyr GlnGly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr LeuAsp Thr Leu Gln Leu Asp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln GlnMet Glu Glu Leu Gly Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala MetPro Ala Phe Ala (SEQ ID NO:56)pMON25185.pepPro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val Ala Asp PheAla Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly Met Ala Pro Ala LeuGln Pro Thr Gln Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gln Arg ArgAla Gly Gly Val Leu Val Ala Ser His Leu Gln Ser Phe Leu Glu Val SerTyr Arg Val Leu Arg His Leu Ala Gln Pro Ser Gly Gly Ser Gly Gly SerGln Ser Phe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly AspGly Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cys His ProGlu Glu Leu Val Leu Leu Gly His Ser Leu Gly Ile Pro Trp Ala Pro LeuSer Ser Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln LeuHis Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gly IleSer (SEQ ID NO:57)pMON25186.pepMet Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Ala Phe Ala SerAla Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser His Leu Gln SerPhe Leu Glu Val Ser Tyr Arg Val Leu Arg His Leu Ala Gln Pro Ser GlyGly Ser Gly Gly Ser Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln Val ArgLys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Ala Thr Tyr Lys LeuCys His Pro Glu Glu Leu Val Leu Leu Gly His Ser Leu Gly Ile Pro TrpAla Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys LeuSer Gln Leu His Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala LeuGlu Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu AspVal Ala Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly(SEQ ID NO:58)pMON25187.pepThr Gln Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gln Arg Arg Ala GlyGly Val Leu Val Ala Ser His Leu Gln Ser Phe Leu Glu Val Ser Tyr ArgVal Leu Arg His Leu Ala Gln Pro Ser Gly Gly Ser Gly Gly Ser Gln SerPhe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly Asp Gly AlaAla Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cys His Pro Glu GluLeu Val Leu Leu Gly His Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser SerCys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu His SerGly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gly Ile Ser ProGlu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val Ala Asp Phe AlaThr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly Met Ala Pro Ala Leu GlnPro (SEQ ID NO:59)pMON25188.pepSer Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser His Leu GlnSer Phe Leu Glu Val Ser Tyr Arg Val Leu Arg His Leu Ala Gln Pro SerGly Gly Ser Gly Gly Ser Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln ValArg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cys Ala ThrTyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu Gly His Ser Leu GlyIle Pro Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu AlaGly Cys Leu Ser Gln Leu His Ser Gly Leu Phe Leu Tyr Gln Gly Leu LeuGln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr LeuGln Leu Asp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu GluLeu Gly Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Ala PheAla (SEQ ID NO:60)pMON3460.PepLeu Leu Gly His Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser SerCys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln LeuHis Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu GluGly Ile Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln LeuAsp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu GluLeu Gly Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met ProAla Phe Ala Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Leu ValAla Ser His Leu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val LeuArg His Leu Ala Gln Pro Thr Pro Leu Gly Pro Ala Ser Ser LeuPro Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys IleGln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr TyrLys Leu Cys His Pro Glu Glu Leu Val (SEQ ID NO:95)pMON3461.PepGln Leu His Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln AlaLeu Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr LeuGln Leu Asp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln Gln MetGlu Glu Leu Gly Met Ala Pro Ala Leu Gln Pro Thr Gln Gly AlaMet Pro Ala Phe Ala Ser Ala Phe Gln Arg Arg Ala Gly Gly ValLeu Val Ala Ser His Leu Gln Ser Phe Leu Glu Val Ser Tyr ArgVal Leu Arg His Leu Ala Gln Pro Thr Pro Leu Gly Pro Ala SerSer Leu Pro Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln Val ArgLys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cys AlaThr Tyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu Gly His'0 - Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro Ser GlnAla Leu Gln Leu Ala Gly Cys Leu Ser (SEQ ID NO:96)3462.PepLeu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gly Ile SerPro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val AlaAsp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly MetAla Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Ala Phe AlaSer Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser HisLeu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Leu Arg His LeuAla Gln Pro Thr Pro Leu Gly Pro Ala Ser Ser Leu Pro Gln SerPhe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly AspGly Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu CysHis Pro Glu Glu Leu Val Leu Leu Gly His Ser Leu Gly Ile ProTrp Ala Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu AlaGly Cys Leu Ser Gln Leu His Ser Gly (SEQ ID NO:97)3463.PepLeu Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pro GluLeu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val Ala Asp PheAla Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly Met Ala ProAla Leu Gln Pro Thr Gln Gly Ala Met Pro Ala Phe Ala Ser AlaPhe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser His Leu GlnSer Phe Leu Glu Val Ser Tyr Arg Val Leu Arg His Leu Ala GlnPro Thr Pro Leu Gly Pro Ala Ser Ser Leu Pro Gln Ser Phe LeuLeu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly Asp Gly AlaAla Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cys His ProGlu Glu Leu Val Leu Leu Gly His Ser Leu Gly Ile Pro Trp AlaPro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly CysLeu Ser Gln Leu His Ser Gly Leu Phe (SEQ ID NO:98)3464.PepAla Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu Asp ThrLeu Gln Leu Asp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln GlnMet Glu Glu Leu Gly Met Ala Pro Ala Leu Gln Pro Thr Gln GlyAla Met Pro Ala Phe Ala Ser Ala Phe Gln Arg Arg Ala Gly GlyVal Leu Val Ala Ser His Leu Gln Ser Phe Leu Glu Val Ser TyrArg Val Leu Arg His Leu Ala Gln Pro Thr Pro Leu Gly Pro AlaSer Ser Leu Pro Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln ValArg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu CysAla Thr Tyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu GlyHis Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro SerGln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu His Ser GlyLeu Phe Leu Tyr Gln Gly Leu Leu Gln (SEQ ID NO:99)3465.PepAsp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly MetAla Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Ala Phe AlaSer Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser HisLeu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Leu Arg His LeuAla Gln Pro Thr Pro Leu Gly Pro Ala Ser Ser Leu Pro Gln SerPhe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly AspGly Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu CysHis Pro Glu Glu Leu Val Leu Leu Gly His Ser Leu Gly Ile ProTrp Ala Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu AlaGly Cys Leu Ser Gln Leu His Ser Gly Leu Phe Leu Tyr Gln GlyLeu Leu Gln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro ThrLeu Asp Thr Leu Gln Leu Asp Val Ala (SEQ ID NO:100)3466.PepIle Trp Gln Gln Met Glu Glu Leu Gly Met Ala Pro Ala Leu GlnPro Thr Gln Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gln ArgArg Ala Gly Gly Val Leu Val Ala Ser His Leu Gln Ser Phe LeuGlu Val Ser Tyr Arg Val Leu Arg His Leu Ala Gln Pro Thr ProLeu Gly Pro Ala Ser Ser Leu Pro Gln Ser Phe Leu Leu Lys SerLeu Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu GlnGlu Lys Leu Cys Ala Thr Tyr Lys Leu Cys His Pro Glu Glu LeuVal Leu Leu Gly His Ser Leu Gly Ile Pro Trp Ala Pro Leu SerSer Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser GlnLeu His Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala LeuGlu Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu GlnLeu Asp Val Ala Asp Phe Ala Thr Thr (SEQ ID NO:101)3467.PepGln Gln Met Glu Glu Leu Gly Met Ala Pro Ala Leu Gln Pro ThrGln Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gln Arg Arg AlaGly Gly Val Leu Val Ala Ser His Leu Gln Ser Phe Leu Glu ValSer Tyr Arg Val Leu Arg His Leu Ala Gln Pro Thr Pro Leu GlyPro Ala Ser Ser Leu Pro Gln Ser Phe Leu Leu Lys Ser Leu GluGln Val Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu LysLeu Cys Ala Thr Tyr Lys Leu Cys His Pro Glu Glu Leu Val LeuLeu Gly His Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser CysPro Ser Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu HisSer Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu GlyIle Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu AspVal Ala Asp Phe Ala Thr Thr Ile Trp (SEQ ID NO:102)3499.PepLeu Leu Gly His Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser SerCys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln LeuHis Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu GluGly Ile Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln LeuAsp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu GluLeu Gly Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met ProAla Phe Ala Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Leu ValAla Ser His Leu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val LeuArg His Leu Ala Gln Pro Thr Pro Leu Gly Pro Ala Ser Ser LeuPro Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys IleGln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr TyrLys Leu Cys His Pro Glu Glu Leu Val (SEQ ID NO:103)pG1110.pepGlnSerPheLeuLeuLysSerLeuGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuValLeuLeuGlyHisSerLeuGlyIleProTrpAlaProLeuSerSerCysProSerGlnAlaLeuGlnLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGluGluLeuGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGlnSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrProLeuGlyProAlaSerSerLeuPro (SEQ ID NO:104)pG123122.pepGluLeuGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGlnSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrProLeuGlyProAlaSerSerLeuProGlnSerPheLeuLeuLysSerLeuGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuValLeuLeuGlyHisSerLeuGlyIleProTrpAlaProLeuSerSerCysProSerGlnAlaLeuGlnLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGlu (SEQ ID NO:105)pG125124.pepGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGlnSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrProLeuGlyProAlaSerSerLeuProGlnSerPheLeuLeuLysSerLeuGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuValLeuLeuGlyHisSerLeuGlyIleProTrpAlaProLeuSerSerCysProSerGlnAlaLeuGlnLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGluGluLeu (SEQ ID NO:106)pG1312.pepPheLeuLeuLysSerLeuGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuValLeuLeuGlyHisSerLeuGlyIleProTrpAlaProLeuSerSerCysProSerGlnAlaLeuGlnLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGluGluLeuGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGlnSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrProLeuGlyProAlaSerSerLeuProGlnSer (SEQ ID NO:107)pG159158.pepSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrProLeuGlyProAlaSerSerLeuProGlnSerPheLeuLeuLysSerLeuGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuValLeuLeuGlyHisSerLeuGlyIleProTrpAlaProLeuSerSerCysProSerGlnAlaLeuGlnLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGluGluLeuGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGln (SEQ ID NO:108)pG1918.pepGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuValLeuLeuGlyHisSerLeuGlyIleProTrpAlaProLeuSerSerCysProSerGlnAlaLeuGlnLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGluGluLeuGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGlnSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrProLeuGlyProAlaSerSerLeuProGlnSerPheLeuLeuLysSerLeu (SEQ ID NO:109)pG32.pepLeuGlyProAlaSerSerLeuProGlnSerPheLeuLeuLysSerLeuGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuValLeuLeuGlyHisSerLeuGlyIleProTrpAlaProLeuSerSerCysProSerGlnAlaLeuGlnLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGluGluLeuGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGlnSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrPro (SEQ ID NO:110)pG4948.pepLeuLeuGlyHisSerLeuGlyIleProTrpAlaProLeuSerSerCysProSerGlnAlaLeuGlnLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGluGluLeuGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGlnSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrProLeuGlyProAlaSerSerLeuProGlnSerPheLeuLeuLysSerLeuGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuVal (SEQ ID NO:111)pG6059.pepProLeuSerSerCysProSerGlnAlaLeuGlnLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGluGluLeuGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGlnSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrProLeuGlyProAlaSerSerLeuProGlnSerPheLeuLeuLysSerLeuGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuValLeuLeuGlyHisSerLeuGlyIleProTrpAla (SEQ ID NO:112)pG6766.pepGlnAlaLeuGlnLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGluGluLeuGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGlnSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrProLeuGlyProAlaSerSerLeuProGlnSerPheLeuLeuLysSerLeuGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuValLeuLeuGlyHisSerLeuGlyIleProTrpAlaProLeuSerSerCysProSer (SEQ ID NO:113)pG6968.pepLeuGlnLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGluGluLeuGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGlnSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrProLeuGlyProAlaSerSerLeuProGlnSerPheLeuLeuLysSerLeuGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuValLeuLeuGlyHisSerLeuGlyIleProTrpAlaProLeuSerSerCysProSerGlnAla (SEQ ID NO:114)pG7170.pepLeuAlaGlyCysLeuSerGlnLeuHisSerGlyLeuPheLeuTyrGlnGlyLeuLeuGlnAlaLeuGluGlyIleSerProGluLeuGlyProThrLeuAspThrLeuGlnLeuAspValAlaAspPheAlaThrThrIleTrpGlnGlnMetGluGluLeuGlyMetAlaProAlaLeuGlnProThrGlnGlyAlaMetProAlaPheAlaSerAlaPheGlnArgArgAlaGlyGlyValLeuValAlaSerHisLeuGlnSerPheLeuGluValSerTyrArgValLeuArgHisLeuAlaGlnProAspMetAlaThrProLeuGlyProAlaSerSerLeuProGlnSerPheLeuLeuLysSerLeuGluGlnValArgLysIleGlnGlyAspGlyAlaAlaLeuGlnGluLysLeuCysAlaThrTyrLysLeuCysHisProGluGluLeuValLeuLeuGlyHisSerLeuGlyIleProTrpAlaProLeuSerSerCysProSerGlnAlaLeuGln (SEQ ID NO:115)p170169.pep 1 His Leu Ala Gln Pro Asp Met Ala Thr Pro Leu Gly Pro Ala Ser 16 Ser Leu Pro Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln Val Arg 31 Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cys Ala 46 Thr Tyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu Gly His 61 Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln 76 Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu His Ser Gly Leu 91 Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pro106 Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val Ala Asp121 Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly Met Ala136 Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Ala Phe Ala Ser151 Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala Ser His Leu166 Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Leu Arg (SEQ ID__________________________________________________________________________NO:128)
Materials and Methods
Recombinant DNA methods
Unless noted otherwise, all specialty chemicals were obtained from Sigma Co., (St. Louis, Mo.). Restriction endonucleases and T4 DNA ligase were obtained from New England Biolabs (Beverly, Mass.) or Boehringer Mannheim (Indianapolis, Ind.).
Transformation of E. coli strains
E. coli strains, such as DH5.alpha..TM. (Life Technologies, Gaithersburg, Md.) and TG1 (Amersham Corp., Arlington Heights, Ill.) are used for transformation of ligation reactions and are the source of plasmid DNA for transfecting mammalian cells. E. coli strains, such as MON105 and JM101, can be used for expressing the G-CSF receptor agonist of the present invention in the cytoplasm or periplasmic space.
MON105 ATCC#55204: F-, lamda-,IN(rrnD, rrE)1, rpoD+, rpoH358
DH5.alpha..TM.: F-, phi80dlacZdeltaM15, delta(lacZYA-argF)U169, deoR, recA1, endA1, hsdR17(rk-,mk+), phoA, supE44lamda-, thi-1, gyrA96, relA1
TG1: delta(lac-pro), supE, thi-1, hsdD5/F'(traD36, proA+B+, lacIq, lacZdeltaM15)
DH5.alpha..TM. Subcloning efficiency cells are purchased as competent cells and are ready for transformation using the manufacturer's protocol, while both E. coli strains TG1 and MON105 are rendered competent to take up DNA using a CaCl.sub.2 method. Typically, 20 to 50 mL of cells are grown in LB medium (1% Bacto-tryptone, 0.5% Bacto-yeast extract, 150 mM NaCl) to a density of approximately 1.0 optical density unit at 600 nanometers (OD600) as measured by a Baush & Lomb Spectronic spectrophotometer (Rochester, N.Y.). The cells are collected by centrifugation and resuspended in one-fifth culture volume of CaCl.sub.2 solution (50 mM CaCl.sub.2, 10 mM Tris-Cl, pH7.4) and are held at 4.degree. C. for 30 minutes. The cells are again collected by centrifugation and resuspended in one-tenth culture volume of CaCl.sub.2 solution. Ligated DNA is added to 0.2 mL of these cells, and the samples are held at 4.degree. C. for 1 hour. The samples are shifted to 42.degree. C. for two minutes and 1 mL of LB is added prior to shaking the samples at 37.degree. C. for one hour. Cells from these samples are spread on plates (LB medium plus 1.5% Bacto-agar) containing either ampicillin (100 micrograms/mL, ug/mL) when selecting for ampicillin-resistant transformants, or spectinomycin (75 ug/mL) when selecting for spectinomycin-resistant transformants. The plates are incubated overnight at 37.degree. C. Single colonies are picked, grown in LB supplemented with appropriate antibiotic for 6-16 hours at 37.degree. C. with shaking. Colonies are picked and inoculated into LB plus appropriate antibiotic (100 ug/mL ampicillin or 75 ug/mL spectinomycin) and are grown at 37.degree. C. while shaking. Before harvesting the cultures, 1 ul of cells are analyzed by PCR for the presence of a G-CSF gene. The PCR is carried out using a combination of primers that anneal to the G-CSF gene and/or vector. After the PCR is complete, loading dye is added to the sample followed by electrophoresis as described earlier. A gene has been ligated to the vector when a PCR product of the expected size is observed.
Methods for creation of genes with new N-terminus/C-terminus
Method I
Creation of genes with new N-terminus/C-terminus which contain a linker region.
Genes with new N-terminus/C-terminus which contain a linker region separating the original C-terminus and N-terminus can be made essentially following the method described in L. S. Mullins, et al. J. Am. Chem. Soc. 116, 5529-5533 (1994). Multiple steps of polymerase chain reaction (PCR) amplifications are used to rearrange the DNA sequence encoding the primary amino acid sequence of the protein. The steps are illustrated in FIG. 2.
In the first step, the primer set ("new start" and "linker start") is used to create and amplify, from the original gene sequence, the DNA fragment ("Fragment Start") that contains the sequence encoding the new N-terminal portion of the new protein followed by the linker that connects the C-terminal and N-terminal ends of the original protein. In the second step, the primer set ("new stop" and "linker stop") is used to create and amplify, from the original gene sequence, the DNA fragment ("Fragment Stop") that encodes the same linker as used above, followed by the new C-terminal portion of the new protein. The "new start" and "new stop" primers are designed to include the appropriate restriction enzyme recognition sites which allow cloning of the new gene into expression plasmids. Typical PCR conditions are one cycle 95.degree. C. melting for two minutes; 25 cycles 94.degree. C. denaturation for one minute, 50.degree. C. annealing for one minute and 72.degree. C. extension for one minute; plus one cycle 72.degree. C. extension for seven minutes. A Perkin Elmer GeneAmp PCR Core Reagents kit is used. A 100 ul reaction contains 100 pmole of each primer and one ug of template DNA; and 1.times. PCR buffer, 200 uM dGTP, 200 uM DATP, 200 uM dTTP, 200 uM dCTP, 2.5 units AmpliTaq DNA polymerase and 2 mM MgCl.sub.2. PCR reactions are performed in a Model 480 DNA thermal cycler (Perkin Elmer Corporation, Norwalk, Conn.).
"Fragment Start" and "Fragment Stop", which have complementary sequence in the linker region and the coding sequence for the two amino acids on both sides of the linker, are joined together in a third PCR step to make the full-length gene encoding the new protein. The DNA fragments "Fragment Start" and "Fragment Stop" are resolved on a 1% TAE gel, stained with ethidium bromide and isolated using a Qiaex Gel Extraction kit (Qiagen). These fragments are combined in equimolar quantities, heated at 70.degree. C. for ten minutes and slow cooled to allow annealing through their shared sequence in "linker start" and "linker stop". In the third PCR step, primers "new start" and "new stop" are added to the annealed fragments to create and amplify the full-length new N-terminus/C-terminus gene. Typical PCR conditions are one cycle 95.degree. C. melting for two minutes; 25 cycles 94.degree. C. denaturation for one minute, 60.degree. C. annealing for one minute and 72.degree. C. extension for one minute; plus one cycle 72.degree. C. extension for seven minutes. A Perkin Elmer GeneAmp PCR Core Reagents kit is used. A 100 ul reaction contains 100 pmole of each primer and approximately 0.5 ug of DNA; and 1.times. PCR buffer, 200 uM dGTP, 200 uM DATP, 200 uM dTTP, 200 uM dCTP, 2.5 units AmpliTaq DNA polymerase and 2 mM MgCl.sub.2. PCR reactions are purified using a Wizard PCR Preps kit (Promega).
Method II
Creation of genes with new N-terminus/C-terminus without a linker region.
New N-terminus/C-terminus genes without a linker joining the original N-terminus and C-terminus can be made using two steps of PCR amplification and a blunt end ligation. The steps are illustrated in FIG. 3. In the first step, the primer set ("new start" and "P-bl start") is used to create and amplify, from the original gene sequence, the DNA fragment ("Fragment Start") that contains the sequence encoding the new N-terminal portion of the new protein. In the second step, the primer set ("new stop" and "P-bl stop") is used to create and amplify, from the original gene sequence, the DNA fragment ("Fragment Stop") that contains the sequence encoding the new C-terminal portion of the new protein. The "new start" and "new stop" primers are designed to include appropriate restriction sites which allow cloning of the new gene into expression vectors. Typical PCR conditions are one cycle 95.degree. C. melting for two minutes; 25 cycles 94.degree. C. denaturation for one minute, 50.degree. C. annealing for 45 seconds and 72.degree. C. extension for 45 seconds. Deep Vent polymerase (New England Biolabs) is used to reduce the occurrence of overhangs in conditions recommended by the manufacturer. The "P-bl start" and "P-bl stop" primers are phosphorylated at the 5' end to aid in the subsequent blunt end ligation of "Fragment Start" and "Fragment Stop" to each other. A 100 ul reaction contained 150 pmole of each primer and one ug of template DNA; and 1.times. Vent buffer (New England Biolabs), 300 uM dGTP, 300 uM DATP, 300 uM dTTP, 300 uM dCTP, and 1 unit Deep Vent polymerase. PCR reactions are performed in a Model 480 DNA thermal cycler (Perkin Elmer Corporation, Norwalk, Conn.). PCR reaction products are purified using a Wizard PCR Preps kit (Promega).
The primers are designed to include appropriate restriction enzyme recognition sites which allow for the cloning of the new gene into expression vectors. Typically "Fragment Start" is designed to create a NcoI restriction site, and "Fragment Stop" is designed to create a HindIII restriction site. Restriction digest reactions are purified using a Magic DNA Clean-up System kit (Promega). Fragments Start and Stop are resolved on a 1% TAE gel, stained with ethidium bromide and isolated using a Qiaex Gel Extraction kit (Qiagen). These fragments are combined with and annealed to the ends of the .about.3800 base pair NcoI/HindIII vector fragment of pMON3934 by heating at 50.degree. C. for ten minutes and allowed to slow cool. The three fragments are ligated together using T4 DNA ligase (Boehringer Mannheim). The result is a plasmid containing the full-length new N-terminus/C-terminus gene. A portion of the ligation reaction is used to transform E. coli strain DH5.alpha.cells (Life Technologies, Gaithersburg, Md.). Plasmid DNA is purified and sequence confirmed as below.
Method III
Creation of new N-terminus/C-terminus genes by tandem-duplication method
New N-terminus/C-terminus genes can be made based on the method described in R. A. Horlick, et al. Protein Eng. 5:427-431 (1992). Polymerase chain reaction (PCR) amplification of the new N-terminus/C-terminus genes is performed using a tandemly duplicated template DNA. The steps are illustrated in FIG. 4.
The tandemly-duplicated template DNA is created by cloning and contains two copies of the gene separated by DNA sequence encoding a linker connecting the original C- and N-terminal ends of the two copies of the gene. Specific primer sets are used to create and amplify a full-length new N terminus/C-terminus gene from the tandemly-duplicated template DNA. These primers are designed to include appropriate restriction sites which allow for the cloning of the new gene into expression vectors. Typical PCR conditions are one cycle 95.degree. C. melting for two minutes; 25 cycles 94.degree. C. denaturation for one minute, 50.degree. C. annealing for one minute and 72.degree. C. extension for one minute; plus one cycle 72.degree. C. extension for seven minutes. A Perkin Elmer GeneAmp PCR Core Reagents kit (Perkin Elmer Corporation, Norwalk, Conn.) is used. A 100 ul reaction contains 100 pmole of each primer and one ug of template DNA; and 1.times. PCR buffer, 200 uM dGTP, 200 uM DATP, 200 uM dTTP, 200 uM dCTP, 2.5 units AmpliTaq DNA polymerase and 2 mM MgCl.sub.2. PCR reactions are performed in a Model 480 DNA thermal cycler (Perkin Elmer Corporation, Norwalk, Conn.). PCR reactions are purified using a Wizard PCR Preps kit (Promega).
DNA Isolation and Characterization
Plasmid DNA can be isolated by a number of different methods and using commercially available kits known to those skilled in the art. A few such methods are shown herein. Plasmid DNA is isolated using the Promega Wizard.TM. Miniprep kit (Madison, Wis.), the Qiagen QIAwell Plasmid isolation kits (Chatsworth, Calif.) or Qiagen Plasmid Midi kit. These kits follow the same general procedure for plasmid DNA isolation. Briefly, cells are pelleted by centrifugation (5000.times.g), plasmid DNA released with sequential NaOH/acid treatment, and cellular debris is removed by centrifugation (10000.times.g). The supernatant (containing the plasmid DNA) is loaded onto a column containing a DNA-binding resin, the column is washed, and plasmid DNA eluted with TE. After screening for the colonies with the plasmid of interest, the E. coli cells are inoculated into 50-100 mLs of LB plus appropriate antibiotic for overnight growth at 37.degree. C. in an air incubator while shaking. The purified plasmid DNA is used for DNA sequencing, further restriction enzyme digestion, additional subcloning of DNA fragments and transfection into mammalian, E. coli or other cells.
Sequence Confirmation
Purified plasmid DNA is resuspended in dH.sub.2 O and quantitated by measuring the absorbance at 260/280 nm in a Bausch and Lomb Spectronic 601 UV spectrometer. DNA samples are sequenced using ABI PRISM.TM. DyeDeoxy.TM. terminator sequencing chemistry (Applied Biosystems Division of Perkin Elmer Corporation, Lincoln City, Calif.) kits (Part Number 401388 or 402078) according to the manufacturers suggested protocol usually modified by the addition of 5% DMSO to the sequencing mixture. Sequencing reactions are performed in a Model 480 DNA thermal cycler (Perkin Elmer Corporation, Norwalk, Conn.) following the recommended amplification conditions. Samples are purified to remove excess dye terminators with Centri-Sep.TM. spin columns (Princeton Separations, Adelphia, N.J.) and lyophilized. Fluorescent dye labeled sequencing reactions are resuspended in deionized formamide, and sequenced on denaturing 4.75% polyacrylamide-8M urea gels using an ABI Model 373A automated DNA sequencer. Overlapping DNA sequence fragments are analyzed and assembled into master DNA contigs using Sequencher v2.1 DNA analysis software (Gene Codes Corporation, Ann Arbor, Mich.).
Expression of G-CSF Receptor Agonists in Mammalian Cells
Mammalian Cell Transfection/Production of Conditioned Media
The BHK-21 cell line can be obtained from the ATCC 10801 University Boulevard, Manassas, Va. 20110-2209. The cells are cultured in Dulbecco's modified Eagle media (DMEM/high-glucose), supplemented to 2mM (mM) L-glutamine and 10% fetal bovine serum (FBS). This formulation is designated BHK growth media. Selective media is BHK growth media supplemented with 453 units/mL hygromycin B (Calbiochem, San Diego, Calif.). The BHK-21 cell line was previously stably transfected with the HSV transactivating protein VP16, which transactivates the IE110 promoter found on the plasmid pMON3359 (See Hippenmeyer et al., Bio/Technology, pp.1037-1041, 1993). The VP16 protein drives expression of genes inserted behind the IE110 promoter. BHK-21 cells expressing the transactivating protein VP16 are designated BHK-VP16. The plasmid pMON1118 (See Highkin et al., Poultry Sci., 70: 970-981, 1991) expresses the hygromycin resistance gene from the SV40 promoter. A similar plasmid is available from ATCC, pSV2-hph.
BHK-VP16 cells are seeded into a 60 millimeter (mm) tissue culture dish at 3.times.10.sup.5 cells per dish 24 hours prior to transfection. Cells are transfected for 16 hours in 3 mL of "OPTIMEM".TM. (Gibco-BRL, Gaithersburg, Md.) containing 10 ug of plasmid DNA containing the gene of interest, 3 ug hygromycin resistance plasmid, pMON1118, and 80 ug of Gibco-BRL "LIPOFECTAMINE".TM. per dish. The media is subsequently aspirated and replaced with 3 mL of growth media. At 48 hours post-transfection, media from each dish is collected and assayed for activity (transient conditioned media). The cells are removed from the dish by trypsin-EDTA, diluted 1:10 and transferred to 100 mm tissue culture dishes containing 10 mL of selective media. After approximately 7 days in selective media, resistant cells grow into colonies several millimeters in diameter. The colonies are removed from the dish with filter paper (cut to approximately the same size as the colonies and soaked in trypsin/EDTA) and transferred to individual wells of a 24 well plate containing 1 mL of selective media. After the clones are grown to confluence, the conditioned media is re-assayed, and positive clones are expanded into growth media.
Expression of G-CSF Receptor Agonists in E. coli
E. coli strain MON105 or JM101 harboring the plasmid of interest are grown at 37.degree. C. in M9 plus casamino acids medium with shaking in a air incubator Model G25 from New Brunswick Scientific (Edison, N.J.). Growth is monitored at OD600 until it reaches a value of 1, at which time nalidixic acid (10 milligrams/mL) in 0.1 N NaOH is added to a final concentration of 50 .mu.g/mL. The cultures are then shaken at 37.degree. C. for three to four additional hours. A high degree of aeration is maintained throughout culture period in order to achieve maximal production of the desired gene product. The cells are examined under a light microscope for the presence of inclusion bodies (IB). One mL aliquots of the culture are removed for analysis of protein content by boiling the pelleted cells, treating them with reducing buffer and electrophoresis via SDS-PAGE (see Maniatis et al. Molecular Cloning: A Laboratory Manual, 1982). The culture is centrifuged (5000.times.g) to pellet the cells.
Inclusion Body Preparation, Extraction, Refolding, Dialysis, DEAE Chromatography, and Characterization of the G-CSF receptor agonists which accumulate as inclusion bodies in E. coli
Isolation of Inclusion Bodies
The cell pellet from a 330 mL E. coli culture is resuspended in 15 mL of sonication buffer (10 mM 2-amino-2-(hydroxymethyl) 1,3-propanediol hydrochloride (Tris-HCl), pH 8.0+1 mM ethylenediaminetetraacetic acid (EDTA)). These resuspended cells are sonicated using the microtip probe of a Sonicator Cell Disruptor (Model W-375, Heat Systems-Ultrasonics, Inc., Farmingdale, N.Y.). Three rounds of sonication in sonication buffer followed by centrifugation are employed to disrupt the cells and wash the inclusion bodies (IB). The first round of sonication is a 3 minute burst followed by a 1 minute burst, and the final two rounds of sonication are for 1 minute each.
Extraction and Refolding of Proteins from Inclusion Body Pellets
Following the final centrifugation step, the IB pellet is resuspended in 10 mL of 50 mM Tris-HCl, pH 9.5, 8 M urea and 5 mM dithiothreitol (DTT) and stirred at room temperature for approximately 45 minutes to allow for denaturation of the expressed protein.
The extraction solution is transferred to a beaker containing 70 mL of 5 mM Tris-HCl, pH 9.5 and 2.3 M urea and gently stirred while exposed to air at 4.degree. C. for 18 to 48 hours to allow the proteins to refold. Refolding is monitored by analysis on a Vydac (Hesperia, Calif.) C18 reversed phase high pressure liquid chromatography (RP-HPLC) column (0.46.times.25 cm). A linear gradient of 40% to 65% acetonitrile, containing 0.1% trifluoroacetic acid (TFA), is employed to monitor the refold. This gradient is developed over 30 minutes at a flow rate of 1.5 mL per minute. Denatured proteins generally elute later in the gradient than the refolded proteins.
Purification
Following the refold, contaminating E. coli proteins are removed by acid precipitation. The pH of the refold solution is titrated to between pH 5.0 and pH 5.2 using 15% (v/v) acetic acid (HOAc). This solution is stirred at 4.degree. C. for 2 hours and then centrifuged for 20 minutes at 12,000.times.g to pellet any insoluble protein.
The supernatant from the acid precipitation step is dialyzed using a Spectra/Por 3 membrane with a molecular weight cut off (MWCO) of 3,500 daltons. The dialysis is against 2 changes of 4 liters (a 50-fold excess) of 10 mM Tris-HCl, pH 8.0 for a total of 18 hours. Dialysis lowers the sample conductivity and removes urea prior to DEAE chromatography. The sample is then centrifuged (20 minutes at 12,000.times.g) to pellet any insoluble protein following dialysis.
A Bio-Rad Bio-Scale DEAE2 column (7.times.52 mm) is used for ion exchange chromatography. The column is equilibrated in a buffer containing 10 mM Tris-HCl, pH 8.0. The protein is eluted using a 0-to-500 mM sodium chloride (NaCl) gradient, in equilibration buffer, over 45 column volumes. A flow rate of 1 mL per minute is used throughout the run. Column fractions (2 mL per fraction) are collected across the gradient and analyzed by RP HPLC on a Vydac (Hesperia, Calif.) C18 column (0.46.times.25 cm). A linear gradient of 40% to 65% acetonitrile, containing 0.1% trifluoroacetic acid (TFA), is employed. This gradient is developed over 30 minutes at a flow rate of 1.5 mL per minute. Pooled fractions are then dialyzed against 2 changes of 4 liters (50-to-500-fold excess) of 10 mM ammonium acetate (NH.sub.4 Ac), pH 4.0 for a total of 18 hours. Dialysis is performed using a Spectra/Por 3 membrane with a MWCO of 3,500 daltons. Finally, the sample is sterile filtered using a 0.22 .mu.m syringe filter (.mu.Star LB syringe filter, Costar, Cambridge, Mass.), and stored at 4.degree. C.
In some cases the folded proteins can be affinity purified using affinity reagents such as mAbs or receptor subunits attached to a suitable matrix. Alternatively, (or in addition) purification can be accomplished using any of a variety of chromatographic methods such as: ion exchange, gel filtration or hydrophobic chromatography or reversed phase HPLC.
These and other protein purification methods are described in detail in Methods in Enzymology, Volume 182 `Guide to Protein Purification` edited by Murray Deutscher, Academic Press, San Diego, Calif. (1990).
Protein Characterization
The purified protein is analyzed by RP-HPLC, electrospray mass spectrometry, and SDS-PAGE. The protein quantitation is done by amino acid composition, RP-HPLC, and Bradford protein determination. In some cases tryptic peptide mapping is performed in conjunction with electrospray mass spectrometry to confirm the identity of the protein.
AML Proliferation Assay
The factor-dependent cell line AML 193 was obtained from the American Type Culture Collection (ATCC, Rockville, Md.). This cell line, established from a patient with acute myelogenous leukemia, is a growth factor dependent cell line which displayed enhanced growth in GM-CSF supplemented medium (Lange, B., et al., Blood 70: 192, 1987; Valtieri, M., et al., J. Immunol. 138:4042, 1987). The ability of AML 193 cells to proliferate in the presence of human IL-3 has also been documented. (Santoli, D., et al., J. Immunol. 139: 348, 1987). A cell line variant was used, AML 193 1.3, which was adapted for long term growth in IL-3 by washing out the growth factors and starving the cytokine dependent AML 193 cells for growth factors for 24 hours. The cells are then replated at 1.times.10.sup.5 cells/well in a 24 well plate in media containing 100 U/mL IL-3. It took approximately 2 months for the cells to grow rapidly in IL-3. These cells are maintained as AML 193 1.3 thereafter by supplementing tissue culture medium (see below) with human IL-3.
AML 193 1.3 cells are washed 6 times in cold Hanks balanced salt solution (HBSS, Gibco, Grand Island, N.Y.) by centrifuging cell suspensions at 250.times.g for 10 minutes followed by decantation of the supernatant. Pelleted cells are resuspended in HBSS and the procedure is repeated until six wash cycles are completed. Cells washed six times by this procedure are resuspended in tissue culture medium at a density ranging from 2.times.10.sup.5 to 5.times.10.sup.5 viable cells/mL. This medium is prepared by supplementing Iscove's modified Dulbecco's Medium (IMDM, Hazelton, Lenexa, Kans.) with albumin, transferrin, lipids and 2-mercaptoethanol. Bovine albumin (Boehringer-Mannheim, Indianapolis, Ind.) is added at 500 .mu.g/mL; human transferrin (Boehringer-Mannheim, Indianapolis, Ind.) is added at 100 .mu.g/mL; soybean lipid (Boehringer-Mannheim, Indianapolis, Ind.) is added at 50 .mu.g/mL; and 2-mercaptoethanol (Sigma, St. Louis, Mo.) is added at 5.times.10.sup.-5 M.
Serial dilutions of G-CSF receptor agonist proteins are made in triplicate series in tissue culture medium supplemented as stated above in 96 well Costar 3596 tissue culture plates. Each well contained 50 .mu.l of medium containing G-CSF receptor agonist proteins once serial dilutions are completed. Control wells contained tissue culture medium alone (negative control). AML 193 1.3 cell suspensions prepared as above are added to each well by pipetting 50 .mu.l (2.5.times.10.sup.4 cells) into each well. Tissue culture plates are incubated at 37.degree. C. with 5% CO.sub.2 in humidified air for 3 days. On day 3, 0.5 .mu.Ci .sup.3 H-thymidine (2 Ci/mM, New England Nuclear, Boston, Mass.) is added in 50 .mu.l of tissue culture medium. Cultures are incubated at 37.degree. C. with 5% CO.sub.2 in humidified air for 18-24 hours. Cellular DNA is harvested onto glass filter mats (Pharmacia LKB, Gaithersburg, Md.) using a TOMTEC cell harvester (TOMTEC, Orange, Conn.) which utilized a water wash cycle followed by a 70% ethanol wash cycle. Filter mats are allowed to air dry and then placed into sample bags to which scintillation fluid (Scintiverse II, Fisher Scientific, St. Louis, Mo. or BetaPlate Scintillation Fluid, Pharmacia LKB, Gaithersburg, Md.) is added. Beta emissions of samples from individual tissue culture wells are counted in a LKB BetaPlate model 1205 scintillation counter (Pharmacia LKB, Gaithersburg, Md.) and data is expressed as counts per minute of .sup.3 H-thymidine incorporated into cells from each tissue culture well. Activity of each G-CSF receptor agonist proteins preparation is quantitated by measuring cell proliferation (.sup.3 H-thymidine incorporation) induced by graded concentrations of G-CSF receptor agonist. Typically, concentration ranges from 0.05 pM-10.sup.5 pM are quantitated in these assays. Activity is determined by measuring the dose of G-CSF receptor agonist protein which provides 50% of maximal proliferation (EC.sub.50 =0.5.times.(maximum average counts per minute of .sup.3 H-thymidine incorporated per well among triplicate cultures of all concentrations of G-CSF receptor agonists tested--background proliferation measured by .sup.3 H-thymidine incorporation observed in triplicate cultures lacking any factor). This EC.sub.50 value is also equivalent to 1 unit of bioactivity. Every assay is performed with native interleukin-3 and G-CSF as reference standards so that relative activity levels could be assigned.
Typically, the G-CSF receptor agonist proteins were tested in a concentration range of 2000 pM to 0.06 pM titrated in serial 2 fold dilutions.
Activity for each sample was determined by the concentration which gave 50% of the maximal response by fitting a four-parameter logistic model to the data. It was observed that the upper plateau (maximal response) for the sample and the standard with which it was compared did not differ. Therefore relative potency calculation for each sample was determined from EC.sub.50 estimations for the sample and the standard as indicated above.
Other in Vitro Cell Based Proliferation Assays
Other in vitro cell based proliferation assays, known to those skilled in the art, may also be useful to determine the activity of the G-CSF receptor agonists in a similar manner as described in the AML 193.1.3 cell proliferation assay.
Transfected Cell Lines
Cell lines, such as BHK or the murine pro B cell line Baf/3, can be transfected with a colony stimulating factor receptor, such as the human G-CSF receptor which the cell line does not have. These transfected cell lines can be used to determine the activity of the ligand of which the receptor has been transfected.
EXAMPLE 1
Construction of pMON3485
The new N-terminus/C-terminus gene in pMON3485 was created using Method I as described in Materials and Methods. Fragment Start was created and amplified from G-CSF Ser.sup.17 sequence in pMON13037 using the primer set, 39 start (SEQ ID NO:7) and L-11 start (SEQ ID NO:3). Fragment Stop was created and amplified from G-CSF Ser.sup.17 sequence in the plasmid, pMON13037 (WO 95/21254), using the primer set, 38 stop (SEQ ID NO:8) and L-11 stop (SEQ ID NO:4). The full-length new N terminus/C-terminus G-CSF Ser.sup.17 gene was created and amplified from the annealed Fragments Start and Stop using the primers 39 start (SEQ ID NO:7) and 38 stop (SEQ ID NO:8).
The resulting DNA fragment which contains the new gene was digested with restriction endonucleases NcoI and HindIII and purified using a Magic DNA Clean-up System kit (Promega, Madison, Wis.). The plasmid, pMON3934 (derivative of pMON3359), was digested with restriction endonucleases HindIII and NcoI, resulting in an approximately 3800 base pair vector fragment, and gel-purified. The purified restriction fragments were combined and ligated using T4 DNA ligase. A portion of the ligation reaction was used to transform E. coli strain DH5.alpha. cells (Life Technologies, Gaithersburg, Md.). Transformant bacteria were selected on ampicillin-containing plates. Plasmid DNA was isolated and sequenced to confirm the correct insert. The resulting plasmid was designated pMON3485.
BHK cells were transfected with the plasmid, pMON3485, for protein expression and bioassay.
The plasmid, pMON3485 containing the gene sequence of (SEQ ID NO:25), encodes the following amino acid sequence:
__________________________________________________________________________Tyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu Gly HisSer Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro SerGln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu His SerGly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu GlyIle Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln LeuAsp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln Gln Met GluGlu Leu Gly Met Ala Pro Ala Leu Gln Pro Thr Gln Gly AlaMet Pro Ala Phe Ala Ser Ala Phe Gln Arg Arg Ala Gly GlyVal Leu Val Ala Ser His Leu Gln Ser Phe Leu Glu Val SerTyr Arg Val Leu Arg His Leu Ala Gln Pro Ser Gly Gly SerGly Gly Ser Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln ValArg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys LeuCys Ala Thr (SEQ ID NO:43)__________________________________________________________________________
EXAMPLE 2
Construction of pMON3486
The new N-terminus/C-terminus gene in pMON3486 was created using Method I as described in Materials and Methods. Fragment Start was created and amplified from G-CSF Ser.sup.17 sequence in the plasmid, pMON13037, using the primer set, 97 start (SEQ ID NO:9) and L-11 start (SEQ ID NO:3). Fragment Stop was created and amplified from G-CSF Ser.sup.17 sequence in pMON13037 using the primer set, 96 stop (SEQ ID NO:10) and L-11 stop (SEQ ID NO:4). The full-length new N terminus/C-terminus G-CSF Ser.sup.17 gene was created and amplified from the annealed Fragments Start and Stop using the primers 97 start (SEQ ID NO:9) and 96 stop (SEQ ID NO:10).
The resulting DNA fragment which contains the new gene was digested with restriction endonucleases NcoI and HindIII and gel-purified using a Magic DNA Clean-up System kit. The plasmid, pMON3934, was digested with restriction endonucleases HindIII and NcoI, resulting in an approximately 3800 base pair vector fragment, and gel-purified. The purified restriction fragments were combined and ligated using T4 DNA ligase. A portion of the ligation reaction was used to transform E. coli strain DH5.alpha. cells. Transformant bacteria were selected on ampicillin-containing plates. Plasmid DNA was isolated and sequenced to confirm the correct insert. The resulting plasmid was designated pMON3486.
BHK cells were transfected with the plasmid, pMON3486, for protein expression and bioassay.
The plasmid, pMON3486 containing the gene sequence of (SEQ ID NO:26), encodes the following amino acid sequence:
__________________________________________________________________________Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp ValAla Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu LeuGly Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met ProAla Phe Ala Ser Ala Phe Gln Arg Arg Ala Gly Gly Val LeuVal Ala Ser His Leu Gln Ser Phe Leu Glu Val Ser Tyr ArgVal Leu Arg His Leu Ala Gln Pro Ser Gly Gly Ser Gly GlySer Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln Val Arg LysIle Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cys AlaThr Tyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu GlyHis Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys ProSer Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu HisSer Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu GluGly Ile Ser (SEQ ID NO:44)__________________________________________________________________________
EXAMPLE 3
Construction of pMON3487
The new N-terminus/C-terminus gene in pMON3487 was created using Method I as described in Materials and Methods. Fragment Start was created and amplified from G-CSF Ser.sup.17 sequence in the plasmid, pMON13037, using the primer set, 126 start (SEQ ID NO:11) and L-11 start (SEQ ID NO:3). Fragment Stop was created and amplified from G-CSF Ser.sup.17 sequence in pMON13037 using the primer set, 125 stop (SEQ ID NO:12) and L-11 stop (SEQ ID NO:4). The full-length new N terminus/C-terminus G-CSF Ser.sup.17 gene was created and amplified from the annealed Fragments Start and Stop using the primers 126 start (SEQ ID NO:11) and 125 stop (SEQ ID NO:12).
The resulting DNA fragment which contains the new gene was digested with restriction endonucleases NcoI and HindIII and purified using a Magic DNA Clean-up System kit. The plasmid, pMON3934, was digested with restriction endonucleases HindIII and NcoI, resulting in an approximately 3800 base pair vector fragment, and gel-purified. The purified restriction fragments were combined and ligated using T4 DNA ligase. A portion of the ligation reaction was used to transform E. coli strain DH5.alpha. cells. Transformant bacteria were selected on ampicillin-containing plates. Plasmid DNA was isolated and sequenced to confirm the correct insert. The resulting plasmid was designated pMON3487.
BHK cells were transfected with the plasmid, pMON3487, for protein expression and bioassay.
The plasmid, pMON3487 containing the gene sequence of (SEQ ID NO:27), encodes the following amino acid sequence:
__________________________________________________________________________Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro AlaPhe Ala Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Leu ValAla Ser His Leu Gln Ser Phe Leu Glu Val Ser Tyr Arg ValLeu Arg His Leu Ala Gln Pro Ser Gly Gly Ser Gly Gly SerGln Ser Phe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys IleGln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cys Ala ThrTyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu Gly HisSer Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro SerGln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu His SerGly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu GlyIle Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln LeuAsp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln Gln Met GluGlu Leu Gly (SEQ ID NO:45)__________________________________________________________________________
EXAMPLE 4
Construction of pMON3488
The new N-terminus/C-terminus gene in pMON3488 was created using Method I as described in Materials and Methods. Fragment Start was created and amplified from G-CSF Ser.sup.17 sequence in the plasmid, pMON13037, using the primer set, 133 start (SEQ ID NO:13) and L-11 start (SEQ ID NO:3). Fragment Stop was created and amplified from G-CSF Ser.sup.17 sequence in the plasmid, pMON13037 using the primer set, 132 stop (SEQ ID NO:14) and L-11 stop (SEQ ID NO:4). The full-length new N terminus/C-terminus G-CSF Ser.sup.17 gene was created and amplified from the annealed Fragments Start and Stop using the primers 133 start (SEQ ID NO:13) and 132 stop (SEQ ID NO:14).
The resulting DNA fragment which contains the new gene was digested with restriction endonucleases NcoI and HindIII and purified using a Magic DNA Clean-up System kit. The plasmid, pMON3934, was digested with restriction endonucleases HindIII and NcoI, resulting in an approximately 3800 base pair vector fragment, and gel-purified. The purified restriction fragments were combined and ligated using T4 DNA ligase. A portion of the ligation reaction was used to transform E. coli strain DH5.alpha. cells. Transformant bacteria were selected on ampicillin-containing plates. Plasmid DNA was isolated and sequenced to confirm the correct insert. The resulting plasmid was designated pMON3488.
BHK cells were transfected with the plasmid, pMON3488, for protein expression and bioassay.
The plasmid, pMON3488 containing the gene sequence of (SEQ ID NO:28), encodes the following amino acid sequence:
__________________________________________________________________________Thr Gln Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gln ArgArg Ala Gly Gly Val Leu Val Ala Ser His Leu Gln Ser PheLeu Glu Val Ser Tyr Arg Val Leu Arg His Leu Ala Gln ProSer Gly Gly Ser Gly Gly Ser Gln Ser Phe Leu Leu Lys SerLeu Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Ala Ala LeuGln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cys His Pro GluGlu Leu Val Leu Leu Gly His Ser Leu Gly Ile Pro Trp AlaPro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu Ala GlyCys Leu Ser Gln Leu His Ser Gly Leu Phe Leu Tyr Gln GlyLeu Leu Gln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly ProThr Leu Asp Thr Leu Gln Leu Asp Val Ala Asp Phe Ala ThrThr Ile Trp Gln Gln Met Glu Glu Leu Gly Met Ala Pro AlaLeu Gln Pro (SEQ ID NO:46)__________________________________________________________________________
EXAMPLE 5
Construction of pMON3489
The new N-terminus/C-terminus gene in pMON3489 was created using Method I as described in Materials and Methods. Fragment Start was created and amplified from G-CSF Ser.sup.17 sequence in the plasmid, pMON13037, using the primer set, 142 start (SEQ ID NO:15) and L-11 start (SEQ ID NO:3). Fragment Stop was created and amplified from G-CSF Ser.sup.17 sequence in pMON13037 using the primer set, 141 stop (SEQ ID NO:16) and L-11 stop (SEQ ID NO:4). The full-length new N terminus/C-terminus G-CSF Ser.sup.17 gene was created and amplified from the annealed Fragments Start and Stop using the primers 142 start (SEQ ID NO:15) and 141 stop (SEQ ID NO:16).
The resulting DNA fragment which contains the new gene was digested with restriction endonucleases NcoI and HindIII and purified using a Magic DNA Clean-up System kit. The plasmid, pMON3934, was digested with restriction endonucleases HindIII and NcoI, resulting in an approximately 3800 base pair vector fragment, and gel-purified. The purified restriction fragments were combined and ligated using T4 DNA ligase. A portion of the ligation reaction was used to transform E. coli strain DH5.alpha. cells. Transformant bacteria were selected on ampicillin-containing plates. Plasmid DNA was isolated and sequenced to confirm the correct insert. The resulting plasmid was designated pMON3489.
BHK cells were transfected with the plasmid, pMON3489, for protein expression and bioassay.
The plasmid, pMON3489 containing the gene sequence of (SEQ ID NO:29), encodes the following amino acid sequence:
__________________________________________________________________________Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala SerHis Leu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Leu ArgHis Leu Ala Gln Pro Ser Gly Gly Ser Gly Gly Ser Gln SerPhe Leu Leu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln GlyAsp Gly Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr Tyr LysLeu Cys His Pro Glu Glu Leu Val Leu Leu Gly His Ser LeuGly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln AlaLeu Gln Leu Ala Gly Cys Leu Ser Gln Leu His Ser Gly LeuPhe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gly Ile SerPro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp ValAla Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu LeuGly Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met ProAla Phe Ala (SEQ ID NO:47)__________________________________________________________________________
EXAMPLE 6
Construction of pMON3490
The new N-terminus/C-terminus gene in pMON3490 was created using Method II as described in Materials and Methods. Fragment Start was created and amplified from G-CSF sequence in the plasmid, pMON13037, using the primer set, 39 start (SEQ ID NO:7) and P-bl start (SEQ ID NO:5). Fragment Stop was created and amplified from G-CSF Ser.sup.17 sequence in pMON13037 using the primer set, 38 stop (SEQ ID NO:8) and P-bl stop (SEQ ID NO:6). Fragment Start was digested with restriction endonuclease NcoI, and Fragment Stop was digested with restriction endonuclease HindIII. After purification, the digested Fragments Start and Stop were combined with and ligated to the approximately 3800 base pair NcoI-HindIII vector fragment of pMON3934. Transformant bacteria were selected on ampicillin-containing plates. Plasmid DNA was isolated and sequenced to confirm the correct insert. The resulting plasmid was designated pMON3490.
BHK cells were transfected with the plasmid, pMON3490, for protein expression and bioassay.
The plasmid, pMON3490 containing the gene sequence of (SEQ ID NO:30), encodes the following amino acid sequence:
__________________________________________________________________________Tyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu Gly HisSer Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pro SerGln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu His SerGly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu GlyIle Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln LeuAsp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln Gln Met GluGlu Leu Gly Met Ala Pro Ala Leu Gln Pro Thr Gln Gly AlaMet Pro Ala Phe Ala Ser Ala Phe Gln Arg Arg Ala Gly GlyVal Leu Val Ala Ser His Leu Gln Ser Phe Leu Glu Val SerTyr Arg Val Leu Arg His Leu Ala Gln Pro Thr Pro Leu GlyPro Ala Ser Ser Leu Pro Gln Ser Phe Leu Leu Lys Ser LeuGlu Gln Val Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu GlnGlu Lys Leu Cys Ala Thr (SEQ ID NO:48)__________________________________________________________________________
EXAMPLE 7
Construction of pMON3491
The new N-terminus/C-terminus gene in pMON3491 was created using Method II as described in Materials and Methods. Fragment Start was created and amplified from G-CSF sequence in the plasmid, pMON13037, using the primer set, 97 start (SEQ ID NO:9) and P-bl start (SEQ ID NO:5). Fragment Stop was created and amplified from G-CSF Ser.sup.17 sequence in pMON13037 using the primer set, 96 stop (SEQ ID NO:10) and P-bl stop (SEQ ID NO:6). Fragment Start was digested with restriction endonuclease NcoI, and Fragment Stop was digested with restriction endonuclease HindIII. After purification, the digested Fragments Start and Stop were combined with and ligated to the approximately 3800 base pair NcoI-HindIII vector fragment of pMON3934. A portion of the ligation reaction was used to transform E. coli strain DH5.alpha. cells. Transformant bacteria were selected on ampicillin-containing plates. Plasmid DNA was isolated and sequenced to confirm the correct insert. The resulting plasmid was designated pMON3491.
BHK cells were transfected with the plasmid, pMON3491, for protein expression and bioassay.
The plasmid, pMON3491 containing the gene sequence of (SEQ ID NO:31), encodes the following amino acid sequence:
__________________________________________________________________________Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp ValAla Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu LeuGly Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met ProAla Phe Ala Ser Ala Phe Gln Arg Arg Ala Gly Gly Val LeuVal Ala Ser His Leu Gln Ser Phe Leu Glu Val Ser Tyr ArgVal Leu Arg His Leu Ala Gln Pro Thr Pro Leu Gly Pro AlaSer Ser Leu Pro Gln Ser Phe Leu Leu Lys Ser Leu Glu GlnVal Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu LysLeu Cys Ala Thr Tyr Lys Leu Cys His Pro Glu Glu Leu ValLeu Leu Gly His Ser Leu Gly Ile Pro Trp Ala Pro Leu SerSer Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Leu SerGln Leu His Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu GlnAla Leu Glu Gly Ile Ser (SEQ ID NO:49)__________________________________________________________________________
EXAMPLE 8
Construction of pMON3492
The new N-terminus/C-terminus gene in pMON3492 was created using Method II as described in Materials and Methods. Fragment Start was created and amplified from G-CSF sequence in the plasmid, pMON13037, using the primer set, 126 start (SEQ ID NO:11) and P-bl start (SEQ ID NO:5). Fragment Stop was created and amplified from G-CSF Ser.sup.17 sequence in pMON13037 using the primer set, 125 stop (SEQ ID NO:12) and P-bl stop (SEQ ID NO:6). Fragment Start was digested with restriction endonuclease NcoI, and Fragment Stop was digested with restriction endonuclease HindIII. After purification, the digested Fragments Start and Stop were combined with and ligated to the approximately 3800 base pair NcoI-HindIII vector fragment of pMON3934. A portion of the ligation reaction was used to transform E. coli strain DH5.alpha. cells. Transformant bacteria were selected on ampicillin-containing plates. Plasmid DNA was isolated and sequenced to confirm the correct insert. The resulting plasmid was designated pMON3492.
BHK cells were transfected with the plasmid, pMON3492, for protein expression and bioassay.
The plasmid, pMON3492 containing the gene sequence of (SEQ ID NO:32), encodes the following amino acid sequence:
__________________________________________________________________________Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pro AlaPhe Ala Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Leu ValAla Ser His Leu Gln Ser Phe Leu Glu Val Ser Tyr Arg ValLeu Arg His Leu Ala Gln Pro Thr Pro Leu Gly Pro Ala SerSer Leu Pro Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln ValArg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys LeuCys Ala Thr Tyr Lys Leu Cys His Pro Glu Glu Leu Val LeuLeu Gly His Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser SerCys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser GlnLeu His Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln AlaLeu Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu Asp ThrLeu Gln Leu Asp Val Ala Asp Phe Ala Thr Thr Ile Trp GlnGln Met Glu Glu Leu Gly (SEQ ID NO:50)'TZ,1/35
EXAMPLE 9
Construction of pMON3493
The new N-terminus/C-terminus gene in pMON3493 was created using Method II as described in Materials and Methods. Fragment Start was created and amplified from G-CSF sequence in the plasmid, pMON13037, using the primer set, 133 start (SEQ ID NO:13) and P-bl start (SEQ ID NO:5). Fragment Stop was created and amplified from G-CSF Ser.sup.17 sequence in pMON13037 using the primer set, 132 stop (SEQ ID NO:14) and P-bl stop (SEQ ID NO:6). Fragment Start was digested with restriction endonuclease NcoI, and Fragment Stop was digested with restriction endonuclease HindIII. After purification, the digested Fragments Start and Stop were combined with and ligated to the approximately 3800 base pair NcoI-HindIII vector fragment of pMON3934. A portion of the ligation reaction was used to transform E. coli strain DH5.alpha. cells. Transformant bacteria were selected on ampicillin-containing plates. Plasmid DNA was isolated and sequenced to confirm the correct insert. The resulting plasmid was designated pMON3493.
BHK cells were transfected with the plasmid, pMON3493, for protein expression and bioassay.
The plasmid, pMON3493 containing the gene sequence of (SEQ ID NO:33), encodes the following amino acid sequence:
__________________________________________________________________________Thr Gln Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gln ArgArg Ala Gly Gly Val Leu Val Ala Ser His Leu Gln Ser PheLeu Glu Val Ser Tyr Arg Val Leu Arg His Leu Ala Gln ProThr Pro Leu Gly Pro Ala Ser Ser Leu Pro Gln Ser Phe LeuLeu Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gly Asp GlyAla Ala Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu CysHis Pro Glu Glu Leu Val Leu Leu Gly His Ser Leu Gly IlePro Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu GlnLeu Ala Gly Cys Leu Ser Gln Leu His Ser Gly Leu Phe LeuTyr Gln Gly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pro GluLeu Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Val Ala AspPhe Ala Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gly MetAla Pro Ala Leu Gln Pro (SEQ ID NO:51)__________________________________________________________________________
EXAMPLE 10
Construction of pMON3494
The new N-terminus/C-terminus gene in pMON3494 was created using Method II as described in Materials and Methods. Fragment Start was created and amplified from G-CSF sequence in the plasmid, pMON13037, using the primer set, 142 start (SEQ ID NO:15) and P-bl start (SEQ ID NO:5). Fragment Stop was created and amplified from G-CSF Ser.sup.17 sequence in pMON13037 using the primer set, 141 stop (SEQ ID NO:16) and P-bl stop (SEQ ID NO:6). Fragment Start was digested with restriction endonuclease NcoI, and Fragment Stop was digested with restriction endonuclease HindIII. After purification, the digested Fragments Start and Stop were combined with and ligated to the approximately 3800 base pair NcoI-HindIII vector fragment of pMON3934. A portion of the ligation reaction was used to transform E. coli strain DH5.alpha. cells. Transformant bacteria were selected on ampicillin-containing plates. Plasmid DNA was isolated and sequenced to confirm the correct insert. The resulting plasmid was designated pMON3494.
BHK cells were transfected with the plasmid, pMON3494, for protein expression and bioassay.
The plasmid, pMON3494 containing the gene sequence of (SEQ ID NO:34), encodes the following amino acid sequence:
__________________________________________________________________________Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Leu Val Ala SerHis Leu Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Leu ArgHis Leu Ala Gln Pro Thr Pro Leu Gly Pro Ala Ser Ser LeuPro Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln Val Arg LysIle Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cys AlaThr Tyr Lys Leu Cys His Pro Glu Glu Leu Val Leu Leu GlyHis Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys ProSer Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu HisSer Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu GluGly Ile Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu GlnLeu Asp Val Ala Asp Phe Ala Thr Thr Ile Trp Gln Gln MetGlu Glu Leu Gly Met Ala Pro Ala Leu Gln Pro Thr Gln GlyAla Met Pro Ala Phe Ala (SEQ ID NO:52)__________________________________________________________________________
EXAMPLES 11-20
The genes encoding the G-CSF receptor agonists of Examples 1-10 were excised from the BHK vectors as a NcoI/HindIII fragment and ligated with the .about.3630 base pair NcoI/HindIII vector fragment of pMON2341 (WO 94/12638). The resulting plasmids (Examples 11-20) are indicated in Table 4. The plasmids were transformed into E. coli strain JM101 cells and expression of the G-CSF receptor agonist protein was evaluated. The proteins expressed are the same as those expressed in the parental BHK expression vector except the proteins were immediately preceded by a Methionine-Alanine dipeptide and the Methionine is processed off by methionine aminopeptidase. Overnight growths of cells (20 Klett units) were inoculated in 10 mL of minimal M9 medium supplemented with vitamin B1 and trace minerals and incubated with shaking at 37.degree. C. until initial Klett readings of .about.120 units were obtained. At 120 Klett units 50 uL of 10 mg/mL nalidixic acid was added. Four hours post-induction, a 1 ml aliquot was removed for protein expression analysis by SDS-PAGE. Cells were also examined using light microscopy for the presence of inclusion bodies. Only pMON3450 and pMON3455 had significant expression levels of the G-CSF receptor agonist protein. In an effort to improve expression levels of G-CSF receptor agonists, the 5' end of the genes were re-engineered to incorporate AT-rich codons and E. coli preferred codons between the unique NcoI and NheI restriction endonuclease recognition sites (Examples 21-28).
TABLE 4______________________________________E. coli expression plasmids Resulting E. coli Parental expression plasmid Break- BHK plasmidExample # pMON # point Linker pMON #______________________________________Example 11 pMON3450 38/39 zero pMON3490Example 12 pMON3455 38/39 .DELTA.1-10 pMON3485Example 13 pMON3451 96/97 zero pMON3491Example 14 pMON3456 96/97 .DELTA.1-10 pMON3486Example 15 pMON3452 125/126 zero pMON3492Example 16 pMON3457 125/126 .DELTA.1-10 pMON3487Example 17 pMON3453 132/133 zero pMON3493Example 18 pMON3458 132/133 .DELTA.1-10 pMON3488Example 19 pMON3454 141/142 zero pMON3494Example 20 pMON3459 141/142 .DELTA.1-10 pMON3489______________________________________
EXAMPLE 21
Construction of pMON25184
The complementary pair of synthetic oligomers, 141for.seq (SEQ ID NO:23) and 141rev.seq (SEQ ID NO:24), (Midland Certified Reagent Co., Midland Tex.) were annealed by heating 2 ug of each synthetic oligomer in a 20 ul reaction mixture containing 20 mM Tris-HCl (7.5), 10 mM MgCl.sub.2, and 50 mM NaCl, at 80.degree. C. for 5 minutes, and allowing the mixture to slowly cool to ambient temperature (approximately 45 minutes). When properly annealed the oligomers create an NcoI site at the 5' end and a NheI site at the 3' end. Approximately 15 ng of the annealed oligomer pair was ligated with the gel-purified .about.4120 base pair NcoI/NheI vector fragment of pMON3454 (.about.molar ratio of 10:1). The resulting gene, had seven codon changes at the 5' end of the gene. The ligation reaction was used to transform E. coli strain DH5.alpha. and the desired codon changes were confirmed by DNA sequence analysis. The resulting plasmid was designated pMON25184. Plasmid, pMON25184 containing the gene sequence of (SEQ ID NO:38), DNA was retransformed into E. coli strain JM101 cells for protein expression. The protein expressed is the same as that expressed from pMON3454.
EXAMPLE 22
Construction of pMON25188
The complementary pair of synthetic oligomers, 141for.seq (SEQ ID NO:23) and 141rev.seq (SEQ ID NO:24), (Midland Certified Reagent Co., Midland Tex.) were annealed by heating 2 ug of each synthetic oligomer in a 20 ul reaction mixture containing 20 mM Tris-HCl (7.5), 10 mM MgCl.sub.2, and 50 mM NaCl, at 80.degree. C. for 5 minutes, and allowing the mixture to slowly cool to ambient temperature (approximately 45 minutes). When properly annealed the oligomers create an NcoI site at the 5' end and a NheI site at the 3' end. Approximately 15 ng of the annealed oligomer pair was ligated with the .about.4110 base pair NcoI/NheI gel-purified pMON3459 (.about.molar ratio of 10:1). The ligation mixture was used to transform E. coli strain DH5.alpha. and the desired codon changes were confirmed by DNA sequence analysis. The resulting plasmid was designated pMON25188. The resulting gene, had seven codon changes at the 5' end of the gene. Plasmid, pMON25188 containing the gene sequence of (SEQ ID NO:42), DNA was retransformed into E. coli strain JM101 cells for protein expression. The protein expressed is the same as that expressed from pMON3459.
EXAMPLE 23
Construction of pMON25183
pMON25183 was constructed using an overlapping PCR primer method. The synthetic oligomers, 132for.seq (SEQ ID NO:321 and 132rev.seq (SEQ ID NO:22), encode the NcoI and NheI restriction recognition sequence, respectively. Amplified DNA was generated by the DNA polymerase chain amplification method using the PCR Optimizer Kit (Invitrogen). The PCR reactions were performed using the manufacturer's recommended conditions using 5.times. buffer B (300 mM Tris-HCl pH8.5, 75 mM (NH.sub.4).sub.2 SO.sub.4, 10 mM MgCl.sub.2) for seven cycles consisting of 94.degree. C. for 1', 65.degree. C. for 2', and 72.degree. C. for 2', followed by 20 cycles of 94.degree. C. for 1', and 72.degree. C. for 3', and a final cycle of 7 minutes at 72.degree. C. using a Perkin Elmer Model 480 DNA thermal cycler (Perkin Elmer). The reaction product was desalted using Centri-Sep spin columns (Princeton Separations) following the manufacturer's recommended protocol, digested with NcoI/NheI, and gel purified from TAE-agarose gels using Gene Clean (Bio 101) and the DNA product was eluted in dH.sub.2 O The purified PCR product was ligated with the .about.4090 base pair NcoI/NheI pMON3453 vector fragment. Positive clones containing the AT-rich replacement insert were identified as described in Example 21. The resulting plasmid was designated pMON25183. The resulting gene, had 14 codon changes at the 5' end of the gene. Plasmid, pMON25183 containing the gene sequence of (SEQ ID NO:37), DNA was retransformed into E. coli strain JM101 cells for protein expression. The protein expressed is the same as that expressed from pMON3453.
EXAMPLE 24
Construction of pMON25187
pMON25187 was constructed using an overlapping PCR primer method. The synthetic oligomers, 132for.seq (SEQ ID NO:21) and 132rev.seq (SEQ ID NO:22), encode the NcoI and NheI restriction recognition sequence, respectively. Amplified DNA was generated by the DNA polymerase chain amplification method using the PCR Optimizer Kit (Invitrogen). The PCR reactions were performed using the manufacturer's recommended conditions, in 5.times. buffer B for seven cycles consisting of 94.degree. C. for 1', 65.degree. C. for 2', and 72.degree. C. for 2', followed by 20 cycles of 94.degree. C. for 1', and 72.degree. C. for 3', and a final cycle of 7 minutes at 72.degree. C. using a Perkin Elmer Model 480 DNA thermal cycler (Perkin Elmer). The reaction product was desalted using Centri-Sep spin columns (Princeton Separations) following the manufacturer's recommended protocol, digested with NcoI/NheI, and gel purified from TAE-agarose gels using Gene Clean (Bio 101) and the DNA product was eluted in dH.sub.2 O. The purified PCR product was ligated with the .about.4080 base pair NcoI/NheI pMON3458 vector fragment. Positive clones containing the AT-rich replacement insert were identified as described in Example 21. The resulting plasmid was designated pMON25187. The resulting gene, had 14 codon changes at the 5' end of the gene. Plasmid, pMON25187 containing the gene sequence of (SEQ ID NO:41), DNA was retransformed into E. coli strain JM101 cells for protein expression. The protein expressed is the same as that expressed from pMON3458.
EXAMPLE 25
Construction of pMON25182
pMON25182 was constructed using the overlapping PCR primer approach described in Example 23. The synthetic oligomer primers 125for.seq (SEQ ID NO:19) and 125rev.seq (SEQ ID NO:20) were used in the PCR reaction. The PCR reaction conditions were identical to those used in Example 23 except the annealing temperature for the first seven cycles was 60.degree. C. The purified PCR product was ligated with .about.4070 base pair NcoI/NheI pMON3452 vector fragment. Positive clones containing the AT-rich replacement insert were identified as described in Example 21. The resulting plasmid was designated pMON25182. The resulting gene, had 19 codon changes at the 5' end of the gene. Plasmid, pMON25182 containing the gene sequence of (SEQ ID NO:36), DNA was retransformed into E. coli strain JM101 cells for protein expression. The protein expressed is the same as that expressed from pMON3452.
EXAMPLE 26
Construction of pMON25186
pMON25186 was constructed using the overlapping PCR primer approach described in Example 23. The synthetic oligomer primers 125for.seq (SEQ ID NO:19) and 125rev.seq (SEQ ID NO:20) were used in the PCR reaction. The PCR reaction conditions were identical to those used in Example 23 except the annealing temperature for the first seven cycles was 60.degree. C. The purified PCR product was ligated with the .about.4060 base pair NcoI/NheI pMON3457 vector fragment. Positive clones containing the AT-rich replacement insert were identified as described in Example 21. The resulting plasmid was designated pMON25186. The resulting gene, had 19 codon changes at the 5' end of the gene. Plasmid, pMON25186 containing the gene sequence of (SEQ ID NO:40), DNA was retransformed into E. coli strain JM101 cells for protein expression. The protein expressed is the same as that expressed from pMON3457.
EXAMPLE 27
Construction of pMON25181
pMON25181 was constructed using PCR to amplify a DNA fragment from pMON3451 as the template using the oligomers 96for.seq (SEQ ID NO:17) and 96rev.seq (SEQ ID NO:18). The oligomer 96for.seq was designed to create six codon changes. The PCR reaction conditions were the same as described in Example 25, except 10 ng of pMON3451 plasmid DNA was added. The purified PCR product was ligated with the .about.3980 base pair NcoI/NheI pMON3451 vector fragment. Positive clones containing the AT-rich replacement insert were identified as described in Example 21. The resulting plasmid was designated pMON25181. The resulting gene, had 6 codon changes at the 5' end of the gene. Plasmid, pMON25181 containing the gene sequence of (SEQ ID NO:35), DNA was retransformed into E. coli strain JM101 cells for protein expression. The protein expressed is the same as that expressed from pMON3451.
EXAMPLE 28
Construction of pMON25185
pMON25185 was constructed using PCR to amplify a DNA fragment from pMON3451 as the template using the oligomers 96for.seq (SEQ ID NO:17) and 96rev.seq (SEQ ID NO:18). The oligomer 9697for.seq was designed to create six codon changes. The PCR reaction conditions were the same as described in Example 25, except 10 ng of pMON3456 plasmid DNA was added. The purified PCR product was ligated with the .about.3970 base pair NcoI/NheI pMON3456 vector fragment. Positive clones containing the AT-rich replacement insert were identified as described in Example 21. The resulting plasmid was designated pMON25185. The resulting gene, had 6 codon changes at the 5' end of the gene. Plasmid, pMON25185 containing the gene sequence of (SEQ ID NO:39), DNA was retransformed into E. coli strain JM101 cells for protein expression. The protein expressed is the same as that expressed from pMON3456.
EXAMPLE 29
The G-CSF amino acid substitution variants of the present invention were made using PCR mutagenesis techniques as described in WO 94/12639 and WO 94/12638. These and other variants (i.e. amino acid substitutions, insertions or deletions and N-terminal or C-terminal extensions) could also be made, by one skilled in the art, using a variety of other methods including synthetic gene assembly or site-directed mutagenesis (see Taylor et al., Nucl. Acids Res., 13:7864-8785, 1985; Kunkel et al., Proc. Natl. Acad. Sci. USA, 82:488-492, 1985; Sambrook et al., Molecular Cloning: A Laboratory Manual, 2nd ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989, WO 94/12639 and WO 94/12638). These substitutions can be made one at a time or in combination with other amino acid substitutions, and/or deletions, and/or insertions and/or extensions. After sequence verification of the changes, the plasmid DNA can be transfected into an appropriate mammalian cell, insect cell or bacterial strain such as E. coli for production. Known variants of G-CSF, which are active, include substitutions at positions 1 (Thr to Ser, Arg or Gly, 2 (Pro to Leu), 3 (Leu to Arg or Ser) and 17 (Cys to Ser) and deletions of amino acids 1-11 (Kuga et al. Biocheinicla and Biophysical Research Comm. 159:103-111, 1989). It is understood that these G-CSF amino acid substitution variants could serve as the template sequence for the rearrangement of the amino acid sequence as described in the other examples.
Bioactivity Determination of G-CSF Amino Acid Substitution Variants
The G-CSF amino acid substitution variants were assayed in the Baf/3 cell line, transfected with the human G-CSF receptor, proliferation assay to determine their bioactivity relative to native G-CSF. The G-CSF variants tested and their relative bioactivity are shown in Table 5. A "+" indicates that the activity was comparable to native G-CSF and "-" indicates that the activity was significantly decreased or not detected.
TABLE 5______________________________________CELL PROLIFERATION ACTIVITY OF G-CSF VARIANTS IN BAF/3CELL LINE TRANSFECTED WITH THE HUMAN G-CSF RECEPTORaa position native aa mutant aa activity *______________________________________13 Phe Ser +13 Phe His +13 Phe Thr +13 Phe Pro +16 Lys Pro +16 Lys Ser +16 Lys Thr +16 Lys His +18 Leu Pro +18 Leu Thr +18 Leu His +18 Leu Cys +18 Leu Ile +19 Glu Ala -19 Glu Thr -19 Glu Arg -19 Glu Pro -19 Glu Leu -19 Glu Gly -19 Glu Ser -22 Arg Tyr +22 Arg Ser +22 Arg Ala +22 Arg Val +22 Arg Thr +24 Ile Pro +24 Ile Leu +24 Ile Tyr +27 Asp Gly +30 Ala Ile +30 Ala Leu +34 Lys Ser +43 His Gly +43 His Thr +43 His Val +43 His Lys +43 His Trp +43 His Ala +43 His Arg +43 His Cys +43 His Leu +44 Pro Arg +44 Pro Asp +44 Pro Val +44 Pro Ala +44 Pro His +44 Pro Gln +44 Pro Trp +44 Pro Gly +44 Pro Thr +46 Glu Ala +46 Glu Arg +46 Glu Phe +46 Glu Ile +47 Leu Thr +49 Leu Phe +49 Leu Arg +49 Leu Ser +50 Leu His +50 Leu Pro +51 Gly Ser +51 Gly Met +54 Leu His +67 Gln Lys +67 Gln Leu +67 Gln Cys +67 Gln Lys +70 Gln Pro +70 Gln Leu +70 Gln Arg +70 Gln Ser +104 Asp Gly +104 Asp Val +108 Leu Ala +108 Leu Val +108 Leu Arg +108 Leu Gly +108 Leu Trp +108 Leu Gln +115 Thr His +115 Thr Leu +115 Thr Ala +115 Thr Ile +120 Gln Gly +120 Gln Arg +120 Gln Lys +120 Gln His +123 Glu Arg +123 Glu Phe +123 Glu Thr +144 Phe His +144 Phe Arg +144 Phe Pro +144 Phe Leu +144 Phe Glu +146 Arg Gln +147 Arg Gln +156 His Asp -156 His Ser +156 His Gly +159 Ser Arg +159 Ser Thr +159 Ser Tyr +159 Ser Val +159 Ser Gly +162 Glu Gly -162 Glu Trp +162 Glu Leu +163 Val Arg +163 Val Ala +163 Val Gly +165 Tyr Cys not determined169 Ser Leu +169 Ser Cys +169 Ser Arg +170 His Arg +170 His Ser +______________________________________
EXAMPLES 30-37
Examples 30-37 were made in a similar manner as described in Example 6 using the plasmid pMON13037 as the template and the oligonucleotide primers indicated in Table 6. The resulting gene and the designated plasmid pMON # and the protein encoded are indicated in Table 6.
TABLE 6______________________________________ resulting resultingExample breakpoint primers gene protein______________________________________30 48/49 49start pMON3460 (SEQ ID (SEQ ID (SEQ ID NO: 95) NO: 68) NO: 86) 48stop (SEQ ID NO: 69)31 76/77 77start pMON3461 (SEQ ID (SEQ ID (SEQ ID NO: 96) NO: 70) NO: 87) 76stop (SEQ ID NO: 71)32 81/82 82start pMON3462 (SEQ ID (SEQ ID (SEQ ID NO: 97) NO: 72) NO: 88) 81stop (SEQ ID NO: 73)33 83/84 84start pMON3463 (SEQ ID (SEQ ID (SEQ ID NO: 98) NO: 74) NO: 88) 83stop (SEQ ID NO: 75)34 90/91 91start pMON3464 (SEQ ID (SEQ ID (SEQ ID NO: 99) NO: 76) NO: 89) 90stop (SEQ ID NO: 77)35 111/112 112start pMON3465 (SEQ ID (SEQ ID (SEQ ID NO: 100) NO: 78) NO: 90) 111stop (SEQ ID NO: 79)36 116/117 117start pMON3466 (SEQ ID (SEQ ID (SEQ ID NO: 101) NO: 80) NO: 91) 116stop (SEQ ID NO: 81)37 118/119 119start pMON3467 (SEQ ID (SEQ ID (SEQ ID NO: 102) NO: 82) NO: 92) 118stop (SEQ ID NO: 83)______________________________________
The G-CSF receptor agonist genes in pMON3640, pMON3461, pMON3462, pMON3463, pMON3464, pMON3465, pMON3466 and pMON3467 were transferred to an E. coli expression vector, pMON2341, as an NcoI/HindIII restriction fragment, resulting in the plasmids pMON3468, pMON3469, pMON3470, pMON3471, pMON3472, pMON3473, pMON3474 and pMON3498 respectively.
EXAMPLE 38
The plasmid, pMON3468, resulted in low expression levels in E. coli of the desired G-CSF receptor agonist. The 5' end of the gene was redesigned to use codon selection that was AT rich to increase expression levels. The oligonucleotides, Z4849AT.for (SEQ ID NO:84) and Z4849AT.rev (SEQ ID NO:85), were used to re-engineer the gene. The resulting plasmid, pMON3499, containing the gene (SEQ ID NO:94) encodes the G-CSF receptor agonist of (SEQ ID NO:103).
EXAMPLE 39
The G-CSF receptor agonists were assayed in the Baf/3 cell line, transfected with the human G-CSF receptor, (Baf/3-G-CSF) proliferation assay to determine their bioactivity relative to native G-CSF. The activity of the receptor agonists is shown in Table 7.
TABLE 7______________________________________G-CSF receptor agonist activity in Baf/3-G-CSF cell proliferation assaypMON # breakpoint Expression E. coli refold EC50 (pM)______________________________________native G-CSF 50 pMpMON25182 125/126 + + 38 pMpMON25183 132/133 + + 58 pMpMON25184 141/142 + + 70 pMpMON25186 125/126 + + 92 pMpMON25187 132/133 + + 83 pMpMON25188 141/142 + + 41 pMpMON3450 38/39 + + 121 pMpMON3455 38/39 + + 102 pMpMON3499 48/49 + + 137 pMpMON3470 81/82 + + no activity detectedpMON3473 111/112 + -______________________________________
EXAMPLES 40-52
The plasmids in Table 8 contain genes encoding sequence rearranged G-CSF receptor agonists that were made by the method of Horlich et al. (Protein Eng. 5:427-431, 1992). As described in Materials and Methods, the tandem repeat of the G-CSF Ser.sup.17 gene was maintained on a pACYC177 based plasmid (Chang and Cohen, J. Bacteriol. 134:1141-1156, 1978), containing the sequence; GAG ATG GCT, encoding; Asp Met Ala, following immediately downstream of amino acid 174 of the first copy of the G-CSF Ser.sup.17 gene and immediately preceeding amino acid 1 of the second copy of the G-CSF Ser.sup.17 gene. The resulting sequence rearranged G-CSF receptor agonists have the linker; Asp Met Ala, between the original C-terminus and original N-terminus of G-CSF Ser.sup.17. The sequence rearranged G-CSF receptor agonists encoded by the plasmids of Table 8 were identified using a G-CSF receptor binding screen (Wantanabe et al. Analyt. Biochem 195:38-44, 1991). The sequence rearranged G-CSF receptor agonists shown in Table 8 had receptor binding comparable to or better than native recombinant hG-CSF.
TABLE 8______________________________________plasmiddesignation breakpoint gene sequence protein sequence______________________________________pG32 2-3 SEQ ID NO: 110 SEQ ID NO: 122pG1110 10-11 SEQ ID NO: 104 SEQ ID NO: 116pG1312 12-13 SEQ ID NO: 107 SEQ ID NO: 119pG4948 48-49 SEQ ID NO: 111 SEQ ID NO: 123pG5960 59-60 SEQ ID NO: 112 SEQ ID NO: 124pG6667 66-67 SEQ ID NO: 113 SEQ ID NO: 125pG6869 68-69 SEQ ID NO: 114 SEQ ID NO: 126 pG123122 122-123 SEQ ID NO: 105 SEQ ID NO: 117 pG159158 158-159 SEQ ID NO: 108 SEQ ID NO: 120pG7170 70-71 SEQ ID NO: 115 SEQ ID NO: 127 pG125124 124-125 SEQ ID NO: 106 SEQ ID NO: 118pG1918 18-19 SEQ ID NO: 109 SEQ ID NO: 121 pG170169 169-170 SEQ ID NO: 129 SEQ ID NO: 128______________________________________
Additional techniques for the construction of the variant genes, recombinant protein expression, protein purification, protein characterization, biological activity determination can be found in WO 94/12639, WO 94/12638, WO 95/20976, WO 95/21197, WO 95/20977, WO 95/21254 which are hereby incorporated by reference in their entirety.
All references, patents or applications cited herein are incorporated by reference in their entirety as if written herein.
Various other examples will be apparent to the person skilled in the art after reading the present disclosure without departing from the spirit and scope of the invention. It is intended that all such other examples be included within the scope of the appended claims.
__________________________________________________________________________# SEQUENCE LISTING- (1) GENERAL INFORMATION:- (iii) NUMBER OF SEQUENCES: 129- (2) INFORMATION FOR SEQ ID NO:1:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: protein- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 1#/note= "Xaa at position 1 is Thr, Ser, Arg, - # Tyr or Gly;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 2#/note= "Xaa at position 2 is Pro or Leu;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 3#/note= "Xaa at position 3 is Leu,#or Ser;" Arg, Tyr- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 13#/note= "Xaa at position 13 is Phe, Ser, His, - # Thr or Pro;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 16#/note= "Xaa at position 16 is Lys, Pro, Ser, - # thr or His;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 17#/note= "Xaa at position 17 is Cys, Ser, Gly, - # Ala, Ile, Tyr or Arg;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 18#/note= "Xaa at position 18 is Leu, Thr, Pro, - # His, Ile or Cys;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 22#/note= "Xaa at position 22 is Arg, Tyr, Ser, - # Thr or Ala;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 24#/note= "Xaa at position 24 is Ile,#or Leu;" Pro, Tyr- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 27#/note= "Xaa at position 27 is Asp, or Gly;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 30#/note= "Xaa at position 30 is Ala,#or Gly;" Ile, Leu- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 34#/note= "Xaa at position 34 is Lys or Ser;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 36#/note= "Xaa at position 36 is Cys or Ser;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 42#/note= "Xaa at position 42 is Cys or Ser;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 43#/note= "Xaa at position 43 is His, Thr, Gly, - # Val, Lys, Trp, Ala, Arg, Cys, or Leu;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 44#/note= "Xaa at position 44 is Pro, Gly, Arg, - # Asp, Val, Ala, His, Trp, Gln, or Thr;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 46#/note= "Xaa at position 46 is Glu, Arg, Phe, - # Arg, Ile or Ala;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 47#/note= "Xaa at position 47 is Leu or Thr;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 49#/note= "Xaa at position 49 is Leu,#or Ser;" Phe, Arg- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 50#/note= "Xaa at position 50 is Leu, Ile, His, - # Pro or Tyr;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 54#/note= "Xaa at position 54 is Leu or His;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 64#/note= "Xaa at position 64 is Cys or Ser;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 67#/note= "Xaa at position 67 is Gln,#or Cys;" Lys, Leu- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 70#/note= "Xaa at position 70 is Gln, Pro, Leu, - # Arg or Ser;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 74#/note= "Xaa at position 74 is Cys or Ser;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 104#/note= "Xaa at position 104 is Asp,#Val;" Gly or- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 108#/note= "Xaa at position 108 is Leu, Ala, Val, - # Arg, Trp, Gln or Gly;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 115#/note= "Xaa at position 115 is Thr,#or Ala;" His, Leu- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 120#/note= "Xaa at position 120 is Gln, Gly, Arg, - # Lys or His"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 123#/note= "Xaa at position 123 is Glu,#or Thr" Arg, Phe- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 144#/note= "Xaa at position 144 is Phe, His, Arg, - # Pro, Leu, Gln or Glu;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 146#/note= "Xaa at position146 is Arg or Gln;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 147#/note= "Xaa ap position 147 is Arg or Gln;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 156#/note= "Xaa at position 156 is His,#Ser;" Gly or- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 159#/note= "Xaa at position 159 is Ser, Arg, Thr, - # Tyr, Val or Gly;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 162#/note= "Xaa at position 162 is Glu,#or Trp;" Leu, Gly- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 163#/note= "Xaa at position 163 is Val,#or Ala;" Gly, Arg- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 169#/note= "Xaa at position 169 is Arg, Ser, Leu, - # Arg or Cys;"- (ix) FEATURE: (A) NAME/KEY: Modified-sit - #e (B) LOCATION: 170#/note= "Xaa at position 170 is His,#Ser;" Arg or- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:- Xaa Xaa Xaa Gly Pro Ala Ser Ser Leu Pro Gl - #n Ser Xaa Leu Leu Xaa# 15- Xaa Xaa Glu Gln Val Xaa Lys Xaa Gln Gly Xa - #a Gly Ala Xaa Leu Gln# 30- Glu Xaa Leu Xaa Ala Thr Tyr Lys Leu Xaa Xa - #a Xaa Glu Xaa Xaa Val# 45- Xaa Xaa Gly His Ser Xaa Gly Ile Pro Trp Al - #a Pro Leu Ser Ser Xaa# 60- Pro Ser Xaa Ala Leu Xaa Leu Ala Gly Xaa Le - #u Ser Gln Leu His Ser#80- Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Al - #a Leu Glu Gly Ile Ser# 95- Pro Glu Leu Gly Pro Thr Leu Xaa Thr Leu Gl - #n Xaa Asp Val Ala Asp# 110- Phe Ala Xaa Thr Ile Trp Gln Gln Met Glu Xa - #a Xaa Gly Met Ala Pro# 125- Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Al - #a Phe Ala Ser Ala Xaa# 140- Gln Xaa Xaa Ala Gly Gly Val Leu Val Ala Se - #r Xaa Leu Gln Xaa Phe145 1 - #50 1 - #55 1 -#60- Leu Xaa Xaa Ser Tyr Arg Val Leu Xaa Xaa Le - #u Ala Gln Pro# 170- (2) INFORMATION FOR SEQ ID NO:2:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 4 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:- Gly Gly Gly Ser- (2) INFORMATION FOR SEQ ID NO:3:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 54 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:- GCTCTGAGAG CCGCCAGAGC CGCCAGAGGG CTGCGCAAGG TGGCGTAGAA CG - #CG 54- (2) INFORMATION FOR SEQ ID NO:4:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 54 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:- CAGCCCTCTG GCGGCTCTGG CGGCTCTCAG AGCTTCCTGC TCAAGTCTTT AG - #AG 54- (2) INFORMATION FOR SEQ ID NO:5:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 18 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:# 18 CG- (2) INFORMATION FOR SEQ ID NO:6:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 21 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:#21 CCAG C- (2) INFORMATION FOR SEQ ID NO:7:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:# 32 CAAG CTGTGCCACC CC- (2) INFORMATION FOR SEQ ID NO:8:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:# 36 GGTG GCACACAGCT TCTCCT- (2) INFORMATION FOR SEQ ID NO:9:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9:# 32 CGAG TTGGGTCCCA CC- (2) INFORMATION FOR SEQ ID NO:10:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:10:# 36 GGAT ATCCCTTCCA GGGCCT- (2) INFORMATION FOR SEQ ID NO:11:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11:# 32 GGCC CCTGCCCTGC AG- (2) INFORMATION FOR SEQ ID NO:12:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12:# 36 TCCC AGTTCTTCCA TCTGCT- (2) INFORMATION FOR SEQ ID NO:13:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13:# 32 CCAG GGTGCCATGC CG- (2) INFORMATION FOR SEQ ID NO:14:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:14:# 36 GGGC TGCAGGGCAG GGGCCA- (2) INFORMATION FOR SEQ ID NO:15:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:15:# 32 TGCT TTCCAGCGCC GG- (2) INFORMATION FOR SEQ ID NO:16:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:16:# 36 GGCG AAGGCCGGCA TGGCAC- (2) INFORMATION FOR SEQ ID NO:17:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 33 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:17:# 33 AACT GGGTCCAACT CTG- (2) INFORMATION FOR SEQ ID NO:18:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 24 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:18:# 24GCAG ATGG- (2) INFORMATION FOR SEQ ID NO:19:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 65 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:19:- TATATCCATG GCTATGGCTC CAGCTCTGCA ACCAACTCAA GGTGCAATGC CA - #GCATTTGC 60# 65- (2) INFORMATION FOR SEQ ID NO:20:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 63 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:20:- GATGGCTAGC AACCAGAACA CCACCTGCAC GACGTTGAAA AGCAGATGCA AA - #TGCTGGCA 60# 63- (2) INFORMATION FOR SEQ ID NO:21:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 57 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:21:- TATATCCATG GCTACTCAAG GTGCTATGCC AGCTTTTGCT TCTGCTTTTC AA - #CGTCG 57- (2) INFORMATION FOR SEQ ID NO:22:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 58 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:22:- GCAGATGGCT AGCAACCAGA ACACCACCTG CACGACGTTG AAAAGCAGAA GC - #AAAAGC 58- (2) INFORMATION FOR SEQ ID NO:23:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 44 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:23:# 44 CAAC GTCGTGCAGG TGGTGTTCTG GTTG- (2) INFORMATION FOR SEQ ID NO:24:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 44 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:24:# 44 CACC TGCACGACGT TGAAAAGCAG AAGC- (2) INFORMATION FOR SEQ ID NO:25:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 525 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:25:- ATGGCTTACA AGCTGTGCCA CCCCGAGGAG CTGGTGCTGC TCGGACACTC TC - #TGGGCATC 60- CCCTGGGCTC CCCTGAGCTC CTGCCCCAGC CAGGCCCTGC AGCTGGCAGG CT - #GCTTGAGC 120- CAACTCCATA GCGGCCTTTT CCTCTACCAG GGGCTCCTGC AGGCCCTGGA AG - #GGATATCC 180- CCCGAGTTGG GTCCCACCTT GGACACACTG CAGCTGGACG TCGCCGACTT TG - #CCACCACC 240- ATCTGGCAGC AGATGGAAGA ACTGGGAATG GCCCCTGCCC TGCAGCCCAC CC - #AGGGTGCC 300- ATGCCGGCCT TCGCCTCTGC TTTCCAGCGC CGGGCAGGAG GGGTCCTGGT TG - #CTAGCCAT 360- CTGCAGAGCT TCCTGGAGGT GTCGTACCGC GTTCTACGCC ACCTTGCGCA GC - #CCTCTGGC 420- GGCTCTGGCG GCTCTCAGAG CTTCCTGCTC AAGTCTTTAG AGCAAGTGAG GA - #AGATCCAG 480# 525CA GGAGAAGCTG TGTGCCACCT AATAA- (2) INFORMATION FOR SEQ ID NO:26:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 525 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:26:- ATGGCTCCCG AGTTGGGTCC CACCTTGGAC ACACTGCAGC TGGACGTCGC CG - #ACTTTGCC 60- ACCACCATCT GGCAGCAGAT GGAAGAACTG GGAATGGCCC CTGCCCTGCA GC - #CCACCCAG 120- GGTGCCATGC CGGCCTTCGC CTCTGCTTTC CAGCGCCGGG CAGGAGGGGT CC - #TGGTTGCT 180- AGCCATCTGC AGAGCTTCCT GGAGGTGTCG TACCGCGTTC TACGCCACCT TG - #CGCAGCCC 240- TCTGGCGGCT CTGGCGGCTC TCAGAGCTTC CTGCTCAAGT CTTTAGAGCA AG - #TGAGGAAG 300- ATCCAGGGCG ATGGCGCAGC GCTCCAGGAG AAGCTGTGTG CCACCTACAA GC - #TGTGCCAC 360- CCCGAGGAGC TGGTGCTGCT CGGACACTCT CTGGGCATCC CCTGGGCTCC CC - #TGAGCTCC 420- TGCCCCAGCC AGGCCCTGCA GCTGGCAGGC TGCTTGAGCC AACTCCATAG CG - #GCCTTTTC 480# 525CA GGCCCTGGAA GGGATATCCT AATAA- (2) INFORMATION FOR SEQ ID NO:27:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 525 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:27:- ATGGCTATGG CCCCTGCCCT GCAGCCCACC CAGGGTGCCA TGCCGGCCTT CG - #CCTCTGCT 60- TTCCAGCGCC GGGCAGGAGG GGTCCTGGTT GCTAGCCATC TGCAGAGCTT CC - #TGGAGGTG 120- TCGTACCGCG TTCTACGCCA CCTTGCGCAG CCCTCTGGCG GCTCTGGCGG CT - #CTCAGAGC 180- TTCCTGCTCA AGTCTTTAGA GCAAGTGAGG AAGATCCAGG GCGATGGCGC AG - #CGCTCCAG 240- GAGAAGCTGT GTGCCACCTA CAAGCTGTGC CACCCCGAGG AGCTGGTGCT GC - #TCGGACAC 300- TCTCTGGGCA TCCCCTGGGC TCCCCTGAGC TCCTGCCCCA GCCAGGCCCT GC - #AGCTGGCA 360- GGCTGCTTGA GCCAACTCCA TAGCGGCCTT TTCCTCTACC AGGGGCTCCT GC - #AGGCCCTG 420- GAAGGGATAT CCCCCGAGTT GGGTCCCACC TTGGACACAC TGCAGCTGGA CG - #TCGCCGAC 480# 525CA GCAGATGGAA GAACTGGGAT AATAA- (2) INFORMATION FOR SEQ ID NO:28:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 525 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:28:- ATGGCTACCC AGGGTGCCAT GCCGGCCTTC GCCTCTGCTT TCCAGCGCCG GG - #CAGGAGGG 60- GTCCTGGTTG CTAGCCATCT GCAGAGCTTC CTGGAGGTGT CGTACCGCGT TC - #TACGCCAC 120- CTTGCGCAGC CCTCTGGCGG CTCTGGCGGC TCTCAGAGCT TCCTGCTCAA GT - #CTTTAGAG 180- CAAGTGAGGA AGATCCAGGG CGATGGCGCA GCGCTCCAGG AGAAGCTGTG TG - #CCACCTAC 240- AAGCTGTGCC ACCCCGAGGA GCTGGTGCTG CTCGGACACT CTCTGGGCAT CC - #CCTGGGCT 300- CCCCTGAGCT CCTGCCCCAG CCAGGCCCTG CAGCTGGCAG GCTGCTTGAG CC - #AACTCCAT 360- AGCGGCCTTT TCCTCTACCA GGGGCTCCTG CAGGCCCTGG AAGGGATATC CC - #CCGAGTTG 420- GGTCCCACCT TGGACACACT GCAGCTGGAC GTCGCCGACT TTGCCACCAC CA - #TCTGGCAG 480# 525AT GGCCCCTGCC CTGCAGCCCT AATAA- (2) INFORMATION FOR SEQ ID NO:29:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 525 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:29:- ATGGCTTCTG CTTTCCAGCG CCGGGCAGGA GGGGTCCTGG TTGCTAGCCA TC - #TGCAGAGC 60- TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC AGCCCTCTGG CG - #GCTCTGGC 120- GGCTCTCAGA GCTTCCTGCT CAAGTCTTTA GAGCAAGTGA GGAAGATCCA GG - #GCGATGGC 180- GCAGCGCTCC AGGAGAAGCT GTGTGCCACC TACAAGCTGT GCCACCCCGA GG - #AGCTGGTG 240- CTGCTCGGAC ACTCTCTGGG CATCCCCTGG GCTCCCCTGA GCTCCTGCCC CA - #GCCAGGCC 300- CTGCAGCTGG CAGGCTGCTT GAGCCAACTC CATAGCGGCC TTTTCCTCTA CC - #AGGGGCTC 360- CTGCAGGCCC TGGAAGGGAT ATCCCCCGAG TTGGGTCCCA CCTTGGACAC AC - #TGCAGCTG 420- GACGTCGCCG ACTTTGCCAC CACCATCTGG CAGCAGATGG AAGAACTGGG AA - #TGGCCCCT 480# 525GG TGCCATGCCG GCCTTCGCCT AATAA- (2) INFORMATION FOR SEQ ID NO:30:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:30:- ATGGCTTACA AGCTGTGCCA CCCCGAGGAG CTGGTGCTGC TCGGACACTC TC - #TGGGCATC 60- CCCTGGGCTC CCCTGAGCTC CTGCCCCAGC CAGGCCCTGC AGCTGGCAGG CT - #GCTTGAGC 120- CAACTCCATA GCGGCCTTTT CCTCTACCAG GGGCTCCTGC AGGCCCTGGA AG - #GGATATCC 180- CCCGAGTTGG GTCCCACCTT GGACACACTG CAGCTGGACG TCGCCGACTT TG - #CCACCACC 240- ATCTGGCAGC AGATGGAAGA ACTGGGAATG GCCCCTGCCC TGCAGCCCAC CC - #AGGGTGCC 300- ATGCCGGCCT TCGCCTCTGC TTTCCAGCGC CGGGCAGGAG GGGTCCTGGT TG - #CTAGCCAT 360- CTGCAGAGCT TCCTGGAGGT GTCGTACCGC GTTCTACGCC ACCTTGCGCA GC - #CCACACCA 420- TTGGGCCCTG CCAGCTCCCT GCCCCAGAGC TTCCTGCTCA AGTCTTTAGA GC - #AAGTGAGA 480- AAGATCCAGG GCGATGGCGC AGCGCTCCAG GAGAAGCTGT GTGCCACCTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:31:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:31:- ATGGCTCCCG AGTTGGGTCC CACCTTGGAC ACACTGCAGC TGGACGTCGC CG - #ACTTTGCC 60- ACCACCATCT GGCAGCAGAT GGAAGAACTG GGAATGGCCC CTGCCCTGCA GC - #CCACCCAG 120- GGTGCCATGC CGGCCTTCGC CTCTGCTTTC CAGCGCCGGG CAGGAGGGGT CC - #TGGTTGCT 180- AGCCATCTGC AGAGCTTCCT GGAGGTGTCG TACCGCGTTC TACGCCACCT TG - #CGCAGCCC 240- ACACCATTGG GCCCTGCCAG CTCCCTGCCC CAGAGCTTCC TGCTCAAGTC TT - #TAGAGCAA 300- GTGAGAAAGA TCCAGGGCGA TGGCGCAGCG CTCCAGGAGA AGCTGTGTGC CA - #CCTACAAG 360- CTGTGCCACC CCGAGGAGCT GGTGCTGCTC GGACACTCTC TGGGCATCCC CT - #GGGCTCCC 420- CTGAGCTCCT GCCCCAGCCA GGCCCTGCAG CTGGCAGGCT GCTTGAGCCA AC - #TCCATAGC 480- GGCCTTTTCC TCTACCAGGG GCTCCTGCAG GCCCTGGAAG GGATATCCTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:32:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (Synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:32:- ATGGCTATGG CCCCTGCCCT GCAGCCCACC CAGGGTGCCA TGCCGGCCTT CG - #CCTCTGCT 60- TTCCAGCGCC GGGCAGGAGG GGTCCTGGTT GCTAGCCATC TGCAGAGCTT CC - #TGGAGGTG 120- TCGTACCGCG TTCTACGCCA CCTTGCGCAG CCCACACCAT TGGGCCCTGC CA - #GCTCCCTG 180- CCCCAGAGCT TCCTGCTCAA GTCTTTAGAG CAAGTGAGAA AGATCCAGGG CG - #ATGGCGCA 240- GCGCTCCAGG AGAAGCTGTG TGCCACCTAC AAGCTGTGCC ACCCCGAGGA GC - #TGGTGCTG 300- CTCGGACACT CTCTGGGCAT CCCCTGGGCT CCCCTGAGCT CCTGCCCCAG CC - #AGGCCCTG 360- CAGCTGGCAG GCTGCTTGAG CCAACTCCAT AGCGGCCTTT TCCTCTACCA GG - #GGCTCCTG 420- CAGGCCCTGG AAGGGATATC CCCCGAGTTG GGTCCCACCT TGGACACACT GC - #AGCTGGAC 480- GTCGCCGACT TTGCCACCAC CATCTGGCAG CAGATGGAAG AACTGGGATA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:33:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:33:- ATGGCTACCC AGGGTGCCAT GCCGGCCTTC GCCTCTGCTT TCCAGCGCCG GG - #CAGGAGGG 60- GTCCTGGTTG CTAGCCATCT GCAGAGCTTC CTGGAGGTGT CGTACCGCGT TC - #TACGCCAC 120- CTTGCGCAGC CCACACCATT GGGCCCTGCC AGCTCCCTGC CCCAGAGCTT CC - #TGCTCAAG 180- TCTTTAGAGC AAGTGAGAAA GATCCAGGGC GATGGCGCAG CGCTCCAGGA GA - #AGCTGTGT 240- GCCACCTACA AGCTGTGCCA CCCCGAGGAG CTGGTGCTGC TCGGACACTC TC - #TGGGCATC 300- CCCTGGGCTC CCCTGAGCTC CTGCCCCAGC CAGGCCCTGC AGCTGGCAGG CT - #GCTTGAGC 360- CAACTCCATA GCGGCCTTTT CCTCTACCAG GGGCTCCTGC AGGCCCTGGA AG - #GGATATCC 420- CCCGAGTTGG GTCCCACCTT GGACACACTG CAGCTGGACG TCGCCGACTT TG - #CCACCACC 480- ATCTGGCAGC AGATGGAAGA ACTGGGAATG GCCCCTGCCC TGCAGCCCTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:34:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:34:- ATGGCTTCTG CTTTCCAGCG CCGGGCAGGA GGGGTCCTGG TTGCTAGCCA TC - #TGCAGAGC 60- TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC AGCCCACACC AT - #TGGGCCCT 120- GCCAGCTCCC TGCCCCAGAG CTTCCTGCTC AAGTCTTTAG AGCAAGTGAG AA - #AGATCCAG 180- GGCGATGGCG CAGCGCTCCA GGAGAAGCTG TGTGCCACCT ACAAGCTGTG CC - #ACCCCGAG 240- GAGCTGGTGC TGCTCGGACA CTCTCTGGGC ATCCCCTGGG CTCCCCTGAG CT - #CCTGCCCC 300- AGCCAGGCCC TGCAGCTGGC AGGCTGCTTG AGCCAACTCC ATAGCGGCCT TT - #TCCTCTAC 360- CAGGGGCTCC TGCAGGCCCT GGAAGGGATA TCCCCCGAGT TGGGTCCCAC CT - #TGGACACA 420- CTGCAGCTGG ACGTCGCCGA CTTTGCCACC ACCATCTGGC AGCAGATGGA AG - #AACTGGGA 480- ATGGCCCCTG CCCTGCAGCC CACCCAGGGT GCCATGCCGG CCTTCGCCTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:35:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:35:- ATGGCTCCGG AACTGGGTCC AACTCTGGAC ACACTGCAGC TGGACGTCGC CG - #ACTTTGCC 60- ACCACCATCT GGCAGCAGAT GGAAGAACTG GGAATGGCCC CTGCCCTGCA GC - #CCACCCAG 120- GGTGCCATGC CGGCCTTCGC CTCTGCTTTC CAGCGCCGGG CAGGAGGGGT CC - #TGGTTGCT 180- AGCCATCTGC AGAGCTTCCT GGAGGTGTCG TACCGCGTTC TACGCCACCT TG - #CGCAGCCC 240- ACACCATTGG GCCCTGCCAG CTCCCTGCCC CAGAGCTTCC TGCTCAAGTC TT - #TAGAGCAA 300- GTGAGAAAGA TCCAGGGCGA TGGCGCAGCG CTCCAGGAGA AGCTGTGTGC CA - #CCTACAAG 360- CTGTGCCACC CCGAGGAGCT GGTGCTGCTC GGACACTCTC TGGGCATCCC CT - #GGGCTCCC 420- CTGAGCTCCT GCCCCAGCCA GGCCCTGCAG CTGGCAGGCT GCTTGAGCCA AC - #TCCATAGC 480# 531ACCAGGG GCTCCTGCAG GCCCTGGAAG GGATATCCTA A- (2) INFORMATION FOR SEQ ID NO:36:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:36:- ATGGCTATGG CTCCAGCTCT GCAACCAACT CAAGGTGCAA TGCCAGCATT TG - #CATCTGCT 60- TTTCAACGTC GTGCAGGTGG TGTTCTGGTT GCTAGCCATC TGCAGAGCTT CC - #TGGAGGTG 120- TCGTACCGCG TTCTACGCCA CCTTGCGCAG CCCACACCAT TGGGCCCTGC CA - #GCTCCCTG 180- CCCCAGAGCT TCCTGCTCAA GTCTTTAGAG CAAGTGAGAA AGATCCAGGG CG - #ATGGCGCA 240- GCGCTCCAGG AGAAGCTGTG TGCCACCTAC AAGCTGTGCC ACCCCGAGGA GC - #TGGTGCTG 300- CTCGGACACT CTCTGGGCAT CCCCTGGGCT CCCCTGAGCT CCTGCCCCAG CC - #AGGCCCTG 360- CAGCTGGCAG GCTGCTTGAG CCAACTCCAT AGCGGCCTTT TCCTCTACCA GG - #GGCTCCTG 420- CAGGCCCTGG AAGGGATATC CCCCGAGTTG GGTCCCACCT TGGACACACT GC - #AGCTGGAC 480# 531CCACCAC CATCTGGCAG CAGATGGAAG AACTGGGATA A- (2) INFORMATION FOR SEQ ID NO:37:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:37:- ATGGCTACTC AAGGTGCTAT GCCAGCTTTT GCTTCTGCTT TTCAACGTCG TG - #CAGGTGGT 60- GTTCTGGTTG CTAGCCATCT GCAGAGCTTC CTGGAGGTGT CGTACCGCGT TC - #TACGCCAC 120- CTTGCGCAGC CCACACCATT GGGCCCTGCC AGCTCCCTGC CCCAGAGCTT CC - #TGCTCAAG 180- TCTTTAGAGC AAGTGAGAAA GATCCAGGGC GATGGCGCAG CGCTCCAGGA GA - #AGCTGTGT 240- GCCACCTACA AGCTGTGCCA CCCCGAGGAG CTGGTGCTGC TCGGACACTC TC - #TGGGCATC 300- CCCTGGGCTC CCCTGAGCTC CTGCCCCAGC CAGGCCCTGC AGCTGGCAGG CT - #GCTTGAGC 360- CAACTCCATA GCGGCCTTTT CCTCTACCAG GGGCTCCTGC AGGCCCTGGA AG - #GGATATCC 420- CCCGAGTTGG GTCCCACCTT GGACACACTG CAGCTGGACG TCGCCGACTT TG - #CCACCACC 480# 531TGGAAGA ACTGGGAATG GCCCCTGCCC TGCAGCCCTA A- (2) INFORMATION FOR SEQ ID NO:38:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:38:- ATGGCTTCTG CTTTTCAACG TCGTGCAGGT GGTGTTCTGG TTGCTAGCCA TC - #TGCAGAGC 60- TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC AGCCCACACC AT - #TGGGCCCT 120- GCCAGCTCCC TGCCCCAGAG CTTCCTGCTC AAGTCTTTAG AGCAAGTGAG AA - #AGATCCAG 180- GGCGATGGCG CAGCGCTCCA GGAGAAGCTG TGTGCCACCT ACAAGCTGTG CC - #ACCCCGAG 240- GAGCTGGTGC TGCTCGGACA CTCTCTGGGC ATCCCCTGGG CTCCCCTGAG CT - #CCTGCCCC 300- AGCCAGGCCC TGCAGCTGGC AGGCTGCTTG AGCCAACTCC ATAGCGGCCT TT - #TCCTCTAC 360- CAGGGGCTCC TGCAGGCCCT GGAAGGGATA TCCCCCGAGT TGGGTCCCAC CT - #TGGACACA 420- CTGCAGCTGG ACGTCGCCGA CTTTGCCACC ACCATCTGGC AGCAGATGGA AG - #AACTGGGA 480# 531TGCAGCC CACCCAGGGT GCCATGCCGG CCTTCGCCTA A- (2) INFORMATION FOR SEQ ID NO:39:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 522 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:39:- ATGGCTCCGG AACTGGGTCC AACTCTGGAC ACACTGCAGC TGGACGTCGC CG - #ACTTTGCC 60- ACCACCATCT GGCAGCAGAT GGAAGAACTG GGAATGGCCC CTGCCCTGCA GC - #CCACCCAG 120- GGTGCCATGC CGGCCTTCGC CTCTGCTTTC CAGCGCCGGG CAGGAGGGGT CC - #TGGTTGCT 180- AGCCATCTGC AGAGCTTCCT GGAGGTGTCG TACCGCGTTC TACGCCACCT TG - #CGCAGCCC 240- TCTGGCGGCT CTGGCGGCTC TCAGAGCTTC CTGCTCAAGT CTTTAGAGCA AG - #TGAGAAAG 300- ATCCAGGGCG ATGGCGCAGC GCTCCAGGAG AAGCTGTGTG CCACCTACAA GC - #TGTGCCAC 360- CCCGAGGAGC TGGTGCTGCT CGGACACTCT CTGGGCATCC CCTGGGCTCC CC - #TGAGCTCC 420- TGCCCCAGCC AGGCCCTGCA GCTGGCAGGC TGCTTGAGCC AACTCCATAG CG - #GCCTTTTC 480# 522 TGCA GGCCCTGGAA GGGATATCCT AA- (2) INFORMATION FOR SEQ ID NO:40:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 522 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:40:- ATGGCTATGG CTCCAGCTCT GCAACCAACT CAAGGTGCAA TGCCAGCATT TG - #CATCTGCT 60- TTTCAACGTC GTGCAGGTGG TGTTCTGGTT GCTAGCCATC TGCAGAGCTT CC - #TGGAGGTG 120- TCGTACCGCG TTCTACGCCA CCTTGCGCAG CCCTCTGGCG GCTCTGGCGG CT - #CTCAGAGC 180- TTCCTGCTCA AGTCTTTAGA GCAAGTGAGA AAGATCCAGG GCGATGGCGC AG - #CGCTCCAG 240- GAGAAGCTGT GTGCCACCTA CAAGCTGTGC CACCCCGAGG AGCTGGTGCT GC - #TCGGACAC 300- TCTCTGGGCA TCCCCTGGGC TCCCCTGAGC TCCTGCCCCA GCCAGGCCCT GC - #AGCTGGCA 360- GGCTGCTTGA GCCAACTCCA TAGCGGCCTT TTCCTCTACC AGGGGCTCCT GC - #AGGCCCTG 420- GAAGGGATAT CCCCCGAGTT GGGTCCCACC TTGGACACAC TGCAGCTGGA CG - #TCGCCGAC 480# 522 GGCA GCAGATGGAA GAACTGGGAT AA- (2) INFORMATION FOR SEQ ID NO:41:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 522 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:41:- ATGGCTACTC AAGGTGCTAT GCCAGCTTTT GCTTCTGCTT TTCAACGTCG TG - #CAGGTGGT 60- GTTCTGGTTG CTAGCCATCT GCAGAGCTTC CTGGAGGTGT CGTACCGCGT TC - #TACGCCAC 120- CTTGCGCAGC CCTCTGGCGG CTCTGGCGGC TCTCAGAGCT TCCTGCTCAA GT - #CTTTAGAG 180- CAAGTGAGAA AGATCCAGGG CGATGGCGCA GCGCTCCAGG AGAAGCTGTG TG - #CCACCTAC 240- AAGCTGTGCC ACCCCGAGGA GCTGGTGCTG CTCGGACACT CTCTGGGCAT CC - #CCTGGGCT 300- CCCCTGAGCT CCTGCCCCAG CCAGGCCCTG CAGCTGGCAG GCTGCTTGAG CC - #AACTCCAT 360- AGCGGCCTTT TCCTCTACCA GGGGCTCCTG CAGGCCCTGG AAGGGATATC CC - #CCGAGTTG 420- GGTCCCACCT TGGACACACT GCAGCTGGAC GTCGCCGACT TTGCCACCAC CA - #TCTGGCAG 480# 522 GAAT GGCCCCTGCC CTGCAGCCCT AA- (2) INFORMATION FOR SEQ ID NO:42:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 522 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:42:- ATGGCTTCTG CTTTTCAACG TCGTGCAGGT GGTGTTCTGG TTGCTAGCCA TC - #TGCAGAGC 60- TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC AGCCCTCTGG CG - #GCTCTGGC 120- GGCTCTCAGA GCTTCCTGCT CAAGTCTTTA GAGCAAGTGA GAAAGATCCA GG - #GCGATGGC 180- GCAGCGCTCC AGGAGAAGCT GTGTGCCACC TACAAGCTGT GCCACCCCGA GG - #AGCTGGTG 240- CTGCTCGGAC ACTCTCTGGG CATCCCCTGG GCTCCCCTGA GCTCCTGCCC CA - #GCCAGGCC 300- CTGCAGCTGG CAGGCTGCTT GAGCCAACTC CATAGCGGCC TTTTCCTCTA CC - #AGGGGCTC 360- CTGCAGGCCC TGGAAGGGAT ATCCCCCGAG TTGGGTCCCA CCTTGGACAC AC - #TGCAGCTG 420- GACGTCGCCG ACTTTGCCAC CACCATCTGG CAGCAGATGG AAGAACTGGG AA - #TGGCCCCT 480# 522 AGGG TGCCATGCCG GCCTTCGCCT AA- (2) INFORMATION FOR SEQ ID NO:43:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 171 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:43:- Tyr Lys Leu Cys His Pro Glu Glu Leu Val Le - #u Leu Gly His Ser Leu# 15- Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pr - #o Ser Gln Ala Leu Gln# 30- Leu Ala Gly Cys Leu Ser Gln Leu His Ser Gl - #y Leu Phe Leu Tyr Gln# 45- Gly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pr - #o Glu Leu Gly Pro Thr# 60- Leu Asp Thr Leu Gln Leu Asp Val Ala Asp Ph - #e Ala Thr Thr Ile Trp#80- Gln Gln Met Glu Glu Leu Gly Met Ala Pro Al - #a Leu Gln Pro Thr Gln# 95- Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gl - #n Arg Arg Ala Gly Gly# 110- Val Leu Val Ala Ser His Leu Gln Ser Phe Le - #u Glu Val Ser Tyr Arg# 125- Val Leu Arg His Leu Ala Gln Pro Ser Gly Gl - #y Ser Gly Gly Ser Gln# 140- Ser Phe Leu Leu Lys Ser Leu Glu Gln Val Ar - #g Lys Ile Gln Gly Asp145 1 - #50 1 - #55 1 -#60- Gly Ala Ala Leu Gln Glu Lys Leu Cys Ala Th - #r# 170- (2) INFORMATION FOR SEQ ID NO:44:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 171 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:44:- Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gl - #n Leu Asp Val Ala Asp# 15- Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Gl - #u Leu Gly Met Ala Pro# 30- Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Al - #a Phe Ala Ser Ala Phe# 45- Gln Arg Arg Ala Gly Gly Val Leu Val Ala Se - #r His Leu Gln Ser Phe# 60- Leu Glu Val Ser Tyr Arg Val Leu Arg His Le - #u Ala Gln Pro Ser Gly#80- Gly Ser Gly Gly Ser Gln Ser Phe Leu Leu Ly - #s Ser Leu Glu Gln Val# 95- Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gl - #n Glu Lys Leu Cys Ala# 110- Thr Tyr Lys Leu Cys His Pro Glu Glu Leu Va - #l Leu Leu Gly His Ser# 125- Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cy - #s Pro Ser Gln Ala Leu# 140- Gln Leu Ala Gly Cys Leu Ser Gln Leu His Se - #r Gly Leu Phe Leu Tyr145 1 - #50 1 - #55 1 -#60- Gln Gly Leu Leu Gln Ala Leu Glu Gly Ile Se - #r# 170- (2) INFORMATION FOR SEQ ID NO:45:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 171 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:45:- Thr Gln Gly Ala Met Pro Ala Phe Ala Ser Al - #a Phe Gln Arg Arg Ala# 15- Gly Gly Val Leu Val Ala Ser His Leu Gln Se - #r Phe Leu Glu Val Ser# 30- Tyr Arg Val Leu Arg His Leu Ala Gln Pro Se - #r Gly Gly Ser Gly Gly# 45- Ser Gln Ser Phe Leu Leu Lys Ser Leu Glu Gl - #n Val Arg Lys Ile Gln# 60- Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cy - #s Ala Thr Tyr Lys Leu#80- Cys His Pro Glu Glu Leu Val Leu Leu Gly Hi - #s Ser Leu Gly Ile Pro# 95- Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln Al - #a Leu Gln Leu Ala Gly# 110- Cys Leu Ser Gln Leu His Ser Gly Leu Phe Le - #u Tyr Gln Gly Leu Leu# 125- Gln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gl - #y Pro Thr Leu Asp Thr# 140- Leu Gln Leu Asp Val Ala Asp Phe Ala Thr Th - #r Ile Trp Gln Gln Met145 1 - #50 1 - #55 1 -#60- Glu Glu Leu Gly Met Ala Pro Ala Leu Gln Pr - #o# 170- (2) INFORMATION FOR SEQ ID NO:46:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 118 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:46:- TGGAATAAAA AAGAGAGAAG GAAAAGGATA GAAGAAGGGG GGGGAAGGGA GA - #AAAGGCAA 60- TTCGGAGGTA ACGAAGAAGC GGTGGGAAGG GGTATGAAAA AAATTTGGTG GG - #TAAAAG 118- (2) INFORMATION FOR SEQ ID NO:47:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 171 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:47:- Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Le - #u Val Ala Ser His Leu# 15- Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Le - #u Arg His Leu Ala Gln# 30- Pro Ser Gly Gly Ser Gly Gly Ser Gln Ser Ph - #e Leu Leu Lys Ser Leu# 45- Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Al - #a Ala Leu Gln Glu Lys# 60- Leu Cys Ala Thr Tyr Lys Leu Cys His Pro Gl - #u Glu Leu Val Leu Leu#80- Gly His Ser Leu Gly Ile Pro Trp Ala Pro Le - #u Ser Ser Cys Pro Ser# 95- Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gl - #n Leu His Ser Gly Leu# 110- Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Gl - #u Gly Ile Ser Pro Glu# 125- Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu As - #p Val Ala Asp Phe Ala# 140- Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gl - #y Met Ala Pro Ala Leu145 1 - #50 1 - #55 1 -#60- Gln Pro Thr Gln Gly Ala Met Pro Ala Phe Al - #a# 170- (2) INFORMATION FOR SEQ ID NO:48:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:48:- Tyr Lys Leu Cys His Pro Glu Glu Leu Val Le - #u Leu Gly His Ser Leu# 15- Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pr - #o Ser Gln Ala Leu Gln# 30- Leu Ala Gly Cys Leu Ser Gln Leu His Ser Gl - #y Leu Phe Leu Tyr Gln# 45- Gly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pr - #o Glu Leu Gly Pro Thr# 60- Leu Asp Thr Leu Gln Leu Asp Val Ala Asp Ph - #e Ala Thr Thr Ile Trp#80- Gln Gln Met Glu Glu Leu Gly Met Ala Pro Al - #a Leu Gln Pro Thr Gln# 95- Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gl - #n Arg Arg Ala Gly Gly# 110- Val Leu Val Ala Ser His Leu Gln Ser Phe Le - #u Glu Val Ser Tyr Arg# 125- Val Leu Arg His Leu Ala Gln Pro Thr Pro Le - #u Gly Pro Ala Ser Ser# 140- Leu Pro Gln Ser Phe Leu Leu Lys Ser Leu Gl - #u Gln Val Arg Lys Ile145 1 - #50 1 - #55 1 -#60- Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Le - #u Cys Ala Thr# 170- (2) INFORMATION FOR SEQ ID NO:49:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:49:- Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gl - #n Leu Asp Val Ala Asp# 15- Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Gl - #u Leu Gly Met Ala Pro# 30- Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Al - #a Phe Ala Ser Ala Phe# 45- Gln Arg Arg Ala Gly Gly Val Leu Val Ala Se - #r His Leu Gln Ser Phe# 60- Leu Glu Val Ser Tyr Arg Val Leu Arg His Le - #u Ala Gln Pro Thr Pro#80- Leu Gly Pro Ala Ser Ser Leu Pro Gln Ser Ph - #e Leu Leu Lys Ser Leu# 95- Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Al - #a Ala Leu Gln Glu Lys# 110- Leu Cys Ala Thr Tyr Lys Leu Cys His Pro Gl - #u Glu Leu Val Leu Leu# 125- Gly His Ser Leu Gly Ile Pro Trp Ala Pro Le - #u Ser Ser Cys Pro Ser# 140- Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gl - #n Leu His Ser Gly Leu145 1 - #50 1 - #55 1 -#60- Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Gl - #u Gly Ile Ser# 170- (2) INFORMATION FOR SEQ ID NO:50:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:50:- Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Al - #a Met Pro Ala Phe Ala# 15- Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Le - #u Val Ala Ser His Leu# 30- Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Le - #u Arg His Leu Ala Gln# 45- Pro Thr Pro Leu Gly Pro Ala Ser Ser Leu Pr - #o Gln Ser Phe Leu Leu# 60- Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gl - #y Asp Gly Ala Ala Leu#80- Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cy - #s His Pro Glu Glu Leu# 95- Val Leu Leu Gly His Ser Leu Gly Ile Pro Tr - #p Ala Pro Leu Ser Ser# 110- Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cy - #s Leu Ser Gln Leu His# 125- Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gl - #n Ala Leu Glu Gly Ile# 140- Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Le - #u Gln Leu Asp Val Ala145 1 - #50 1 - #55 1 -#60- Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Gl - #u Glu Leu Gly# 170- (2) INFORMATION FOR SEQ ID NO:51:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:51:- Thr Gln Gly Ala Met Pro Ala Phe Ala Ser Al - #a Phe Gln Arg Arg Ala# 15- Gly Gly Val Leu Val Ala Ser His Leu Gln Se - #r Phe Leu Glu Val Ser# 30- Tyr Arg Val Leu Arg His Leu Ala Gln Pro Th - #r Pro Leu Gly Pro Ala# 45- Ser Ser Leu Pro Gln Ser Phe Leu Leu Lys Se - #r Leu Glu Gln Val Arg# 60- Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Gl - #u Lys Leu Cys Ala Thr#80- Tyr Lys Leu Cys His Pro Glu Glu Leu Val Le - #u Leu Gly His Ser Leu# 95- Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pr - #o Ser Gln Ala Leu Gln# 110- Leu Ala Gly Cys Leu Ser Gln Leu His Ser Gl - #y Leu Phe Leu Tyr Gln# 125- Gly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pr - #o Glu Leu Gly Pro Thr# 140- Leu Asp Thr Leu Gln Leu Asp Val Ala Asp Ph - #e Ala Thr Thr Ile Trp145 1 - #50 1 - #55 1 -#60- Gln Gln Met Glu Glu Leu Gly Met Ala Pro Al - #a Leu Gln Pro# 170- (2) INFORMATION FOR SEQ ID NO:52:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:52:- Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Le - #u Val Ala Ser His Leu# 15- Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Le - #u Arg His Leu Ala Gln# 30- Pro Thr Pro Leu Gly Pro Ala Ser Ser Leu Pr - #o Gln Ser Phe Leu Leu# 45- Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gl - #y Asp Gly Ala Ala Leu# 60- Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cy - #s His Pro Glu Glu Leu#80- Val Leu Leu Gly His Ser Leu Gly Ile Pro Tr - #p Ala Pro Leu Ser Ser# 95- Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cy - #s Leu Ser Gln Leu His# 110- Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gl - #n Ala Leu Glu Gly Ile# 125- Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Le - #u Gln Leu Asp Val Ala# 140- Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Gl - #u Glu Leu Gly Met Ala145 1 - #50 1 - #55 1 -#60- Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pr - #o Ala Phe Ala# 170- (2) INFORMATION FOR SEQ ID NO:53:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:53:- Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gl - #n Leu Asp Val Ala Asp# 15- Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Gl - #u Leu Gly Met Ala Pro# 30- Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Al - #a Phe Ala Ser Ala Phe# 45- Gln Arg Arg Ala Gly Gly Val Leu Val Ala Se - #r His Leu Gln Ser Phe# 60- Leu Glu Val Ser Tyr Arg Val Leu Arg His Le - #u Ala Gln Pro Thr Pro#80- Leu Gly Pro Ala Ser Ser Leu Pro Gln Ser Ph - #e Leu Leu Lys Ser Leu# 95- Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Al - #a Ala Leu Gln Glu Lys# 110- Leu Cys Ala Thr Tyr Lys Leu Cys His Pro Gl - #u Glu Leu Val Leu Leu# 125- Gly His Ser Leu Gly Ile Pro Trp Ala Pro Le - #u Ser Ser Cys Pro Ser# 140- Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gl - #n Leu His Ser Gly Leu145 1 - #50 1 - #55 1 -#60- Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Gl - #u Gly Ile Ser# 170- (2) INFORMATION FOR SEQ ID NO:54:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:54:- Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Al - #a Met Pro Ala Phe Ala# 15- Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Le - #u Val Ala Ser His Leu# 30- Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Le - #u Arg His Leu Ala Gln# 45- Pro Thr Pro Leu Gly Pro Ala Ser Ser Leu Pr - #o Gln Ser Phe Leu Leu# 60- Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gl - #y Asp Gly Ala Ala Leu#80- Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cy - #s His Pro Glu Glu Leu# 95- Val Leu Leu Gly His Ser Leu Gly Ile Pro Tr - #p Ala Pro Leu Ser Ser# 110- Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cy - #s Leu Ser Gln Leu His# 125- Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gl - #n Ala Leu Glu Gly Ile# 140- Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Le - #u Gln Leu Asp Val Ala145 1 - #50 1 - #55 1 -#60- Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Gl - #u Glu Leu Gly# 170- (2) INFORMATION FOR SEQ ID NO:55:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:55:- Thr Gln Gly Ala Met Pro Ala Phe Ala Ser Al - #a Phe Gln Arg Arg Ala# 15- Gly Gly Val Leu Val Ala Ser His Leu Gln Se - #r Phe Leu Glu Val Ser# 30- Tyr Arg Val Leu Arg His Leu Ala Gln Pro Th - #r Pro Leu Gly Pro Ala# 45- Ser Ser Leu Pro Gln Ser Phe Leu Leu Lys Se - #r Leu Glu Gln Val Arg# 60- Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Gl - #u Lys Leu Cys Ala Thr#80- Tyr Lys Leu Cys His Pro Glu Glu Leu Val Le - #u Leu Gly His Ser Leu# 95- Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pr - #o Ser Gln Ala Leu Gln# 110- Leu Ala Gly Cys Leu Ser Gln Leu His Ser Gl - #y Leu Phe Leu Tyr Gln# 125- Gly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pr - #o Glu Leu Gly Pro Thr# 140- Leu Asp Thr Leu Gln Leu Asp Val Ala Asp Ph - #e Ala Thr Thr Ile Trp145 1 - #50 1 - #55 1 -#60- Gln Gln Met Glu Glu Leu Gly Met Ala Pro Al - #a Leu Gln Pro# 170- (2) INFORMATION FOR SEQ ID NO:56:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:56:- Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Le - #u Val Ala Ser His Leu# 15- Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Le - #u Arg His Leu Ala Gln# 30- Pro Thr Pro Leu Gly Pro Ala Ser Ser Leu Pr - #o Gln Ser Phe Leu Leu# 45- Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gl - #y Asp Gly Ala Ala Leu# 60- Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cy - #s His Pro Glu Glu Leu#80- Val Leu Leu Gly His Ser Leu Gly Ile Pro Tr - #p Ala Pro Leu Ser Ser# 95- Cys Pro Ser Gln Ala Leu Gln Leu Ala Gly Cy - #s Leu Ser Gln Leu His# 110- Ser Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gl - #n Ala Leu Glu Gly Ile# 125- Ser Pro Glu Leu Gly Pro Thr Leu Asp Thr Le - #u Gln Leu Asp Val Ala# 140- Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Gl - #u Glu Leu Gly Met Ala145 1 - #50 1 - #55 1 -#60- Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pr - #o Ala Phe Ala# 170- (2) INFORMATION FOR SEQ ID NO:57:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 171 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:57:- Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gl - #n Leu Asp Val Ala Asp# 15- Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Gl - #u Leu Gly Met Ala Pro# 30- Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Al - #a Phe Ala Ser Ala Phe# 45- Gln Arg Arg Ala Gly Gly Val Leu Val Ala Se - #r His Leu Gln Ser Phe# 60- Leu Glu Val Ser Tyr Arg Val Leu Arg His Le - #u Ala Gln Pro Ser Gly#80- Gly Ser Gly Gly Ser Gln Ser Phe Leu Leu Ly - #s Ser Leu Glu Gln Val# 95- Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gl - #n Glu Lys Leu Cys Ala# 110- Thr Tyr Lys Leu Cys His Pro Glu Glu Leu Va - #l Leu Leu Gly His Ser# 125- Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cy - #s Pro Ser Gln Ala Leu# 140- Gln Leu Ala Gly Cys Leu Ser Gln Leu His Se - #r Gly Leu Phe Leu Tyr145 1 - #50 1 - #55 1 -#60- Gln Gly Leu Leu Gln Ala Leu Glu Gly Ile Se - #r# 170- (2) INFORMATION FOR SEQ ID NO:58:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 169 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:58:- Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Al - #a Met Pro Ala Phe Ala# 15- Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Le - #u Val Ala Ser His Leu# 30- Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Le - #u Arg His Leu Ala Gln# 45- Pro Ser Gly Gly Ser Gly Gly Ser Gln Ser Ph - #e Leu Leu Lys Ser Leu# 60- Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Al - #a Ala Leu Gln Glu Lys#80- Ala Thr Tyr Lys Leu Cys His Pro Glu Glu Le - #u Val Leu Leu Gly His# 95- Ser Leu Gly Ile Pro Trp Ala Pro Leu Ser Se - #r Cys Pro Ser Gln Ala# 110- Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu Hi - #s Ser Gly Leu Phe Leu# 125- Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gly Il - #e Ser Pro Glu Leu Gly# 140- Pro Thr Leu Asp Thr Leu Gln Leu Asp Val Al - #a Asp Phe Ala Thr Thr145 1 - #50 1 - #55 1 -#60- Ile Trp Gln Gln Met Glu Glu Leu Gly 165- (2) INFORMATION FOR SEQ ID NO:59:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 171 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:59:- Thr Gln Gly Ala Met Pro Ala Phe Ala Ser Al - #a Phe Gln Arg Arg Ala# 15- Gly Gly Val Leu Val Ala Ser His Leu Gln Se - #r Phe Leu Glu Val Ser# 30- Tyr Arg Val Leu Arg His Leu Ala Gln Pro Se - #r Gly Gly Ser Gly Gly# 45- Ser Gln Ser Phe Leu Leu Lys Ser Leu Glu Gl - #n Val Arg Lys Ile Gln# 60- Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cy - #s Ala Thr Tyr Lys Leu#80- Cys His Pro Glu Glu Leu Val Leu Leu Gly Hi - #s Ser Leu Gly Ile Pro# 95- Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln Al - #a Leu Gln Leu Ala Gly# 110- Cys Leu Ser Gln Leu His Ser Gly Leu Phe Le - #u Tyr Gln Gly Leu Leu# 125- Gln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gl - #y Pro Thr Leu Asp Thr# 140- Leu Gln Leu Asp Val Ala Asp Phe Ala Thr Th - #r Ile Trp Gln Gln Met145 1 - #50 1 - #55 1 -#60- Glu Glu Leu Gly Met Ala Pro Ala Leu Gln Pr - #o# 170- (2) INFORMATION FOR SEQ ID NO:60:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 171 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:60:- Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Le - #u Val Ala Ser His Leu# 15- Gln Ser Phe Leu Glu Val Ser Tyr Arg Val Le - #u Arg His Leu Ala Gln# 30- Pro Ser Gly Gly Ser Gly Gly Ser Gln Ser Ph - #e Leu Leu Lys Ser Leu# 45- Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Al - #a Ala Leu Gln Glu Lys# 60- Leu Cys Ala Thr Tyr Lys Leu Cys His Pro Gl - #u Glu Leu Val Leu Leu#80- Gly His Ser Leu Gly Ile Pro Trp Ala Pro Le - #u Ser Ser Cys Pro Ser# 95- Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gl - #n Leu His Ser Gly Leu# 110- Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Gl - #u Gly Ile Ser Pro Glu# 125- Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu As - #p Val Ala Asp Phe Ala# 140- Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gl - #y Met Ala Pro Ala Leu145 1 - #50 1 - #55 1 -#60- Gln Pro Thr Gln Gly Ala Met Pro Ala Phe Al - #a# 170- (2) INFORMATION FOR SEQ ID NO:61:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 8 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:61:- Gly Gly Gly Ser Gly Gly Gly Ser1 5- (2) INFORMATION FOR SEQ ID NO:62:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 12 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:62:- Gly Gly Gly Ser Gly Gly Gly Ser Gly Gly Gl - #y Ser# 10- (2) INFORMATION FOR SEQ ID NO:63:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 7 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:63:- Ser Gly Gly Ser Gly Gly Ser1 5- (2) INFORMATION FOR SEQ ID NO:64:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 5 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:64:- Glu Phe Gly Asn Met1 5- (2) INFORMATION FOR SEQ ID NO:65:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 6 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:65:- Glu Phe Gly Gly Asn Met1 5- (2) INFORMATION FOR SEQ ID NO:66:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 9 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:66:- Glu Phe Gly Gly Asn Gly Gly Asn Met1 5- (2) INFORMATION FOR SEQ ID NO:67:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 7 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:67:- Gly Gly Ser Asp Met Ala Gly1 5- (2) INFORMATION FOR SEQ ID NO:68:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:68:# 32 GCTC GGACACTCTC TG- (2) INFORMATION FOR SEQ ID NO:69:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:69:# 36 CACC AGCTCCTCGG GGTGGC- (2) INFORMATION FOR SEQ ID NO:70:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:70:# 32 ACTC CATAGCGGCC TT- (2) INFORMATION FOR SEQ ID NO:71:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:71:# 36 GCTC AAGCAGCCTG CCAGCT- (2) INFORMATION FOR SEQ ID NO:72:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:72:# 32 TTTC CTCTACCAGG GG- (2) INFORMATION FOR SEQ ID NO:73:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:73:# 36 GCCG CTATGGAGTT GGCTCA- (2) INFORMATION FOR SEQ ID NO:74:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:74:# 32 CTAC CAGGGGCTCC TG- (2) INFORMATION FOR SEQ ID NO:75:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:75:# 36 GAAA AGGCCGCTAT GGAGTT- (2) INFORMATION FOR SEQ ID NO:76:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:76:# 32 CCTG GAAGGGATAT CC- (2) INFORMATION FOR SEQ ID NO:77:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:77:# 36 CTGC AGGAGCCCCT GGTAGA- (2) INFORMATION FOR SEQ ID NO:78:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:78:# 32 CTTT GCCACCACCA TC- (2) INFORMATION FOR SEQ ID NO:79:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:79:# 36 GGCG ACGTCCAGCT GCAGTG- (2) INFORMATION FOR SEQ ID NO:80:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:80:# 32 CTGG CAGCAGATGG AA- (2) INFORMATION FOR SEQ ID NO:81:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:81:# 36 GGTG GTGGCAAAGT CGGCGA- (2) INFORMATION FOR SEQ ID NO:82:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 32 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:82:# 32 GCAG ATGGAAGAAC TG- (2) INFORMATION FOR SEQ ID NO:83:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 36 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:83:# 36 CCAG ATGGTGGTGG CAAAGT- (2) INFORMATION FOR SEQ ID NO:84:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 50 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:84:# 50GACATT CTTTAGGTAT TCCATGGGCT CCTCTGAGCT- (2) INFORMATION FOR SEQ ID NO:85:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 40 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:85:# 40 ATAC CTAAAGAATG TCCTAACAAA- (2) INFORMATION FOR SEQ ID NO:86:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:86:- ATGGCTCTGC TCGGACACTC TCTGGGCATC CCCTGGGCTC CCCTGAGCTC CT - #GCCCCAGC 60- CAGGCCCTGC AGCTGGCAGG CTGCTTGAGC CAACTCCATA GCGGCCTTTT CC - #TCTACCAG 120- GGGCTCCTGC AGGCCCTGGA AGGGATATCC CCCGAGTTGG GTCCCACCTT GG - #ACACACTG 180- CAGCTGGACG TCGCCGACTT TGCCACCACC ATCTGGCAGC AGATGGAAGA AC - #TGGGAATG 240- GCCCCTGCCC TGCAGCCCAC CCAGGGTGCC ATGCCGGCCT TCGCCTCTGC TT - #TCCAGCGC 300- CGGGCAGGAG GGGTCCTGGT TGCTAGCCAT CTGCAGAGCT TCCTGGAGGT GT - #CGTACCGC 360- GTTCTACGCC ACCTTGCGCA GCCCACACCA TTGGGCCCTG CCAGCTCCCT GC - #CCCAGAGC 420- TTCCTGCTCA AGTCTTTAGA GCAAGTGAGA AAGATCCAGG GCGATGGCGC AG - #CGCTCCAG 480- GAGAAGCTGT GTGCCACCTA CAAGCTGTGC CACCCCGAGG AGCTGGTGTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:87:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:87:- ATGGCTCAAC TCCATAGCGG CCTTTTCCTC TACCAGGGGC TCCTGCAGGC CC - #TGGAAGGG 60- ATATCCCCCG AGTTGGGTCC CACCTTGGAC ACACTGCAGC TGGACGTCGC CG - #ACTTTGCC 120- ACCACCATCT GGCAGCAGAT GGAAGAACTG GGAATGGCCC CTGCCCTGCA GC - #CCACCCAG 180- GGTGCCATGC CGGCCTTCGC CTCTGCTTTC CAGCGCCGGG CAGGAGGGGT CC - #TGGTTGCT 240- AGCCATCTGC AGAGCTTCCT GGAGGTGTCG TACCGCGTTC TACGCCACCT TG - #CGCAGCCC 300- ACACCATTGG GCCCTGCCAG CTCCCTGCCC CAGAGCTTCC TGCTCAAGTC TT - #TAGAGCAA 360- GTGAGAAAGA TCCAGGGCGA TGGCGCAGCG CTCCAGGAGA AGCTGTGTGC CA - #CCTACAAG 420- CTGTGCCACC CCGAGGAGCT GGTGCTGCTC GGACACTCTC TGGGCATCCC CT - #GGGCTCCC 480- CTGAGCTCCT GCCCCAGCCA GGCCCTGCAG CTGGCAGGCT GCTTGAGCTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:88:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:88:- ATGGCTCTTT TCCTCTACCA GGGGCTCCTG CAGGCCCTGG AAGGGATATC CC - #CCGAGTTG 60- GGTCCCACCT TGGACACACT GCAGCTGGAC GTCGCCGACT TTGCCACCAC CA - #TCTGGCAG 120- CAGATGGAAG AACTGGGAAT GGCCCCTGCC CTGCAGCCCA CCCAGGGTGC CA - #TGCCGGCC 180- TTCGCCTCTG CTTTCCAGCG CCGGGCAGGA GGGGTCCTGG TTGCTAGCCA TC - #TGCAGAGC 240- TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC AGCCCACACC AT - #TGGGCCCT 300- GCCAGCTCCC TGCCCCAGAG CTTCCTGCTC AAGTCTTTAG AGCAAGTGAG AA - #AGATCCAG 360- GGCGATGGCG CAGCGCTCCA GGAGAAGCTG TGTGCCACCT ACAAGCTGTG CC - #ACCCCGAG 420- GAGCTGGTGC TGCTCGGACA CTCTCTGGGC ATCCCCTGGG CTCCCCTGAG CT - #CCTGCCCC 480- AGCCAGGCCC TGCAGCTGGC AGGCTGCTTG AGCCAACTCC ATAGCGGCTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:89:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:89:- ATGGCTCTCT ACCAGGGGCT CCTGCAGGCC CTGGAAGGGA TATCCCCCGA GT - #TGGGTCCC 60- ACCTTGGACA CACTGCAGCT GGACGTCGCC GACTTTGCCA CCACCATCTG GC - #AGCAGATG 120- GAAGAACTGG GAATGGCCCC TGCCCTGCAG CCCACCCAGG GTGCCATGCC GG - #CCTTCGCC 180- TCTGCTTTCC AGCGCCGGGC AGGAGGGGTC CTGGTTGCTA GCCATCTGCA GA - #GCTTCCTG 240- GAGGTGTCGT ACCGCGTTCT ACGCCACCTT GCGCAGCCCA CACCATTGGG CC - #CTGCCAGC 300- TCCCTGCCCC AGAGCTTCCT GCTCAAGTCT TTAGAGCAAG TGAGAAAGAT CC - #AGGGCGAT 360- GGCGCAGCGC TCCAGGAGAA GCTGTGTGCC ACCTACAAGC TGTGCCACCC CG - #AGGAGCTG 420- GTGCTGCTCG GACACTCTCT GGGCATCCCC TGGGCTCCCC TGAGCTCCTG CC - #CCAGCCAG 480- GCCCTGCAGC TGGCAGGCTG CTTGAGCCAA CTCCATAGCG GCCTTTTCTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:90:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:90:- ATGGCTGCCC TGGAAGGGAT ATCCCCCGAG TTGGGTCCCA CCTTGGACAC AC - #TGCAGCTG 60- GACGTCGCCG ACTTTGCCAC CACCATCTGG CAGCAGATGG AAGAACTGGG AA - #TGGCCCCT 120- GCCCTGCAGC CCACCCAGGG TGCCATGCCG GCCTTCGCCT CTGCTTTCCA GC - #GCCGGGCA 180- GGAGGGGTCC TGGTTGCTAG CCATCTGCAG AGCTTCCTGG AGGTGTCGTA CC - #GCGTTCTA 240- CGCCACCTTG CGCAGCCCAC ACCATTGGGC CCTGCCAGCT CCCTGCCCCA GA - #GCTTCCTG 300- CTCAAGTCTT TAGAGCAAGT GAGAAAGATC CAGGGCGATG GCGCAGCGCT CC - #AGGAGAAG 360- CTGTGTGCCA CCTACAAGCT GTGCCACCCC GAGGAGCTGG TGCTGCTCGG AC - #ACTCTCTG 420- GGCATCCCCT GGGCTCCCCT GAGCTCCTGC CCCAGCCAGG CCCTGCAGCT GG - #CAGGCTGC 480- TTGAGCCAAC TCCATAGCGG CCTTTTCCTC TACCAGGGGC TCCTGCAGTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:91:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:91:- ATGGCTGACT TTGCCACCAC CATCTGGCAG CAGATGGAAG AACTGGGAAT GG - #CCCCTGCC 60- CTGCAGCCCA CCCAGGGTGC CATGCCGGCC TTCGCCTCTG CTTTCCAGCG CC - #GGGCAGGA 120- GGGGTCCTGG TTGCTAGCCA TCTGCAGAGC TTCCTGGAGG TGTCGTACCG CG - #TTCTACGC 180- CACCTTGCGC AGCCCACACC ATTGGGCCCT GCCAGCTCCC TGCCCCAGAG CT - #TCCTGCTC 240- AAGTCTTTAG AGCAAGTGAG AAAGATCCAG GGCGATGGCG CAGCGCTCCA GG - #AGAAGCTG 300- TGTGCCACCT ACAAGCTGTG CCACCCCGAG GAGCTGGTGC TGCTCGGACA CT - #CTCTGGGC 360- ATCCCCTGGG CTCCCCTGAG CTCCTGCCCC AGCCAGGCCC TGCAGCTGGC AG - #GCTGCTTG 420- AGCCAACTCC ATAGCGGCCT TTTCCTCTAC CAGGGGCTCC TGCAGGCCCT GG - #AAGGGATA 480- TCCCCCGAGT TGGGTCCCAC CTTGGACACA CTGCAGCTGG ACGTCGCCTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:92:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:92:- ATGGCTATCT GGCAGCAGAT GGAAGAACTG GGAATGGCCC CTGCCCTGCA GC - #CCACCCAG 60- GGTGCCATGC CGGCCTTCGC CTCTGCTTTC CAGCGCCGGG CAGGAGGGGT CC - #TGGTTGCT 120- AGCCATCTGC AGAGCTTCCT GGAGGTGTCG TACCGCGTTC TACGCCACCT TG - #CGCAGCCC 180- ACACCATTGG GCCCTGCCAG CTCCCTGCCC CAGAGCTTCC TGCTCAAGTC TT - #TAGAGCAA 240- GTGAGAAAGA TCCAGGGCGA TGGCGCAGCG CTCCAGGAGA AGCTGTGTGC CA - #CCTACAAG 300- CTGTGCCACC CCGAGGAGCT GGTGCTGCTC GGACACTCTC TGGGCATCCC CT - #GGGCTCCC 360- CTGAGCTCCT GCCCCAGCCA GGCCCTGCAG CTGGCAGGCT GCTTGAGCCA AC - #TCCATAGC 420- GGCCTTTTCC TCTACCAGGG GCTCCTGCAG GCCCTGGAAG GGATATCCCC CG - #AGTTGGGT 480- CCCACCTTGG ACACACTGCA GCTGGACGTC GCCGACTTTG CCACCACCTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:93:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:93:- ATGGCTCAGC AGATGGAAGA ACTGGGAATG GCCCCTGCCC TGCAGCCCAC CC - #AGGGTGCC 60- ATGCCGGCCT TCGCCTCTGC TTTCCAGCGC CGGGCAGGAG GGGTCCTGGT TG - #CTAGCCAT 120- CTGCAGAGCT TCCTGGAGGT GTCGTACCGC GTTCTACGCC ACCTTGCGCA GC - #CCACACCA 180- TTGGGCCCTG CCAGCTCCCT GCCCCAGAGC TTCCTGCTCA AGTCTTTAGA GC - #AAGTGAGA 240- AAGATCCAGG GCGATGGCGC AGCGCTCCAG GAGAAGCTGT GTGCCACCTA CA - #AGCTGTGC 300- CACCCCGAGG AGCTGGTGCT GCTCGGACAC TCTCTGGGCA TCCCCTGGGC TC - #CCCTGAGC 360- TCCTGCCCCA GCCAGGCCCT GCAGCTGGCA GGCTGCTTGA GCCAACTCCA TA - #GCGGCCTT 420- TTCCTCTACC AGGGGCTCCT GCAGGCCCTG GAAGGGATAT CCCCCGAGTT GG - #GTCCCACC 480- TTGGACACAC TGCAGCTGGA CGTCGCCGAC TTTGCCACCA CCATCTGGTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:94:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 534 base (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: other nucleic acid#= "DNA (synthetic)"PTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:94:- ATGGCTTTGT TAGGACATTC TTTAGGTATT CCATGGGCTC CTCTGAGCTC CT - #GCCCCAGC 60- CAGGCCCTGC AGCTGGCAGG CTGCTTGAGC CAACTCCATA GCGGCCTTTT CC - #TCTACCAG 120- GGGCTCCTGC AGGCCCTGGA AGGGATATCC CCCGAGTTGG GTCCCACCTT GG - #ACACACTG 180- CAGCTGGACG TCGCCGACTT TGCCACCACC ATCTGGCAGC AGATGGAAGA AC - #TGGGAATG 240- GCCCCTGCCC TGCAGCCCAC CCAGGGTGCC ATGCCGGCCT TCGCCTCTGC TT - #TCCAGCGC 300- CGGGCAGGAG GGGTCCTGGT TGCTAGCCAT CTGCAGAGCT TCCTGGAGGT GT - #CGTACCGC 360- GTTCTACGCC ACCTTGCGCA GCCCACACCA TTGGGCCCTG CCAGCTCCCT GC - #CCCAGAGC 420- TTCCTGCTCA AGTCTTTAGA GCAAGTGAGA AAGATCCAGG GCGATGGCGC AG - #CGCTCCAG 480- GAGAAGCTGT GTGCCACCTA CAAGCTGTGC CACCCCGAGG AGCTGGTGTA AT - #AA 534- (2) INFORMATION FOR SEQ ID NO:95:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:95:- Leu Leu Gly His Ser Leu Gly Ile Pro Trp Al - #a Pro Leu Ser Ser Cys# 15- Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Le - #u Ser Gln Leu His Ser# 30- Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Al - #a Leu Glu Gly Ile Ser# 45- Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gl - #n Leu Asp Val Ala Asp# 60- Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Gl - #u Leu Gly Met Ala Pro#80- Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Al - #a Phe Ala Ser Ala Phe# 95- Gln Arg Arg Ala Gly Gly Val Leu Val Ala Se - #r His Leu Gln Ser Phe# 110- Leu Glu Val Ser Tyr Arg Val Leu Arg His Le - #u Ala Gln Pro Thr Pro# 125- Leu Gly Pro Ala Ser Ser Leu Pro Gln Ser Ph - #e Leu Leu Lys Ser Leu# 140- Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Al - #a Ala Leu Gln Glu Lys145 1 - #50 1 - #55 1 -#60- Leu Cys Ala Thr Tyr Lys Leu Cys His Pro Gl - #u Glu Leu Val# 170- (2) INFORMATION FOR SEQ ID NO:96:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:96:- Gln Leu His Ser Gly Leu Phe Leu Tyr Gln Gl - #y Leu Leu Gln Ala Leu# 15- Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr Le - #u Asp Thr Leu Gln Leu# 30- Asp Val Ala Asp Phe Ala Thr Thr Ile Trp Gl - #n Gln Met Glu Glu Leu# 45- Gly Met Ala Pro Ala Leu Gln Pro Thr Gln Gl - #y Ala Met Pro Ala Phe# 60- Ala Ser Ala Phe Gln Arg Arg Ala Gly Gly Va - #l Leu Val Ala Ser His#80- Leu Gln Ser Phe Leu Glu Val Ser Tyr Arg Va - #l Leu Arg His Leu Ala# 95- Gln Pro Thr Pro Leu Gly Pro Ala Ser Ser Le - #u Pro Gln Ser Phe Leu# 110- Leu Lys Ser Leu Glu Gln Val Arg Lys Ile Gl - #n Gly Asp Gly Ala Ala# 125- Leu Gln Glu Lys Leu Cys Ala Thr Tyr Lys Le - #u Cys His Pro Glu Glu# 140- Leu Val Leu Leu Gly His Ser Leu Gly Ile Pr - #o Trp Ala Pro Leu Ser145 1 - #50 1 - #55 1 -#60- Ser Cys Pro Ser Gln Ala Leu Gln Leu Ala Gl - #y Cys Leu Ser# 170- (2) INFORMATION FOR SEQ ID NO:97:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:97:- Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Le - #u Glu Gly Ile Ser Pro# 15- Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Le - #u Asp Val Ala Asp Phe# 30- Ala Thr Thr Ile Trp Gln Gln Met Glu Glu Le - #u Gly Met Ala Pro Ala# 45- Leu Gln Pro Thr Gln Gly Ala Met Pro Ala Ph - #e Ala Ser Ala Phe Gln# 60- Arg Arg Ala Gly Gly Val Leu Val Ala Ser Hi - #s Leu Gln Ser Phe Leu#80- Glu Val Ser Tyr Arg Val Leu Arg His Leu Al - #a Gln Pro Thr Pro Leu# 95- Gly Pro Ala Ser Ser Leu Pro Gln Ser Phe Le - #u Leu Lys Ser Leu Glu# 110- Gln Val Arg Lys Ile Gln Gly Asp Gly Ala Al - #a Leu Gln Glu Lys Leu# 125- Cys Ala Thr Tyr Lys Leu Cys His Pro Glu Gl - #u Leu Val Leu Leu Gly# 140- His Ser Leu Gly Ile Pro Trp Ala Pro Leu Se - #r Ser Cys Pro Ser Gln145 1 - #50 1 - #55 1 -#60- Ala Leu Gln Leu Ala Gly Cys Leu Ser Gln Le - #u His Ser Gly# 170- (2) INFORMATION FOR SEQ ID NO:98:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:98:- Leu Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gl - #y Ile Ser Pro Glu Leu# 15- Gly Pro Thr Leu Asp Thr Leu Gln Leu Asp Va - #l Ala Asp Phe Ala Thr# 30- Thr Ile Trp Gln Gln Met Glu Glu Leu Gly Me - #t Ala Pro Ala Leu Gln# 45- Pro Thr Gln Gly Ala Met Pro Ala Phe Ala Se - #r Ala Phe Gln Arg Arg# 60- Ala Gly Gly Val Leu Val Ala Ser His Leu Gl - #n Ser Phe Leu Glu Val#80- Ser Tyr Arg Val Leu Arg His Leu Ala Gln Pr - #o Thr Pro Leu Gly Pro# 95- Ala Ser Ser Leu Pro Gln Ser Phe Leu Leu Ly - #s Ser Leu Glu Gln Val# 110- Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gl - #n Glu Lys Leu Cys Ala# 125- Thr Tyr Lys Leu Cys His Pro Glu Glu Leu Va - #l Leu Leu Gly His Ser# 140- Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cy - #s Pro Ser Gln Ala Leu145 1 - #50 1 - #55 1 -#60- Gln Leu Ala Gly Cys Leu Ser Gln Leu His Se - #r Gly Leu Phe# 170- (2) INFORMATION FOR SEQ ID NO:99:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:99:- Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly Pr - #o Thr Leu Asp Thr Leu# 15- Gln Leu Asp Val Ala Asp Phe Ala Thr Thr Il - #e Trp Gln Gln Met Glu# 30- Glu Leu Gly Met Ala Pro Ala Leu Gln Pro Th - #r Gln Gly Ala Met Pro# 45- Ala Phe Ala Ser Ala Phe Gln Arg Arg Ala Gl - #y Gly Val Leu Val Ala# 60- Ser His Leu Gln Ser Phe Leu Glu Val Ser Ty - #r Arg Val Leu Arg His#80- Leu Ala Gln Pro Thr Pro Leu Gly Pro Ala Se - #r Ser Leu Pro Gln Ser# 95- Phe Leu Leu Lys Ser Leu Glu Gln Val Arg Ly - #s Ile Gln Gly Asp Gly# 110- Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr Ty - #r Lys Leu Cys His Pro# 125- Glu Glu Leu Val Leu Leu Gly His Ser Leu Gl - #y Ile Pro Trp Ala Pro# 140- Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Le - #u Ala Gly Cys Leu Ser145 1 - #50 1 - #55 1 -#60- Gln Leu His Ser Gly Leu Phe Leu Tyr Gln Gl - #y Leu Leu Gln# 170- (2) INFORMATION FOR SEQ ID NO:100:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:100:- Asp Phe Ala Thr Thr Ile Trp Gln Gln Met Gl - #u Glu Leu Gly Met Ala# 15- Pro Ala Leu Gln Pro Thr Gln Gly Ala Met Pr - #o Ala Phe Ala Ser Ala# 30- Phe Gln Arg Arg Ala Gly Gly Val Leu Val Al - #a Ser His Leu Gln Ser# 45- Phe Leu Glu Val Ser Tyr Arg Val Leu Arg Hi - #s Leu Ala Gln Pro Thr# 60- Pro Leu Gly Pro Ala Ser Ser Leu Pro Gln Se - #r Phe Leu Leu Lys Ser#80- Leu Glu Gln Val Arg Lys Ile Gln Gly Asp Gl - #y Ala Ala Leu Gln Glu# 95- Lys Leu Cys Ala Thr Tyr Lys Leu Cys His Pr - #o Glu Glu Leu Val Leu# 110- Leu Gly His Ser Leu Gly Ile Pro Trp Ala Pr - #o Leu Ser Ser Cys Pro# 125- Ser Gln Ala Leu Gln Leu Ala Gly Cys Leu Se - #r Gln Leu His Ser Gly# 140- Leu Phe Leu Tyr Gln Gly Leu Leu Gln Ala Le - #u Glu Gly Ile Ser Pro145 1 - #50 1 - #55 1 -#60- Glu Leu Gly Pro Thr Leu Asp Thr Leu Gln Le - #u Asp Val Ala# 170- (2) INFORMATION FOR SEQ ID NO:101:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:101:- Ile Trp Gln Gln Met Glu Glu Leu Gly Met Al - #a Pro Ala Leu Gln Pro# 15- Thr Gln Gly Ala Met Pro Ala Phe Ala Ser Al - #a Phe Gln Arg Arg Ala# 30- Gly Gly Val Leu Val Ala Ser His Leu Gln Se - #r Phe Leu Glu Val Ser# 45- Tyr Arg Val Leu Arg His Leu Ala Gln Pro Th - #r Pro Leu Gly Pro Ala# 60- Ser Ser Leu Pro Gln Ser Phe Leu Leu Lys Se - #r Leu Glu Gln Val Arg#80- Lys Ile Gln Gly Asp Gly Ala Ala Leu Gln Gl - #u Lys Leu Cys Ala Thr# 95- Tyr Lys Leu Cys His Pro Glu Glu Leu Val Le - #u Leu Gly His Ser Leu# 110- Gly Ile Pro Trp Ala Pro Leu Ser Ser Cys Pr - #o Ser Gln Ala Leu Gln# 125- Leu Ala Gly Cys Leu Ser Gln Leu His Ser Gl - #y Leu Phe Leu Tyr Gln# 140- Gly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pr - #o Glu Leu Gly Pro Thr145 1 - #50 1 - #55 1 -#60- Leu Asp Thr Leu Gln Leu Asp Val Ala Asp Ph - #e Ala Thr Thr# 170- (2) INFORMATION FOR SEQ ID NO:102:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:102:- Gln Gln Met Glu Glu Leu Gly Met Ala Pro Al - #a Leu Gln Pro Thr Gln# 15- Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gl - #n Arg Arg Ala Gly Gly# 30- Val Leu Val Ala Ser His Leu Gln Ser Phe Le - #u Glu Val Ser Tyr Arg# 45- Val Leu Arg His Leu Ala Gln Pro Thr Pro Le - #u Gly Pro Ala Ser Ser# 60- Leu Pro Gln Ser Phe Leu Leu Lys Ser Leu Gl - #u Gln Val Arg Lys Ile#80- Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Le - #u Cys Ala Thr Tyr Lys# 95- Leu Cys His Pro Glu Glu Leu Val Leu Leu Gl - #y His Ser Leu Gly Ile# 110- Pro Trp Ala Pro Leu Ser Ser Cys Pro Ser Gl - #n Ala Leu Gln Leu Ala# 125- Gly Cys Leu Ser Gln Leu His Ser Gly Leu Ph - #e Leu Tyr Gln Gly Leu# 140- Leu Gln Ala Leu Glu Gly Ile Ser Pro Glu Le - #u Gly Pro Thr Leu Asp145 1 - #50 1 - #55 1 -#60- Thr Leu Gln Leu Asp Val Ala Asp Phe Ala Th - #r Thr Ile Trp# 170- (2) INFORMATION FOR SEQ ID NO:103:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 174 amino (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: protein- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:103:- Leu Leu Gly His Ser Leu Gly Ile Pro Trp Al - #a Pro Leu Ser Ser Cys# 15- Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Le - #u Ser Gln Leu His Ser# 30- Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Al - #a Leu Glu Gly Ile Ser# 45- Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gl - #n Leu Asp Val Ala Asp# 60- Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Gl - #u Leu Gly Met Ala Pro#80- Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Al - #a Phe Ala Ser Ala Phe# 95- Gln Arg Arg Ala Gly Gly Val Leu Val Ala Se - #r His Leu Gln Ser Phe# 110- Leu Glu Val Ser Tyr Arg Val Leu Arg His Le - #u Ala Gln Pro Thr Pro# 125- Leu Gly Pro Ala Ser Ser Leu Pro Gln Ser Ph - #e Leu Leu Lys Ser Leu# 140- Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Al - #a Ala Leu Gln Glu Lys145 1 - #50 1 - #55 1 -#60- Leu Cys Ala Thr Tyr Lys Leu Cys His Pro Gl - #u Glu Leu Val# 170- (2) INFORMATION FOR SEQ ID NO:104:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:104:- CAGAGCTTCC TGCTCAAGTC TTTAGAGCAA GTGAGGAAGA TCCAGGGCGA TG - #GCGCAGCG 60- CTCCAGGAGA AGCTGTGTGC CACCTACAAG CTGTGCCACC CCGAGGAGCT GG - #TGCTGCTC 120- GGACACTCTC TGGGCATCCC CTGGGCTCCC CTGAGCTCCT GCCCCAGCCA GG - #CCCTGCAG 180- CTGGCAGGCT GCTTGAGCCA ACTCCATAGC GGCCTTTTCC TCTACCAGGG GC - #TCCTGCAG 240- GCCCTGGAAG GGATATCCCC CGAGTTGGGT CCCACCTTGG ACACACTGCA GC - #TGGACGTC 300- GCCGACTTTG CCACCACCAT CTGGCAGCAG ATGGAAGAAC TGGGAATGGC CC - #CTGCCCTG 360- CAGCCCACCC AGGGTGCCAT GCCGGCCTTC GCCTCTGCTT TCCAGCGCCG GG - #CAGGAGGG 420- GTCCTGGTTG CTAGCCATCT GCAGAGCTTC CTGGAGGTGT CGTACCGCGT TC - #TACGCCAC 480# 531ACATGGC TACACCATTA GGCCCTGCCA GCTCCCTGCC C- (2) INFORMATION FOR SEQ ID NO:105:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:105:- GAACTGGGAA TGGCCCCTGC CCTGCAGCCC ACCCAGGGTG CCATGCCGGC CT - #TCGCCTCT 60- GCTTTCCAGC GCCGGGCAGG AGGGGTCCTG GTTGCTAGCC ATCTGCAGAG CT - #TCCTGGAG 120- GTGTCGTACC GCGTTCTACG CCACCTTGCG CAGCCCGACA TGGCTACACC AT - #TAGGCCCT 180- GCCAGCTCCC TGCCCCAGAG CTTCCTGCTC AAGTCTTTAG AGCAAGTGAG GA - #AGATCCAG 240- GGCGATGGCG CAGCGCTCCA GGAGAAGCTG TGTGCCACCT ACAAGCTGTG CC - #ACCCCGAG 300- GAGCTGGTGC TGCTCGGACA CTCTCTGGGC ATCCCCTGGG CTCCCCTGAG CT - #CCTGCCCC 360- AGCCAGGCCC TGCAGCTGGC AGGCTGCTTG AGCCAACTCC ATAGCGGCCT TT - #TCCTCTAC 420- CAGGGGCTCC TGCAGGCCCT GGAAGGGATA TCCCCCGAGT TGGGTCCCAC CT - #TGGACACA 480# 531TCGCCGA CTTTGCCACC ACCATCTGGC AGCAGATGGA A- (2) INFORMATION FOR SEQ ID NO:106:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:106:- GGAATGGCCC CTGCCCTGCA GCCCACCCAG GGTGCCATGC CGGCCTTCGC CT - #CTGCTTTC 60- CAGCGCCGGG CAGGAGGGGT CCTGGTTGCT AGCCATCTGC AGAGCTTCCT GG - #AGGTGTCG 120- TACCGCGTTC TACGCCACCT TGCGCAGCCC GACATGGCTA CACCATTAGG CC - #CTGCCAGC 180- TCCCTGCCCC AGAGCTTCCT GCTCAAGTCT TTAGAGCAAG TGAGGAAGAT CC - #AGGGCGAT 240- GGCGCAGCGC TCCAGGAGAA GCTGTGTGCC ACCTACAAGC TGTGCCACCC CG - #AGGAGCTG 300- GTGCTGCTCG GACACTCTCT GGGCATCCCC TGGGCTCCCC TGAGCTCCTG CC - #CCAGCCAG 360- GCCCTGCAGC TGGCAGGCTG CTTGAGCCAA CTCCATAGCG GCCTTTTCCT CT - #ACCAGGGG 420- CTCCTGCAGG CCCTGGAAGG GATATCCCCC GAGTTGGGTC CCACCTTGGA CA - #CACTGCAG 480# 531ACTTTGC CACCACCATC TGGCAGCAGA TGGAAGAACT G- (2) INFORMATION FOR SEQ ID NO:107:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:107:- TTCCTGCTCA AGTCTTTAGA GCAAGTGAGG AAGATCCAGG GCGATGGCGC AG - #CGCTCCAG 60- GAGAAGCTGT GTGCCACCTA CAAGCTGTGC CACCCCGAGG AGCTGGTGCT GC - #TCGGACAC 120- TCTCTGGGCA TCCCCTGGGC TCCCCTGAGC TCCTGCCCCA GCCAGGCCCT GC - #AGCTGGCA 180- GGCTGCTTGA GCCAACTCCA TAGCGGCCTT TTCCTCTACC AGGGGCTCCT GC - #AGGCCCTG 240- GAAGGGATAT CCCCCGAGTT GGGTCCCACC TTGGACACAC TGCAGCTGGA CG - #TCGCCGAC 300- TTTGCCACCA CCATCTGGCA GCAGATGGAA GAACTGGGAA TGGCCCCTGC CC - #TGCAGCCC 360- ACCCAGGGTG CCATGCCGGC CTTCGCCTCT GCTTTCCAGC GCCGGGCAGG AG - #GGGTCCTG 420- GTTGCTAGCC ATCTGCAGAG CTTCCTGGAG GTGTCGTACC GCGTTCTACG CC - #ACCTTGCG 480# 531CTACACC ATTAGGCCCT GCCAGCTCCC TGCCCCAGAG C- (2) INFORMATION FOR SEQ ID NO:108:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:108:- AGCTTCCTGG AGGTGTCGTA CCGCGTTCTA CGCCACCTTG CGCAGCCCGA CA - #TGGCTACA 60- CCATTAGGCC CTGCCAGCTC CCTGCCCCAG AGCTTCCTGC TCAAGTCTTT AG - #AGCAAGTG 120- AGGAAGATCC AGGGCGATGG CGCAGCGCTC CAGGAGAAGC TGTGTGCCAC CT - #ACAAGCTG 180- TGCCACCCCG AGGAGCTGGT GCTGCTCGGA CACTCTCTGG GCATCCCCTG GG - #CTCCCCTG 240- AGCTCCTGCC CCAGCCAGGC CCTGCAGCTG GCAGGCTGCT TGAGCCAACT CC - #ATAGCGGC 300- CTTTTCCTCT ACCAGGGGCT CCTGCAGGCC CTGGAAGGGA TATCCCCCGA GT - #TGGGTCCC 360- ACCTTGGACA CACTGCAGCT GGACGTCGCC GACTTTGCCA CCACCATCTG GC - #AGCAGATG 420- GAAGAACTGG GAATGGCCCC TGCCCTGCAG CCCACCCAGG GTGCCATGCC GG - #CCTTCGCC 480# 531GCCGGGC AGGAGGGGTC CTGGTTGCTA GCCATCTGCA G- (2) INFORMATION FOR SEQ ID NO:109:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:109:- AGCTTCCTGG AGGTGTCGTA CCGCGTTCTA CGCCACCTTG CGCAGCCCGA CA - #TGGCTACA 60- CCATTAGGCC CTGCCAGCTC CCTGCCCCAG AGCTTCCTGC TCAAGTCTTT AG - #AGCAAGTG 120- AGGAAGATCC AGGGCGATGG CGCAGCGCTC CAGGAGAAGC TGTGTGCCAC CT - #ACAAGCTG 180- TGCCACCCCG AGGAGCTGGT GCTGCTCGGA CACTCTCTGG GCATCCCCTG GG - #CTCCCCTG 240- AGCTCCTGCC CCAGCCAGGC CCTGCAGCTG GCAGGCTGCT TGAGCCAACT CC - #ATAGCGGC 300- CTTTTCCTCT ACCAGGGGCT CCTGCAGGCC CTGGAAGGGA TATCCCCCGA GT - #TGGGTCCC 360- ACCTTGGACA CACTGCAGCT GGACGTCGCC GACTTTGCCA CCACCATCTG GC - #AGCAGATG 420- GAAGAACTGG GAATGGCCCC TGCCCTGCAG CCCACCCAGG GTGCCATGCC GG - #CCTTCGCC 480# 531GCCGGGC AGGAGGGGTC CTGGTTGCTA GCCATCTGCA G- (2) INFORMATION FOR SEQ ID NO:110:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:110:- TTAGGCCCTG CCAGCTCCCT GCCCCAGAGC TTCCTGCTCA AGTCTTTAGA GC - #AAGTGAGG 60- AAGATCCAGG GCGATGGCGC AGCGCTCCAG GAGAAGCTGT GTGCCACCTA CA - #AGCTGTGC 120- CACCCCGAGG AGCTGGTGCT GCTCGGACAC TCTCTGGGCA TCCCCTGGGC TC - #CCCTGAGC 180- TCCTGCCCCA GCCAGGCCCT GCAGCTGGCA GGCTGCTTGA GCCAACTCCA TA - #GCGGCCTT 240- TTCCTCTACC AGGGGCTCCT GCAGGCCCTG GAAGGGATAT CCCCCGAGTT GG - #GTCCCACC 300- TTGGACACAC TGCAGCTGGA CGTCGCCGAC TTTGCCACCA CCATCTGGCA GC - #AGATGGAA 360- GAACTGGGAA TGGCCCCTGC CCTGCAGCCC ACCCAGGGTG CCATGCCGGC CT - #TCGCCTCT 420- GCTTTCCAGC GCCGGGCAGG AGGGGTCCTG GTTGCTAGCC ATCTGCAGAG CT - #TCCTGGAG 480# 531TTCTACG CCACCTTGCG CAGCCCGACA TGGCTACACC A- (2) INFORMATION FOR SEQ ID NO:111:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:111:- CTGCTCGGAC ACTCTCTGGG CATCCCCTGG GCTCCCCTGA GCTCCTGCCC CA - #GCCAGGCC 60- CTGCAGCTGG CAGGCTGCTT GAGCCAACTC CATAGCGGCC TTTTCCTCTA CC - #AGGGGCTC 120- CTGCAGGCCC TGGAAGGGAT ATCCCCCGAG TTGGGTCCCA CCTTGGACAC AC - #TGCAGCTG 180- GACGTCGCCG ACTTTGCCAC CACCATCTGG CAGCAGATGG AAGAACTGGG AA - #TGGCCCCT 240- GCCCTGCAGC CCACCCAGGG TGCCATGCCG GCCTTCGCCT CTGCTTTCCA GC - #GCCGGGCA 300- GGAGGGGTCC TGGTTGCTAG CCATCTGCAG AGCTTCCTGG AGGTGTCGTA CC - #GCGTTCTA 360- CGCCACCTTG CGCAGCCCGA CATGGCTACA CCATTAGGCC CTGCCAGCTC CC - #TGCCCCAG 420- AGCTTCCTGC TCAAGTCTTT AGAGCAAGTG AGGAAGATCC AGGGCGATGG CG - #CAGCGCTC 480# 531GTGCCAC CTACAAGCTG TGCCACCCCG AGGAGCTGGT G- (2) INFORMATION FOR SEQ ID NO:112:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:112:- CCCCTGAGCT CCTGCCCCAG CCAGGCCCTG CAGCTGGCAG GCTGCTTGAG CC - #AACTCCAT 60- AGCGGCCTTT TCCTCTACCA GGGGCTCCTG CAGGCCCTGG AAGGGATATC CC - #CCGAGTTG 120- GGTCCCACCT TGGACACACT GCAGCTGGAC GTCGCCGACT TTGCCACCAC CA - #TCTGGCAG 180- CAGATGGAAG AACTGGGAAT GGCCCCTGCC CTGCAGCCCA CCCAGGGTGC CA - #TGCCGGCC 240- TTCGCCTCTG CTTTCCAGCG CCGGGCAGGA GGGGTCCTGG TTGCTAGCCA TC - #TGCAGAGC 300- TTCCTGGAGG TGTCGTACCG CGTTCTACGC CACCTTGCGC AGCCCGACAT GG - #CTACACCA 360- TTAGGCCCTG CCAGCTCCCT GCCCCAGAGC TTCCTGCTCA AGTCTTTAGA GC - #AAGTGAGG 420- AAGATCCAGG GCGATGGCGC AGCGCTCCAG GAGAAGCTGT GTGCCACCTA CA - #AGCTGTGC 480# 531TGGTGCT GCTCGGACAC TCTCTGGGCA TCCCCTGGGC T- (2) INFORMATION FOR SEQ ID NO:113:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:113:- CAGGCCCTGC AGCTGGCAGG CTGCTTGAGC CAACTCCATA GCGGCCTTTT CC - #TCTACCAG 60- GGGCTCCTGC AGGCCCTGGA AGGGATATCC CCCGAGTTGG GTCCCACCTT GG - #ACACACTG 120- CAGCTGGACG TCGCCGACTT TGCCACCACC ATCTGGCAGC AGATGGAAGA AC - #TGGGAATG 180- GCCCCTGCCC TGCAGCCCAC CCAGGGTGCC ATGCCGGCCT TCGCCTCTGC TT - #TCCAGCGC 240- CGGGCAGGAG GGGTCCTGGT TGCTAGCCAT CTGCAGAGCT TCCTGGAGGT GT - #CGTACCGC 300- GTTCTACGCC ACCTTGCGCA GCCCGACATG GCTACACCAT TAGGCCCTGC CA - #GCTCCCTG 360- CCCCAGAGCT TCCTGCTCAA GTCTTTAGAG CAAGTGAGGA AGATCCAGGG CG - #ATGGCGCA 420- GCGCTCCAGG AGAAGCTGTG TGCCACCTAC AAGCTGTGCC ACCCCGAGGA GC - #TGGTGCTG 480# 531TGGGCAT CCCCTGGGCT CCCCTGAGCT CCTGCCCCAG C- (2) INFORMATION FOR SEQ ID NO:114:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:114:- CTGCAGCTGG CAGGCTGCTT GAGCCAACTC CATAGCGGCC TTTTCCTCTA CC - #AGGGGCTC 60- CTGCAGGCCC TGGAAGGGAT ATCCCCCGAG TTGGGTCCCA CCTTGGACAC AC - #TGCAGCTG 120- GACGTCGCCG ACTTTGCCAC CACCATCTGG CAGCAGATGG AAGAACTGGG AA - #TGGCCCCT 180- GCCCTGCAGC CCACCCAGGG TGCCATGCCG GCCTTCGCCT CTGCTTTCCA GC - #GCCGGGCA 240- GGAGGGGTCC TGGTTGCTAG CCATCTGCAG AGCTTCCTGG AGGTGTCGTA CC - #GCGTTCTA 300- CGCCACCTTG CGCAGCCCGA CATGGCTACA CCATTAGGCC CTGCCAGCTC CC - #TGCCCCAG 360- AGCTTCCTGC TCAAGTCTTT AGAGCAAGTG AGGAAGATCC AGGGCGATGG CG - #CAGCGCTC 420- CAGGAGAAGC TGTGTGCCAC CTACAAGCTG TGCCACCCCG AGGAGCTGGT GC - #TGCTCGGA 480# 531TCCCCTG GGCTCCCCTG AGCTCCTGCC CCAGCCAGGC C- (2) INFORMATION FOR SEQ ID NO:115:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:115:- CTGGCAGGCT GCTTGAGCCA ACTCCATAGC GGCCTTTTCC TCTACCAGGG GC - #TCCTGCAG 60- GCCCTGGAAG GGATATCCCC CGAGTTGGGT CCCACCTTGG ACACACTGCA GC - #TGGACGTC 120- GCCGACTTTG CCACCACCAT CTGGCAGCAG ATGGAAGAAC TGGGAATGGC CC - #CTGCCCTG 180- CAGCCCACCC AGGGTGCCAT GCCGGCCTTC GCCTCTGCTT TCCAGCGCCG GG - #CAGGAGGG 240- GTCCTGGTTG CTAGCCATCT GCAGAGCTTC CTGGAGGTGT CGTACCGCGT TC - #TACGCCAC 300- CTTGCGCAGC CCGACATGGC TACACCATTA GGCCCTGCCA GCTCCCTGCC CC - #AGAGCTTC 360- CTGCTCAAGT CTTTAGAGCA AGTGAGGAAG ATCCAGGGCG ATGGCGCAGC GC - #TCCAGGAG 420- AAGCTGTGTG CCACCTACAA GCTGTGCCAC CCCGAGGAGC TGGTGCTGCT CG - #GACACTCT 480# 531GGGCTCC CCTGAGCTCC TGCCCCAGCC AGGCCCTGCA G- (2) INFORMATION FOR SEQ ID NO:116:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:116:- Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln Va - #l Arg Lys Ile Gln Gly# 15- Asp Gly Ala Ala Leu Gln Glu Lys Leu Cys Al - #a Thr Tyr Lys Leu Cys# 30- His Pro Glu Glu Leu Val Leu Leu Gly His Se - #r Leu Gly Ile Pro Trp# 45- Ala Pro Leu Ser Ser Cys Pro Ser Gln Ala Le - #u Gln Leu Ala Gly Cys# 60- Leu Ser Gln Leu His Ser Gly Leu Phe Leu Ty - #r Gln Gly Leu Leu Gln#80- Ala Leu Glu Gly Ile Ser Pro Glu Leu Gly Pr - #o Thr Leu Asp Thr Leu# 95- Gln Leu Asp Val Ala Asp Phe Ala Thr Thr Il - #e Trp Gln Gln Met Glu# 110- Glu Leu Gly Met Ala Pro Ala Leu Gln Pro Th - #r Gln Gly Ala Met Pro# 125- Ala Phe Ala Ser Ala Phe Gln Arg Arg Ala Gl - #y Gly Val Leu Val Ala# 140- Ser His Leu Gln Ser Phe Leu Glu Val Ser Ty - #r Arg Val Leu Arg His145 1 - #50 1 - #55 1 -#60- Leu Ala Gln Pro Asp Met Ala Thr Pro Leu Gl - #y Pro Ala Ser Ser Leu# 175- Pro- (2) INFORMATION FOR SEQ ID NO:117:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:117:- Glu Leu Gly Met Ala Pro Ala Leu Gln Pro Th - #r Gln Gly Ala Met Pro# 15- Ala Phe Ala Ser Ala Phe Gln Arg Arg Ala Gl - #y Gly Val Leu Val Ala# 30- Ser His Leu Gln Ser Phe Leu Glu Val Ser Ty - #r Arg Val Leu Arg His# 45- Leu Ala Gln Pro Asp Met Ala Thr Pro Leu Gl - #y Pro Ala Ser Ser Leu# 60- Pro Gln Ser Phe Leu Leu Lys Ser Leu Glu Gl - #n Val Arg Lys Ile Gln#80- Gly Asp Gly Ala Ala Leu Gln Glu Lys Leu Cy - #s Ala Thr Tyr Lys Leu# 95- Cys His Pro Glu Glu Leu Val Leu Leu Gly Hi - #s Ser Leu Gly Ile Pro# 110- Trp Ala Pro Leu Ser Ser Cys Pro Ser Gln Al - #a Leu Gln Leu Ala Gly# 125- Cys Leu Ser Gln Leu His Ser Gly Leu Phe Le - #u Tyr Gln Gly Leu Leu# 140- Gln Ala Leu Glu Gly Ile Ser Pro Glu Leu Gl - #y Pro Thr Leu Asp Thr145 1 - #50 1 - #55 1 -#60- Leu Gln Leu Asp Val Ala Asp Phe Ala Thr Th - #r Ile Trp Gln Gln Met# 175- Glu- (2) INFORMATION FOR SEQ ID NO:118:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:118:- Gly Met Ala Pro Ala Leu Gln Pro Thr Gln Gl - #y Ala Met Pro Ala Phe# 15- Ala Ser Ala Phe Gln Arg Arg Ala Gly Gly Va - #l Leu Val Ala Ser His# 30- Leu Gln Ser Phe Leu Glu Val Ser Tyr Arg Va - #l Leu Arg His Leu Ala# 45- Gln Pro Asp Met Ala Thr Pro Leu Gly Pro Al - #a Ser Ser Leu Pro Gln# 60- Ser Phe Leu Leu Lys Ser Leu Glu Gln Val Ar - #g Lys Ile Gln Gly Asp#80- Gly Ala Ala Leu Gln Glu Lys Leu Cys Ala Th - #r Tyr Lys Leu Cys His# 95- Pro Glu Glu Leu Val Leu Leu Gly His Ser Le - #u Gly Ile Pro Trp Ala# 110- Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gl - #n Leu Ala Gly Cys Leu# 125- Ser Gln Leu His Ser Gly Leu Phe Leu Tyr Gl - #n Gly Leu Leu Gln Ala# 140- Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro Th - #r Leu Asp Thr Leu Gln145 1 - #50 1 - #55 1 -#60- Leu Asp Val Ala Asp Phe Ala Thr Thr Ile Tr - #p Gln Gln Met Glu Glu# 175- Leu- (2) INFORMATION FOR SEQ ID NO:119:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:119:- Phe Leu Leu Lys Ser Leu Glu Gln Val Arg Ly - #s Ile Gln Gly Asp Gly# 15- Ala Ala Leu Gln Glu Lys Leu Cys Ala Thr Ty - #r Lys Leu Cys His Pro# 30- Glu Glu Leu Val Leu Leu Gly His Ser Leu Gl - #y Ile Pro Trp Ala Pro# 45- Leu Ser Ser Cys Pro Ser Gln Ala Leu Gln Le - #u Ala Gly Cys Leu Ser# 60- Gln Leu His Ser Gly Leu Phe Leu Tyr Gln Gl - #y Leu Leu Gln Ala Leu#80- Glu Gly Ile Ser Pro Glu Leu Gly Pro Thr Le - #u Asp Thr Leu Gln Leu# 95- Asp Val Ala Asp Phe Ala Thr Thr Ile Trp Gl - #n Gln Met Glu Glu Leu# 110- Gly Met Ala Pro Ala Leu Gln Pro Thr Gln Gl - #y Ala Met Pro Ala Phe# 125- Ala Ser Ala Phe Gln Arg Arg Ala Gly Gly Va - #l Leu Val Ala Ser His# 140- Leu Gln Ser Phe Leu Glu Val Ser Tyr Arg Va - #l Leu Arg His Leu Ala145 1 - #50 1 - #55 1 -#60- Gln Pro Asp Met Ala Thr Pro Leu Gly Pro Al - #a Ser Ser Leu Pro Gln# 175- Ser- (2) INFORMATION FOR SEQ ID NO:120:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:120:- Ser Phe Leu Glu Val Ser Tyr Arg Val Leu Ar - #g His Leu Ala Gln Pro# 15- Asp Met Ala Thr Pro Leu Gly Pro Ala Ser Se - #r Leu Pro Gln Ser Phe# 30- Leu Leu Lys Ser Leu Glu Gln Val Arg Lys Il - #e Gln Gly Asp Gly Ala# 45- Ala Leu Gln Glu Lys Leu Cys Ala Thr Tyr Ly - #s Leu Cys His Pro Glu# 60- Glu Leu Val Leu Leu Gly His Ser Leu Gly Il - #e Pro Trp Ala Pro Leu#80- Ser Ser Cys Pro Ser Gln Ala Leu Gln Leu Al - #a Gly Cys Leu Ser Gln# 95- Leu His Ser Gly Leu Phe Leu Tyr Gln Gly Le - #u Leu Gln Ala Leu Glu# 110- Gly Ile Ser Pro Glu Leu Gly Pro Thr Leu As - #p Thr Leu Gln Leu Asp# 125- Val Ala Asp Phe Ala Thr Thr Ile Trp Gln Gl - #n Met Glu Glu Leu Gly# 140- Met Ala Pro Ala Leu Gln Pro Thr Gln Gly Al - #a Met Pro Ala Phe Ala145 1 - #50 1 - #55 1 -#60- Ser Ala Phe Gln Arg Arg Ala Gly Gly Val Le - #u Val Ala Ser His Leu# 175- Gln- (2) INFORMATION FOR SEQ ID NO:121:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:121:- Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Al - #a Ala Leu Gln Glu Lys# 15- Leu Cys Ala Thr Tyr Lys Leu Cys His Pro Gl - #u Glu Leu Val Leu Leu# 30- Gly His Ser Leu Gly Ile Pro Trp Ala Pro Le - #u Ser Ser Cys Pro Ser# 45- Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gl - #n Leu His Ser Gly Leu# 60- Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Gl - #u Gly Ile Ser Pro Glu#80- Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu As - #p Val Ala Asp Phe Ala# 95- Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gl - #y Met Ala Pro Ala Leu# 110- Gln Pro Thr Gln Gly Ala Met Pro Ala Phe Al - #a Ser Ala Phe Gln Arg# 125- Arg Ala Gly Gly Val Leu Val Ala Ser His Le - #u Gln Ser Phe Leu Glu# 140- Val Ser Tyr Arg Val Leu Arg His Leu Ala Gl - #n Pro Asp Met Ala Thr145 1 - #50 1 - #55 1 -#60- Pro Leu Gly Pro Ala Ser Ser Leu Pro Gln Se - #r Phe Leu Leu Lys Ser# 175- Leu- (2) INFORMATION FOR SEQ ID NO:122:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:122:- Leu Gly Pro Ala Ser Ser Leu Pro Gln Ser Ph - #e Leu Leu Lys Ser Leu# 15- Glu Gln Val Arg Lys Ile Gln Gly Asp Gly Al - #a Ala Leu Gln Glu Lys# 30- Leu Cys Ala Thr Tyr Lys Leu Cys His Pro Gl - #u Glu Leu Val Leu Leu# 45- Gly His Ser Leu Gly Ile Pro Trp Ala Pro Le - #u Ser Ser Cys Pro Ser# 60- Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gl - #n Leu His Ser Gly Leu#80- Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Gl - #u Gly Ile Ser Pro Glu# 95- Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu As - #p Val Ala Asp Phe Ala# 110- Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gl - #y Met Ala Pro Ala Leu# 125- Gln Pro Thr Gln Gly Ala Met Pro Ala Phe Al - #a Ser Ala Phe Gln Arg# 140- Arg Ala Gly Gly Val Leu Val Ala Ser His Le - #u Gln Ser Phe Leu Glu145 1 - #50 1 - #55 1 -#60- Val Ser Tyr Arg Val Leu Arg His Leu Ala Gl - #n Pro Asp Met Ala Thr# 175- Pro- (2) INFORMATION FOR SEQ ID NO:123:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:123:- Leu Leu Gly His Ser Leu Gly Ile Pro Trp Al - #a Pro Leu Ser Ser Cys# 15- Pro Ser Gln Ala Leu Gln Leu Ala Gly Cys Le - #u Ser Gln Leu His Ser# 30- Gly Leu Phe Leu Tyr Gln Gly Leu Leu Gln Al - #a Leu Glu Gly Ile Ser# 45- Pro Glu Leu Gly Pro Thr Leu Asp Thr Leu Gl - #n Leu Asp Val Ala Asp# 60- Phe Ala Thr Thr Ile Trp Gln Gln Met Glu Gl - #u Leu Gly Met Ala Pro#80- Ala Leu Gln Pro Thr Gln Gly Ala Met Pro Al - #a Phe Ala Ser Ala Phe# 95- Gln Arg Arg Ala Gly Gly Val Leu Val Ala Se - #r His Leu Gln Ser Phe# 110- Leu Glu Val Ser Tyr Arg Val Leu Arg His Le - #u Ala Gln Pro Asp Met# 125- Ala Thr Pro Leu Gly Pro Ala Ser Ser Leu Pr - #o Gln Ser Phe Leu Leu# 140- Lys Ser Leu Glu Gln Val Arg Lys Ile Gln Gl - #y Asp Gly Ala Ala Leu145 1 - #50 1 - #55 1 -#60- Gln Glu Lys Leu Cys Ala Thr Tyr Lys Leu Cy - #s His Pro Glu Glu Leu# 175- Val- (2) INFORMATION FOR SEQ ID NO:124:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:124:- Pro Leu Ser Ser Cys Pro Ser Gln Ala Leu Gl - #n Leu Ala Gly Cys Leu# 15- Ser Gln Leu His Ser Gly Leu Phe Leu Tyr Gl - #n Gly Leu Leu Gln Ala# 30- Leu Glu Gly Ile Ser Pro Glu Leu Gly Pro Th - #r Leu Asp Thr Leu Gln# 45- Leu Asp Val Ala Asp Phe Ala Thr Thr Ile Tr - #p Gln Gln Met Glu Glu# 60- Leu Gly Met Ala Pro Ala Leu Gln Pro Thr Gl - #n Gly Ala Met Pro Ala#80- Phe Ala Ser Ala Phe Gln Arg Arg Ala Gly Gl - #y Val Leu Val Ala Ser# 95- His Leu Gln Ser Phe Leu Glu Val Ser Tyr Ar - #g Val Leu Arg His Leu# 110- Ala Gln Pro Asp Met Ala Thr Pro Leu Gly Pr - #o Ala Ser Ser Leu Pro# 125- Gln Ser Phe Leu Leu Lys Ser Leu Glu Gln Va - #l Arg Lys Ile Gln Gly# 140- Asp Gly Ala Ala Leu Gln Glu Lys Leu Cys Al - #a Thr Tyr Lys Leu Cys145 1 - #50 1 - #55 1 -#60- His Pro Glu Glu Leu Val Leu Leu Gly His Se - #r Leu Gly Ile Pro Trp# 175- Ala- (2) INFORMATION FOR SEQ ID NO:125:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:125:- Gln Ala Leu Gln Leu Ala Gly Cys Leu Ser Gl - #n Leu His Ser Gly Leu# 15- Phe Leu Tyr Gln Gly Leu Leu Gln Ala Leu Gl - #u Gly Ile Ser Pro Glu# 30- Leu Gly Pro Thr Leu Asp Thr Leu Gln Leu As - #p Val Ala Asp Phe Ala# 45- Thr Thr Ile Trp Gln Gln Met Glu Glu Leu Gl - #y Met Ala Pro Ala Leu# 60- Gln Pro Thr Gln Gly Ala Met Pro Ala Phe Al - #a Ser Ala Phe Gln Arg#80- Arg Ala Gly Gly Val Leu Val Ala Ser His Le - #u Gln Ser Phe Leu Glu# 95- Val Ser Tyr Arg Val Leu Arg His Leu Ala Gl - #n Pro Asp Met Ala Thr# 110- Pro Leu Gly Pro Ala Ser Ser Leu Pro Gln Se - #r Phe Leu Leu Lys Ser# 125- Leu Glu Gln Val Arg Lys Ile Gln Gly Asp Gl - #y Ala Ala Leu Gln Glu# 140- Lys Leu Cys Ala Thr Tyr Lys Leu Cys His Pr - #o Glu Glu Leu Val Leu145 1 - #50 1 - #55 1 -#60- Leu Gly His Ser Leu Gly Ile Pro Trp Ala Pr - #o Leu Ser Ser Cys Pro# 175- Ser- (2) INFORMATION FOR SEQ ID NO:126:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:126:- Leu Gln Leu Ala Gly Cys Leu Ser Gln Leu Hi - #s Ser Gly Leu Phe Leu# 15- Tyr Gln Gly Leu Leu Gln Ala Leu Glu Gly Il - #e Ser Pro Glu Leu Gly# 30- Pro Thr Leu Asp Thr Leu Gln Leu Asp Val Al - #a Asp Phe Ala Thr Thr# 45- Ile Trp Gln Gln Met Glu Glu Leu Gly Met Al - #a Pro Ala Leu Gln Pro# 60- Thr Gln Gly Ala Met Pro Ala Phe Ala Ser Al - #a Phe Gln Arg Arg Ala#80- Gly Gly Val Leu Val Ala Ser His Leu Gln Se - #r Phe Leu Glu Val Ser# 95- Tyr Arg Val Leu Arg His Leu Ala Gln Pro As - #p Met Ala Thr Pro Leu# 110- Gly Pro Ala Ser Ser Leu Pro Gln Ser Phe Le - #u Leu Lys Ser Leu Glu# 125- Gln Val Arg Lys Ile Gln Gly Asp Gly Ala Al - #a Leu Gln Glu Lys Leu# 140- Cys Ala Thr Tyr Lys Leu Cys His Pro Glu Gl - #u Leu Val Leu Leu Gly145 1 - #50 1 - #55 1 -#60- His Ser Leu Gly Ile Pro Trp Ala Pro Leu Se - #r Ser Cys Pro Ser Gln# 175- Ala- (2) INFORMATION FOR SEQ ID NO:127:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:127:- Leu Ala Gly Cys Leu Ser Gln Leu His Ser Gl - #y Leu Phe Leu Tyr Gln# 15- Gly Leu Leu Gln Ala Leu Glu Gly Ile Ser Pr - #o Glu Leu Gly Pro Thr# 30- Leu Asp Thr Leu Gln Leu Asp Val Ala Asp Ph - #e Ala Thr Thr Ile Trp# 45- Gln Gln Met Glu Glu Leu Gly Met Ala Pro Al - #a Leu Gln Pro Thr Gln# 60- Gly Ala Met Pro Ala Phe Ala Ser Ala Phe Gl - #n Arg Arg Ala Gly Gly#80- Val Leu Val Ala Ser His Leu Gln Ser Phe Le - #u Glu Val Ser Tyr Arg# 95- Val Leu Arg His Leu Ala Gln Pro Asp Met Al - #a Thr Pro Leu Gly Pro# 110- Ala Ser Ser Leu Pro Gln Ser Phe Leu Leu Ly - #s Ser Leu Glu Gln Val# 125- Arg Lys Ile Gln Gly Asp Gly Ala Ala Leu Gl - #n Glu Lys Leu Cys Ala# 140- Thr Tyr Lys Leu Cys His Pro Glu Glu Leu Va - #l Leu Leu Gly His Ser145 1 - #50 1 - #55 1 -#60- Leu Gly Ile Pro Trp Ala Pro Leu Ser Ser Cy - #s Pro Ser Gln Ala Leu# 175- Gln- (2) INFORMATION FOR SEQ ID NO:128:- (i) SEQUENCE CHARACTERISTICS:#acids (A) LENGTH: 177 amino (B) TYPE: amino acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: peptide- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:128:- His Leu Ala Gln Pro Asp Met Ala Thr Pro Le - #u Gly Pro Ala Ser Ser# 15- Leu Pro Gln Ser Phe Leu Leu Lys Ser Leu Gl - #u Gln Val Arg Lys Ile# 30- Gln Gly Asp Gly Ala Ala Leu Gln Glu Lys Le - #u Cys Ala Thr Tyr Lys# 45- Leu Cys His Pro Glu Glu Leu Val Leu Leu Gl - #y His Ser Leu Gly Ile# 60- Pro Trp Ala Pro Leu Ser Ser Cys Pro Ser Gl - #n Ala Leu Gln Leu Ala#80- Gly Cys Leu Ser Gln Leu His Ser Gly Leu Ph - #e Leu Tyr Gln Gly Leu# 95- Leu Gln Ala Leu Glu Gly Ile Ser Pro Glu Le - #u Gly Pro Thr Leu Asp# 110- Thr Leu Gln Leu Asp Val Ala Asp Phe Ala Th - #r Thr Ile Trp Gln Gln# 125- Met Glu Glu Leu Gly Met Ala Pro Ala Leu Gl - #n Pro Thr Gln Gly Ala# 140- Met Pro Ala Phe Ala Ser Ala Phe Gln Arg Ar - #g Ala Gly Gly Val Leu145 1 - #50 1 - #55 1 -#60- Val Ala Ser His Leu Gln Ser Phe Leu Glu Va - #l Ser Tyr Arg Val Leu# 175- Arg- (2) INFORMATION FOR SEQ ID NO:129:- (i) SEQUENCE CHARACTERISTICS:#pairs (A) LENGTH: 531 base (B) TYPE: nucleic acid (C) STRANDEDNESS: unknown (D) TOPOLOGY: unknown- (ii) MOLECULE TYPE: other nucleic acid#= "synthetic"DESCRIPTION: /desc- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:129:- CACCTTGCGC AGCCCGACAT GGCTACACCA TTAGGCCCTG CCAGCTCCCT GC - #CCCAGAGC 60- TTCCTGCTCA AGTCTTTAGA GCAAGTGAGG AAGATCCAGG GCGATGGCGC AG - #CGCTCCAG 120- GAGAAGCTGT GTGCCACCTA CAAGCTGTGC CACCCCGAGG AGCTGGTGCT GC - #TCGGACAC 180- TCTCTGGGCA TCCCCTGGGC TCCCCTGAGC TCCTGCCCCA GCCAGGCCCT GC - #AGCTGGCA 240- GGCTGCTTGA GCCAACTCCA TAGCGGCCTT TTCCTCTACC AGGGGCTCCT GC - #AGGCCCTG 300- GAAGGGATAT CCCCCGAGTT GGGTCCCACC TTGGACACAC TGCAGCTGGA CG - #TCGCCGAC 360- TTTGCCACCA CCATCTGGCA GCAGATGGAA GAACTGGGAA TGGCCCCTGC CC - #TGCAGCCC 420- ACCCAGGGTG CCATGCCGGC CTTCGCCTCT GCTTTCCAGC GCCGGGCAGG AG - #GGGTCCTG 480# 531TGCAGAG CTTCCTGGAG GTGTCGTACC GCGTTCTACG C__________________________________________________________________________

Number	Name	Date
4810643	Souza et al.	Mar 1989
4999291	Sousa	Mar 1991
5399345	Schumacher et al.	Mar 1995
5635599	Pastan et al.	Jun 1997

Number	Date	Country
0 396 158 A1	Aug 1986	EPX
0 272 703 B2	Jun 1988	EPX
0 299 782 A2	Jan 1989	EPX
WO9527732	Oct 1995	WOX

G-CSF receptor agonists

Information

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Date Filed

Date Issued

Inventors

Original Assignees

Examiners

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CPC

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Abstract

Description

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Parent Case Info

US Referenced Citations (4)

Foreign Referenced Citations (4)

Non-Patent Literature Citations (27)

Continuation in Parts (1)

Entry
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