Altered major histocompatibility complex (MHC) determinant and methods of using the determinant

BACKGROUND OF THE INVENTION
This invention relates to an altered major histocompatibility complex (MHC) determinant and to the altered MHC determinant in association with an antigen. This invention also relates to the use of the altered MHC determinant in diagnostic applications and for treating or immunizing a mammal.
The major histocompatibility complex is a series of genes that code for protein molecules responsible for cell--cell recognition and interaction. The MHC of mammalian species contains three groups of genes: class I, class II, and class III. Class I and class II genes code for cell surface recognition molecules. Class III genes code for certain complement components.
The ability of cells to recognize other cells as self or as originating from another genetically different individual (non-self) is an important property in maintaining the integrity of tissue and organ structure. Class I and class II MHC products control recognition of self and non-self. The major histocompatibility system thus prevents an individual from being invaded by cells from another individual. For example, transplants from one individual generally cannot survive in another individual because of histocompatibility differences.
Histocompatibility similarities are required for cellular cooperation in induction of the immune response, and they provide a mechanism to ensure that T cells and B cells of a given individual can recognize each other for cooperation, yet recognize foreign structures at the same time. For instance, T lymphocytes, when presented with an antigen in the proper manner, react in one of two ways: through the generation of T cytotoxic lymphocytes (T.sub.c) or through amplification by T helper cells (T.sub.h) or suppression by T suppressor cells (T.sub.s) of the effects of other T or B cells. In general, T lymphocytes only recognize the antigen and respond to it when it is presented on the surface of antigen-presenting cell. This antigen-presenting cell may vary according to the type of T lymphocyte involved. Thus, in the generation of cytotoxic responses, lymphocytes and possibly macrophages present the antigen to the T.sub.c cells, while in the other types of T response the presenting cell may be a macrophage and perhaps dendritic cells.
T cells need to recognize two structures, a foreign antigen and an MHC gene product, for their subsequent activation. The process of generating T.sub.c cells and a cytotoxic response requires that the antigen be presented to the T cells in association with an MHC class I gene product. On the other hand, for B cells to be activated, binding to the antigen is necessary, plus a second signal usually given by a T.sub.h lymphocyte. However, the T.sub.h lymphocytes require the presentation of the antigen in a processed form by an antigen-presenting cell in the context of an MHC class II determinant.
In the case of B cell activation, it has been established that whatever the antigen-presenting cell is, it must process the antigen before presenting it to the T.sub.h lymphocytes. This involves taking up the antigen, sequestering it in intracellular compartments, and re-expressing the antigen or a portion thereof on the surface of the antigen-presenting cell in association with a class II MHC determinant. The T.sub.h cell must be able to recognize the processed antigen and class II markers on both the antigen-presenting cell and the B cell. When each of these requirements is fulfilled, the B cell will be stimulated to proliferate, which greatly increases the number of cells capable of synthesizing specific antibody. These then differentiate into plasma cells, which secrete large amounts of antibody. A similar response employing class II receptors on T.sub.S suppressor cells and class II MHC markers on macrophages and B cells may be operative in induction of T suppressor activity, which turns off antibody production.
Much remains to be understood of the interactions between antigens and MHC class I and class II molecules, and of the way in which T cell receptors recognize MHC-antigen complexes. For instance, a large proportion of MHC molecules is likely to be occupied by a variety of preexisting (probably endogenous) peptides. This obscures the interpretation of peptide-binding assays and hampers crystallographic studies of peptide-MHC complexes. It would be extremely useful to be able to isolate peptide-free MHC molecules, which could be loaded by a single type of peptide.
In addition, there exists a need in the art for knowledge of the peptide motifs of individual MHC alleles to aid in making T-cell epitope predictions, to aid in synthetic or recombinant vaccine development, and for intervention in autoimmune diseases or graft rejection.
SUMMARY OF THE INVENTION
This invention aids in fulfilling these needs in the art. More particularly, this invention provides a MHC class I determinant comprising .alpha..sub.1, .alpha..sub.2, .alpha..sub.3, and .beta..sub.2 -microglobulin polypeptide domains encoded by a mammalian MHC class I locus. The .alpha..sub.3 domain has a carboxyl terminus, and the .beta..sub.2 -microglobulin domain has an amino terminus that is covalently linked to the carboxyl terminus of the .alpha..sub.3 domain.
This invention also provides a MHC class II determinant comprising .alpha..sub.1, .alpha..sub.2, .beta..sub.1, and .beta..sub.2 polypeptide domains encoded by a mammalian MHC class II locus. The domains are covalently linked to form a polypeptide comprising the .beta..sub.2 -.sub.60 .sub.2 -.alpha..sub.1 -.beta..sub.1 domains in sequence.
In addition, this invention provides a recombinant DNA molecule comprising the MHC class I determinant or the MHC class II determinant of the invention inserted in a vector.
Further, this invention provides a host transformed with the vector of the invention.
Also, this invention provides a composition comprising an antigen bound to the MHC class I determinant or the MHC class II determinant of the invention.
Moreover, this invention provides a method of eliciting an immune system response in a mammal. The method comprises administering to the mammal an effective amount of the MHC class I or class II determinant of the invention, with or without association with an antigen.
Although native MHC molecules can be highly complicated structures not lending themselves to convenient manipulation, the present invention demonstrates the feasibility of creating MHC-antigen complexes between any of a variety of molecules capable of fulfilling the task of target recognition. These molecules are easier to handle and refold during and after denaturing treatments. These constructs are useful in the analysis of functional interactions between the various domains comprising the MHC molecules.
Moreover, this invention makes it possible to intervene in the functioning of the immune system. The immune system cells are capable of recognizing the altered MHC determinants and compositions of the invention and to respond to the presence of a potential pathogen with an effector appropriate to its lineage, e.g., cytotoxic T lymphocytes would respond by cytotoxic activity against the target, and B lymphocytes are activated to synthesize antibody. Macrophages and granulocytes carry out their effector functions, including cytokine release, phagocytosis, and reactive oxygen generation after intervention by the altered MHC determinants and compositions of the invention. Similarly, with an antigen or peptide portion typical as a marker for tumor cells, the immune system response to the tumor is beneficially elevated. In addition, with an antigen capable of causing recognition of immune cells having an inappropriate reactivity with self-determinants, this invention makes it possible to selectively target cells for destruction.

BRIEF DESCRIPTION OF THE DRAWINGS
This invention will be described in greater detail by referring to the drawings in which:
FIG. 1 depicts the orientation of an MHC class I molecule and .beta..sub.2 -microglobulin in a cell membrane.
FIG. 2 depicts the orientation of an MHC class II molecule in a cell membrane.
FIG. 3A diagrammatically depicts an altered class I MHC determinant of the invention.
FIG. 3B is a block diagram showing the altered class I MHC determinant of the invention and a spacer covalently linking the MHC gene produce to .beta..sub.2 -microglobulin.
FIG. 4A depicts an altered class II MHC determinant of the invention.
FIG. 4B is a block diagram showing the domains of the altered class II MHC determinant of the invention linked by spacers.
FIG. 5 depicts DNA constructs of the parental plasmid, pSC-K.sup.d -2, in (A) (SEQ ID NO:1 and SEQ ID NO:2). Various spacers are depicted in (B) Spacer SC-10 corresponds to SEQ ID NO:3 and SEQ ID NO:4; spacer SC-13 corresponds to SEQ ID NO:5 and SEQ ID NO:6; spacer SC-15 corresponds to SEQ ID NO:7 and SEQ ID NO:8; spacer SC-17 corresponds to SEQ ID NO:9 and SEQ ID NO:10; spacer SC-19 corresponds to SEQ ID NO:11 and SEQ ID NO:12; and spacer SC-21 corresponds to SEQ ID NO:13 and SEQ ID NO:14.
FIG. 6 shows the immunodetection of intracellular SC-K.sup.d molecules:
(A) Immunoprecipitation of SC-K.sup.d -2, -10, -13, -17, -19, -21 by mAb 34-1-2. NT refers to "non-transfected" and pKC refers to transfection by the vector. Transfections were made in the absence (-) or in the presence (+) of a peptide (NPR.sup.-) added at a concentration of 10.sup.-4 M in the culture medium.
(B) Immunoprecipitation of SC-K.sup.d -2, -15 by monoclonal antibody (mAb) 34-1-2 (left), F23-1 (middle) and 20-8-4 (right). Symbols as above.
(C) Immunoprecipitation of SC-K.sup.d -15 treated (+) and non-treated (0) with Endo H.
(D) Overexposed autoradiogram [3 weeks instead of 2 days in (A) and (B)] showing the presumptive monkey .beta..sub.2 -microglobulin band, which is co-precipitated by 34-1-2 in larger relative amounts with SC-K.sup.d -2 than with SC-K.sup.d -15 (on top, with a 2-day exposure).
FIG. 7 depicts the CD3-TCR complex.
FIG. 8 depicts the TCR.alpha.-.xi./.beta.-.xi. fusion construct.
FIG. 9 is the nucleotide sequence of the .alpha. and .beta. chains of the TCR of the CW3/1.1 CTL clone.
FIG. 10 is a plasmid map of pCDL-SR.alpha.296.
FIG. 11 is the nucleotide sequence of peptides CW3 and Y81.
FIG. 12 is a diagram which shows that the altered MHC K.sup.d molecule does not activate the RBL-transfectant.
FIG. 13 is a diagram showing that the altered K.sup.d molecule activates the RBL transfectant in the presence of the SF1-1.1.1 antibody.
FIG. 14 is a graph which shows the release of serotonin from RBL-2H3 transfectant cells expressing the modified TCR .alpha.-.xi.-/.beta..xi. which were incubated with altered K.sup.d molecules complexed with the SF1-1.1.1 antibody (anti-K.sup.d) and the CW.sup.3 peptide or with anti-C.beta. antibody.
FIG. 15 is a schematic diagram showing the TCR-peptide-MHC complex and the TCR aggregation induced by the anti-K.sup.d antibody.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENT
The invention concerns construction of functional molecules capable of activating the immune system and capable of presenting antigens to the immune system to elicit an antigenic response. More particularly, it concerns the regulation of the immune system response by presenting antigen via an altered MHC determinant so as to cause T-cells to respond to the determinant or the presented antigen. The invention also concerns a method of immunization and therapy for diseases as varied as AIDS, lupus erythematatosus, multiple sclerosis, toxic shock, and snake bite.
1. Major Histocompatibility Complex ("MHC")
All nucleated cells express class I MHC gene products on their surface. Class II gene products are expressed on some cells, such as B cells and macrophages, but not on other cells. This invention provides an altered major histocompatibility complex determinant of a mammal.
The term "major histocompatibility complex" is abbreviated herein as "MHC". The term is used in describing this invention in a generic sense to refer to the set of genes that code for histocompatibility markers in mammals. Exemplary of the mammalian species from which the altered MHC determinants of the invention can be based are the species identified in Table 1.
TABLE 1______________________________________MHC nomenclature of mammalian species Species MHC designation______________________________________Chimpanzee ChLA Dog DLA Guinea pig GPLA Human HLA Mouse H-2 Pig SLA Rabbit RLA Rat RT1 Rhesus monkey RhLA______________________________________ Where reference is made herein to the MHC of a particular mammalian species, the MHC designation in TABLE 1 will be employed.
2. Class I And Class II Major Histocompatibility Complex Gene Products
Class I MHC gene products are glycoproteins that are noncovalently bound to a peptide termed .beta..sub.2 -microglobulin, which is abbreviated ".beta..sub.2 m" or ".beta..sub.2 M". The class I component is referred to as the heavy chain and the .beta..sub.2 -microglobulin as the light chain. The orientation of the MHC class I molecule and .beta..sub.2 -microglobulin in a cell membrane is illustrated in FIG. 1.
Referring to the Figure, the heavy chain structure is organized with three exposed domains, .alpha..sub.1, .alpha..sub.2, and .alpha..sub.3, which extend from the cell surface and are attached to a hydrophobic transmembrane domain 1 and a short cytoplasmic anchor segment 2 within the cell. Two of the outer domains (.alpha..sub.2 and .alpha..sub.3) have intrachain disulfide bonds (forming loops with considerable homology with Ig).
The light chain (.beta..sub.2 -microglobulin) shown in the Figure is about the same size as one of the .alpha. domains of the heavy chain. Each domain is immunoglobulin-like, consisting of a folded .beta. pleated sheet structure held together by a disulfide bond at the ends, giving a plane-like surface. The .beta..sub.2 chain folds with the .alpha..sub.3 domain of the heavy chain, and the .alpha..sub.1 and .alpha..sub.2 domains also pair.
The .beta..sub.2 -microglobulin gene is located on a chromosome different from that containing the MHC class I gene product. Its structure is highly conserved, whereas that of the heavy chains varies extensively from one individual to another because of differences in amino acid sequences of the external domains. The polymorphism of the heavy chain is contributed primarily by the .alpha..sub.1 domain and to a lesser degree by the .alpha..sub.2 domain.
The products of the class II genes are less well characterized. In the mouse, the class II gene product (Ia) consists of two polypeptide chains (.alpha. and .beta., FIG. 2). The .alpha. and .beta. chains are divided into two external domains (.alpha..sub.1 and .alpha..sub.2 or .beta..sub.1 and .beta..sub.2), transmembrane domains 3 and 4 in FIG. 2, and cytoplasmic domains 5 and 6. Cystein residues that participate in disulfide bridge formation are indicated by S in FIG. 2.
The class I and class II MHC gene products may be glycosylated.
3. Altered Class I And Class II MHC Determinants Of The Invention
This invention involves altered determinants corresponding to products of class I and class II MHC loci. This invention also involves an altered MHC class I or class II determinant with an antigen to form a composition that can be recognized by the immune system of a mammal to initiate an immune or cytolytic response.
An altered class I MHC determinant substantially free of associated antigen is diagrammatically depicted in FIG. 3A in which the .alpha..sub.3 domain of the heavy chain is linked to the .beta..sub.2 -microglobulin domain by means of a spacer (shown as a broken line in the Figure). The resulting product, which is depicted in block diagram form in FIG. 3B, is the altered class I MHC determinant of this invention and comprises the .alpha..sub.1, .alpha..sub.2, .alpha..sub.3, and .beta..sub.2 -microglobulin domains covalently linked in sequence. As shown in FIG. 3A, the .alpha..sub.3 domain of the heavy chain is free of the region proximate the transmembrane domain region 1 in FIG. 1 to the carboxyl terminus of the cytoplasmic segment 2.
The altered class I MHC determinant can be prepared by appropriate selection of the MHC locus encoding the .alpha..sub.1, .alpha..sub.2, .alpha..sub.3 domains, and a gene encoding the .beta..sub.2 -microglobulin domain so that each of these domains will retain their functions in activating cytotoxic T cells and in antigen presentation to mammalian T cell receptors. Expression of the polypeptide coded by the MHC locus can be achieved by recombinant DNA techniques described in detail hereinafter.
An altered class II MHC determinant of the invention is shown in diagrammatic form in FIG. 4A. Referring to the Figure, the amino terminus of the .alpha..sub.1 domain is joined to the carboxyl terminus of the .beta..sub.1 domain, such as by means of a spacer (broken line). Similarly, the carboxyl terminus of the .alpha..sub.2 domain is joined to the amino terminus of the .beta..sub.2 domain, such as by means of another spacer (broken line). The resulting product is the altered class II MHC determinant of this invention, which can be represented by the block diagram shown in FIG. 4B. The altered determinant comprises the .beta..sub.2, .alpha..sub.2, .alpha..sub.1, and .beta..sub.1 domains covalently linked in sequence. As shown in FIG. 4A, the altered determinant is free of the regions proximate the transmembrane domains 3 and 4 in FIG. 2 extending to the carboxyl termini of the cytoplasmic segments 5 and 6, which are normally affixed to the .alpha..sub.1 -.alpha..sub.2 chain and the .beta..sub.1 -.beta..sub.2 chain, respectively. Once again, the portions of the MHC loci are selected to preserve the function of the domains in stimulating a cytotoxic response or in presenting antigen to mammalian T cell receptors.
4. Polypeptides Encoded By MHC
The altered major histocompatibility complex determinant of the invention is a polypeptide encoded by the genetic loci of class I or class II mammalian MHC and .beta..sub.2 m genes, where the polypeptide contains a binding site for an antigen that may be associated with the polypeptide, and when associated, the polypeptide and the antigen together are recognizable by a mammalian T cell receptor. In the case of human class I determinants, the determinant can be a polypeptide encoded by any of genetic loci identified in Table 2, as well as genetic loci not listed and/or not yet discovered.
TABLE 2______________________________________HLA class I loci HLA-A HLA-B HLA-C Allele Allele Allele______________________________________A1 B7 Cw1.sup.b A2 B7 Cw2 A3 B13 Cw3 A11 B18 Cw4 A23 B27 Cw5 A24 B35 Cw6 A25 B37 Cw7 A26 B38 Cw8 A28 B39 A29 Bw31 A30 Bw42 A31 B44 A32 B45 AW33 B49 Bw50 B51 Bw52 Bw53 Bw54 Bw55 Bw57 Bw58 Bw60 Bw61 Bw62 Bw63 Bw64 Bw65______________________________________ "w" designates workshop specificity not yet given accepted status according to WHO nomenclature rules.
In the case of human class II MHC determinants, the polypeptide employed in this invention can be encoded by any of the genetic loci in Table 3, as well as loci not listed here or not yet discovered.
TABLE 3______________________________________HLA class II loci Allele Allele Allele Allele______________________________________Dw1a DR1 DQw1 DPw1 Dw2 DR2 DQw2 DPw2 Dw3 DR3 DQw3 DPw3 Dw4 DR4 DPw4 Dw5 DR7 DPw5 Dw8 DRw8 DPw6 Dw9 DRw9 Dw10 DRw10 Dw11 DRw11 Dw12 DRw12 Dw13 DRw13 Dw14 DRw14 Dw17 Dw18 Dw19______________________________________ "w" designates workshop specificity not yet given accepted status according to WHO nomenclature rules.
The polypeptide employed in this invention can be based on an MHC determinant other than human species. Thus, for example, the polypeptide can be encoded by any of the genetic loci described in Table 4, which identifies MHC loci of the mouse.
TABLE 4______________________________________H-2 MHC lociClass I II II II II I I Products K A.beta. A.alpha. E.beta. E.alpha. D L______________________________________
It will be understood that the present invention is intended to encompass the altered MHC class I and class II determinants of the invention in the form in which they are prepared in situ or in purified form. In addition, the invention encompasses the altered determinants whether or not fully glycosylated and whether obtained using the techniques described herein or other methods. In a preferred embodiment of this invention, the altered MHC class I and class II determinants are totally free or substantially free of one or more of the following components: mammalian tissue and mammalian tissue components, nucleic acids, extraneous proteins and lipids, and adventitious microorganisms, such as bacteria and viruses. It will also be understood that the invention encompasses equivalent determinants having substantially the same biological and immunogenic properties. Thus, this invention is intended to cover variants of MHC determinants.
Depending upon the use to be made of the altered MHC class I and class II determinants, it may be desirable to label them. Examples of suitable labels are radioactive labels, enzymatic labels, fluorescent labels, chemiluminescent labels, and chromophores. The methods for labeling the altered determinants of the invention do not differ in essence from those widely used for labeling immunoglobulin. The need to label may be avoided using labeled antibody to the altered determinants or anti-immunoglobulin to the antibodies to the altered determinants as an indirect marker.
5. Joining The Polypeptide Domains Of the Altered MHC Determinant
The domains of the altered MHC determinants correspond to domains encoded by naturally occurring MHC loci and variants thereof that encode MHC products capable of effecting a cytotoxic response by appropriate T cells or inducing an immune response by the lymphocyte. The altered MHC class I and class II determinants of the invention differ from naturally occurring mammalian MHC gene products in that domains of the gene products are covalently linked, such as by means of a spacer. For example, in class I NHC gene products in nature, the class I heavy chain is always non-covalently associated with .beta..sub.2 -microglobulin. In contrast, the altered class I determinant of the invention comprises the class I heavy chain covalently linked to the .beta..sub.2 m domain. Similarly, the altered MHC class II determinant of the invention is comprised of a polypeptide chain in which the .beta..sub.2 -.alpha..sub.2 -.alpha..sub.1 -.beta..sub.1 domains are covalently linked. These domains are never linked in this way in nature. The altered MHC class I and class II determinants are the same as the corresponding MHC gene products in nature in other respects.
The altered MHC determinants of the invention can be obtained from DNA constructs encoding the MHC domains such that there is readthrough translation. For example, in the case of class I MHC determinants, the DNA construct contains a DNA sequence encoding the .alpha..sub.1, .alpha..sub.2, and .alpha..sub.3 domains linked to a DNA sequence encoding the .beta..sub.2 m domain so that there is readthrough translation from the 5' end of the DNA encoding the .alpha..sub.1 domain to the 3' end of the DNA sequence encoding the .beta..sub.2 m domain. Similarly, the altered class II MHC determinants of the invention can be obtained from DNA constructs in which there can be readthrough translation of a DNA sequence encoding the .beta..sub.2 -.alpha..sub.2 -.alpha..sub.1 -.beta..sub.1 domains.
It was surprisingly discovered that despite the covalent linkage of the MHC domains, the resulting altered MHC class I and class II determinants of the invention mimic the unaltered MHC class I and class II gene products that occur in nature.
In one embodiment of this invention, the MHC domains are covalently linked by a spacer, which is a nucleotide sequence encoding a polypeptide that functions as a hinge in the altered determinant. The spacer allows efficient folding or refolding of the domains with respect to each other such that the altered determinant has the ability to bind antigen or to stimulate the immune system.
The nucleotide sequence of the spacer and the corresponding amino acid sequence have not been found to be critical to the successful practice of this invention. Similarly, the size of the spacer has not been found to be critical. The spacer will generally be of a size to encode a polypeptide of about 2 to about 30 amino acids, and preferably about 5 to about 15 amino acids. Particularly preferred spacers encode polypeptides having about 10 to about 15 amino acids.
A typical spacer for use in a DNA construct encoding an altered H-2 determinant of the invention comprises all or part of the following nucleotide sequence:
(SEQ ID NO:15) 5' GATCGGATCCGGAGGCGGTGGATCCGGTGGCGGCGGTTC 3'
(SEQ ID NO:16) 3' CCTAGGCCTCCGCCACCTAGGCCACCGCCGCCAAGCTAG 5'
As another example, all or part of the following nucleotide sequence can be employed to form a spacer of up to 15 amino acids for an altered HLA-A2 determinant of the invention: (SEQ ID NO:17)5 " GGT GGC GGT GGA TCA GGC GGT GGT CCA CCG CCA CCT AGT CCG CCA CCA Gly Gly Gly Gly Ser Gly Gly Gly - (SEQ ID NO:18) GGG TCG GGT GGC GGC GGA TCC 3' CCC AGC CCA CCG CCG CCT AGG Gly Ser Gly Gly Gly Gly Ser
This sequence can be inserted after the nucleotides encoding amino acid 274 of HLA-A2 and before the nucleotides encoding amino acid 1 of human .beta..sub.2 -microglobulin resulting in the construction depicted in block diagram form in FIG. 3B.
It will be understood that this invention contemplates the use of the altered MHC determinants in non-cross-linked or cross-linked form. It will also be understood that the altered MHC determinant can be loaded with antigen without unfolding the antigen binding domain. Nevertheless, the invention contemplates unfolding the domain, for example in 7M urea, and dialysis.
6. Antigens Presented In Association With The Altered MHC Determinant
T cells can recognize synthetic peptides loaded on MHC class I and class II molecules. This phenomenon is called MHC restriction. The altered MHC class I determinants and class II determinants of this invention are capable of MHC restriction by association with antigens that are recognizable by T cell receptors of mammalian cells. Crystallography of human MHC class I molecules, HLA-A2 and Aw68, revealed a groove made up by the .alpha..sub.1 and .alpha..sub.2 domains of heavy chains. This groove is believed to be the binding site for antigens. The altered MHC class I determinants of the invention include a binding site of this type for antigens.
More particularly, this invention makes it possible to present antigens to the mammalian immune system and to elicit an immune response in vivo or in vitro. The antigen presented in association with the altered MHC determinant of this invention is generally a peptide. The antigens recognized by MHC class I and class II restricted T cells can be mimicked by artificial peptides. The peptide can also be a naturally occurring peptide. Thus, the peptide can be isolated from a source in which it occurs in nature or the peptide can be chemically synthesized.
When the antigen associated with the altered MHC determinant of this invention is a peptide, the peptide will typically contain about 5 to about 20 amino acid residues, preferably 8, 9 or 10 amino acid residues, when altered class I MHC molecules are used. Longer peptides can be employed with the altered MHC class II determinants of the invention. Octamers, nonomers, and decamers are particularly preferred peptides.
The naturally occurring peptides that normally bind to MHC gene products can be modified at one or more positions by other amino acids. In this event, it will be understood that the modified peptide will not necessarily have the same binding characteristics as the native or unmodified peptide; that is, a distinct allele-specific peptide motif capable of being presented by each MHC determinant may be observed. In any event, the peptide motifs typically contain two anchor positions occupied by a fixed amino acid residue or by one of a few residues with closely related side chains. These anchor positions are not in the same place in the different motifs. In general, the structure of the peptide should match the peptide-binding cleft of the altered MHC determinant. Thus, the allele-specific pockets in the altered MHC determinants of this invention and the side chains of the allele-specific anchor residues should preferably have complementary structures. Following are guidelines for selecting peptide/MHC combinations.
The physical association of antigenic peptides and altered MHC class I and class II determinants of the invention can be monitored using a direct peptide binding assay (PBA) in solid phase or an inhibition peptide binding assay (IPBA) in which the competing peptide is present in a soluble phase. Other tests measuring changes in fluorescence of an appropriately labeled peptide in soluble form when binding to a soluble MHC, or altered MHC molecule, are also available. The ability of different peptides to inhibit the lytic activity of human antiviral cytolytic T cells toward cells incubated with the corresponding target peptide can also be examined as a measure of the effectiveness of antigen binding and presentation.
In general: (a) Binding of a given human T cell-recognized peptide to several HLA class I and class II molecules occurs occasionally. Nevertheless, preferential binding of peptides to their respective restriction molecules is also observed. (b) Binding of HLA molecules to peptides recognized by murine T cells occurs less frequently, but such mechanisms are contemplated by this invention. (c) There exist HIV-1 peptides containing agretopic residues which allow their binding to HLA molecules and are particularly interesting in the scope of the invention. (d) The kinetics of HLA/peptide association depend on the peptide tested and are faster than or similar to those for Ia molecules. (e) Peptide/HLA molecule binding is frequently dependent on length, number of positive charges, and presence of hydrophobic residues in the peptide. (f) A correlation may be observed between a peptide inhibitory effect in the IPBA and its blocking effect in the cytolytic test.
Examples of typical peptides that can be combined with the altered MHC determinants of this invention are given in Table 6.
Table 6__________________________________________________________________________Peptides for Binding to Altered MHC Deteriminants Restricting PeptideSequenceElement__________________________________________________________________________Influenza A virus Matrix M.57-68KGILGFVFTLTVHLA-A2 M.Y.sup.+ 57-68YKGILGFVFTLTVHLA-A2 - NUCLEOPROTEIN N.147-158R.sup.- TYQRTRALVTGH-2 K.sup.D N.335-349Y.sup.+ SAAFEDLRVLSFIRGYHLA-B37 - Haemagglutinin H.130-142HNTNGVTAACSHEIa.sup.d H.305-329CPKYVKQNTLKLATGMRNVPEKQTRHLA-DR Lysozyme; Lys.46-61NTDGSTDYGILQINSRIa.sup.k repressor: R.12-26LEDARRLKAIYEKKKIa.sup.d HLA-A2: A2.170-185RYLENGKETLQRTDAPH-2 K.sup.d - HIV 1GAG. 51-65 LETSEGCRQILGQLQ 205-219ETINEEAAEWDRVHP-- 219-233HAGPIAPGQMREPRG-- 265-279KRWIILGLNKIVRMYHLA-B27 378-391MQRGNFRNQRKIVK-- 418-433KEGHQMKDCTERQANFHLA-A2 Env.105-117HEDIISLWDQSLKIa* 312-327IRIQRGPGRAFVTIGKH-2 D.sup.d 428-445FINMWQEVGKAMYAPPISIa* 474-489RPGGGDMRDNWRSELY-- 510-521VVQREKRAVGIG-- 584-604RILAVERYLKDQQLLGIWGCSHLA,C1 II* 827-843YVAEGTDRVIEVVQGACR-- 846-860RHIPRRIRQGLERIL-- Nef.66-80VGFPVTPQVPLRPMT-- 79-94MTYKAAVDLSHFLKEK-- 113-128WIYHTQGYFPDWQNYTHLA-B17.37 132-147GVRYPLTFGWCYKLVPHLA-B18 137-145LTFGWCYKL-- 160-174ENTSLLHPVSLHGMD-- Vif.1-15MENRWQVMIVWQVDR-- 25-40VKHHMYVSGKARGWFY-- 46-60SPHPRISSEVHIPLG-- 60-72GDARLVITTYWGL-- 71-85GLHTGERDWHLGQGV-- Ref. 1-16MAGRSGDSDEDLLKAV-- 18-30LIKFLYQSNPPPN-- 37-50ARRNRRRRWRERQR-- Vpr.1-14MEQAPEDQGPQREP-- 55-68AGVAEIIRILQQLL-- 68-80LFIHFRIGCRHSR--__________________________________________________________________________ *Not precisely identified restricting element.
Examples of other peptide epitopes that can be associated with the altered MHC determinants of this invention are shown in Table 7.
TABLE 7______________________________________Additional Peptides for Binding - to Altered MHC Determinants - Sequence Protein source______________________________________T Y Q R T R A L V Influenza PR8 NP 147-154 - S Y F P E I T H I Self-peptide of P815 - I Y A T V A G S LInfluenza JAP HA 523-549 V Y Q I L A I Y AInfluenza JAP HA 523-549 - - N V G T Y VInfluenza PR8 HA 518-528 - - E N G K E THLA-A24 170-18233 R Y L K N G K E THLA-Cw3 170-186 K Y Q A V T T T LP815 tumour antigen S Y I P S A E K IPlasmodium berghei CSP 249-260 S Y V P S A E Q IPlasmodium yoelii CSP 276-288 - Known epitopes, aligned A S N E N M E T M Influenza NP366-374 S G P S N T P P E I.sctn.Adenovirus E1A S G V E N P G G Y C L.sctn.Lymphocyte choriomeningitis virus GP 272-293 S A I N N Y . . .Simian virus 40 T 192-211 - Known epitopes, - aligned R G Y V Y Q G L Vesicular stomatitis virus NP 52-59 S I I N F E K LOvalbumin 258-276.sctn. A P G N Y P A LSendai Virus NP 321-332 - Known epitopes, aligned I L K E P V H G VHIV reverse transcriptase 461-485 F L Q S R P E P THIV Gag protein 446-460.sctn. A M Q M L K E . .HIV Gag protein 193-203.sctn. Q M K D C T E R QHIV Gag protein 418-443.sctn.______________________________________
The antigens described in Tables 6 and 7 are merely representative of antigens that can be presented to cell receptors in association with the altered MHC determinants of this invention. Other antigens that form complexes with the determinants can also be employed. Using both the direct peptide binding assay (PBA) and the inhibition of peptide binding assay (IPBA), the physical interactions between HLA molecules and peptides can be analyzed. More particularly, the assays can be carried out as follows.
Direct Peptide Binding Assay. Wells of microtiter plates are pretreated with 100 .mu.l 2.5% glutaraldehyde in distilled water for 2 h at 20.degree. C., washed with distilled water, and coated for 16 h at 4.degree. C. with 100 .mu.l of peptide diluted at 5 .mu.g/ml either in carbonate-bicarbonate buffer, pH 9.6, or in PBS, pH 7.4 or pH 5.0. Remaining free sites are blocked by incubation for 2 h at 20.degree. C. with BSA diluted 1% in PBS containing 0.05% Tween 20 (Tw) and 0.02% sodium azoture. After washing, purified .sup.125 I-HLA molecules (100 .mu.l containing 1.5.times.10.sup.5 cpm, 10.sup.-9 M) diluted in PBS containing 1% BSA, 0.05% Tw, 0.02% sodium azoture, 1 mM PMSF, and 10 .mu.g/ml trypsin inhibitor are added and incubated for 20 h at 20.degree. C. After extensive washing, the radioactivity of each well is counted.
Inhibition Peptide Binding Assay. Concentrations of 0.1-100 .mu.M of competitor peptides are incubated in tubes for 0-3 h at 20.degree. C. with .sup.125 I-HLA (10.sup.-9 M) diluted in PBS-BSA-Tw containing the protease inhibitors as mentioned above. Then the mixture is added to microtiter plate wells coated with a peptide that shows significant binding to HLA molecules in the direct test and incubated 20 h at 20.degree. C. After extensive washing, the radioactivity in each well is counted and the percent of inhibition is calculated.
Competition between Peptides in a Lytic Assay. Human antipeptide CTL is generated (37). Briefly, 6-8.times.10.sup.7 PBMC are stimulated with 100 .mu.g of a synthetic peptide in 10 ml culture medium (RPMI 1640 supplemented with 100 .mu.g/ml penicillin, 100 .mu.g/ml streptomycin, 2 mM L-glutamin, 2 mM nonessential amino acids, 1 mM sodium pyruvate, 10 mM Hepes, and 10% pooled heat-inactivated human AB serum). After a 7-d incubation, a secondary in vitro stimulation is performed by mixing 5-7.times.10.sup.6 effector cells with 2-3.times.10.sup.7 irradiated (4,000 rad) autologous PBMC in 10 ml culture medium containing 50-100 .mu.g of peptide.
In most cases, T cell epitopes are recognized in association with only a few, if not a single, MHC restriction elements. In contrast, some peptides can be recognized in association with several H-2 or HLA molecules. Furthermore, a single peptide can be recognized by both MHC class I and class II restricted T cells. Since class I and class II molecules have a similar predicted tertiary structure, including a single antigen binding site, interactions between peptides and these two types of molecules are also contemplated by this invention. Moreover, it will be understood that this invention contemplates the binding of antigens normally associated with the MHC of one species, such as H-2, to the altered MHC determinant of another species, such as HLA.
The formation of compositions comprising antigens bound to the altered MHC determinants of the invention can be based on peptides known to be antigenically involved in diseases such as AIDS (gag, nef, vif, ret, vpr, or env proteins or peptides), multiple sclerosis (myelin basic protein), toxic shock (bacteria), or snake venom (antigenic region for particular snake venom, alkaloid based and proteinaceous based; current snake bite therapy is based on administration of antibodies to the particular venom). These compositions can be formulated so as to allow the target recognition potential of an immune system cell to be specifically redirected to the antigen in presentation with the altered MHC determinant. It will be understood that libraries comprised of different altered MHC determinants of the invention and associated antigens can be prepared. It is thus possible to formulate compositions comprising two or more of the members of the library in any combination or amount, such as for simultaneously or sequentially targeting different receptors.
The extent of loading of the altered MHC determinant with peptide varies. The altered MHC determinant is typically employed in an amount of about 10 to about 1000 .mu.g/ml and the peptide is employed in an amount of about 10 to about 1000 .mu.g/ml.
While this invention has been described with reference to the use of peptides for binding altered MHC determinants, it will be understood that other antigenic materials can be employed. For example, peptides combined with haptens in general can be employed. Peptides can be combined with metals, such as nickel. Peptides can also be combined with carbohydrates. Certain chemicals, such as p-benzoyl arsonate, also bind directly in the groove of MHC materials. Suitable antigens are reviewed by P. Kourilsky and J. M. Claverie in "Advances in Immunology" (1989).
Similarly, the altered MHC determinants of the invention can be loaded with conventional immunotoxins and directed to a T cell associated with autoimmune disease for the purpose of disabling the T cell. Diptheria toxin, or subunits thereof, and Pseudomonas A toxin are examples of suitable immunotoxins.
7. Binding To Lymphocyte Cell Receptors
The altered MHC class I and class II determinants of the invention and compositions comprising antigens bound to the altered determinants are recognizable by receptors on T lymphocytes.
More particularly, the antigen and MHC recognition structure of T cells is referred to herein as the T cell receptor. The T cell receptor involved in antigen and MHC recognition is characterized in Table 8. Variable regions of the .alpha.- and .beta.-chains form the antigen binding site and also determine MHC specificity. In the presence of antigen and MHC, the T cell is activated. This results in phosphorylation of at least two subunits of the receptor complex, the .delta.- and .epsilon.-chains.
TABLE 8______________________________________Surface Structures Involved in Antigen Recognition by Human T Lymphocytes Molecular WeightChains Nonreduced Reduced Function______________________________________A. T Cell 90,000 41,000-43,000 Dual recognition receptor complex (two chains) of antigen and .alpha. and .beta. MHC "T.sub.3 complex" - .delta. 23,000 23,000 Phosphorylated during cell activation .gamma. 20,000-23,000 20,000-23,000 Unknown .epsilon. 20,000 20,000 Phosphorylated during cell activation .zeta. 32,000 16(two chains) Unknown B. T.sub.4 (CD4) 62,000 62,000 MHC class II recognition C. T.sub.8 (CD8) 76,000 31,000-33,000 MHC class I recognition______________________________________
Two other chains on the T cell surface, T.sub.4 (CD4) and T.sub.8 (CD8), are associated with the recognition of the altered class I or class II MHC determinants of the invention, without interacting with antigen. These molecules may normally bind non polymorphic (constant) determinants on class I or class II gene products of the antigen presenting cell. These molecules may also be associated with the T cell receptor.
A summary of the relationship between MHC class I and class II molecules and the type of immune reactive T cells is given in Table 9.
TABLE 9______________________________________Restrictions On Lymphoid Cell Activation Function Phenotype Restriction______________________________________T helper CD4.sup.+ CD8.sup.- Class II MHC + Antigen DTH CD4.sup.+ CD8.sup.- Class II MHC + Antigen CTL CD4.sup.- CD8.sup.+ or CD4.sup.+ CD8.sup.- Class I or II MHC + Antigen Suppressor CD4.sup.- CD8.sup.+ Class I MHC______________________________________
T helper cell activation and delayed hypersensitivity effector (DTH) cells are antigen and class II MHC restricted; CTL activities are antigen and class I or class II MHC restricted. Suppression can be class I restricted or unrestricted. Surface phenotype (CD4 or CD8) correlates mainly with MHC recognition of class II (CD4.sup.+) or class I (CD8.sup.+).
Considering the important regulatory role of class II restricted inducer cells (all of which are CD4.sup.+), it is not surprising that a virus such as the AIDS-related virus, which infects T cells through the CD4 marker and thus selectively depletes the CD4 population, can cause the severe immune suppression and other abnormalities of lymphocyte growth seen in AIDS patients. This invention should make it possible to inhibit infection of cells by blocking the susceptible cell surface marker with either the altered MHC class I or class II determinant or by the composition comprising antigen bound to the altered determinant. This invention should also make it possible to mimic antigen binding to the T cell receptor .alpha.- and .beta.-chains or to the .delta.-chains. By cross-linking receptors with the altered determinant of the invention, T cell activation is facilitated. This invention thus makes it possible to stimulate or enhance the function of the immune system.
8. Methods Of Preparing Altered MHC Class I And Class II Determinants
The altered MHC class I and class II determinants of the invention can be prepared according to well known recombinant DNA techniques. More particularly, nucleic acid sequences encoding the domains of class I and class II MHC gene products and .beta..sub.2 m, and spacers where appropriate, are employed in this invention. A nucleic acid fragment of interest can be ligated to a cloning vehicle. The nucleic acid can be obtained from any source, for example, from plasmids, from cloned DNA or RNA, or from natural DNA or RNA from any source. DNA or RNA can be extracted from a biological material, such as biological fluids or tissue, by a variety of techniques including those described by Maniatis et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, New York (1982). The nucleic acid will generally be obtained from a higher organism, such as an animal. The nucleic acid sequence can also be chemically synthesized using conventional techniques.
It is not necessary that the nucleic acid fragment to be ligated be present in a pure form. The nucleic acid to be ligated can contain more than one specific nucleic acid sequence, which can be the same or different. The specific nucleic acid fragment to be ligated can be a fraction of a larger molecule or the fragment can constitute an entire gene or assembly of genes encoding the domains of interest. The DNA can be a single-stranded or double-stranded form. If the fragment is in single-stranded form, it can be converted to double-stranded form using DNA polymerase according to conventional techniques.
The nucleic acid fragment to be ligated can have cohesive ends compatible with any combination of sites in a cloning vehicle. Alternatively, the nucleic acid fragment can have one or more blunt ends that can be ligated to corresponding blunt ends in the cloning sites of the vehicle. The nucleic acid fragment to be ligated can be further processed, if desired, by successive exonuclease deletion, such as with the enzyme Bal 31. In the event that the nucleic acid fragment to be ligated does not contain a desired combination of cohesive ends, the fragment can be modified by adding a linker, an adaptor, or homopolymer tailing.
If it is difficult to determine which fragment in a complicated mixture of nucleic acid sequences is desired for ligation, or if it is desired to ligate more than a single nucleic acid fragment, mixtures of nucleic acid fragments can be employed. This procedure can be utilized to generate a small library of clones that contain all compatible fragments in the original nucleic acid mixture.
The cloning vehicle employed in practicing the invention can be any double-stranded DNA molecule capable of transporting the nucleic acid fragment to be ligated into the host cell and capable of replicating within the cell. More particularly, the cloning vehicle must contain at least one DNA sequence that can act as the origin of replication in a host cell. In addition, the cloning vehicle must contain two or more sites for insertion of the nucleic acid sequence to be ligated. These sites will ordinarily correspond to restriction enzyme sites at which cohesive ends can be formed, and which are complementary to the cohesive ends on the nucleic acid fragment to be ligated to the vehicle. In general, this invention can be carried out with plasmid, bacteriophage, or cosmid cloning vehicles having these characteristics.
It is preferred that the plasmid carry one or more genes responsible for a useful characteristic, such as selectable marker, displayed by the host cell. In one type of strategy, plasmids having genes for resistance to two different drugs are chosen. For example, insertion of the DNA fragment of interest into a gene for an antibiotic inactivates the gene and destroys drug resistance. The second drug resistance gene is not affected when bacterial cells are transformed with the recombinants, and colonies containing the gene of interest can be selected by resistance to the second drug and susceptibility to the first drug. Preferred antibiotic markers are genes imparting chloramphenicol, ampicillin, or tetracycline resistance to the host cell.
When a plasmid is employed, the plasmid can be derived from bacteria or some other organism or the plasmid can be synthetically prepared. The plasmid can replicate independently of the host cell chromosome or an integrative plasmid (episome) can be employed. The plasmid can make use of the DNA replicative enzymes of the host cell in order to replicate or the plasmid can carry genes that code for the enzymes required for plasmid replication. A number of different plasmids can be employed in practicing this invention. Typical of the plasmids that can be utilized are pBR322, pBR325, Co1E1, RP4, and the 2 .mu.m circle that occurs in many strains of the yeast Saccharomyces cerevisiae. The cloning vehicle can also be a bacteriophage. It will be understood that this invention can be practiced with phage vectors that proliferate by a lytic cycle or by lysogenic infection.
Cloning can be carried in procaryotic or eucaryotic cells. The host for replicating the cloning vehicle will of course be one that is compatible with the vehicle and in which the vehicle can replicate. Cloning can be carried out in bacterial or yeast cells, although cells of fungal, animal, and plant origin can also be employed. The preferred host cells for conducting cloning work are bacterial cells, such as E. coli, as well as species of Streptomyces, Bacillus, and Pseudomonas. The use of E. coli cells is particularly preferred because most cloning vehicles, such as bacterial plasmids and bacteriophages, replicate in these cells. Yeast cells can also be employed for cloning work. Also preferred are strains of Saccharomyces cerevisiae. Animal cells, such as COS monkey cells, are preferred where post-translational processing of the altered MHC determinant is desired. For example, the altered MHC class I and class II determinants of the invention can be prepared in glycosylated form in COS cells. This invention thus contemplates the preparation and use of the altered determinants of the invention in glycosylated or non-glycosylated form.
Expression control sequences can be included in the vector of this invention. These include the operator, promoter and ribosome binding and interaction sequences (including sequences such as the Shine-Dalgarno sequences), the lactose operon of E. coli ("the lac system"), the corresponding sequences of the tryptophan synthetase system of E. coli ("the trp system"), the major operator and promoter regions of phage .lambda. (O.sub.L P.sub.L and O.sub.R P.sub.R.sup.I), and the control region of the phage fd coat protein. DNA fragments containing these sequences can be excised by cleavage with restriction enzymes from the DNA isolated from transducing phages that carry the lac or trp operons, or from the DNA of phage .lambda. or fd. These fragments can then be manipulated in order to obtain a limited population of molecules such that the essential controlling sequences can be joined very close to, or in juxtaposition with, the initiation codon of the coding sequence for the desired gene product. The product is then inserted into a cloning vehicle for transformation of the appropriate hosts and the level of production measured. Cells giving the most efficient expression can be selected.
To shorten the distance between the particular expression control sequence and the initiation codon of the chosen gene fragment, the particular fragment may be treated lightly with a combination of nucleases acting specifically at or near its terminus or used in exonuclease and polymerase-linked repair reactions to remove some or all of those nucleotides of the fragment preceding the fragment's start codon. Alternatively, a fragment can be similarly shortened with exonuclease treatment or polymerase-linked repair reactions and then cleaved to produce one fragment to permit fusion to another fragment before attachment to the expression control sequence.
The nucleotide sequences encoding domains of class I and class II mammalian gene products are known in the art and can be employed in practicing this invention. For example, following are primary structural data for .beta..sub.2 m molecules from several different species that can be employed in practicing this invention.
__________________________________________________________________________SEQ ID NO:__________________________________________________________________________ 10 20 30 40 50 .vertline. .vertline. .vertline. .vertline. .vertline. 59 Mouse .beta.2m IQKTPQIQVYSRHPPENGKPNILNCYVTQFHPPHIEIQMLKNGKKIPKVE - 60 Rat .beta.2m F-----S-----Q---EL--------NI- - 61 Guinea Pig .beta.2m VHLA-RV-------A----Q-FI----SG----Q--VEL------- DN-- - 62 Rabbit .beta.2m V-RA-NV-------A------F-----SG----Q-D-EL---V---EN-- - 63 Human .beta.2m R--K---------A----S-F-----SG---SD-VDL--D-ER-E--- - 64 Bovine .beta.2m RP-K---------------Y-----YG----Q---DL----E--KS-- - 60 70 80 90 99 .vertline. .vertline. .vertline. .vertline. .vertline. Mouse .beta.2m MSDMSFSKDWSFYILAHTEFTPTETDTYACRVKH SMAEPKTVYWDRDM - Rat .beta.2m L----------------------V-------VTLK----------- - Guinea Pig .beta.2m L------T--L-V-AA---NDS-E-S---S-ITLS---I-K--PNK - Rabbit .beta.2m Q--L--N------L-V------NNKNE-S-----VTLK--M--K----Y - Human .beta.2m H--L---------L-YY-------K-E-----N-VTLS Q--I-K----- - Bovine .beta.2m Q--L---------L-S-A----DSK-E-S-----VTLEQ-RI------L__________________________________________________________________________
The straight lines indicate homology to the sequence listed at the top. The single letter code for amino acids is used where A is Ala; C, Cys; D, Asp; E, Glu; F, Phe; G, Gly; H, His; I, Ile; K, Lys; L, Leu; M. Met; N, Asn; P, Pro; Q, Gln; R, Arg; S, Ser; T, Thr; V, Val; W, Trp; Y, Tyr. Position 85 of mouse .beta..sub.2 m is Ala for C57BL/6 mice and Asp for BALB/c. Source: Paul, Fundamental Immunology, 2nd Ed., Raven Press, N.Y. (1989), page 500.
Exemplary of other sequences that can be employed in this invention are those in the following compilation of sequences for murine class I molecules encoded within H-2, Q, and TL subregions.
- SEQ ID NO: EXON 2 1 5 10 15 20 25 30 35 40 45 50 55 60 65 70 75 80 85 90 65 H-2K.sup.b GPHSLRYFVTAVSRPGLGEPRYMEVGYVDDTEFVRFDSDAENPRYEPRARWMEQEGPEYWERETQKAKGNEQS FRVDLRTLLGYYNGSKG 66 H-2K.sup.d FIA-------Q--------D---F----P-----------EQ--R--SD--W---S---AQR------- 67 H-2K.sup.k H---------K--FIS-------Q----------------V-----VE------N--I------I---N--- A-R-----A- 68 H-2K.sup.q H------*-*K--FIS------------------------------VE------N--I--D----S------ --R-----A- 69 H-2D.sup.d S--------------F------------N---------------------I------------RR------- -------A-R-----A- 70 H-2D.sup.p K----------N--------------MK--V------------Q---N--DH------S--N---------- 71 H-2D.sup.b M---E--------E----IS-----NK------------------P-------------------Q--W--- S--N--------A- 72 H-2L.sup.d M---E-------------IS-----NK----------------Q-P------------I--I---Q--W--- N-----------A- 73 Q-7.sup.d (27.1) Q---Q--H---- -------WFIS-------Q------------M--------------------M---H-----GS---AQS-- ----- 74 Q-7.sup.b Q---Q--H-----------WFIS-------Q------------M--------------------I---H--- --GS---AQS------- 75 Q-8.sup.b H----W---V---FII-------Q------------M------------------------H-E----S--- AQR------- 76 Q-9.sup.b Q---Q--H-----------WFIS-------Q------------M--------------------I---H--- --GS---AQS------- 77 Q-10.sup.b S--M---E-S----------FII-------Q---------T--M----P---------------R------- -H-S------H----ES 78 PH-2.sup.d -37 S-------T------------FII-------Q------------M------I------------W--R DMGRN---N-----------ND 79 17.3A S------Y--L---AIS--W-IA---L---Q-A----AG-TGT-KLS-P-V--------A---EIVTA-A-F --EN-Q-M-D---L-QN 80 C25.1 S------Y--L---AIS--W-IA---L---Q----N-SG-TAT-KLS-P-V--------A---EIVTS-A-F --EN-Q-M-D---L-QN 81 and 82 T1a.sup.a -1 S---K--Y--L--AIS--W- -IAG--L---Q-RC-E-AG-SAT-KL--P-V--------A---EIVTS-A-F--EN-Q-M-D--SL-QN EXON 3 91 95 100 105 110 115 120 125 130 135 140 145 150 155 160 165 170 175 180 65 H-2K.sup.b GSHTIQVISGCEVGSDGRLLRGYQQYAYDGCDYIALNEDLKTWTAADMAALITKHKWEQAGEAERLRAYLEGT CVEWLRRYLKNGNATLLRT 66 H-2K.sup.d F-RMF--D----W--------F----R----------------T-----RR------D--YY------E--- ------EL--E----- 67 H-2K.sup.k F-RMY-------W------E-------------------------------------D---D---------- ------QL-----P-- 68 H-2K.sup.q RMY--D-----------E-V-----------------------------------A---R------A----- S-H----------- 69 H-2D.sup.d L-WMA--D-E---------W-F------------------------Q--RR------A---D------E--- ---------------- 70 H-2D.sup.p GMR--D----W------E-F----P-------------------Q--RR------A--T-------A----- ----EL------C- 71 H-2D.sup.b L-QM---DL---W------L-F--E-R-------------------Q--RR----S-A--HYK-----E--- --H------------- 72 H-2L.sup.d T--L-WMY--D-----------E-F----R-------------------Q--RR------A--YY------E -----H------------- 73 Q-7.sup.d (27.1) L-WMY--DM----------L-F--E-R--------------V----Q--RR------I--KDQ-------MQ S-----QL-KE----- 74 Q-7.sup.b L-WMY--DM----------L-F--E-R--------------V----Q--RR------I--KDQ-------MQ S-----QL-KE----- 75 Q-8.sup.b L-WMY--D----E------L-F--E-R-------------------Q--L-------I---D------A--Q S-----QLRKE---C- 76 Q-9.sup.b L-WMY--DM----------L-F--E-R--------------V----Q--RR------I--KDQ-------M- S-----QL-KE----- 77 Q-10.sup.b WMY--K------F----L------R----------------V--I--RR------A--YY-----AE----- L---EL-KE----- 78 PH-2.sup.d -37 E---L-WMY--D--P--------C-E----Q---S-----RS---N-I-SQ-S---S-AVD--HQQ-- --Q-P-----H---RL--E--Q-S 79 17.3A MY----EFF-S-F-A-E-HG---Q-------------------E--RS------YT-LR-T----P-KDS-L ---E-RKK-QEC- 80 C25.1 MY----EFF-S-F-A-E-HG---R----------------T--E--RS------YT-LR-T----P-KDS-L ---E-RKK-QEC- 81 and 82 T1a.sup.a- 1 MY----.sctn..sctn..sctn.-N-F-A-E-HG---R-------------------E--RS------YT- LR-T----P-KDS-F-----RKK-QECA 83 T1a.sup.a -3 F.sctn..sctn..sctn.-S-F-A-E-HG---R--------V----------E--RS------YT-LR-T- ---P-KDS-L---E-RKK-QEC-
- SEQ ID NO: EXON 4 185 190 195 200 205 210 215 220 225 230 235 240 245 250 255 260 265 270 65 cont. H-2K.sup. b DSPKAHVTHHSRPEDKVTLRCWALGFYPADITLTWQLNGEELIQDMELVETRPAGDGTFQKWASVVVPLG KEQYYTCHVYHQGLPEPLTLRW 66 cont. H-2K.sup.d Y-P-SQVD------------------------D-T--------------------A---------N-----H -K---------- and 85 67 cont. H-2K.sup.k R---------------------------------T------------------------------------- ------------ 68 cont. H-2K.sup.q T------------------------------------------K------ and 86 69 cont. H-2D.sup.d P--------R---GD--------------------------T-E---------------------------- K-----E-E----------GKE and 87 70 cont. H-2D.sup.p P------P-S-G-----------------------------T--------------------AL-------- N-----E-E---------- and 88 71 cont. H-2D.sup.b P-SKGE--------------------------T------------------------------N---R---E ---------- and 89 72 cont. H-2L.sup.d P-SKGE--------------------------T------------------------------N---R---E ---------- and 89 73 cont. Q-7.sup.d (27.1) P--------P-SYGA--- -----------------------T--T---------V-----------------N-----N-E--------- -GRW 74 cont. Q-7.sup.b P--------P-SYGA--------------------------T------------------------------ N-----N-E----------GRW 75 cont. Q-8.sup.b P--------P-SYGA--------------------------T------------------------------ N-----N-E---------- 77 cont. Q-10.sup.b P--T-----PGS-GD------P-------------------T-----Q------------------------ N-------E---------- 78 cont. PH-2.sup.d -37 P--------P-S--E---- ----------------------T--------------------A-----------------E---------- and 90 and 91 79 cont. 17.3A P--T-----A---GD-------------H---------------T-----------------A----S-E-- K-------E---------- and 92 80 cont. C25.1 P--T-----P---GY--------R--------------------T-----------------A--------- K-------E---------- and 93 82 cont. T1a.sup.a -1 P--T-----P---GY--- --------------------------------------------AL---S-E--K-------K--------- - and 94 84 and 95 T1a.sup.a -2 T-----------------AL---S-E--K-------K---------- 83 cont. T1a.sup.a -3 P--T-----P---GY----- ------------------------------------------A----S-E--K-------E---------- and 96 EXON 5 EXON 6 EXON 7 EXON 8 275 280 285 290 295 300 305 310 315 320 325 330 335 340 345 350 65 cont. H-2K.sup.b EPPPSTVSNMATVAVLVVLGAAIVTGAVVAFVMKMRRRNT GGKGGDYALAP GSQTSDLSLPDCK YMVHDPHSLA 66 cont. H-2K.sup.d KL-------TVII------------------------S-- VN----- G- and 85 67 cont. H-2K.sup.k TVII--------------------------- 68 cont. H-2K.sup.q A---TVII--------------------S------ and 86 69 cont. H-2D.sup.d S--KT-TVII--P-----VVIL---M-----S----- S--M------ and 87 70 cont. H-2D.sup.p D-Y-VI---------VFII--------M---S-- T--- S-EM--R--- A and 88 71 cont. H-2D.sup.b D-Y-VI----G----MAII---------S----- S-EM--R--- A and 89 73 cont. Q-7.sup.d (27.1) Y-------I--V-D---VAII--------NS--X 74 cont. Q-7.sup.b Y-------I--V-D---VAII--------NS--X 75 cont. Q-8.sup.b M--I----V-WPSLELWWILX 77 cont. Q-10.sup.b D-I-SHI-D-LWPSLKLWWYLX 78 cont. PH-2.sup.d -37 VII--------V-IL---------S---HI V--CS--HVL KSFQT-DWPQ- A and 90 and 91 79 cont. 17.3A Q-SMP-RT--RA-SS---M-IL-FMSGS--MWM-K-N N-D-NTA-Y QNEREH---TSGX and 92 80 cont. C25.1 L-QTSMP-RT--RA-SS---M-IL-FMSGS--MWM-K-N N-D-NTA-Y QNEREH---TPRAESEALGVEAGMKDLPSAPPLVSX and 93 82 cont. T1a.sup.a -1 Q-SMP-RT--RA-SS---M-IL-FMSGG--MWM-K-N N-D-NTA-C QNEREH---SPRAESEALGVEAGMKDLPSAPPLVSX and 94 84 and 95 T1a.sup.a -2 Q-SMP-RT--RA-SS---M-IL-FMSGS--MWM-K-K N-D-NTA-C QNEREH---SPRAESEALGVEAGLKDLPS 83 cont. T1a.sup.a -3 Q-SMPTRTI-RA-AA---MVIL-VMTGSG-MWM-K-K NRD-NTA-C QNEREH---SAGDESDALGVEAGLKELPTAPPLVPX
The above sequences are grouped by exon where exons 2, 3, and 4 encode the extracellular domains, exon 5 encodes the transmembrane region, and exons 6, 7, and 8 encode the intracytoplasmic portions of the molecules. A indicates identity with the prototype; * indicates an unidentified residue; and .sctn. indicates a deletion used to facilitate alignment of the sequences. Stop codons are represented by x in some sequences. Source: Paul, supra, at pages 502-503.
The deduced protein sequences for members of the HLA-A2/A28 family are shown below. Sequences designated with A2 are serologically indistinguishable and have been selected by functional assays. The A28 family is divided into A68 and A69 specificities based on serologic data. Paul, supra, at page 511.
- SEQ ID NO: LEADER PEPTIDE 20 -10 97 HLA-A2.1 MAVMAPRTLVLLLSGALALTQTWA 98 A2.4a 99 A2.3 100 A2(Lee) 101 A2.2Y 102 AW69 103 AW68.2 104 AW68.1 .alpha..sub.1 DOMAIN 10 20 30 40 50 60 70 80 90 97 cont. HLA-A2.1 GSHSMRYFFTSVSRPGRGEPRFLAVGYVDDTCFVRFDSDAASQRMEPRAPWIEQEGPEYWDGET RKVKAHSQTHRVDLGTLRGYYNISEA 98 cont. A2.4a Y----------------------------------------------------------------------- ---------- 105 A2.4b 106 A2.1/.3 99 cont. A2.3 100 cont. A2(Lee) Y----------------------------------------------------------------------- ---------- 107 A2.2F R----------------------------------------------- 101 cont. A2.2Y Y---------------------------------R------------------------------------- ---------- 108 A2.4c Y---------------------------------R----------------------N-------------- ---------- 102 cont. AW69 Y----------------------------------------------------RN--N---Q---D------ ---------- 103 cont. AW68.2 Y--M-------------------------------------------------RN--N---Q---D------ ---------- 104 cont. AW68.1 Y----------------------------------------------------RN--N---Q---D------ ---------- .alpha..sub.2 DOMAIN 100 110 120 130 140 150 160 170 180 97 cont. HLA-A2.1 DSHTVQRMYGCDVGSDWRFLRGYHQYAYDGKDYIALKEDLRSWTAADMAAQTTKHKWEAAHVAE QLRAYLEGTCVEWLRRYLENGKETLQRT 98 cont. A2.4a 105 cont. A2.4b C----------------------------------------------------------------------- ------------ 106 cont. A2.1/.3 99 cont. A2.3 T--E---W-------------------------- 100 cont. A2(Lee) F-------G--------------------------------------------------------------- ------------ 107 cont. A2.2F L------------------------------------------------------------W---------- ---------------- 101 cont. A2.2Y L------------------------------------------------------------W---------- ---------------- 108 cont. A2.4c L------------------------------------------------------------W---------- ---------------- 102 cont. AW69 103 cont. AW68.2 L---------P-G------------------------------------------------W---------- ---------------- 104 cont. AW68.1 L-M---------G------R-D---------------------------------------W---------- ---------------- .alpha..sub.3 DOMAIN 190 200 210 220 230 240 250 260 270 97 cont. HLA-A2.1 DAPKTHMTHHAVSDHEATLRCWALSFYPAEITLTWQRDGEDQTQDTELVETRPAGDGTFQKWAA VVVPSGQEQRYTCHVQHEGLPKPLTLRW 98 cont. A2.4a 105 cont. A2.4b 106 cont. A2.1/.3 E-------------------------------------- 99 cont. A2.3 100 cont. A2(Lee) 107 cont. A2.2F 101 cont. A2.2Y 108 cont. A2.4c 102 cont. AW69 103 cont. AW68.2 V----------------------------- 104 cont. AW68.2 V----------------------------- TRANSMEMBRANE REGION CYTO. 1 CYTO. 2 CYTO. 3 280 290 300 310 320 330 340 97 cont. HLA-A2.1 EPSSQPTIPIVGIIAGLVLFGAVITGAVVAAVMWRRKSS DRKGGSYSQAA SSDSAQGSDVSLTACK V 98 cont. A2.4a 99 cont. A2.3 100 cont. A2(Lee) 101 cont. A2.2Y 102 cont. AW69 103 cont. AW68.1 104 cont. AW68.2
Amino acid sequences of representative class II .alpha. chains deduced from cDNA clones are shown below. Residues identical to DR.alpha. sequence are indicated by hyphens. Numbering is in reference to the DRa sequence. Paul, supra, at page 519.
__________________________________________________________________________SIGNAL SEQUENCES20 -10 .vertline. .vertline. DR.alpha. MAISGVPVLGFFIIAVLMSAQESWA DQ.alpha.1 -ILNKALL--ALALTTV--PCGG DP.alpha. (MRPEDR)-FHIRAVI-RALSL-F-L-LRGAG- DN.alpha. --LRAGL----HTLMT-L-P--AG- I-A.alpha. -PR-RALI--VLALTTML-LCGG I-E.alpha. --TIGAL--R--F------S-K--- -.alpha.1 DOMAIN 10 20 30 40 50 60 70 80 .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. DR.alpha. IKEEHV IIQAEFYLNPDQSGEFMFDFDGDEIFHVDMAKKETVWRLEEFGRFASFEAQG ALANIAVDKANLEIMTKRSNYTPITN DQ.alpha.1 ED-VAD--ASCGVNL-QFYGP--QYTHE-----Q-Y--LER---A--WP--SK-GG-DP- ---R-M--A-H--N--I--Y-S-AA-- DP.alpha. --AD-- STY-A-VQTHRPT-----E--E--M-Y--LD------H-----QAF------ G-----ILNN--NTLIQ---H-QA-- DN.alpha. T-AD-MGSYGPA--QSYGA--Q-THE--EEQL-S--LK-S-A----P---D--R-DP-- G--G--AI--H-D-LVE---RSRAI- I-A.alpha. EDDIEAD--GSYGIT--QS-GDI-QYT-E-----L-Y--LD------M-P--AQLRR--P- -G-Q---TG-H----L-----S--A-- I-E.alpha. -----T --------L--KR----------------IE-S--I------AK------- -------------DV-KE---N--DA- -.alpha.2 DOMAIN 90 100 110 120 130 140 150 160 170 .vertline. .vertline. .vertline. .vertline . .vertline. .vertline. .vertline. .vertline. .vertline. DR.alpha. VPPEVTVLTNSPVELREPNVLICFIDKFTPPVVNVTWLRNGKPVTTGVSETVFLPREDHLFR KFHYLPFLPSTEDVYDCRVEHWGLDEPLLKHW DQ.alpha.1 EV-----FSK---T-GQ--T---LV-NIF-----I---S--QS--ED----S--SKS--S- F-IS--T----ADEI---K-------Q------ DP.alpha. D------FPKE----GQ--T---H----F---L-----C--EL--E--A-SL----T-YS-H -----T-V--A--F-----------Q------ DN.alpha. R----PK-R---GQ--I---IV-NIF---I-I------QT--E--AQ-SFYSQP------------V--A--- ---Q-------A---R-- I-A.alpha. EA-QA--FPK---L-GQ--T----V-NIF---I-I-----S-S--D--Y--S-FVNR-YS- H-LS--T-I--DD-I---K------E--V---- I-E.alpha. A------SR---N-G---I--------S------------R---E----------D----------T-----D -F---E-D----E---R-A- - CONNECTING PEPTIDE TRANSMEMBRANE REGION CYTOPLASMIC REGION 180 190 200 210 220 .vertline. .vertline. .vertline. .vertline. .vertline. DR.alpha. EFDAPSPLPETTE NVVCALGLTVGLVGIIIGTIFII KGLRKSNAAERRGPL DQ.alpha.1 PEI-A-MS-L-- T-------S---M--VV--V--- Q---SVG-SRHQ--- DP.alpha. AQE-IQM----- T-L-----VL----F-V--VL-- S--SGHDPRAQ-T- DN.alpha. LQV-I-P-DAM- TL------AI----FLV--VL-- M-TYV-SVPR I-A.alpha. PEI-A-MS-L-- T-------S------VV------ Q---SGGTSRHP--- I-E.alpha. EEKTL----K- F------VV-I-L-M IK-R-VV---QGAL__________________________________________________________________________
Amino acid sequences of representative class II .beta. chains deduced from cDNA clones are shown below. Residues identical to DR.epsilon. sequence are indicated by hyphens. Numbering is in reference to the DR.beta. sequence. Paul, supra, at page 520.
__________________________________________________________________________SIGNAL SEQUENCES30 -20 -10 .vertline. .vertline. .vertline. DR.beta. MVCLKLPGGSCMTALTVTLMVLSSPLALA DQ.beta. MSWKKS-RI--DLRVATV-LM-AI---S--EG DP.beta. MV-QVSAAPRTV---AL----LTSVVQG DO.beta. MGSGWVPWVV--L-N-TR-D-SMTQG I-A.alpha. MALQIPSLLLS-AV-V-------RTEG I-E.alpha. MVW--RVP-VA-VILL-T---P-V--V -.alpha.1 DOMAIN 10 20 30 40 50 60 70 80 90 .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. DR.beta. GDTRPRFLWQLKFECHFFNGTERVRLLERCIYNQEESVRFDSDVGEYRAVTELGRPDAEYWNS QKDLLEQRRAAVDTYCRHNYGVGESFTVQRR DQ.beta.1 R-SPED-VY-F-GL-Y-T-------GVT-H---R--Y--------V-----PQ---V----- ---EV--GA--S--RV-----E-AYRGIL--- DP.beta. RA-PENY-F-GRQ--YA----Q- F---Y---R--F---------F----------E----- ---I--EE--VP-RM-----EL-GPM-L--- DO.beta. T-SPED-VI-A-AD-Y-T----K-QFVV-F-F-L--Y--------MFV-L-K--Q----Q--- RL----RS-Q---GV-----RL-AP---G-K I-A.alpha. NSERH-VA---G--Y-T---Q-I-SVN-Y---R--W---------------------------PEI--RT--E ---V-----EGV-TH-SL-- I-E.alpha. R--P----EYVTS----Y---QH--F---F---R--NL---------------------N- ---PEI--DA--S---------EISDKFL-R-- -.alpha.2 DOMAIN 100 110 120 130 140 150 160 170 180 .vertline. .vertline. .vertline. .vertline . .vertline. .vertline. .vertline. .vertline. .vertline. DR.beta. VEPKVTVYPSKTQPLQHHNLLVCSVSGFYPGSIEVRWFRNGQEEKAGVVSTGLIQNGDWTFQT LVMLETVPRSGEVYTCQVEHPSVTSPLTVEW DQ.beta. T--IS--R-EA-N-----I---TD---SQ-K------D---T------P--R-------I-----MT-QR-D- ---H-----LQ--I---- DP.beta. Q-R-N-S---KG----------H-TD------Q----L-----T------N--R-------I-----MT-QQ- D--------T-LD--V---- DO.beta. Q-E-----ER-PL-HQ----H---T-----D-KIK--L-----R---M---P-R--------V----MT-EL- H----L-D-S-LL--VS--- I-A.alpha. EQ-N-AISL-R-EA-N---T-----TD---AK-K----------TV--S--Q--R------ -V-----MT-HQ------H-----LK--I---- I-E.alpha. T-----T-----E----------D----N---------K--ET-I-----VR-------------W--Q---- ---------L-D-V---- - CONNECTING PEPTIDE TRANSMEMBRANE REGION CYTOPLASMIC REGION 190 200 210 220 230 .vertline. .vertline. .vertline. .vertline. .vertline. DR.beta. RARSESAQSKM LSGVGGFVLGLLFLGAGLFI YFRNQKGHSGLQPTGFLS DQ.beta. Q-------- -----------I---L--I- RQ-SR- -L-H DP.beta. K-Q-D--R--T -T-A-------IIC-V-I-M HR-SK-VQR-SA DO.beta. Q--YSWR-- ---IAA-L---I--LV-IV- QL-A---YVRT-MS-NEVSRAVLLPQSC I-A.alpha. Q----R--- ---I--C---VI---L---- RH-S---PR-PP-A-L-Q I-E.alpha. K-Q-T---N-- -------------------- -------Q-E-----L--__________________________________________________________________________
It will be understood that this invention encompasses biochemical variants of class I and class II MHC domains. For example, following is a comparison of the polymorphic residues in DQ.alpha. first domain sequences. Numbers correspond to amino acid residues. Identity with the DR1 DQw1.1 sequence is indicated by a hyphen; parentheses mark deleted amino acids; and a blank space indicates that no sequence data are available. Paul, supra, at page 524.
__________________________________________________________________________ 11 18 25 26 34 40 41 45 47 48 50 51 52 53 54 55 61 64 66 69 75 76 80 - .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. - DR1 DQw1.1 C F Y T E E R A R W E F S K F G G R M A I M Y - DR2 DQw1.2 - - - - Q - - - - - - - - - - - - - - - - - - - DR2 DQw1.AZH - - - - Q - - - - - - - - - - - - - - - - - - - DRw6 DQw1.18 F - Q - K - - - - - - - - - - - - - - - - - DRw6 DQw1.19 - - Q - - - - - - - - - - - - - - - - - - - DRw8 DQ1 F - Q - K - - - - - - - - - - - - - - - - - DR3 DQw2 Y S - - Q G - V C L V L R Q R [ ] F T I L S L S - DR4 DQw3.1 Y S - S - - - V Q L L - R R R R F T I L - V S - DR4 DQw3.2 Y S - S - - - V Q L L - R R R R F T I L - V S - DR5 DQw3.1 Y S - - Q G - V C L V L R Q R [ ] F T I L S L S - DR9 DQw3 Y S - S - - - V Q L L - R R R R F T I L - V S - DR8 DQblank Y S - - Q G - V C L V L R Q R [ ] F T I T - L S__________________________________________________________________________
Similarly, following is a comparison of the polymorphic residues in DQ.beta. first domain sequences. Numbers correspond to amino acid residues. Identity with the DR1 DQw1.1 sequence is indicated by a hyphen, and a blank space indicates that no sequence data are available. Paul, supra, at page 525.
__________________________________________________________________________ 3 9 13 14 26 28 30 37 38 45 46 47 52 53 55 56 57 66 67 70 71 74 75 77 84 85 86 87 89 90 - .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. .vertline. - DR1 DQw1.1 S Y G L G T H Y V G V Y P Q R P V E V G A S V R E V A Y G - - DR2 DQw1.2 F - M L - Y - A - - - - - - - D - - - T E L T - - - F - - - DR2 DQw1.12 P L A M Y - Y D - - - - - - - - D D I R T E L T - - - F - - - DR2 DQw1.AZH - - - - - - - - - - - - - - - S - - - - - - - - - - - - - - DRw6 DQw1.18 L - - - A - - - - - - - D - - - T E L T - DRw6 DQw1.19 - - M L - - - A - - - - - - - - - - R T E L T - - - G - - - DR3 DQw2 M L S S I - - E F L L L - A D I R K A - - Q L E L T - - DR7 DQw2 - - M L S S I - - E F L L L - A D I R K A - - Q L E L T T - DR4 DQw3.1 - A M Y - Y - A E - - - L P - D - - R T E L T Q L E L T T - DR4 DQw3.2 - - M L - Y - A - - - - L P - A - - R T E L T Q L E L T T - DR5 DQw3.1 - A M Y - Y - A E - - - L P - D - - R T E L T Q L E L T T - DR9 DQw3.3 - - M L - Y - A - - - - L P - D - - R T E L T Q L E L T T - DR8 DQblank F - M - - Y - A - - - - L - L D D I E D - - T Q L E L T T__________________________________________________________________________
Genes encoding other MHC gene products can be determined from the physical map of the MHC gene complex for the mammalian species of interest.
9. Antibodies To Altered Determinants And Compositions Of The Invention
The altered MHC class I and class II determinants of the invention and compositions containing antigens bound to the determinants are useful for the preparation of antibodies that recognize these substances. The antibodies have diagnostic uses, application in mammalian therapy, and use in the study of MHC and cellular processes.
More particularly, polyclonal or monoclonal antibodies can be used in a variety of applications. Among these the neutralization of MHC gene products by binding to the gene products on cell surfaces. They can also be used to detect MHC gene products in biological preparations or in purifying corresponding MHC gene products or the altered MHC class I and class II determinants of the invention, such as by affinity chromatography.
Antibodies according to the present invention can be prepared by any of a variety of methods. For example, cells expressing an altered determinant or a functional derivative thereof can be administered to an animal in order to induce the production of sera containing polyclonal antibodies that are capable of binding the altered determinant. In addition, antibodies can be prepared to a variety of altered MHC class I and class II determinants of the invention and compositions containing antigens bound to the determinants in a similar manner.
In a preferred method, the antibodies are monoclonal antibodies, which can be prepared using hybridoma technology (Kohler et al., Nature 256:495 (1975); Kohler et al., Eur. J. Immunol. 6:511 (1976); Kohler et al., Eur. J. Immunol. 6:292 1976); Hammerling et al., In: Monoclonal Antibodies and T-Cell Hybridomas, Elsevier, N.Y., pp. 563-681 (1981)). In general, such procedures involve immunizing an animal with the altered MHC determinant or the altered MHC-antigen composition. Splenocytes of the animals are extracted and fused with a myeloma cell line. After fusion, the resulting hybridoma cells can be selectively maintained in HAT medium, and then cloned by limiting dilution as described by Wands, J. R., et al. Gastroenterology 80:225-232 (1981). The hybridoma cells obtained are then assayed to identify clones secreting antibodies capable of binding the altered MHC determinant or the composition.
See also 2,658,197 (A1) [90 01769], Feb. 14, 1990, "Restricted Monoclonal Antibodies That Recognize A Peptide That Is Associated With An Antigen Of A Major Histocompatibility Complex, Use In Diagnosis and Treatment," Huynh Thien Duc Guy, Pririe Rucay, Philippe Kourilsky; National Institute of Health and Medical Research.
The antibodies can be detectably labeled. Examples of labels that can be employed in the present invention include, but are not limited to, enzymes, radioisotypes, fluorescent compounds, chemiluminescent compounds, bioluminescent compounds and metal chelates.
Examples of enzymes include malate dehydrogenase, staphylococcal nuclease, delta-V-steroid isomerase, yeast alcohol dehydrogenase, alpha-glycerophosphate dehydrogenase, triose phosphate isomerase, biotin-avidin peroxidase, horseradish peroxidase, alkaline phosphatase, asparaginase, glucose oxidase, .beta.-galactosidase, ribonuclease, urease, catalase, glucose-VI-phosphate dehydrogenase, glucoamylase and acetylcholine esterase.
Examples of isotopes are .sup.3 H, .sup.125 I, .sup.32 P, .sup.35 S, .sup.14 C, .sup.51 Cr, .sup.36 Cl, .sup.57 Co, .sup.58 Co, .sup.59 Fe, and .sup.75 Se. Among the most commonly used fluorescent labeling compounds are fluoroscein, isothiocyanate, rhodamine, phycoerythrin, phycocyanin, allophycocyanin, o-phthaldehyde and fluorescamine.
Examples of typical chemiluminescent labeling compounds are luminal, isoluminol, theromatic acridinium ester, imidazole, acridinium salts, oxalate ester, and dioxetane.
Those of ordinary skill in the art will know of other suitable labels for binding to antibodies, or will be able to ascertain the same by the use of routine experimentation. Furthermore, the binding of these labels to antibodies can be accomplished using standard techniques commonly known to those of ordinary skill in the art. Bioluminescent compounds for purposes of labeling include luciferin, luciferase and aequorin.
The antibodies and antigen of the present invention are ideally suited for the preparation of a kit. Such kit may comprise a carrier means being compartmentalized to receive one or more container means, such as vials, tubes and the like, each of said container means comprising the separate elements of the assay to be used.
10. Diagnostic Applications
The altered MHC class I and class II determinants, compositions containing antigens bound to the altered determinants, and antibodies to these substances are useful in diagnostic applications. For example, the altered determinants can be used to target lymphocyte receptors, such as CD4.sup.+ and CD8.sup.+ receptors of T lymphocytes, and the resulting bound determinant can be assayed, for instance, by means of an antibody to the bound determinant. In addition, it will be understood that the altered MHC determinants of the invention can be labeled in the manner previously described for antibodies. In this case, the label on the altered MHC determinant can be detected and quantified. Compositions comprising an antigen bound to an altered determinant of the invention can be used in a similar manner with MHC-restricted receptors recognizing the antigen and the determinant.
Typical examples of assays based on the antibodies of the invention are radioimmunoassays (RIA), enzyme immunoassays (EIA), enzyme-linked immunosorbent assays (ELISA), and immunometric or sandwich immunoassays, including simultaneous sandwich, forward sandwich, and reverse sandwich immunoassays.
In the preferred mode for preforming the assays it is desirable to employ blockers in the incubation medium to assure that non-specific proteins, protease, or human antibodies to immunoglobulins present in the experimental sample do not cross-link or destroy the antibodies and yield false positive or false negative results. Nonrelevant (i.e. non-specific) antibodies of the same class or subclass (isotype) as those used in the assays (e.g. IgG, IgM, etc.) can be used as blockers. In addition, a buffer system should be employed. Preferred buffers are those based on weak organic acids, such as imidazole, HEPPS, MOPS, TES, ADA, ACES, HEPES, PIPES, TRIS, and the like, at physiological pH ranges. Somewhat less preferred buffers are inorganic buffers such as phosphate, borate or carbonate. Finally, known protease inhibitors can be added to the buffer.
Well known solid phase immunoadsorbents, such as glass, polystyrene, polypropylene, dextran, nylon and other materials, in the form of tubes, beads, and microtiter plates formed from or coated with such materials, can be employed in the present invention. Immobilized antibodies can be either covalently or physically bound to the solid phase immunoadsorbent by techniques, such as covalent bonding via an amide or ester linkage, or by adsorption.
11. Immunization and Therapeutic Administration
In another embodiment of this invention, the altered MHC class I and class II determinants and compositions containing antigens bound to the determinants and antibodies to these substances can be administered to a mammal to produce a therapeutic effect. For example, immune responses to self components represent a failure of immunological tolerance. As a result, clones of T cells and B cells emerge bearing receptors for self-antigens, which can lead to the production of self-directed antibodies, cytotoxic T cells, and inflammatory T cells. Such a breakdown in tolerance produces an autoimmune response that can cause autoimmune diseases. Administration of the altered determinants, compositions, or antibodies of the invention can intervene in these processes. Thus, for example, this invention can be utilized to treat T cell mediated autoimmune diseases, such as thyroiditis and multiple sclerosis.
This invention also provides altered MHC class I and class II determinants for use in therapeutic or vaccine compositions. Conventional modes of administration can be employed. For example, administration can be carried out by oral, respiratory, or parenteral routes. Intradermal, subcutaneous, and intramuscular routes of administration are preferred when the vaccine is administered parenterally.
The ability of the altered determinants and compositions of the invention to exhibit a therapeutic or immunizing effect can be enhanced by emulsification with an adjuvant, incorporation in a liposome, coupling to a suitable carrier, or even in cells, or by combinations of these techniques. For example, the altered determinants and compositions can be administered with a conventional adjuvant, such as aluminum phosphate and aluminum hydroxide gel, in an amount sufficient to mediate humoral or cellular immune response in the host. Similarly, these reagents can be bound to lipid membranes or incorporated in lipid membranes to form liposomes. The use of nonpyrogenic lipids free of nucleic acids and other extraneous matter can be employed for this purpose.
In addition, any of the common liquid or solid vehicles can be employed, which are acceptable to the host and do not have any adverse side effects on the host nor any detrimental effects on the reagents of the invention. Conveniently, phosphate buffered saline at a physiological pH can be employed as the carrier. One or more injections may be required, particularly one or two additional booster injections. It will be understood that conventional adjuvants, such as SAF-1, complete Freund's adjuvant and incomplete Freund's adjuvant, or oil-based adjuvants, such as mineral oil, can be administered with the reagents of the invention to elicit an increased antibody or cell-mediated immune response.
The immunization schedule will depend upon several factors, such as the susceptibility of the host and the age of the host. A single dose of the reagents of the invention can be administered to the host or a primary course of immunization can be followed in which several doses at intervals of time are administered. Subsequent doses used as boosters can be administered as needed following the primary course.
In an initial protocol, the mouse can be injected with about 10 to about 20 .mu.g of the altered MHC determinant of the invention per injection. The usual vaccine dosages can be employed in humans.
In addition to the antibodies produced for kits and diagnostic assays, antibodies of the present invention can be humanized by procedures well known in the art (using either chimeric antibody production or CDR grafting technology). U.S. Pat. No. 4,816,567 Cabilly et al., EPA 0120694 Publication No., assigned to Celltech, EPA 0173494 Publication No. assigned to Stanford University, and EPA 0125023 Publication No. assigned to Genentech, describing chimeric antibody procedures and EPA 0194276 Publication No. assigned to Celltech describing CDR grafting procedures.
The humanized antibodies would be prepared from antibodies obtained against specific MHC-antigen complexes. The humanized antibodies could then be used therapeutically in humans so as to avoid the problems associated with the use of non-human antibodies in human therapy.
This invention will now be described in greater detail in the following Examples.
EXAMPLE I
Engineering of Single-Chain Murine Class I Major Transplantation Antigen
Single-chain mouse K.sup.d molecules (SC-K.sup.d) were engineered by connecting residue 276 of K.sup.d heavy chain to the first residue of .beta..sub.2 -microglobulin through spacers of various lengths, and expressed intracellularly in monkey COS-1 cells. Labeled SC-K.sup.d molecules were found to react with several monoclonal antibodies, which recognize native K.sup.d molecules. SC K.sup.d -15 (with a spacer of 15 residues) was studied in more detail. It could be purified and shown to regain a native-like structure after treatment with denaturing agents. Purified SC-K.sup.d -15 could bind certain peptides in a manner qualitatively similar to that of K.sup.d.
Plasmid constructs
A full-length K.sup.d cDNA (Lalanne, J. -L., Delarbre, C., Gachelin, G., and Kourilsky, P., Nucleic Acids Res., 1983. 11:1567) was cut by Hind III (at the level of residue 276) and fused in phase, by a Gly--Gly coding linker, to .beta..sub.2 m cDNA (Daniel, F., Morello, D., LeBail, O., Chambon, P., Cayre, Y., and Kourilsky, P., EMBO J. 1983. 2:1061) in which a Bam HI site overlapping the first Ile codon of mature .beta..sub.2 m had been introduced by site-directed mutagenesis. The block was cloned in a mammalian expression vector, pKC3 (kindly provided by Dr. Hanahan, U.C.S.F.), which contains the SV40 promoter and origin of replication, yielding pSC-K.sup.d -2 (shown in Gene Constructs discussion, FIG. 5A). Synthetic linkers of different lengths were then ligated at the Bam HI site of pSC-K.sup.d -2 (FIG. 5B). For example, the SC-K.sup.d -15 liner was:
5' GATCGGATCCGGAGGCGGTGGATCCGGTGGCGGCGGTTC 3'
3' CCTAGGCCTCCGCCACCTAGGCCACCGCCGCCAAGCTAG 5'
Bam HI digestion of pSC-K.sup.d -15 and religation yielded pSC-K.sup.d -10. pSC-K.sup.d -13, -17, -19 and -21 were obtained by cloning the appropriate linkers into the Bam HI site of pSC-K.sup.d -10. All spacers and junctions were sequenced.
Transfection and immunoprecipitation
COS-1 cells (about 3.5.times.10.sup.6 cells in 60-mm plates) grown in DMEM supplemented with 10% newborn serum, penicillin, streptomycin and L-glutamine, were transfected one day after plating with 0.5 ml calcium phosphate mixture containing 5 .mu.g of CsCl-purified plasmid DNA. Transfection efficiencies were occasionally monitored with pCH110 plasmid expressing E. coli .beta.-galactosidase (Pharmacia, Uppsala, Sweden). Thirty-six hours after transfection, cells were radiolabeled with [.sup.35 S] methionine (45 .mu.Ci/plate=1.67 m Bq/plate) for 4 h at 37.degree. C., then washed once in PBS and collected in 1 ml lysis buffer (10 mM Tris-HCl, pH 7.4, 1 mM EDTA, 150 mM NaCl, 1% w/v NP40, BSA 10 mg/ml) containing 20 mM iodoacetamide and 1 IU/ml aprotinin. Lysates were precleared with protein A-Sepharose for 1 h at 4.degree. C., and SN were incubated for 18 h at 4.degree. C. with either 30 .mu.l of culture SN or 5 .mu.l of purified mAb and protein A-Sepharose. The beads were washed three times and the proteins were eluted in Laemmli buffer with 2-ME and analyzed by SDS-PAGE on 12% gels. Gels were fixed, treated with Amplify (Amersham Int., Amersham, GB), dried and visualized by autoradiography with use of Kodak (Rochester, N.Y.) XAR-X-ray film.
For endoglycosidase H (Endo H) treatments, samples were equilibrated in 0.5% SDS, 1 M 2-ME, boiled for 2 min., precipitated with 15% trichloroacetic, rinsed with acetone and resuspended in 50 .mu.l 50 mM sodium citrate, pH 5.5, 0.1% SDS, 20 mM2-ME. Endo H (Boehringer-Mannheim, Mannheim, FRG) was added to a final concentration of 150 mU/ml, samples were incubated at 37.degree. C. for 24 h, and then analyzed by SDS PAGE.
Immunoaffinity purification of SC-K.sup.d -15 protein
COS-1 cells (usually 10.sup.7 cells) were transfected with pSC-K.sup.d -15 DNA, labeled and lysed as above. SN were precleared with protein A-Sepharose for 1 h at 4.degree. C. then incubated for 18 h at 4.degree. C. with 100 .mu.l mAb 34.1.2 covalently bound to protein A beads. After the final wash in PBS, SC-K.sup.d -15 was eluted from the matrix with an equal volume of 3 M thiocyanate for 10 min on ice. After an overnight dialysis in PBS containing 0.1% NP40, 0.05% Tween and 0.2% BSA, SC-K.sup.d -15 was used in direct binding test as below. Its purity was assessed by SDS-PAGE.
Peptides and Peptide Binding Assays
Peptides used in this study are described in Choppin et al. (Choppin, J., Martinon, F., Gomard, E., Bahraoui, E., Connan, F., Bouillot, F., and Levy, J. -P, J. Exp. Med., 1990. 172:889 and references therein), except for HLA-Cw3 and HLA-A24 described in Maryanski, J. Ll, Pala, P., Cerottini, J. -C, and Corradin, G., J. Exp. Med. 1988. 167:1391. Binding assays were performed as described in Choppin, J., Martinon, F., Gomard, E., Bahraoui, E., Connan, F., Bouillot, F., and Levy, J. -P, J. Exp. Med., 1990. 172:889. DR3, DRw13, and K.sup.d molecules were also purified and iodinated as in Choppin, J., Martinon, F., Gomard, E., Bahraoui, E., Connan, F., Bouillot, F., and Levy, J. -P, J. Exp. Med., 1990. 172:889.
Gene Constructs
The C-terminal part of the K.sup.d heavy chain truncated in the hinge region was hooked to the N-terminal part of .beta..sub.2 -microglobulin with an appropriate spacer. From the 3-D structure of K.sup.d (Prochnicka-Chalufour, A., Casanova, J. -L, Kourilsky, P., and Claverie, J. -M, Res. Immunol., 1989. 140:133) modeled after the HLA-A2 structure of Bjorkmann et al. (Bjorkmann, P. J., Saper, M. A., Samraoui, B., Bennet, W. S., Strominger, J. L., and Wiley, D. C., Nature 1987. 329:506), the minimal length of a polyglycine type of spacer was estimated to be 11 residues, starting from residue 276 in the K.sup.d amino acid sequence (which allows the use of a convenient restriction site in the K.sup.d cDNA).
Two full-length cDNA clones encoding K.sup.d (Lalanne, J. -L, Delarbe, C., Gachelin, G., and Kourilsky, P., Nucleic Acids Res., 1983. 11:1567) and .beta..sub.2 -microglobulin (Daniel, F., Morello, D., LeBail, O., Chambon, P., Cayre, Y. and Kourilsky, P., EMBO J. 1983. 2:106) were connected by synthetic oligonucleotides encoding the spacers. The latter were designed as repeats of several glycines and one serine, (see discussion Plasmid Constructs). A series of pSC-K.sup.d -coding of cDNA with spacers of 2, 10, 13, 15, 17, 19 and 21 amino acid residues were thus obtained. The verified sequences are shown in FIG. 6.
Expression of SC-Kd in transfected monkey COS-1 cells
COS-1 cells (in which the recombinant plasmids replicate) were transiently transfected for 36 h and labeled with [.sup.35 ] methionine for 4 h. SC-K.sup.d molecules were not directly detectable by electrophoresis of SN or cell extracts. For immunoprecipitation, mAb 34-1-2 (Ozato, L., Mayer, N. and Sachs, D. H., Transplantation, 1982. 34:113), which reacts with native K.sup.d and D.sup.d.
SN contained 20-50 fold less immunoprecipitable material than cellular extracts. This is not unexpected because the K.sup.d heavy chain truncated at the level of the Hind III site is not secreted by COS-1 cells (Chambon, P., D.E.A.. thesis, University of Paris, 1987). In cellular extracts, bands corresponding to proteins with an apparent molecular mass of about 52 kDa were specifically precipitated, and their mobility decreased slightly as the length of the spacer increased (FIG. 6A, SC-K.sup.d -2,-10, -13,-17,-19,-21; for SC-K.sup.d -15, see FIG. 6B). No band was seen with mock-transfected cells and 34-1-2 (FIG. 8A, lanes NT and pKC), nor with transfected cells and an irrelevant antibody (F23, 1; FIG. 6B). After the results of Townsend et al. (Townsend, A., Ohlen, C., Bastin, J., Ljunggren, H. -G., Foster, L., and Karre, K., Nature 1989. 340:443) with the RMA-S mutant cell line, whether the addition of large amounts of an immunogenic peptide (influenza NPR.sup.-) was investigated and found to have no effect (FIGS. 6A and 6B). In much of the following work, SC-K.sup.d -15 was arbitrarily chosen as the prototype SC-K.sup.d molecule.
In separate studies using baculovirus vectors, it has been verified that 34-1-2 reacts very poorly with the K.sup.d heavy chain expressed in insect cells in the absence of mouse .beta..sub.2 -microglobulin (about 20- to 50-fold fold less than K.sup.d associated to .beta..sub.2 -microglobulin). Reactivity with 34-1-2 is thus a strong indication that K.sup.d heavy chain is properly associated with .beta..sub.2 -microglobulin. To probe other parts of the K.sup.d molecule, other K.sup.d -specific mAb (97-G and 20-8-4 (Ozato, L., Mayer, N. and Sachs, D. H., Transplantation, 1982. 34:113 and Rebai, N., Mercier, P., Kristensen, T., Devaux, C., Malissen, B., MAwas, C., and Pierres, M., Immunogenetics 1983. 17:57) were used and identical results were obtained. As an example, the SC-K.sup.d -2 and SC-K.sup.d -15 bands precipitated by mAb 20-8-4 are shown in FIG. 6B. The exact specificity of 97-G is not known, but the epitope recognized by 20-8-4 has been shown to include residues 82 and 89 belonging to the first domain of K.sup.d (Abastado, J. -P., Jaulin, C., Schutze, M. -P., Langlade-Demoyen, P., Plata, F., Ozato, K., and Kourilsky, P., J. Exp. Med. 1987. 166:327. Thus, this epitope is properly folded in SC-K.sup.d -2 and SC-K.sup.d -15 (as well as in other SC-K.sup.d molecules.
The state of glycosylation of intracellular SC-K.sup.d -15 was assessed by treatment with Endo H. The molecule appears to be fully Endo H sensitive (FIG. 6C) and, after treatment, its apparent molecular mass is about 45 kDa, which fits the expected molecular mass of non-glycosylated SC-K.sup.d -15 devoid of its signal peptide (390 amino acids). These results suggest that most of the SC-K.sup.d -15 molecules are found in the endoplasmic reticulum in a high-mannose form.
With all three mAb, the precipitated SC-K.sup.d -2 band was always 5-10 fold less intense than that obtained with SC-K.sup.d molecules with longer spacers. However, the Gly--Gly spacer is unlikely to allow proper association of .beta..sub.2 -microglobulin to the heavy chain. A 12-kDa band, presumably monkey .beta..sub.2 -microglobulin, is co-precipitated in relatively much higher amounts with SC-K.sup.d -2 than with other SC-K.sup.d (FIG. 6D). This suggests that monkey .beta..sub.2 -microglobulin may associate better with SC-K.sup.d -2 than with other SC-K.sup.d where the longer spacer permits proper folding of the murine .beta..sub.2 -microglobulin over the K.sup.d heavy chain, which could explain the detection of some SC-K.sup.d -2 molecules. In any case, monkey .beta..sub.2 -microglobulin does not play a compulsory role in the folding of SC-K.sup.d -15 since it has been possible to produce immunoprecipitable SC-K.sup.d -15 in insect cells infected by a recombinant baculovirus.
Purification and peptide binding
The reactivity of SC-K.sup.d molecules with three distinct mAb provided evidence for their native-like character Nevertheless, it was necessary to purify these molecules, check their ability to fold back after treatments which separate heavy chain from .beta..sub.2 m, and finally test whether they were able to bind peptides.
A solid-phase matrix, made of 34-1-2 coupled to protein A beads, was used to purify .sup.35 S-labeled SC-K.sup.d -15 from lysates of transiently transfected COS-1 cells. Treatment with 3 M sodium thiocyanate eluted the protein with a reasonable yield (about 70%) as assessed by a second immunoprecipitation with 34-1-2. After electrophoresis, the purified material ran as a single 52-kDa band. This confirmed that reactivity with 34-1-2 can be regained in the absence of detectable monkey .beta..sub.2 -microglobulin. This eluting treatment would normally dissociate heavy chain from .beta..sub.2 -microglobulin (Elliott, T., and Eisen, H. N., Proc. Natl. Acad. Sci., USA 1990. 87:5213). In addition 6 M urea was also used with similar results (not shown).
K.sup.d molecules isolated from the spleen of BALB/c mice were then purified and iodinated. They were purified by affinity chromatography on a 20-8-4 mAb column and compared binding of peptides by the latter and by .sup.35 S-labeled SC-K.sup.d -15 in the assay of Bouillot et al. (Bouillot, M., Choppin, J., Cornille, F., Martinon, F., Papo, T., Gomard, E., Fournie-Zaluski, M. -C., and Levey, J. -P., Nature 1989. 339:473 and Choppin, J., Martinon, F., Gomard, E., Bahraoui, E., Connan, F., Bouillot, F., and Levy, J. -P, J. Exp. Med., 1990. 172:889).
Two peptides from HIV viral proteins (env 312-327 and vpr 68-80), known to bind strongly to several MHC molecules (Choppin, J., Martinon, F., Gomard, E., Bahraoui, E., Connan, F., Bouillot, F., and Levy, J. -P, J. Exp. Med., 1990. 172:889), showed significant binding to SC-K.sup.d -15 as well as to the HLA-DR3 or DR213 positive control (Table 10; results shown in duplicate). In a separate experiment, the binding of SC-K.sup.d -15) and that of conventional K.sup.d were compared (Table 10). As above, peptide env 312-327 was found to bind to both molecules, but three peptides known to be immunogenic (HLA-A24 170-182, HLA-Cw3 170-182 and influenza NPR- 147-158; (Maryanski, J. L., Pala, P., Cerottini, J. -C. and Corradin, G., J. Exp. Med. 1988. 167:1391 and Bodmer, H. C., Pemberton, R. M., Rothbard, J. B., Askonas, B. A., Cell 1989. 52:253), showed no detectable binding, either to the SC-K.sup.d nor to the K.sup.d molecules. In a competition experiment in which the env 312-327 peptide is bound to plastic, it was seen that the vpr 68-80 peptide competed efficiently, while the Cw3 170-182 peptide (which did not bind in the direct assay) did not. In summary, SC-K.sup.d -15 bound in the HIV peptides env 312-327 and vpr 68-80 to a significant extent, albeit somewhat less efficiently than conventional K.sup.d (but the optimal conditions may be different for K.sup.d and SC-K.sup.d -15 and efforts have not been made to optimize binding to SC-K.sup.d -15 at this stage).
There was no detectable binding of three immunogenic peptides neither to SC-K.sup.d -15 nor to K.sup.d. It is possible that these peptides bind much less efficiently than the two above-described HIV peptides and that the assay, as carried out here, is not sensitive enough to detect binding. Similar observations have been made before (Choppin, J., Martinon, F., Gomard, E., Bahraoui, E., Connan, F., Bouillot, F., and Levy, J. -P, J. Exp. Med., 1990. 172:889).
In conclusion, not ignoring the difficulties associated with the interpretation of such peptide binding experiments, this example demonstrates that the behavior of SC-K.sup.d -15 is qualitatively similar to that of conventional K.sup.d. This is clear preliminary evidence that SC-K.sup.d -15 is capable of binding peptides in a manner similar to that of K.sup.d.
In conclusion, this example demonstrates the engineering of single-chain K.sup.d molecules which so far display the expected properties with respect to (a) reactivity with three mAb, one of which probes proper association with .beta..sub.2 -microglobulin and another one an epitope belonging to the first domain, (b) efficient refolding upon treatment with 3 M sodium thiocyanate or 6 M urea, and (c) binding of certain peptides. Above 10 residues or so, the length of the spacer between K.sup.d heavy chain and murine .beta..sub.2 -microglobulin does not seem critical. All experiments described have been performed with trace amounts of metabolically labeled SC-K.sup.d molecules. Production in large amounts should yield material useful for peptide and TcR binding studies.
TABLE 10______________________________________Binding of peptides to purified MHC molecules.sup.1/ .sup.35 S-labeled .sup.125 I-labeled SC-Kd HLA-DR3/DRw13______________________________________(A) Input (cpm) 10,000 200000/200000 nef 66-80 475 2325/1388 (30 .mu.g/ml; pH 9.6) 397 1822/1290 env 312-327 750 6782/19957 (30 .mu.g/ml; pH 9.6) 712 3778/22637 vpr 68-80 710 18582/21838 (10 .mu.g/ml, pH 5) 621 18245/20593______________________________________
.sup.1/ Experiments were carried out in duplicate.
______________________________________ .sup.35 S-labeled .sup.125 I-labeled SC-Kd H-2K______________________________________(B) Input (cpm) 6000 100000 No coated peptide 228 1471 223 1595 A24 170-182 284 1060 (10 .mu.g/ml; pH 9.6) 229 1302 Cw3 170-182 169 1340 (10 .mu.g/ml; pH 9.6) 117 1384 NPR 147-158 214 1257 (10 .mu.g/ml; pH 9.6) 171 1259 env 312-327 390 13772 (5 .mu.g/ml; pH 9.6) 377 13764 env 312-327 42 359 + vpr 68-80 41 409 env 312-327 367 15378 + Cw3 170-182 375 15835______________________________________
EXAMPLE II
Preparation of an HLA-.beta.2-Microglobulin (MHC Class I) Peptide Complex
The "empty" (i.e. devoid of peptide) MHC class I molecule is produced in vast amounts in the periplasm of the E. coli strain harboring the recombinant plasmid. Inclusion bodies can be isolated, washed briefly in 6 M urea, and then dissolved in 8 M urea, or 6 M urea+3 M isothiocyanate. The solubilized MHC class I molecules are then mixed with a 100 fold (or more) molar excess of a peptide specifically presented by HLA-A2 or MHC class I, such as Influenza virus or HIV peptides described as optimal nonapeptides by Falk et al. (Nature (1991) 351, 290). The MHC class I peptide mixture in a dialysis bag is then dialyzed in a small volume of 6 M urea plus peptide, then 4 M urea plus peptide, then 2 M urea plus peptide, then large volumes of buffer. The MHC class I peptide complex is then purified by conventional methods (such as those described in "Protein Purification Applications", Harris E. L. V. & Angal S. (Eds.) IRL Press, Oxford, 1990).
EXAMPLE III
Immunization
For immunization, the complex is usually coupled to a protein carrier, as it is done for synthetic vaccines. Usual vaccination protocols (with several immunizations and a recall injection) should be used. The antibody response should be mainly focussed on the peptide presented by the SC-A2 molecule. In a typical experiment, mice will be injected on the base of the tail of 100 .mu.l of complete Freund adjuvant together with 100 .lambda. of the SC-A2 peptide complex itself coupled to a carrier such as ovalbumin of KLM. Immunization is repeated once or twice, in the following weeks. One month later, mice are boosted and the response is tested.
EXAMPLE IV
Identification and Sequencing of T-cell Region Capable of Binding HLA-A2-.beta.2 Microglobulin
The sequences disclosed by the invention in Examples I and II provide for a method of identifying the interaction responsible for the T-cell recognition of HLA-A.sub.2 -.beta..sub.2 -microglobulin (MHCI).
In detail, using the sequences disclosed in Examples I and II, it is possible to isolate the proteins which bind to these sequences. This is accomplished using one of the methods of purifying a protein which binds to a specific DNA sequence. Such procedures are well known in the art. Preferably, a protein which binds to a specific DNA sequence can be purified using affinity chromatography.
Specifically the amino acid sequence corresponding to the HLA-A.sub.2 -.beta..sub.2 -microglobulin binding domain is immobilized on an appropriate matrix, such as Sepharose, and used as an affinity matrix for the purification of the proteins which bind to the particular sequence (Arcangioli B, et al., Eur. J. Biochem. 179:359-364 (1989).
Preferably the DNA binding protein is extracted from human T-cells. The protein extract, obtained from the T cell is applied to a column which contains the immobilized DNA sequence of interest. Proteins which are not capable of binding to the DNA sequence are washed off the column. Proteins which bind to the DNA sequence are removed from the column using a salt gradient. The proteins eluted from such a column are enriched for the proteins which bind to the specific DNA sequences immobilized on the matrix. The DNA binding protein can then be further purified using procedures known in the art such as ion exchange chromatography, high performance liquid chromatography, and size exclusion chromatography.
During the purification of the DNA binding protein, the protein can be assayed using a gel retardation assay. (Garner, M. M. et al., Nucl. Acid Res. 9:3047 and Fried, M. et al., Nucl. Acid Res. 9:6506 (1981).
Once the DNA binding protein has been purified, a partial amino acid sequence can be obtained from the N-terminal of the protein. Alternatively, the protein can be tryptically mapped and the amino acid sequence at one of the fragments can be determined by one of the methods known in the art.
The deduced amino acid sequence can be used to generate an oligonucleotide probe. The encoding sequence can be based on codons which are known to be more frequently used by the organism. Alternatively, the probe can consist of a mixture of all the possible codon combinations which could encode the polypeptide.
A probe complementary to the amino acid sequence can be used to screen either a cDNA or genomic library for the genomic sequences which encode the DNA binding protein. Once the gene encoding the DNA binding protein has been obtained, the sequence of the DNA can be determined, the gene can be used to obtain large amounts of the protein from a recombinant host, or the sequence can be used in mutational analysis to further define the functional regions within the protein which interacts with the DNA.
Alternatively, proteins which bind to T-cell epitope can be isolated by identifying a clone expressing the protein using the technique of Southwestern blotting (Sharp, Z. D. et al., Biochim Biophys Acta, 1048:306-309 (1990), Gunther, C. V. et al., Genes Dev. 4:6657-679 (1990), and Walker, M. D. et al., Nucleic Acids Res. 18:1159-1166 (1990)).
In a Southwestern blot, a labeled DNA sequence is used to screen a cDNA expression library whose expressed proteins have been immobilized on a filter via colony or plaque transfer. The labeled DNA sequences will bind to colonies or plaques which express a protein capable of binding to the particular DNA sequence. Clones expressing a protein which binds to the labeled DNA sequence can be purified and the cDNA insert which encodes the DNA binding protein can be isolated sequenced. The isolated DNA can be used to express large amounts of the protein for further purification and study, used in isolating the genomic sequences corresponding to the cDNA, or used to generate functional derivative of the binding protein.
EXAMPLE V
Cell Activation Due to Recognition of the Antigenic CW3 Peptide Presented by the Altered MHC K.sup.d determinant
Specific interactions between the T-cell receptor (TCR) and the peptide-MHC complex were studied using a very sensitive functional assay. The test results showed that the peptide-MHC complex formed with the altered K.sup.d is biologically functional. Further, the complex is not only capable of interacting with and being recognized by the TCR in a specific manner, but is also capable of triggering a cellular response.
The functional assay employed below was developed in light of several observations. The different chains constituting the TCR complex share a number of salient characteristics with the immunoglobulin family. Namely, they are organized into functional domains, and the domains carry out their functions independently of each other. Hence, the association of two different domains gives rise to the accumulation of the two functions. A schematic representation of the TCR .alpha./.beta. chains and the associated components of the CD3 complex is shown in FIG. 7.
In the case of the .alpha./.beta. chains of the TCR, the variable domain, V.alpha./V.beta., is responsible for the specific interaction with and the recognition of the peptide-MHC complex. Concerning the .xi. chain of the CD3 complex, the cytoplasmic domain transduces the signal from the TCR ectodomain to the inside of the cell, where it sets off a cascade of intracellular events. The transmembrane domain on the .xi. chain, on the other hand, regulates the levels of the TCR complex that reach the cell surface. Thus, in forming a complex with the TCR .alpha. and .beta. chains, the .xi. chain stabilizes the complex and permits its export to the surface.
For further discussion see, Irving et al., (1991) Cell 64, 891-901; and Romeo et al., (1991) Cell 64, 1037-1046. In addition, Letourneur et al., ((1991) PNAS, USA 88, 8905-8909) show that when the cytoplasmic domain of .xi. is attached to heterologous proteins such as CD4 and CD8, the cytoplasmic domain of .xi. is sufficient for inducing cell activation when the extracellular domains of CD4 or CD8 are cross-linked by antibodies against CD4 or CD8. Engel et al., ((1992) Science 256, 1318-1321) demonstrate that when the transmembrane and cytoplasmic domains of the CD3 .xi. chain are attached to the extracellular domains of the TCR .alpha. and .beta. chains, the cytoplasmic domain of .xi. can induce cell activation when the .alpha./.beta. extracellular domains bind to the antigen-MHC determinant or are cross-linked by an antibody against the TCR.
Chimeric TCRs were constructed by attaching the transmembrane and cytoplasmic domains of the CD3 .xi. chain to domains of the TCR .alpha. and .beta. chains. As the .xi. chain, when attached to heterologous proteins, induces dimerization and export of the dimer to the cell surface, the .xi. chain was attached to the extracellular domains of the .alpha. and .beta. chains as shown in FIG. 8. The nucleotide sequence for the .alpha./.beta. chains was derived from the TCR of a murine cytotoxic CD8+ clone (CW3/1.1) specific for an HLA CW3 peptide (amino acids 170-179). This TCR recognizes the CW3 peptide when it is presented by the MHC molecule, K.sup.d (for a complete description of this cytotoxic clone, see Pala et al. (1988) J. Immunol. 140: 871-877). The detailed sequences of the .alpha./.beta. chains is shown in FIGS. 9a and 9b.
All chimeras .alpha.-.xi./.beta.-.xi. were constructed by the polymerase chain reaction (PCR). PCR products were directly cloned into the expression vector pCDL-SR.alpha.296, and their sequence was confirmed by complete DNA sequencing. Construction of the chimeric protein in the expression vector pCDL-SR.alpha.296 is shown in FIG. 10.
Chimeric constructs were stably transfected into the rat basophilic leukemia line, RBL-2H3. Cells were harvested by trypsinisation and resuspended in complete media (DMEM), 10% fetal calf serum, 20 mM Hepes, 2mM glutamine, penicillin (100 U/ml), streptomycin (100 .mu.g/ml), and gentamicin (150 .mu.g/ml), to a concentration of 1.times.10.sup.7 cells per 0.25 ml of culture media. Cells were transfected with 20 .mu.g of Sal I-linearised DNA, consisting of 10 .mu.g of the CW3 1.1 .alpha. and 10 .mu.g of the CW3 1.1 .beta. constructs; to this were added 2 .mu.g of pfneo linearised by EcoRI, which was used to confer resistance to G418 (Geneticin, Gibco). A charge of 250 V and 450 .mu.F was applied at room temperature with a gene electroporator, and after a 10 min recovery period the cells were put into culture. Selection with active G418 (0.5 mg/ml) was begun after 18 to 24 hours, and the concentration was increased to 1 mg/ml 2 to 4 days later.
Cell activation was induced in the transfected RBL cells and resulted in the secretion of serotonin. Transfected RBL cells that expressed the TCR .alpha.-.xi./.beta.-.xi.0 heterodimer on their cell surface were cultured for 24 hours in complete media at 4.times.10.sup.4 cells/200 .mu.l per well in 96-well flat-bottom plates (Costar) with [.sup.3 H]Serotonin (Dupont) at a final concentration of 2 .mu.Ci/ml (0.2 .mu.Ci per well).
For studies involving cell activation by antibody, cells were washed twice with medium and incubated for 1 hr at 37.degree. C. with serial dilutions of monoclonal antibody (mAb) H57-197 (anti-TCR .alpha./.beta.) or mAb 145-2C11 (anti-CD3). Monoclonal antibodies H57-197 (anti-TCR .alpha./.beta.) and 145-2C11 (anti-CD3) are available from PharMingen (San Diego, Calif.) (Cat. Nos. 01301D and 01081D, respectively).
Following centrifugation, the [.sup.3 H]serotonin levels in the supernatant were measured by counting the radioactivity of 100 .mu.l aliquots from each well using a Packard liquid scintillation counter.
Cell activation was also studied by incubating washed cells for 1 hr at 37.degree. C. with serial dilutions of one of the following: (i) altered K.sup.d molecule complexed with CW3 peptide; (ii) altered K.sup.d molecule complexed with an irrelevant peptide (Y81); or (iii) altered K.sup.d molecule complexed with the SF1-1.1.1 antibody (anti-K.sup.d) and either the CW3 peptide or the Y81 peptide. (The sequence of peptides CW3 and Y81 are shown in FIG. 11.) After incubating for 1 hr, the percentage of serotonin released into the culture medium was measured as described above.
When the .alpha./.beta. chains were cross-linked using the monoclonal antibody H57-197, which is directed against the TCR, the transfected cells secreted serotonin as shown in FIG. 12. As expected, an antibody against the CD3 complex had no effect on RBL-2H3 degranulation. However, neither soluble K.sup.d molecules loaded with the CW3 peptide nor with a peptide derived from Plasmodium berghei (Y81, a negative control) had an effect on cell activation (FIG. 12). This lack of effect of the soluble K.sup.d was overcome when K.sup.d was incubated with the RBL-2H3 cells in the presence of SF1-1.1.1, a monoclonal antibody specific for a region of K.sup.d that does not interfere with TCR interaction. Monoclonal antibody SF1-1.1.1 (anti-K.sup.d) is available from the American Type Culture Collection (Rockville, Md.) (Cat. No. HB158). Thus, a bivalent K.sup.d /SF1-1.1.1 complex, formed from the co-incubation of K.sup.d and SF1-1.1.1 at a concentration ratio of 5 to 1, was able to trigger serotonin release (FIG. 13). Furthermore, the effect is specific, since cells are activated if the K.sup.d is preloaded with CW3, but not when K.sup.d is preloaded with Y81. FIG. 14 shows the concentration dependence of the RBL-2H3 stimulation when K.sup.d and SF1-1.1.1 are co-incubated at a molar ratio of 2 to 1.
The experimental results described above demonstrate that the peptide-MHC complex formed with the single-chain K.sup.d molecule is biologically functional, in the sense that it is recognized by a TCR in the same manner as the native MHC molecule loaded with the right peptide. In addition, the recognition event retains the same specificity as expected for the TCR sequence used. Thus, the peptide/MHC complex is properly recognized when the recombinant K.sup.d protein is loaded with the CW3 peptide, but not when it is loaded with another peptide that is capable of binding to K.sup.d but which was not used for generating the specific CTL clone. Since a bivalent peptide/MHC complex was required to trigger a response of the TCR-transfected cells, any approach in which multivalent K.sup.d structures are formed, such as recombinant techniques linking the K.sup.d proteins through covalent bonds or latex beads to which monovalent K.sup.d proteins could be absorbed, would be expected to stimulate the cells in a comparable manner. Finally, the specific interaction between the CW3/K.sup.d -specific TCR leads to activation of the transfected cells, presumably through the .xi. chains attached to the extracellular .alpha./.beta. domains of the TCR. Hence, both the single-chain MHC protein and the .alpha.-.xi./.beta.-.xi. TCR heterodimer are biochemically and biologically functional in every sense of the word. The recombinant proteins described herein should therefore be useful in therapeutic strategies in which specific immune responses are required.
While this invention has been described in connection with specific embodiments thereof, it will be understood that it is capable of further modifications and this application is intended to cover variations, uses, or adaptations of the invention following, in general, the principles of the invention and including such departures from the present disclosure as come within the art to which the invention pertains and as may be applied to the essential features hereinbefore set forth as follows in the scope of the appended claims.
__________________________________________________________________________# SEQUENCE LISTING - - - - (1) GENERAL INFORMATION: - - (iii) NUMBER OF SEQUENCES: 127 - - - - (2) INFORMATION FOR SEQ ID NO:1: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 18 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1: - - AAGCTGGGGG GGATCCAG - # - # - # 18 - - - - (2) INFORMATION FOR SEQ ID NO:2: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 6 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2: - - Lys Leu Gly Gly Ile Gln 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:3: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 42 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3: - - AAGCTGGGGG GGATCGGATC CGGTGGCGGC GGTTCGATCC AG - # - # 42 - - - - (2) INFORMATION FOR SEQ ID NO:4: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4: - - Gly Gly Ile Gly Ser Gly Gly Gly Gly Ser 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:5: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 51 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5: - - AAGCTGGGGG GGATCGGATC AGGCGGATCC GGTGGCGGCG GTTCGATCCA G - # 51 - - - - (2) INFORMATION FOR SEQ ID NO:6: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 13 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6: - - Gly Gly Ile Gly Ser Gly Gly Ser Gly Gly Gl - #y Gly Ser 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:7: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 57 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7: - - AAGCTGGGGG GGATCGGATC CGGAGGCGGT GGATCCGGTG GCGGCGGTTC GA - #TCCAG 57 - - - - (2) INFORMATION FOR SEQ ID NO:8: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8: - - Gly Gly Ile Gly Ser Gly Gly Gly Gly Ser Gl - #y Gly Gly Gly Ser 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:9: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 63 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9: - - AAGCTGGGGG GGATCGGATC AGGCTCTGGA GGTGGCGGAT CCGGTGGCGG CG -#GTTCGATC 60 - - CAG - # - # - # 63 - - - - (2) INFORMATION FOR SEQ ID NO:10: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 17 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:10: - - Gly Gly Ile Gly Ser Gly Ser Gly Gly Gly Gl - #y Ser Gly Gly Gly Gly 1 5 - # 10 - # 15 - - Ser - - - - (2) INFORMATION FOR SEQ ID NO:11: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 69 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11: - - AAGCTGGGGG GGATCGGATC AGGTGGAGGA TCTGGAGGTG GCGGATCCGG TG -#GCGGCGGT 60 - - TCGATCCAG - # - #- # 69 - - - - (2) INFORMATION FOR SEQ ID NO:12: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 19 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:12: - - Gly Gly Ile Gly Ser Gly Gly Gly Ser Gly Gl - #y Gly Gly Ser Gly Gly 1 5 - # 10 - # 15 - - Gly Gly Ser - - - - (2) INFORMATION FOR SEQ ID NO:13: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 75 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:13: - - AAGCTGGGGG GGATCGGATC AGGCGGAGGT GGAGGATCTG GAGGTGGCGG AT -#CCGGTGGC 60 - - GGCGGTTCGA TCCAG - # - # - # 75 - - - - (2) INFORMATION FOR SEQ ID NO:14: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 21 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:14: - - Gly Gly Ile Gly Ser Gly Gly Gly Gly Gly Se - #r Gly Gly Gly Gly Ser 1 5 - # 10 - # 15 - - Gly Gly Gly Gly Ser 20 - - - - (2) INFORMATION FOR SEQ ID NO:15: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 39 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:15: - - GATCGGATCC GGAGGCGGTG GATCCGGTGG CGGCGGTTC - # - # 39 - - - - (2) INFORMATION FOR SEQ ID NO:16: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 39 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:16: - - GATCGAACCG CCGCCACCGG ATCCACCGCC TCCGGATCC - # - # 39 - - - - (2) INFORMATION FOR SEQ ID NO:17: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 45 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 1..45 (xi) SEQUENCE DESCRIPTION: SEQ ID NO:17: - - GGT GGC GGT GGA TCA GGC GGT GGT GGG TCG GG - #T GGC GGC GGA TCC - #45 Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gl - #y Gly Gly Gly Ser 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:18: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:18: - - Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Gl - #y Gly Gly Gly Ser 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:19: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 12 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:19: - - Lys Gly Ile Leu Gly Phe Val Phe Thr Leu Th - #r Val 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:20: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 13 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:20: - - Tyr Lys Gly Ile Leu Gly Phe Val Phe Thr Le - #u Thr Val 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:21: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 11 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:21: - - Thr Tyr Gln Arg Thr Arg Ala Leu Val Thr Gl - #y 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:22: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 16 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:22: - - Ser Ala Ala Phe Glu Asp Leu Arg Val Leu Se - #r Phe Ile Arg Gly Tyr 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:23: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 13 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:23: - - His Asn Thr Asn Gly Val Thr Ala Ala Cys Se - #r His Glu 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:24: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 25 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:24: - - Cys Pro Lys Tyr Val Lys Gln Asn Thr Leu Ly - #s Leu Ala Thr Gly Met 1 5 - # 10 - # 15 - - Arg Asn Val Pro Glu Lys Gln Thr Arg 20 - # 25 - - - - (2) INFORMATION FOR SEQ ID NO:25: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 16 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:25: - - Asn Thr Asp Gly Ser Thr Asp Tyr Gly Ile Le - #u Gln Ile Asn Ser Arg 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:26: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:26: - - Leu Glu Asp Ala Arg Arg Leu Lys Ala Ile Ty - #r Glu Lys Lys Lys 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:27: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 16 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:27: - - Arg Tyr Leu Glu Asn Gly Lys Glu Thr Leu Gl - #n Arg Thr Asp Ala Pro 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:28: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:28: - - Leu Glu Thr Ser Glu Gly Cys Arg Gln Ile Le - #u Gly Gln Leu Gln 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:29: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:29: - - Glu Thr Ile Asn Glu Glu Ala Ala Glu Trp As - #p Arg Val His Pro 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:30: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:30: - - His Ala Gly Pro Ile Ala Pro Gly Gln Met Ar - #g Glu Pro Arg Gly 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:31: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:31: - - Lys Arg Trp Ile Ile Leu Gly Leu Asn Lys Il - #e Val Arg Met Tyr 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:32: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 14 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:32: - - Met Gln Arg Gly Asn Phe Arg Asn Gln Arg Ly - #s Ile Val Lys 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:33: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 16 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:33: - - Lys Glu Gly His Gln Met Lys Asp Cys Thr Gl - #u Arg Gln Ala Asn Phe 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:34: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 13 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:34: - - His Glu Asp Ile Ile Ser Leu Trp Asp Gln Se - #r Leu Lys 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:35: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 16 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:35: - - Ile Arg Ile Gln Arg Gly Pro Gly Arg Ala Ph - #e Val Thr Ile Gly Lys 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:36: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 18 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:36: - - Phe Ile Asn Met Trp Gln Glu Val Gly Lys Al - #a Met Tyr Ala Pro Pro 1 5 - # 10 - # 15 - - Ile Ser - - - - (2) INFORMATION FOR SEQ ID NO:37: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 16 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:37: - - Arg Pro Gly Gly Gly Asp Met Arg Asp Asn Tr - #p Arg Ser Glu Leu Tyr 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:38: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 12 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:38: - - Val Val Gln Arg Glu Lys Arg Ala Val Gly Il - #e Gly 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:39: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 21 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:39: - - Arg Ile Leu Ala Val Glu Arg Tyr Leu Lys As - #p Gln Gln Leu Leu Gly 1 5 - # 10 - # 15 - - Ile Trp Gly Cys Ser 20 - - - - (2) INFORMATION FOR SEQ ID NO:40: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 18 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:40: - - Tyr Val Ala Glu Gly Thr Asp Arg Val Ile Gl - #u Val Val Gln Gly Ala 1 5 - # 10 - # 15 - - Cys Arg - - - - (2) INFORMATION FOR SEQ ID NO:41: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:41: - - Arg His Ile Pro Arg Arg Ile Arg Gln Gly Le - #u Glu Arg Ile Leu 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:42: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:42: - - Val Gly Phe Pro Val Thr Pro Gln Val Pro Le - #u Arg Pro Met Thr 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:43: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 16 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:43: - - Met Thr Tyr Lys Ala Ala Val Asp Leu Ser Hi - #s Phe Leu Lys Glu Lys 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:44: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 16 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:44: - - Trp Ile Tyr His Thr Gln Gly Tyr Phe Pro As - #p Trp Gln Asn Tyr Thr 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:45: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 16 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:45: - - Gly Val Arg Tyr Pro Leu Thr Phe Gly Trp Cy - #s Tyr Lys Leu Val Pro 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:46: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 9 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:46: - - Leu Thr Phe Gly Trp Cys Tyr Lys Leu 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:47: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:47: - - Glu Asn Thr Ser Leu Leu His Pro Val Ser Le - #u His Gly Met Asp 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:48: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:48: - - Met Glu Asn Arg Trp Gln Val Met Ile Val Tr - #p Gln Val Asp Arg 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:49: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 16 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:49: - - Val Lys His His Met Tyr Val Ser Gly Lys Al - #a Arg Gly Trp Phe Tyr 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:50: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:50: - - Ser Pro His Pro Arg Ile Ser Ser Glu Val Hi - #s Ile Pro Leu Gly 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:51: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 13 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:51: - - Gly Asp Ala Arg Leu Val Ile Thr Thr Tyr Tr - #p Gly Leu 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:52: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 15 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:52: - - Gly Leu His Thr Gly Glu Arg Asp Trp His Le - #u Gly Gln Gly Val 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:53: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 16 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:53: - - Met Ala Gly Arg Ser Gly Asp Ser Asp Glu As - #p Leu Leu Lys Ala Val 1 5 - # 10 - # 15 - - - - (2) INFORMATION FOR SEQ ID NO:54: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 13 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:54: - - Leu Ile Lys Phe Leu Tyr Gln Ser Asn Pro Pr - #o Pro Asn 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:55: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 14 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:55: - - Ala Arg Arg Asn Arg Arg Arg Arg Trp Arg Gl - #u Arg Gln Arg 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:56: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 14 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:56: - - Met Glu Gln Ala Pro Glu Asp Gln Gly Pro Gl - #n Arg Glu Pro 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:57: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 14 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:57: - - Ala Gly Val Ala Glu Ile Ile Arg Ile Leu Gl - #n Gln Leu Leu 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:58: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 13 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:58: - - Leu Phe Ile His Phe Arg Ile Gly Cys Arg Hi - #s Ser Arg 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:59: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 98 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:59: - - Ile Gln Lys Thr Pro Gln Ile Gln Val Tyr Se - #r Arg His Pro Pro Glu 1 5 - # 10 - # 15 - - Asn Gly Lys Pro Asn Ile Leu Asn Cys Tyr Va - #l Thr Gln Phe His Pro 20 - # 25 - # 30 - - Pro His Ile Glu Ile Gln Met Leu Lys Asn Gl - #y Lys Lys Ile Pro Lys 35 - # 40 - # 45 - - Val Glu Met Ser Asp Met Ser Phe Ser Lys As - #p Trp Ser Phe Tyr Ile 50 - # 55 - # 60 - - Leu Ala His Thr Glu Phe Thr Pro Thr Glu Th - #r Asp Thr Tyr Ala Cys 65 - #70 - #75 - #80 - - Arg Val Lys His Ser Met Ala Glu Pro Lys Th - #r Val Tyr Trp Asp Arg 85 - # 90 - # 95 - - Asp Met - - - - (2) INFORMATION FOR SEQ ID NO:60: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 99 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:60: - - Ile Gln Lys Thr Pro Gln Ile Gln Val Tyr Se - #r Arg His Pro Pro Glu 1 5 - # 10 - # 15 - - Asn Gly Lys Pro Asn Phe Leu Asn Cys Tyr Va - #l Ser Gln Phe His Pro 20 - # 25 - # 30 - - Pro Gln Ile Glu Ile Glu Leu Leu Lys Asn Gl - #y Lys Lys Ile Pro Asn 35 - # 40 - # 45 - - Ile Glu Met Ser Asp Leu Ser Phe Ser Lys As - #p Trp Ser Phe Tyr Ile 50 - # 55 - # 60 - - Leu Ala His Thr Glu Phe Thr Pro Thr Glu Th - #r Asp Val Tyr Ala Cys 65 - #70 - #75 - #80 - - Arg Val Lys His Val Thr Leu Lys Glu Pro Ly - #s Thr Val Tyr Trp Asp 85 - # 90 - # 95 - - Arg Asp Met - - - - (2) INFORMATION FOR SEQ ID NO:61: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 99 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:61: - - Val His Leu Ala Pro Arg Val Gln Val Tyr Se - #r Arg His Pro Ala Glu 1 5 - # 10 - # 15 - - Asn Gly Lys Gln Asn Phe Ile Asn Cys Tyr Va - #l Ser Gly Phe His Pro 20 - # 25 - # 30 - - Pro Gln Ile Glu Val Glu Leu Leu Lys Asn Gl - #y Lys Lys Ile Asp Asn 35 - # 40 - # 45 - - Val Glu Met Ser Asp Leu Ser Phe Ser Lys As - #p Trp Thr Phe Tyr Leu 50 - # 55 - # 60 - - Leu Val His Ala Ala Phe Thr Pro Asn Asp Se - #r Asp Glu Tyr Ser Cys 65 - #70 - #75 - #80 - - Arg Val Ser His Ile Thr Leu Ser Glu Pro Ly - #s Ile Val Lys Trp Asp 85 - # 90 - # 95 - - Pro Asn Lys - - - - (2) INFORMATION FOR SEQ ID NO:62: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 99 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:62: - - Val Gln Arg Ala Pro Asn Val Gln Val Tyr Se - #r Arg His Pro Ala Glu 1 5 - # 10 - # 15 - - Asn Gly Lys Pro Asn Phe Leu Asn Cys Tyr Va - #l Ser Gly Phe His Pro 20 - # 25 - # 30 - - Pro Gln Ile Asp Ile Glu Leu Leu Lys Asn Va - #l Lys Lys Ile Glu Asn 35 - # 40 - # 45 - - Val Glu Gln Ser Asp Leu Ser Phe Asn Lys As - #p Trp Thr Phe Tyr Leu 50 - # 55 - # 60 - - Leu Val His Thr Glu Phe Thr Pro Asn Asn Ly - #s Asn Glu Tyr Ser Cys 65 - #70 - #75 - #80 - - Arg Val Lys His Val Thr Leu Lys Glu Pro Me - #t Thr Val Lys Trp Asp 85 - # 90 - # 95 - - Arg Asp Tyr - - - - (2) INFORMATION FOR SEQ ID NO:63: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 100 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 7 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentifed amino acid resi - #due." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:63: - - Ile Gln Arg Thr Pro Lys Xaa Gln Val Tyr Se - #r Arg His Pro Pro Ala 1 5 - # 10 - # 15 - - Asn Gly Lys Pro Ser Ile Phe Asn Cys Tyr Va - #l Thr Ser Gly His Pro 20 - # 25 - # 30 - - Ser Asp Ile Glu Ile Val Asp Leu Leu Lys As - #p Gly Glu Arg Ile Glu 35 - # 40 - # 45 - - Lys Val Glu His Ser Asp Leu Ser Phe Ser Ly - #s Asp Trp Ser Phe Tyr 50 - # 55 - # 60 - - Leu Leu Tyr Tyr Thr Glu Phe Thr Pro Thr Gl - #u Lys Asp Glu Tyr Ala 65 - #70 - #75 - #80 - - Cys Arg Val Asn His Val Thr Leu Ser Gln Pr - #o Lys Ile Val Lys Trp 85 - # 90 - # 95 - - Asp Arg Asp Met 100 - - - - (2) INFORMATION FOR SEQ ID NO:64: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 99 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:64: - - Ile Gln Arg Pro Pro Lys Ile Gln Val Tyr Se - #r Arg His Pro Pro Glu 1 5 - # 10 - # 15 - - Asn Gly Lys Pro Asn Tyr Leu Asn Cys Tyr Va - #l Tyr Gly Phe His Pro 20 - # 25 - # 30 - - Pro Gln Ile Glu Ile Asp Leu Leu Lys Asn Gl - #y Glu Lys Ile Lys Ser 35 - # 40 - # 45 - - Val Glu Gln Ser Asp Leu Ser Phe Ser Lys As - #p Trp Ser Phe Tyr Leu 50 - # 55 - # 60 - - Leu Ser His Ala Glu Phe Thr Pro Asp Ser Ly - #s Asp Glu Tyr Ser Cys 65 - #70 - #75 - #80 - - Arg Val Lys His Val Thr Leu Glu Gln Pro Ar - #g Ile Val Tyr Trp Asp 85 - # 90 - # 95 - - Arg Asp Leu - - - - (2) INFORMATION FOR SEQ ID NO:65: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 350 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 326..327 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:65: - - Gly Pro His Ser Leu Arg Tyr Phe Val Thr Al - #a Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Leu Gly Glu Pro Arg Tyr Met Glu Val Gly Ty - #r Val Asp Asp Thr Glu 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Tyr Glu Pro Arg 35 - # 40 - # 45 - - Ala Arg Trp Met Glu Gln Glu Gly Pro Glu Ty - #r Trp Glu Arg Glu Thr 50 - # 55 - # 60 - - Gln Lys Ala Lys Gly Asn Glu Gln Ser Phe Ar - #g Val Asp Leu Arg Thr 65 - #70 - #75 - #80 - - Leu Leu Gly Tyr Tyr Asn Gln Ser Lys Gly Gl - #y Ser His Thr Ile Gln 85 - # 90 - # 95 - - Val Ile Ser Gly Cys Glu Val Gly Ser Asp Gl - #y Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Gln Gln Tyr Ala Tyr Asp Gly Cys Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Ala Asp Met Al - #a Ala Leu Ile Thr Lys 130 - # 135 - # 140 - - His Lys Trp Glu Gln Ala Gly Glu Ala Glu Ar - #g Leu Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Thr Cys Val Glu Trp Leu Arg Arg Ty - #r Leu Lys Asn GlyAsn 165 - # 170 - # 175 - - Ala Thr Leu Leu Arg Thr Asp Ser Pro Lys Al - #a His Val Thr His His 180 - # 185 - # 190 - - Ser Arg Pro Glu Asp Lys Val Thr Leu Arg Cy - #s Trp Ala Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Ile Gln Asp Met Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ser Val Val Val Pro Le - #u Gly Lys Glu GlnTyr 245 - # 250 - # 255 - - Tyr Thr Cys His Val Tyr His Gln Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Glu Pro Pro Pro Ser Thr Val Ser As - #n Met Ala Thr Val Ala 275 - # 280 - # 285 - - Val Leu Val Val Leu Gly Ala Ala Ile Val Th - #r Gly Ala Val Val Ala 290 - # 295 - # 300 - - Phe Val Met Lys Met Arg Arg Arg Asn Thr Gl - #y Gly Lys Gly Gly Asp 305 3 - #10 3 - #15 3 -#20 - - Tyr Ala Leu Ala Pro Xaa Xaa Gly Ser Gln Th - #r Ser Asp Leu SerLeu 325 - # 330 - # 335 - - Pro Asp Cys Lys Val Met Val His Asp Pro Hi - #s Ser Leu Ala 340 - # 345 - # 350 - - - - (2) INFORMATION FOR SEQ ID NO:66: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 310 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:66: - - Gly Pro His Ser Leu Arg Tyr Phe Val Thr Al - #a Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Leu Gly Glu Pro Arg Phe Ile Ala Val Gly Ty - #r Val Asp Thr Gln Phe 20 - # 25 - # 30 - - Val Arg Phe Asp Ser Asp Ala Asp Asn Pro Ar - #g Phe Glu Pro Arg Ala 35 - # 40 - # 45 - - Pro Trp Met Glu Gln Glu Gly Pro Glu Tyr Tr - #p Glu Glu Gln Thr Gln 50 - # 55 - # 60 - - Arg Ala Lys Ser Asp Glu Gln Trp Phe Arg Va - #l Ser Leu Arg Thr Ala 65 - #70 - #75 - #80 - - Gln Arg Tyr Tyr Asn Gln Ser Lys Gly Gly Se - #r His Thr Phe Gln Arg 85 - # 90 - # 95 - - Met Phe Gly Cys Asp Val Gly Ser Asp Trp Ar - #g Leu Leu Arg Gly Tyr 100 - # 105 - # 110 - - Gln Gln Phe Ala Tyr Asp Gly Arg Asp Tyr Il - #e Ala Leu Met Glu Asp 115 - # 120 - # 125 - - Leu Lys Thr Trp Thr Ala Ala Asp Thr Ala Al - #a Leu Ile Thr Arg Arg 130 - # 135 - # 140 - - Lys Trp Glu Gln Ala Gly Asp Ala Glu Tyr Ty - #r Arg Ala Tyr Leu Glu 145 1 - #50 1 - #55 1 -#60 - - Gly Glu Cys Val Glu Trp Leu Arg Arg Tyr Le - #u Glu Leu Gly AsnGlu 165 - # 170 - # 175 - - Thr Leu Leu Arg Thr Asp Ser Pro Lys Ala Hi - #s Val Thr Tyr His Pro 180 - # 185 - # 190 - - Arg Ser Gln Val Asp Val Thr Leu Arg Cys Tr - #p Ala Leu Gly Phe Tyr 195 - # 200 - # 205 - - Pro Ala Asp Ile Thr Leu Thr Trp Gln Leu As - #n Gly Glu Asp Leu Thr 210 - # 215 - # 220 - - Gln Asp Met Glu Leu Val Glu Thr Arg Pro Al - #a Gly Asp Gly Thr Phe 225 2 - #30 2 - #35 2 -#40 - - Gln Lys Trp Ala Ala Val Val Val Pro Leu Gl - #y Lys Glu Gln AsnTyr 245 - # 250 - # 255 - - Thr Cys His Val His His Lys Gly Leu Pro Gl - #u Pro Leu Thr Leu Arg 260 - # 265 - # 270 - - Trp Lys Leu Pro Pro Ser Thr Val Ser Asn Th - #r Val Ile Ile Ala Val 275 - # 280 - # 285 - - Leu Val Val Leu Gly Ala Ala Ile Val Thr Gl - #y Ala Val Val Ala Phe 290 - # 295 - # 300 - - Val Met Lys Met Arg Arg 305 3 - #10 - - - - (2) INFORMATION FOR SEQ ID NO:67: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 350 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 326..327 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:67: - - Gly Pro His Ser Leu Arg Tyr Phe His Thr Al - #a Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Leu Gly Lys Pro Arg Phe Ile Ser Val Gly Ty - #r Val Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Tyr Glu Pro Arg 35 - # 40 - # 45 - - Val Arg Trp Met Glu Gln Val Glu Pro Glu Ty - #r Trp Glu Arg Met Thr 50 - # 55 - # 60 - - Gln Ile Ala Lys Gly Asn Glu Gln Ile Phe Ar - #g Val Asn Leu Arg Thr 65 - #70 - #75 - #80 - - Ala Leu Arg Tyr Tyr Asn Gln Ser Ala Gly Gl - #y Ser His Thr Phe Gln 85 - # 90 - # 95 - - Arg Met Phe Tyr Cys Glu Val Gly Ser Asp Tr - #p Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Glu Gln Tyr Ala Tyr Asp Gly Cys Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Ala Asp Met Al - #a Ala Leu Ile Thr Lys 130 - # 135 - # 140 - - His Lys Trp Glu Gln Ala Gly Asp Ala Glu Ar - #g Asp Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Thr Cys Val Glu Trp Leu Arg Arg Ty - #r Leu Gln Leu GlyAsn 165 - # 170 - # 175 - - Ala Thr Leu Pro Arg Thr Asp Ser Pro Lys Al - #a His Val Thr Arg His 180 - # 185 - # 190 - - Ser Arg Pro Glu Asp Lys Val Thr Leu Arg Cy - #s Trp Ala Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Thr Gln Asp Met Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ser Val Val Val Pro Le - #u Gly Lys Glu GlnTyr 245 - # 250 - # 255 - - Tyr Thr Cys His Val Tyr His Gln Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Glu Pro Pro Pro Ser Thr Val Ser As - #n Thr Val Ile Ile Ala 275 - # 280 - # 285 - - Val Leu Val Val Leu Gly Ala Ala Ile Val Th - #r Gly Ala Val Val Ala 290 - # 295 - # 300 - - Phe Val Met Lys Met Arg Arg Arg Asn Thr Gl - #y Gly Lys Gly Gly Asp 305 3 - #10 3 - #15 3 -#20 - - Tyr Ala Leu Ala Pro Xaa Xaa Gly Ser Gln Th - #r Ser Asp Leu SerLeu 325 - # 330 - # 335 - - Pro Asp Cys Lys Val Met Val His Asp Pro Hi - #s Ser Leu Ala 340 - # 345 - # 350 - - - - (2) INFORMATION FOR SEQ ID NO:68: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 307 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 16 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 18 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:68: - - Gly Pro His Ser Leu Arg Tyr Phe His Thr Al - #a Val Ser Arg Pro Xaa 1 5 - # 10 - # 15 - - Leu Xaa Lys Pro Arg Phe Ile Ser Val Gly Ty - #r Val Asp Asp Thr Glu 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Tyr Glu Pro Arg 35 - # 40 - # 45 - - Ala Arg Trp Met Glu Gln Val Glu Pro Glu Ty - #r Trp Glu Arg Asn Thr 50 - # 55 - # 60 - - Gln Ile Ala Lys Asp Asn Glu Gln Ser Ser Ar - #g Val Asp Leu Arg Thr 65 - #70 - #75 - #80 - - Leu Leu Arg Tyr Tyr Asn Gln Ser Ala Gly Gl - #y Ser His Thr Ile Gln 85 - # 90 - # 95 - - Arg Met Tyr Gly Cys Asp Val Gly Ser Asp Gl - #y Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Glu Gln Val Ala Tyr Asp Gly Cys Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Ala Asp Met Al - #a Ala Leu Ile Thr Lys 130 - # 135 - # 140 - - His Lys Trp Glu Gln Ala Gly Ala Ala Glu Ar - #g Arg Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Ala Cys Val Glu Trp Leu Ser Arg Hi - #s Leu Lys Asn GlyAsn 165 - # 170 - # 175 - - Ala Thr Leu Leu Arg Thr Asp Ser Pro Lys Al - #a His Val Thr His His 180 - # 185 - # 190 - - Ser Arg Pro Glu Asp Lys Val Thr Leu Arg Cy - #s Trp Ala Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Thr Gln Asp Met Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ser Val Val Val Pro Le - #u Gly Lys Glu GlnTyr 245 - # 250 - # 255 - - Tyr Thr Cys His Val Tyr His Gln Gly Leu Pr - #o Lys Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Glu Pro Pro Pro Ser Ala Val Ser As - #n Thr Val Ile Ile Ala 275 - # 280 - # 285 - - Val Leu Val Val Leu Gly Ala Ala Ile Val Th - #r Gly Ala Val Val Ala 290 - # 295 - # 300 - - Phe Val Met 305 - - - - (2) INFORMATION FOR SEQ ID NO:69: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 311 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:69: - - Gly Ser His Ser Leu Arg Tyr Phe Val Thr Al - #a Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Phe Gly Glu Pro Arg Tyr Met Glu Val Gly Ty - #r Val Asp Asn Thr Glu 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Tyr Glu Pro Arg 35 - # 40 - # 45 - - Ala Arg Trp Ile Glu Gln Glu Gly Pro Glu Ty - #r Trp Glu Arg Glu Thr 50 - # 55 - # 60 - - Arg Arg Ala Lys Gly Asn Glu Gln Ser Phe Ar - #g Val Asp Leu Arg Thr 65 - #70 - #75 - #80 - - Ala Leu Arg Tyr Tyr Asn Gln Ser Ala Gly Gl - #y Ser His Thr Leu Gln 85 - # 90 - # 95 - - Trp Met Ala Gly Cys Asp Val Glu Ser Asp Gl - #y Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Trp Gln Phe Ala Tyr Asp Gly Cys Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Ala Asp Met Al - #a Ala Gln Ile Thr Arg 130 - # 135 - # 140 - - Arg Lys Trp Glu Gln Ala Gly Ala Ala Glu Ar - #g Asp Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Glu Cys Val Glu Trp Leu Arg Arg Ty - #r Leu Lys Asn GlyAsn 165 - # 170 - # 175 - - Ala Thr Leu Leu Arg Thr Asp Pro Pro Lys Al - #a His Val Thr His His 180 - # 185 - # 190 - - Arg Arg Pro Glu Gly Asp Val Thr Leu Arg Cy - #s Trp Ala Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Thr Gln Glu Met Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ser Val Val Val Pro Le - #u Gly Lys Glu GlnLys 245 - # 250 - # 255 - - Tyr Thr Cys His Val Glu His Glu Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Gly Lys Glu Glu Pro Pro Ser Ser Th - #r Lys Thr Asn Thr Val 275 - # 280 - # 285 - - Ile Ile Ala Val Pro Val Val Leu Gly Ala Va - #l Val Ile Leu Gly Ala 290 - # 295 - # 300 - - Val Met Ala Phe Val Met Lys 305 3 - #10 - - - - (2) INFORMATION FOR SEQ ID NO:70: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 311 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:70: - - Gly Pro His Ser Leu Arg Tyr Phe Val Thr Al - #a Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Leu Gly Lys Pro Arg Tyr Met Glu Val Gly Ty - #r Val Asp Asn Thr Glu 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Met Lys Pro Arg 35 - # 40 - # 45 - - Val Arg Trp Met Glu Gln Glu Gly Pro Glu Ty - #r Trp Glu Gln Glu Thr 50 - # 55 - # 60 - - Gln Asn Ala Lys Asp His Glu Gln Ser Phe Ar - #g Val Ser Leu Arg Thr 65 - #70 - #75 - #80 - - Asn Leu Gly Tyr Tyr Asn Gln Ser Lys Gly Gl - #y Ser His Thr Ile Gln 85 - # 90 - # 95 - - Gly Met Arg Gly Cys Asp Val Gly Ser Asp Tr - #p Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Glu Gln Phe Ala Tyr Asp Gly Pro Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Ala Asp Met Al - #a Ala Gln Ile Thr Arg 130 - # 135 - # 140 - - Arg Lys Trp Glu Gln Ala Gly Ala Ala Glu Th - #r Leu Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Ala Cys Val Glu Trp Leu Arg Arg Ty - #r Leu Glu Leu GlyAsn 165 - # 170 - # 175 - - Ala Thr Leu Leu Cys Thr Asp Pro Pro Lys Al - #a His Val Thr His His 180 - # 185 - # 190 - - Pro Arg Ser Glu Gly Lys Val Thr Leu Arg Cy - #s Trp Ala Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Thr Gln Asp Met Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ala Leu Val Val Pro Le - #u Gly Lys Glu GlnAsn 245 - # 250 - # 255 - - Tyr Thr Cys His Val Glu His Glu Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Glu Pro Pro Pro Ser Thr Asp Ser Ty - #r Met Val Ile Val Ala 275 - # 280 - # 285 - - Val Leu Val Val Leu Gly Ala Val Phe Ile Il - #e Gly Ala Val Val Ala 290 - # 295 - # 300 - - Phe Val Met Met Met Arg Arg 305 3 - #10 - - - - (2) INFORMATION FOR SEQ ID NO:71: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 308 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:71: - - Gly Pro His Ser Met Arg Tyr Phe Glu Thr Al - #a Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Leu Glu Glu Pro Arg Tyr Ile Ser Val Gly Ty - #r Val Asp Asn Lys Glu 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Tyr Glu Pro Arg 35 - # 40 - # 45 - - Ala Pro Trp Met Glu Gln Glu Gly Pro Glu Ty - #r Trp Glu Arg Glu Thr 50 - # 55 - # 60 - - Gln Lys Ala Lys Gly Gln Glu Gln Trp Phe Ar - #g Val Ser Leu Arg Asn 65 - #70 - #75 - #80 - - Leu Leu Gly Tyr Tyr Asn Gln Ser Ala Gly Gl - #y Ser His Thr Leu Gln 85 - # 90 - # 95 - - Gln Met Ser Gly Cys Asp Leu Gly Ser Asp Tr - #p Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Leu Gln Phe Ala Tyr Glu Gly Arg Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Ala Asp Met Al - #a Ala Gln Ile Thr Arg 130 - # 135 - # 140 - - Arg Lys Trp Glu Gln Ser Gly Ala Ala Glu Hi - #s Tyr Lys Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Glu Cys Val Glu Trp Leu His Arg Ty - #r Leu Lys Asn GlyAsn 165 - # 170 - # 175 - - Ala Thr Leu Leu Arg Thr Asp Ser Pro Lys Al - #a His Val Thr His His 180 - # 185 - # 190 - - Pro Arg Ser Lys Gly Glu Val Thr Leu Arg Cy - #s Trp Ala Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Thr Gln Asp Met Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ser Val Val Val Pro Le - #u Gly Lys Glu GlnAsn 245 - # 250 - # 255 - - Tyr Thr Cys Arg Val Tyr His Glu Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Glu Pro Pro Pro Ser Thr Asp Ser Ty - #r Met Val Ile Val Ala 275 - # 280 - # 285 - - Val Leu Val Val Leu Gly Ala Met Ala Ile Il - #e Gly Ala Val Val Ala 290 - # 295 - # 300 - - Phe Val Met Lys 305 - - - - (2) INFORMATION FOR SEQ ID NO:72: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 308 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:72: - - Gly Pro His Ser Met Arg Tyr Phe Glu Thr Al - #a Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Leu Gly Glu Pro Arg Tyr Ile Ser Val Gly Ty - #r Val Asn Lys Thr Glu 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Tyr Glu Pro Gln 35 - # 40 - # 45 - - Ala Pro Trp Met Glu Gln Glu Gly Pro Glu Ty - #r Trp Glu Arg Ile Thr 50 - # 55 - # 60 - - Gln Ile Ala Lys Gly Gln Glu Gln Trp Phe Ar - #g Val Asn Leu Arg Thr 65 - #70 - #75 - #80 - - Leu Leu Gly Tyr Tyr Asn Gln Ser Ala Gly Gl - #y Thr His Thr Leu Gln 85 - # 90 - # 95 - - Trp Met Tyr Gly Cys Asp Val Gly Ser Asp Gl - #y Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Glu Gln Phe Ala Tyr Asp Gly Arg Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Ala Asp Met Al - #a Ala Gln Ile Thr Arg 130 - # 135 - # 140 - - Arg Lys Trp Glu Gln Ala Gly Ala Ala Glu Ty - #r Tyr Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Glu Cys Val Glu Trp Leu His Arg Ty - #r Leu Lys Asn GlyAsn 165 - # 170 - # 175 - - Ala Thr Leu Leu Arg Thr Asp Ser Pro Lys Al - #a His Val Thr His His 180 - # 185 - # 190 - - Pro Arg Ser Lys Gly Glu Val Thr Leu Arg Cy - #s Trp Ala Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Thr Gln Asp Met Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ser Val Val Val Pro Le - #u Gly Lys Glu GlnAsn 245 - # 250 - # 255 - - Tyr Thr Cys Arg Val Tyr His Glu Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Glu Pro Pro Pro Ser Thr Asp Ser Ty - #r Met Val Ile Val Ala 275 - # 280 - # 285 - - Val Leu Val Val Leu Gly Ala Met Ala Ile Il - #e Gly Ala Val Val Ala 290 - # 295 - # 300 - - Phe Val Met Lys 305 - - - - (2) INFORMATION FOR SEQ ID NO:73: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 311 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:73: - - Gly Gln His Ser Leu Gln Tyr Phe His Thr Al - #a Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Leu Gly Glu Pro Trp Phe Ile Ser Val Gly Ty - #r Val Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Met Glu Pro Arg 35 - # 40 - # 45 - - Ala Arg Trp Met Glu Gln Glu Gly Pro Glu Ty - #r Trp Glu Arg Glu Thr 50 - # 55 - # 60 - - Gln Met Ala Lys Gly His Glu Gln Ser Phe Ar - #g Gly Ser Leu Arg Thr 65 - #70 - #75 - #80 - - Ala Gln Ser Tyr Tyr Asn Gln Ser Lys Gly Gl - #y Ser His Thr Leu Gln 85 - # 90 - # 95 - - Trp Met Tyr Gly Cys Asp Met Gly Ser Asp Gl - #y Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Leu Gln Phe Ala Tyr Glu Gly Arg Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Val Asp Met Al - #a Ala Gln Ile Thr Arg 130 - # 135 - # 140 - - Arg Lys Trp Glu Gln Ala Gly Ile Ala Glu Ly - #s Asp Gln Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Thr Cys Met Gln Ser Leu Arg Arg Ty - #r Leu Gln Leu GlyLys 165 - # 170 - # 175 - - Glu Thr Leu Leu Arg Thr Asp Pro Pro Lys Al - #a His Val Thr His His 180 - # 185 - # 190 - - Pro Arg Ser Tyr Gly Ala Val Thr Leu Arg Cy - #s Trp Ala Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Thr Gln Asp Thr Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Val Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ser Val Val Val Pro Le - #u Gly Lys Glu GlnAsn 245 - # 250 - # 255 - - Tyr Thr Cys His Val Asn His Glu Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Gly Arg Trp Glu Pro Pro Pro Tyr Th - #r Val Ser Asn Met Ala 275 - # 280 - # 285 - - Thr Ile Ala Val Val Val Asp Leu Gly Ala Va - #l Ala Ile Ile Gly Ala 290 - # 295 - # 300 - - Val Val Ala Phe Val Met Asn 305 3 - #10 - - - - (2) INFORMATION FOR SEQ ID NO:74: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 310 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:74: - - Gly Gln His Ser Leu Gln Tyr Phe His Thr Al - #a Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Leu Gly Glu Pro Trp Phe Ile Ser Val Gly Ty - #r Val Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Met Glu Pro Arg 35 - # 40 - # 45 - - Ala Arg Trp Met Glu Gln Glu Gly Pro Glu Ty - #r Trp Glu Arg Glu Thr 50 - # 55 - # 60 - - Gln Ile Ala Lys Gly His Glu Gln Ser Phe Ar - #g Gly Ser Leu Arg Thr 65 - #70 - #75 - #80 - - Ala Gln Ser Tyr Tyr Asn Gln Ser Lys Gly Gl - #y Ser His Thr Leu Gln 85 - # 90 - # 95 - - Trp Met Tyr Gly Cys Asp Met Gly Ser Asp Gl - #y Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Leu Gln Phe Ala Tyr Glu Gly Arg Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Val Asp Met Al - #a Ala Gln Ile Thr Arg 130 - # 135 - # 140 - - Arg Lys Trp Glu Gln Ala Gly Ile Ala Glu Ly - #s Asp Gln Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Thr Cys Met Asp Ser Leu Arg Arg Ty - #r Leu Gln Leu GlyLys 165 - # 170 - # 175 - - Glu Thr Leu Leu Arg Thr Asp Pro Pro Lys Al - #a His Val Thr His His 180 - # 185 - # 190 - - Pro Arg Ser Tyr Gly Ala Val Thr Leu Arg Cy - #s Trp Ala Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Thr Gln Asp Met Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ser Val Val Val Pro Le - #u Gly Lys Glu GlnAsn 245 - # 250 - # 255 - - Tyr Thr Cys His Val Asn His Glu Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Gly Arg Trp Glu Pro Pro Pro Tyr Th - #r Val Ser Asn Met Ala 275 - # 280 - # 285 - - Thr Ile Ala Val Val Val Leu Gly Ala Val Al - #a Ile Ile Gly Ala Val 290 - # 295 - # 300 - - Val Ala Phe Val Met Asn 305 3 - #10 - - - - (2) INFORMATION FOR SEQ ID NO:75: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 306 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:75: - - Gly Pro His Ser Leu Arg Tyr Phe His Thr Al - #a Val Ser Trp Pro Gly 1 5 - # 10 - # 15 - - Leu Val Glu Pro Arg Phe Ile Ile Val Gly Ty - #r Val Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Met Glu Pro Arg 35 - # 40 - # 45 - - Ala Arg Trp Met Glu Gln Glu Gly Pro Glu Ty - #r Trp Glu Arg Glu Thr 50 - # 55 - # 60 - - Gln Lys Ala Lys Gly His Glu Glu Ser Phe Ar - #g Val Ser Leu Arg Thr 65 - #70 - #75 - #80 - - Ala Gln Arg Tyr Tyr Asn Gln Ser Lys Gly Gl - #y Ser His Thr Leu Gln 85 - # 90 - # 95 - - Trp Met Tyr Gly Cys Asp Val Gly Ser Asp Gl - #u Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Leu Gln Phe Ala Tyr Glu Gly Arg Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Ala Asp Met Al - #a Ala Gln Ile Thr Leu 130 - # 135 - # 140 - - His Lys Trp Glu Gln Ala Gly Ile Ala Glu Ar - #g Asp Asp Arg Ala Tyr 145 1 - #50 1 - #55 1 -#60 - - Leu Glu Gly Ala Cys Val Gln Ser Leu Arg Ar - #g Tyr Leu Gln LeuArg 165 - # 170 - # 175 - - Lys Glu Thr Leu Leu Cys Thr Asp Pro Pro Ly - #s Ala His Val Thr His 180 - # 185 - # 190 - - His Pro Arg Ser Tyr Gly Ala Val Thr Leu Ar - #g Cys Trp Ala Leu Gly 195 - # 200 - # 205 - - Phe Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gl - #n Leu Asn Gly Glu Glu 210 - # 215 - # 220 - - Leu Thr Gln Asp Met Glu Leu Val Glu Thr Ar - #g Pro Ala Gly Asp Gly 225 2 - #30 2 - #35 2 -#40 - - Thr Phe Gln Lys Trp Ala Ser Val Val Val Pr - #o Leu Gly Lys GluGln 245 - # 250 - # 255 - - Asn Tyr Thr Cys His Val Asn His Glu Gly Le - #u Pro Glu Pro Leu Thr 260 - # 265 - # 270 - - Leu Arg Trp Glu Pro Pro Pro Ser Thr Val Se - #r Asn Met Ala Asn Val 275 - # 280 - # 285 - - Ala Ile Leu Val Val Leu Val Ala Trp Pro Se - #r Leu Glu Leu Trp Trp 290 - # 295 - # 300 - - Ile Leu 305 - - - - (2) INFORMATION FOR SEQ ID NO:76: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 182 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:76: - - Gly Gln His Ser Leu Gln Tyr Phe His Thr Al - #a Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Leu Gly Glu Pro Trp Phe Ile Ser Val Gly Ty - #r Val Asp Gln Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Met Glu Pro Arg 35 - # 40 - # 45 - - Ala Arg Trp Met Glu Gln Glu Gly Pro Glu Ty - #r Trp Glu Arg Glu Thr 50 - # 55 - # 60 - - Gln Ile Ala Lys Gly His Glu Gln Ser Phe Ar - #g Gly Ser Leu Arg Thr 65 - #70 - #75 - #80 - - Ala Gln Ser Tyr Tyr Asn Gln Ser Lys Gly Gl - #y Ser His Thr Leu Gln 85 - # 90 - # 95 - - Trp Met Tyr Gly Cys Asp Met Gly Ser Asp Gl - #y Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Leu Gln Phe Ala Tyr Glu Gly Arg Asp Ty - #r Ile Ala Leu Asn Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Val Asp Met Al - #a Ala Gln Ile Thr Arg 130 - # 135 - # 140 - - Arg Lys Trp Glu Gln Ala Gly Ile Ala Glu Ly - #s Asp Gln Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Thr Cys Met Glu Ser Leu Arg Arg Ty - #r Leu Gln Leu GlyLys 165 - # 170 - # 175 - - Glu Thr Leu Leu Arg Thr 180 - - - - (2) INFORMATION FOR SEQ ID NO:77: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 301 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:77: - - Gly Ser His Ser Met Arg Tyr Phe Glu Thr Se - #r Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Leu Gly Glu Pro Arg Phe Ile Ile Val Gly Ty - #r Val Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Thr Pr - #o Arg Met Glu Pro Arg 35 - # 40 - # 45 - - Ala Pro Trp Met Glu Gln Glu Gly Pro Glu Ty - #r Trp Glu Arg Glu Thr 50 - # 55 - # 60 - - Gln Arg Ala Lys Gly Asn Glu Gln Ser Phe Hi - #s Val Ser Leu Arg Thr 65 - #70 - #75 - #80 - - Leu Leu Gly His Tyr Asn Gln Ser Glu Ser Gl - #y Ser His Thr Ile Gln 85 - # 90 - # 95 - - Trp Met Tyr Gly Cys Lys Val Gly Ser Asp Gl - #y Arg Phe Leu Arg Gly 100 - # 105 - # 110 - - Tyr Leu Gln Tyr Ala Tyr Asp Gly Arg Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Ala Asp Val Al - #a Ala Ile Ile Thr Arg 130 - # 135 - # 140 - - Arg Lys Trp Glu Gln Ala Gly Ala Ala Glu Ty - #r Tyr Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Ala Glu Cys Val Glu Trp Leu Leu Arg Ty - #r Leu Glu Leu GlyLys 165 - # 170 - # 175 - - Glu Thr Leu Leu Arg Thr Asp Pro Pro Lys Th - #r His Val Thr His His 180 - # 185 - # 190 - - Pro Gly Ser Glu Gly Asp Val Thr Leu Arg Cy - #s Trp Pro Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Thr Gln Asp Met Glu Leu Gln Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ser Val Val Val Pro Le - #u Gly Lys Glu GlnAsn 245 - # 250 - # 255 - - Tyr Thr Cys His Val Tyr His Glu Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Glu Pro Pro Pro Ser Thr Asp Ser Il - #e Met Ser His Ile Ala 275 - # 280 - # 285 - - Asp Leu Leu Trp Pro Ser Leu Lys Leu Trp Tr - #p Tyr Leu 290 - # 295 - # 300 - - - - (2) INFORMATION FOR SEQ ID NO:78: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 308 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:78: - - Ser Pro His Ser Leu Arg Tyr Phe Thr Thr Al - #a Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Leu Gly Glu Pro Arg Phe Ile Ile Val Gly Ty - #r Val Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Glu Asn Pr - #o Arg Met Glu Pro Arg 35 - # 40 - # 45 - - Ala Arg Trp Ile Glu Gln Glu Gly Pro Glu Ty - #r Trp Glu Arg Glu Thr 50 - # 55 - # 60 - - Trp Lys Ala Arg Asp Met Gly Arg Asn Phe Ar - #g Val Asn Leu Arg Thr 65 - #70 - #75 - #80 - - Leu Leu Gly Tyr Tyr Asn Gln Ser Asn Asp Gl - #u Ser His Thr Leu Gln 85 - # 90 - # 95 - - Trp Met Tyr Gly Cys Asp Val Gly Pro Asp Gl - #y Arg Leu Leu Arg Gly 100 - # 105 - # 110 - - Tyr Cys Gln Glu Ala Tyr Asp Gly Gln Asp Ty - #r Ile Ser Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Arg Ser Trp Thr Ala Asn Asp Ile Al - #a Ser Gln Ile Ser Lys 130 - # 135 - # 140 - - His Lys Ser Glu Ala Val Asp Glu Ala His Gl - #n Gln Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Gln Gly Pro Cys Val Glu Trp Leu His Arg Ty - #r Leu Arg Leu GlyAsn 165 - # 170 - # 175 - - Glu Thr Leu Gln Arg Ser Asp Pro Pro Lys Al - #a His Val Thr His His 180 - # 185 - # 190 - - Pro Arg Ser Glu Asp Glu Val Thr Leu Arg Cy - #s Trp Ala Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Thr Gln Asp Met Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ala Val Val Val Pro Le - #u Gly Lys Glu GlnTyr 245 - # 250 - # 255 - - Tyr Thr Cys His Val Tyr His Glu Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Glu Pro Pro Pro Ser Thr Val Ser As - #n Met Val Ile Ile Ala 275 - # 280 - # 285 - - Val Leu Val Val Leu Gly Ala Val Ile Ile Le - #u Gly Ala Val Val Ala 290 - # 295 - # 300 - - Phe Val Met Lys 305 - - - - (2) INFORMATION FOR SEQ ID NO:79: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 289 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:79: - - Gly Ser His Ser Leu Arg Tyr Phe Tyr Thr Al - #a Leu Ser Arg Pro Ala 1 5 - # 10 - # 15 - - Ile Ser Glu Pro Trp Tyr Ile Ala Val Gly Ty - #r Leu Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Ala Arg Phe Asp Ser Ala Gly Glu Thr Gl - #y Thr Tyr Lys Leu Ser 35 - # 40 - # 45 - - Ala Pro Trp Val Glu Gln Glu Gly Pro Glu Ty - #r Trp Ala Arg Glu Thr 50 - # 55 - # 60 - - Glu Ile Val Thr Ser Asn Ala Gln Phe Phe Ar - #g Glu Asn Leu Gln Thr 65 - #70 - #75 - #80 - - Met Leu Asp Tyr Tyr Asn Leu Ser Gln Asn Gl - #y Ser His Thr Ile Gln 85 - # 90 - # 95 - - Val Met Tyr Gly Cys Glu Val Glu Phe Phe Gl - #y Ser Leu Phe Arg Ala 100 - # 105 - # 110 - - Tyr Glu Gln His Gly Tyr Asp Gly Gln Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Ala Asp Met Al - #a Ala Glu Ile Thr Arg 130 - # 135 - # 140 - - Ser Lys Trp Glu Gln Ala Gly Tyr Thr Glu Le - #u Arg Arg Thr Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Pro Cys Lys Asp Ser Leu Leu Arg Ty - #r Leu Glu Asn ArgLys 165 - # 170 - # 175 - - Lys Thr Gln Glu Cys Thr Asp Pro Pro Lys Th - #r His Val Thr His His 180 - # 185 - # 190 - - Ala Arg Pro Glu Gly Asp Val Thr Leu Arg Cy - #s Trp Ala Leu Gly Phe 195 - # 200 - # 205 - - Tyr Pro Ala His Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Ile Gln Asp Thr Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ala Val Val Val Pro Se - #r Gly Glu Glu GlnLys 245 - # 250 - # 255 - - Tyr Thr Cys His Val Tyr His Glu Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Glu Pro Pro Ser Ser Met Pro Asn Ar - #g Thr Thr Val Arg Ala 275 - # 280 - # 285 - - Leu - - - - (2) INFORMATION FOR SEQ ID NO:80: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 290 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:80: - - Gly Ser His Ser Leu Arg Tyr Phe Tyr Thr Al - #a Leu Ser Arg Pro Ala 1 5 - # 10 - # 15 - - Ile Ser Glu Pro Trp Tyr Ile Ala Val Gly Ty - #r Leu Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asn Ser Ser Gly Glu Thr Al - #a Thr Tyr Lys Leu Ser 35 - # 40 - # 45 - - Ala Pro Trp Val Glu Gln Glu Gly Pro Glu Ty - #r Trp Ala Arg Glu Thr 50 - # 55 - # 60 - - Glu Ile Val Thr Ser Asn Ala Gln Phe Phe Ar - #g Glu Asn Leu Gln Thr 65 - #70 - #75 - #80 - - Met Leu Asp Tyr Tyr Asn Leu Ser Gln Asn Gl - #y Ser His Thr Ile Gln 85 - # 90 - # 95 - - Val Met Tyr Gly Cys Glu Val Glu Phe Phe Gl - #y Ser Leu Phe Arg Ala 100 - # 105 - # 110 - - Tyr Glu Gln His Gly Tyr Asp Gly Arg Asp Ty - #r Ile Ala Leu Met Glu 115 - # 120 - # 125 - - Asp Leu Lys Thr Trp Thr Ala Ala Asp Thr Al - #a Ala Glu Ile Thr Arg 130 - # 135 - # 140 - - Ser Lys Trp Glu Gln Ala Gly Tyr Thr Glu Le - #u Arg Arg Thr Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Pro Cys Lys Asp Ser Leu Arg Leu Ty - #r Leu Glu Asn ArgLys 165 - # 170 - # 175 - - Lys Thr Gln Glu Cys Thr Asp Pro Pro Lys Th - #r His Val Thr His His 180 - # 185 - # 190 - - Pro Arg Pro Glu Gly Tyr Val Thr Leu Arg Cy - #s Trp Ala Leu Arg Phe 195 - # 200 - # 205 - - Tyr Pro Ala Asp Ile Thr Leu Thr Trp Gln Le - #u Asn Gly Glu Glu Leu 210 - # 215 - # 220 - - Ile Gln Asp Thr Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ala Val Val Val Pro Le - #u Gly Lys Glu GlnLys 245 - # 250 - # 255 - - Tyr Thr Cys His Val Tyr His Glu Gly Leu Pr - #o Glu Pro Leu Thr Leu 260 - # 265 - # 270 - - Arg Trp Glu Leu Pro Gln Thr Ser Met Pro As - #n Arg Thr Thr Val Arg 275 - # 280 - # 285 - - Ala Leu 290 - - - - (2) INFORMATION FOR SEQ ID NO:81: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 104 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:81: - - Gly Ser His Ser Leu Lys Tyr Phe Tyr Thr Al - #a Leu Ser Arg Pro Ala 1 5 - # 10 - # 15 - - Ile Ser Glu Pro Trp Tyr Ile Ala Gly Gly Ty - #r Leu Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Arg Cys Phe Glu Ser Ala Gly Glu Ser Al - #a Thr Tyr Lys Leu Arg 35 - # 40 - # 45 - - Ala Pro Trp Val Glu Gln Glu Gly Pro Glu Ty - #r Trp Ala Arg Glu Thr 50 - # 55 - # 60 - - Glu Ile Val Thr Ser Asn Ala Gln Phe Phe Ar - #g Val Glu Asn Leu Gln 65 - #70 - #75 - #80 - - Thr Met Leu Asp Tyr Tyr Ser Leu Ser Gln As - #n Gly Ser His Thr Ile 85 - # 90 - # 95 - - Gln Val Met Tyr Gly Cys Glu Val 100 - - - - (2) INFORMATION FOR SEQ ID NO:82: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 108 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:82: - - Asp Pro Pro Lys Thr His Val Thr His His Pr - #o Arg Pro Glu Gly Tyr 1 5 - # 10 - # 15 - - Val Thr Leu Arg Cys Trp Ala Leu Arg Phe Ty - #r Pro Ala Asp Ile Thr 20 - # 25 - # 30 - - Leu Thr Trp Gln Leu Asn Gly Glu Glu Leu Il - #e Gln Asp Thr Glu Leu 35 - # 40 - # 45 - - Val Glu Thr Arg Pro Ala Gly Asp Gly Thr Ph - #e Gln Lys Trp Ala Ala 50 - # 55 - # 60 - - Val Val Val Pro Leu Gly Lys Glu Gln Lys Ty - #r Thr Cys His Val Tyr 65 - #70 - #75 - #80 - - His Glu Gly Leu Pro Glu Pro Leu Thr Leu Ar - #g Trp Glu Leu Pro Gln 85 - # 90 - # 95 - - Thr Ser Met Pro Asn Arg Thr Thr Val Arg Al - #a Leu 100 - # 105 - - - - (2) INFORMATION FOR SEQ ID NO:83: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 184 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:83: - - Gly Ser Leu Phe Arg Ala Tyr Glu Gln His Gl - #y Tyr Asp Gly Arg Asp 1 5 - # 10 - # 15 - - Tyr Ile Ala Leu Met Glu Asp Val Lys Thr Tr - #p Thr Ala Ala Asp Met 20 - # 25 - # 30 - - Ala Ala Glu Ile Thr Arg Ser Lys Trp Glu Gl - #n Ala Gly Tyr Thr Glu 35 - # 40 - # 45 - - Leu Arg Arg Thr Tyr Leu Glu Gly Pro Cys Ly - #s Asp Ser Leu Leu Arg 50 - # 55 - # 60 - - Tyr Leu Glu Asn Arg Lys Lys Gln Glu Cys Th - #r Asp Pro Pro Lys Thr 65 - #70 - #75 - #80 - - Ala His Val Thr His His Pro Arg Pro Glu Gl - #y Tyr Val Thr Leu Arg 85 - # 90 - # 95 - - Cys Trp Ala Leu Gly Phe Tyr Pro Ala Asp Il - #e Thr Leu Thr Trp Gln 100 - # 105 - # 110 - - Leu Asn Gly Glu Glu Leu Ile Gln Asp Met Gl - #u Leu Val Glu Thr Arg 115 - # 120 - # 125 - - Pro Ala Gly Asp Gly Thr Phe Gln Lys Trp Al - #a Ala Val Val Val Pro 130 - # 135 - # 140 - - Ser Gly Glu Glu Gln Lys Tyr Thr Cys His Va - #l Tyr His Glu Gly Leu 145 1 - #50 1 - #55 1 -#60 - - Pro Glu Pro Leu Thr Leu Arg Trp Glu Pro Pr - #o Gln Ser Ser MetPro 165 - # 170 - # 175 - - Thr Arg Thr Ile Val Arg Ala Leu 180 - - - - (2) INFORMATION FOR SEQ ID NO:84: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 92 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:84: - - Val Thr Leu Arg Cys Trp Ala Leu Gly Phe Ty - #r Pro Ala Asp Ile Thr 1 5 - # 10 - # 15 - - Leu Thr Trp Gln Leu Asn Gly Glu Glu Leu Il - #e Gln Asp Thr Glu Leu 20 - # 25 - # 30 - - Val Glu Thr Arg Pro Ala Gly Asp Gly Thr Ph - #e Gln Lys Trp Ala Ala 35 - # 40 - # 45 - - Leu Val Val Pro Ser Gly Glu Glu Gln Lys Ty - #r Thr Cys His Val Tyr 50 - # 55 - # 60 - - His Lys Gly Leu Pro Glu Pro Leu Thr Leu Ar - #g Trp Glu Pro Pro Gln 65 - #70 - #75 - #80 - - Ser Ser Met Pro Asn Arg Thr Thr Val Arg Al - #a Leu 85 - # 90 - - - - (2) INFORMATION FOR SEQ ID NO:85: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 38 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 14..15 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:85: - - Asn Thr Gly Gly Lys Gly Val Asn Tyr Ala Le - #u Ala Pro Xaa Xaa Gly 1 5 - # 10 - # 15 - - Ser Gln Thr Ser Asp Leu Ser Leu Pro Asp Gl - #y Lys Val Met Val His 20 - # 25 - # 30 - - Asp Pro His Ser Leu Ala 35 - - - - (2) INFORMATION FOR SEQ ID NO:86: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 42 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 18..19 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:86: - - Met Arg Arg Arg Asn Thr Gly Gly Lys Gly Gl - #y Asp Tyr Ala Leu Ala 1 5 - # 10 - # 15 - - Pro Xaa Xaa Gly Ser Gln Thr Ser Asp Leu Se - #r Leu Pro Asp Cys Lys 20 - # 25 - # 30 - - Val Met Val His Asp Pro His Ser Leu Ala 35 - # 40 - - - - (2) INFORMATION FOR SEQ ID NO:87: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 32 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 17..18 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:87: - - Arg Arg Arg Asn Thr Gly Gly Lys Gly Gly As - #p Tyr Ala Leu Ala Pro 1 5 - # 10 - # 15 - - Xaa Xaa Gly Ser Gln Ser Ser Asp Met Ser Le - #u Pro Asp Cys Lys Val 20 - # 25 - # 30 - - - - (2) INFORMATION FOR SEQ ID NO:88: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 29 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 14..15 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:88: - - Asn Thr Gly Gly Lys Gly Gly Asp Tyr Thr Le - #u Ala Pro Xaa Xaa Gly 1 5 - # 10 - # 15 - - Ser Gln Ser Ser Glu Met Ser Leu Arg Asp Cy - #s Lys Ala 20 - # 25 - - - - (2) INFORMATION FOR SEQ ID NO:89: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 32 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 17..18 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:89: - - Arg Arg Arg Asn Thr Gly Gly Lys Gly Gly As - #p Tyr Ala Leu Ala Pro 1 5 - # 10 - # 15 - - Xaa Xaa Gly Ser Gln Ser Ser Glu Met Ser Le - #u Arg Asp Cys Lys Ala 20 - # 25 - # 30 - - - - (2) INFORMATION FOR SEQ ID NO:90: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 10 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:90: - - Arg Arg Arg His Ile Gly Val Lys Gly Cys 1 5 - # 10 - - - - (2) INFORMATION FOR SEQ ID NO:91: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 21 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 6..7 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:91: - - Tyr Ala His Val Leu Xaa Xaa Gly Ser Lys Se - #r Phe Gln Thr Ser Asp 1 5 - # 10 - # 15 - - Trp Pro Gln Lys Ala 20 - - - - (2) INFORMATION FOR SEQ ID NO:92: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 47 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 34..35 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:92: - - Leu Gly Ala Met Ile Ile Leu Gly Phe Met Se - #r Gly Ser Val Met Met 1 5 - # 10 - # 15 - - Trp Met Arg Lys Asn Asn Gly Gly Asn Gly As - #p Asp Asn Thr Ala Ala 20 - # 25 - # 30 - - Tyr Xaa Xaa Gln Met Glu Arg Glu His Leu Se - #r Leu Trp Ser Gln 35 - # 40 - # 45 - - - - (2) INFORMATION FOR SEQ ID NO:93: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 70 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 34..35 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:93: - - Leu Gly Ala Met Ile Ile Leu Gly Phe Met Se - #r Gly Ser Val Met Met 1 5 - # 10 - # 15 - - Trp Met Arg Lys Asn Asn Gly Gly Asn Gly As - #p Asp Asn Thr Ala Ala 20 - # 25 - # 30 - - Tyr Xaa Xaa Gln Asn Glu Arg Glu His Leu Se - #r Leu Thr Pro Arg Ala 35 - # 40 - # 45 - - Glu Ser Glu Ala Leu Gly Val Glu Ala Gly Me - #t Lys Asp Leu Pro Ser 50 - # 55 - # 60 - - Ala Pro Pro Leu Val Ser 65 - #70 - - - - (2) INFORMATION FOR SEQ ID NO:94: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 70 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 34..35 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:94: - - Leu Gly Ala Met Ile Ile Leu Gly Phe Met Se - #r Gly Gly Val Met Met 1 5 - # 10 - # 15 - - Trp Met Arg Lys Asn Asn Gly Gly Asn Gly As - #p Asp Asn Thr Ala Ala 20 - # 25 - # 30 - - Cys Xaa Xaa Gln Met Glu Arg Glu His Leu Se - #r Leu Ser Pro Arg Ala 35 - # 40 - # 45 - - Glu Ser Glu Ala Leu Gly Val Glu Ala Gly Me - #t Lys Asp Leu Pro Ser 50 - # 55 - # 60 - - Ala Pro Pro Leu Val Ser 65 - #70 - - - - (2) INFORMATION FOR SEQ ID NO:95: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 64 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 34..35 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:95: - - Leu Gly Ala Met Ile Ile Leu Gly Ile Met Se - #r Gly Ser Val Met Met 1 5 - # 10 - # 15 - - Trp Met Arg Lys Asn Lys Gly Gly Asn Gly Gl - #n Asp Asn Thr Ala Ala 20 - # 25 - # 30 - - Cys Xaa Xaa Gln Met Glu Arg Glu His Leu Se - #r Leu Ser Pro Arg Ala 35 - # 40 - # 45 - - Glu Ser Glu Ala Leu Gly Val Glu Ala Gly Le - #u Lys Asp Leu Pro Ser 50 - # 55 - # 60 - - - - (2) INFORMATION FOR SEQ ID NO:96: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 70 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 34..35 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:96: - - Leu Gly Ala Met Val Ile Leu Gly Val Met Ar - #g Gly Ser Gly Met Met 1 5 - # 10 - # 15 - - Trp Met Arg Lys Asn Lys Gly Gly Asn Arg As - #p Asp Asn Thr Ala Ala 20 - # 25 - # 30 - - Cys Xaa Xaa Gln Met Glu Arg Glu His Leu Se - #r Leu Ser Ala Gly Asp 35 - # 40 - # 45 - - Glu Ser Asp Ala Leu Gly Val Glu Ala Gly Le - #u Lys Glu Leu Pro Thr 50 - # 55 - # 60 - - Ala Pro Pro Leu Val Pro 65 - #70 - - - - (2) INFORMATION FOR SEQ ID NO:97: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 365 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:97: - - Met Ala Val Met Ala Pro Arg Thr Leu Val Le - #u Leu Leu Ser Gly Ala24 -20 - # -15 - # -10 - - Leu Ala Leu Thr Gln Thr Trp Ala Gly Ser Hi - #s Ser Met Arg Tyr Phe -5 - # 1 - # 5 - - Phe Thr Ser Val Ser Arg Pro Gly Arg Gly Gl - #u Pro Arg Phe Ile Ala 10 - # 15 - # 20 - - Val Gly Tyr Val Asp Asp Thr Gln Phe Val Ar - #g Phe Asp Ser Asp Ala 25 - # 30 - # 35 - #40 - - Ala Ser Gln Arg Met Glu Pro Arg Ala Pro Tr - #p Ile Glu Gln Glu Gly 45 - # 50 - # 55 - - Pro Glu Tyr Trp Asp Gly Glu Thr Arg Lys Va - #l Lys Ala His Ser Gln 60 - # 65 - # 70 - - Thr His Arg Val Asp Leu Ser Thr Leu Arg Gl - #y Tyr Tyr Asn Gln Ser 75 - # 80 - # 85 - - Glu Ala Gly Ser His Thr Val Gln Arg Met Ty - #r Gly Cys Asp Val Gly 90 - # 95 - # 100 - - Ser Asp Trp Arg Phe Leu Arg Gly Tyr His Gl - #n Tyr Ala Tyr Asp Gly 105 1 - #10 1 - #15 1 -#20 - - Lys Asp Tyr Ile Ala Leu Lys Glu Asp Leu Ar - #g Ser Trp Thr AlaAla 125 - # 130 - # 135 - - Asp Met Ala Ala Gln Thr Thr Lys His Lys Tr - #p Glu Ala Ala His Val 140 - # 145 - # 150 - - Ala Glu Gln Leu Arg Ala Tyr Leu Glu Gly Th - #r Cys Val Glu Trp Leu 155 - # 160 - # 165 - - Arg Arg Tyr Leu Glu Asn Gly Lys Glu Thr Le - #u Gln Arg Thr Asp Ala 170 - # 175 - # 180 - - Pro Lys Thr His Met Thr His His Ala Val Se - #r Asp His Glu Ala Thr 185 1 - #90 1 - #95 2 -#00 - - Leu Arg Cys Trp Ala Leu Ser Phe Tyr Pro Al - #a Glu Ile Thr LeuThr 205 - # 210 - # 215 - - Trp Gln Arg Asp Gly Glu Asp Gln Thr Gln As - #p Thr Glu Leu Val Glu 220 - # 225 - # 230 - - Thr Arg Pro Ala Gly Asp Gly Thr Phe Gln Ly - #s Trp Ala Ala Val Val 235 - # 240 - # 245 - - Val Pro Ser Gly Gln Glu Gln Arg Tyr Thr Cy - #s His Val Gln His Glu 250 - # 255 - # 260 - - Gly Leu Pro Lys Pro Leu Thr Leu Pro Trp Gl - #u Pro Ser Ser Gln Pro 265 2 - #70 2 - #75 2 -#80 - - Thr Ile Pro Ile Val Gly Ile Ile Ala Gly Le - #u Val Leu Phe GlyAla 285 - # 290 - # 295 - - Val Ile Thr Gly Ala Val Val Ala Ala Val Me - #t Trp Arg Arg Lys Ser 300 - # 305 - # 310 - - Ser Asp Arg Lys Gly Gly Ser Tyr Ser Gln Al - #a Ala Ser Ser Asp Ser 315 - # 320 - # 325 - - Ala Gln Gly Ser Asp Val Ser Leu Thr Ala Cy - #s Lys Val 330 - # 335 - # 340 - - - - (2) INFORMATION FOR SEQ ID NO:98: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 365 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:98: - - Met Ala Val Met Ala Pro Arg Thr Leu Val Le - #u Leu Leu Ser Gly Ala24 -20 - # -15 - # -10 - - Leu Ala Leu Thr Gln Thr Trp Ala Gly Ser Hi - #s Ser Met Arg Tyr Phe -5 - # 1 - # 5 - - Tyr Thr Ser Val Ser Arg Pro Gly Arg Gly Gl - #u Pro Arg Phe Ile Ala 10 - # 15 - # 20 - - Val Gly Tyr Val Asp Asp Thr Gln Phe Val Ar - #g Phe Asp Ser Asp Ala 25 - # 30 - # 35 - # 40 - - Ala Ser Gln Arg Met Glu Pro Arg Ala Pro Tr - #p Ile Glu Gln Glu Gly 45 - # 50 - # 55 - - Pro Glu Tyr Trp Asp Gly Glu Thr Arg Lys Va - #l Lys Ala His Ser Gln 60 - # 65 - # 70 - - Thr His Arg Val Asp Leu Ser Thr Leu Arg Gl - #y Tyr Tyr Asn Gln Ser 75 - # 80 - # 85 - - Glu Ala Gly Ser His Thr Val Gln Arg Met Ty - #r Gly Cys Asp Val Gly 90 - # 95 - # 100 - - Ser Asp Trp Arg Phe Leu Arg Gly Tyr His Gl - #n Tyr Ala Tyr Asp Gly 105 1 - #10 1 - #15 1 -#20 - - Lys Asp Tyr Ile Ala Leu Lys Glu Asp Leu Ar - #g Ser Trp Thr AlaAla 125 - # 130 - # 135 - - Asp Met Ala Ala Gln Thr Thr Lys His Lys Tr - #p Glu Ala Ala His Val 140 - # 145 - # 150 - - Ala Glu Gln Leu Arg Ala Tyr Leu Glu Gly Th - #r Cys Val Glu Trp Leu 155 - # 160 - # 165 - - Arg Arg Tyr Leu Glu Asn Gly Lys Glu Thr Le - #u Gln Arg Thr Asp Ala 170 - # 175 - # 180 - - Pro Lys Thr His Met Thr His His Ala Val Se - #r Asp His Glu Ala Thr 185 1 - #90 1 - #95 2 -#00 - - Leu Arg Cys Trp Ala Leu Ser Phe Tyr Pro Al - #a Glu Ile Thr LeuThr 205 - # 210 - # 215 - - Trp Gln Arg Asp Gly Glu Asp Gln Thr Gln As - #p Thr Glu Leu Val Glu 220 - # 225 - # 230 - - Thr Arg Pro Ala Gly Asp Gly Thr Phe Gln Ly - #s Trp Ala Ala Val Val 235 - # 240 - # 245 - - Val Pro Ser Gly Gln Glu Gln Arg Tyr Thr Cy - #s His Val Gln His Glu 250 - # 255 - # 260 - - Gly Leu Pro Lys Pro Leu Thr Leu Pro Trp Gl - #u Pro Ser Ser Gln Pro 265 2 - #70 2 - #75 2 -#80 - - Thr Ile Pro Ile Val Gly Ile Ile Ala Gly Le - #u Val Leu Phe GlyAla 285 - # 290 - # 295 - - Val Ile Thr Gly Ala Val Val Ala Ala Val Me - #t Trp Arg Arg Lys Ser 300 - # 305 - # 310 - - Ser Asp Arg Lys Gly Gly Ser Tyr Ser Gln Al - #a Ala Ser Ser Asp Ser 315 - # 320 - # 325 - - Ala Gln Gly Ser Asp Val Ser Leu Thr Ala Cy - #s Lys Val 330 - # 335 - # 340 - - - - (2) INFORMATION FOR SEQ ID NO:99: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 365 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:99: - - Met Ala Val Met Ala Pro Arg Thr Leu Val Le - #u Leu Leu Ser Gly Ala24 -20 - # -15 - # -10 - - Leu Ala Leu Thr Gln Thr Trp Ala Gly Ser Hi - #s Ser Met Arg Tyr Phe -5 - # 1 - # 5 - - Phe Thr Ser Val Ser Arg Pro Gly Arg Gly Gl - #u Pro Arg Phe Ile Ala 10 - # 15 - # 20 - - Val Gly Tyr Val Asp Asp Thr Gln Phe Val Ar - #g Phe Asp Ser Asp Ala 25 - #30 - #35 - #40 - - Ala Ser Gln Arg Met Glu Pro Arg Ala Pro Tr - #p Ile Glu Gln Glu Gly 45 - # 50 - # 55 - - Pro Glu Tyr Trp Asp Gly Glu Thr Arg Lys Va - #l Lys Ala His Ser Gln 60 - # 65 - # 70 - - Thr His Arg Val Asp Leu Ser Thr Leu Arg Gl - #y Tyr Tyr Asn Gln Ser 75 - # 80 - # 85 - - Glu Ala Gly Ser His Thr Val Gln Arg Met Ty - #r Gly Cys Asp Val Gly 90 - # 95 - # 100 - - Ser Asp Gly Arg Phe Leu Arg Gly Tyr His Gl - #n Tyr Ala Tyr Asp Gly 105 1 - #10 1 - #15 1 -#20 - - Lys Asp Tyr Ile Ala Leu Lys Glu Asp Leu Ar - #g Ser Trp Thr AlaAla 125 - # 130 - # 135 - - Asp Met Ala Ala Gln Thr Thr Lys His Lys Tr - #p Glu Thr Ala His Glu 140 - # 145 - # 150 - - Ala Glu Gln Trp Arg Ala Tyr Leu Glu Gly Th - #r Cys Val Glu Trp Leu 155 - # 160 - # 165 - - Arg Arg Tyr Leu Glu Asn Gly Lys Glu Thr Le - #u Gln Arg Thr Asp Ala 170 - # 175 - # 180 - - Pro Lys Thr His Met Thr His His Ala Val Se - #r Asp His Glu Ala Thr 185 1 - #90 1 - #95 2 -#00 - - Leu Arg Cys Trp Ala Leu Ser Phe Tyr Pro Al - #a Glu Ile Thr LeuThr 205 - # 210 - # 215 - - Trp Gln Arg Asp Gly Glu Asp Gln Thr Gln As - #p Thr Glu Leu Val Glu 220 - # 225 - # 230 - - Thr Arg Pro Ala Gly Asp Gly Thr Phe Gln Ly - #s Trp Ala Ala Val Val 235 - # 240 - # 245 - - Val Pro Ser Gly Gln Glu Gln Arg Tyr Thr Cy - #s His Val Gln His Glu 250 - # 255 - # 260 - - Gly Leu Pro Lys Pro Leu Thr Leu Pro Trp Gl - #u Pro Ser Ser Gln Pro 265 2 - #70 2 - #75 2 -#80 - - Thr Ile Pro Ile Val Gly Ile Ile Ala Gly Le - #u Val Leu Phe GlyAla 285 - # 290 - # 295 - - Val Ile Thr Gly Ala Val Val Ala Ala Val Me - #t Trp Arg Arg Lys Ser 300 - # 305 - # 310 - - Ser Asp Arg Lys Gly Gly Ser Tyr Ser Gln Al - #a Ala Ser Ser Asp Ser 315 - # 320 - # 325 - - Ala Gln Gly Ser Asp Val Ser Leu Thr Ala Cy - #s Lys Val 330 - # 335 - # 340 - - - - (2) INFORMATION FOR SEQ ID NO:100: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 365 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:100: - - Met Ala Val Met Ala Pro Arg Thr Leu Val Le - #u Leu Leu Ser Gly Ala24 -20 - # -15 - # -10 - - Leu Ala Leu Thr Gln Thr Trp Ala Gly Ser Hi - #s Ser Met Arg Tyr Phe -5 - # 1 - # 5 - - Tyr Thr Ser Val Ser Arg Pro Gly Arg Gly Gl - #u Pro Arg Phe Ile Ala 10 - # 15 - # 20 - - Val Gly Tyr Val Asp Asp Thr Gln Phe Val Ar - #g Phe Asp Ser Asp Ala 25 - #30 - #35 - #40 - - Ala Ser Gln Arg Met Glu Pro Arg Ala Pro Tr - #p Ile Glu Gln Glu Gly 45 - # 50 - # 55 - - Pro Glu Tyr Trp Asp Gly Glu Thr Arg Lys Va - #l Lys Ala His Ser Gln 60 - # 65 - # 70 - - Thr His Arg Val Asp Leu Ser Thr Leu Arg Gl - #y Tyr Tyr Asn Gln Ser 75 - # 80 - # 85 - - Glu Ala Gly Ser His Thr Val Gln Arg Met Ph - #e Gly Cys Asp Val Gly 90 - # 95 - # 100 - - Ser Asp Gly Arg Phe Leu Arg Gly Tyr His Gl - #n Tyr Ala Tyr Asp Gly 105 1 - #10 1 - #15 1 -#20 - - Lys Asp Tyr Ile Ala Leu Lys Glu Asp Leu Ar - #g Ser Trp Thr AlaAla 125 - # 130 - # 135 - - Asp Met Ala Ala Gln Thr Thr Lys His Lys Tr - #p Glu Ala Ala His Val 140 - # 145 - # 150 - - Ala Glu Gln Leu Arg Ala Tyr Leu Glu Gly Th - #r Cys Val Glu Trp Leu 155 - # 160 - # 165 - - Arg Arg Tyr Leu Glu Asn Gly Lys Glu Thr Le - #u Gln Arg Thr Asp Ala 170 - # 175 - # 180 - - Pro Lys Thr His Met Thr His His Ala Val Se - #r Asp His Glu Ala Thr 185 1 - #90 1 - #95 2 -#00 - - Leu Arg Cys Trp Ala Leu Ser Phe Tyr Pro Al - #a Glu Ile Thr LeuThr 205 - # 210 - # 215 - - Trp Gln Arg Asp Gly Glu Asp Gln Thr Gln As - #p Thr Glu Leu Val Glu 220 - # 225 - # 230 - - Thr Arg Pro Ala Gly Asp Gly Thr Phe Gln Ly - #s Trp Ala Ala Val Val 235 - # 240 - # 245 - - Val Pro Ser Gly Gln Glu Gln Arg Tyr Thr Cy - #s His Val Gln His Glu 250 - # 255 - # 260 - - Gly Leu Pro Lys Pro Leu Thr Leu Pro Trp Gl - #u Pro Ser Ser Gln Pro 265 2 - #70 2 - #75 2 -#80 - - Thr Ile Pro Ile Val Gly Ile Ile Ala Gly Le - #u Val Leu Phe GlyAla 285 - # 290 - # 295 - - Val Ile Thr Gly Ala Val Val Ala Ala Val Me - #t Trp Arg Arg Lys Ser 300 - # 305 - # 310 - - Ser Asp Arg Lys Gly Gly Ser Tyr Ser Gln Al - #a Ala Ser Ser Asp Ser 315 - # 320 - # 325 - - Ala Gln Gly Ser Asp Val Ser Leu Thr Ala Cy - #s Lys Val 330 - # 335 - # 340 - - - - (2) INFORMATION FOR SEQ ID NO:101: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 365 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:101: - - Met Ala Val Met Ala Pro Arg Thr Leu Val Le - #u Leu Leu Ser Gly Ala24 -20 - # -15 - # -10 - - Leu Ala Leu Thr Gln Thr Trp Ala Gly Ser Hi - #s Ser Met Arg Tyr Phe -5 - # 1 - # 5 - - Tyr Thr Ser Val Ser Arg Pro Gly Arg Gly Gl - #u Pro Arg Phe Ile Ala 10 - # 15 - # 20 - - Val Gly Tyr Val Asp Asp Thr Gln Phe Val Ar - #g Phe Asp Ser Asp Ala 25 - #30 - #35 - #40 - - Ala Ser Arg Arg Met Glu Pro Arg Ala Pro Tr - #p Ile Glu Gln Glu Gly 45 - # 50 - # 55 - - Pro Glu Tyr Trp Asp Gly Glu Thr Arg Lys Va - #l Lys Ala His Ser Gln 60 - # 65 - # 70 - - Thr His Arg Val Asp Leu Ser Thr Leu Arg Gl - #y Tyr Tyr Asn Gln Ser 75 - # 80 - # 85 - - Glu Ala Gly Ser His Leu Val Gln Arg Met Ty - #r Gly Cys Asp Val Gly 90 - # 95 - # 100 - - Phe Asp Trp Arg Phe Leu Arg Gly Tyr His Gl - #n Tyr Ala Tyr Asp Gly 105 1 - #10 1 - #15 1 -#20 - - Lys Asp Tyr Ile Ala Leu Lys Glu Asp Leu Ar - #g Ser Trp Thr AlaAla 125 - # 130 - # 135 - - Asp Met Ala Ala Gln Thr Thr Lys His Lys Tr - #p Glu Thr Ala His Val 140 - # 145 - # 150 - - Ala Glu Gln Leu Arg Ala Tyr Leu Glu Gly Th - #r Cys Val Glu Trp Leu 155 - # 160 - # 165 - - Arg Arg Tyr Leu Glu Asn Gly Lys Glu Thr Le - #u Gln Arg Thr Asp Ala 170 - # 175 - # 180 - - Pro Lys Thr His Met Thr His His Ala Val Se - #r Asp His Glu Ala Thr 185 1 - #90 1 - #95 2 -#00 - - Leu Arg Cys Trp Ala Leu Ser Phe Tyr Pro Al - #a Glu Ile Thr LeuThr 205 - # 210 - # 215 - - Trp Gln Arg Asp Gly Glu Asp Gln Thr Gln As - #p Thr Glu Leu Val Glu 220 - # 225 - # 230 - - Thr Arg Pro Ala Gly Asp Gly Thr Phe Gln Ly - #s Trp Ala Ala Val Val 235 - # 240 - # 245 - - Val Pro Ser Gly Gln Glu Gln Arg Tyr Thr Cy - #s His Val Gln His Glu 250 - # 255 - # 260 - - Gly Leu Pro Lys Pro Leu Thr Leu Pro Trp Gl - #u Pro Ser Ser Gln Pro 265 2 - #70 2 - #75 2 -#80 - - Thr Ile Pro Ile Val Gly Ile Ile Ala Gly Le - #u Val Leu Phe GlyAla 285 - # 290 - # 295 - - Val Ile Thr Gly Ala Val Val Ala Ala Val Me - #t Trp Arg Arg Lys Ser 300 - # 305 - # 310 - - Ser Asp Arg Lys Gly Gly Ser Tyr Ser Gln Al - #a Ala Ser Ser Asp Ser 315 - # 320 - # 325 - - Ala Gln Gly Ser Asp Val Ser Leu Thr Ala Cy - #s Lys Val 330 - # 335 - # 340 - - - - (2) INFORMATION FOR SEQ ID NO:102: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 365 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:102: - - Met Ala Val Met Ala Pro Arg Thr Leu Val Le - #u Leu Leu Ser Gly Ala24 -20 - # -15 - # -10 - - Leu Ala Leu Thr Gln Thr Trp Ala Gly Ser Hi - #s Ser Met Arg Tyr Phe -5 - # 1 - # 5 - - Tyr Thr Ser Met Ser Arg Pro Gly Arg Gly Gl - #u Pro Arg Phe Ile Ala 10 - # 15 - # 20 - - Val Gly Tyr Val Asp Asp Thr Gln Phe Val Ar - #g Phe Asp Ser Asp Ala 25 - #30 - #35 - #40 - - Ala Ser Arg Arg Met Glu Pro Arg Ala Pro Tr - #p Ile Glu Gln Glu Gly 45 - # 50 - # 55 - - Pro Glu Tyr Trp Asp Arg Asn Thr Arg Asn Va - #l Lys Ala Gln Ser Gln 60 - # 65 - # 70 - - Thr Asp Arg Val Asp Leu Ser Thr Leu Arg Gl - #y Tyr Tyr Asn Gln Ser 75 - # 80 - # 85 - - Glu Ala Gly Ser His Thr Ile Gln Arg Met Ty - #r Gly Cys Asp Val Gly 90 - # 95 - # 100 - - Phe Asp Gly Arg Phe Leu Arg Gly Tyr Arg Gl - #n Asp Ala Tyr Asp Gly 105 1 - #10 1 - #15 1 -#20 - - Lys Asp Tyr Ile Ala Leu Lys Glu Asp Leu Ar - #g Ser Trp Thr AlaAla 125 - # 130 - # 135 - - Asp Met Ala Ala Gln Thr Thr Lys His Lys Tr - #p Glu Ala Ala His Val 140 - # 145 - # 150 - - Ala Glu Gln Trp Arg Ala Tyr Leu Glu Gly Th - #r Cys Val Glu Trp Leu 155 - # 160 - # 165 - - Arg Arg Tyr Leu Glu Asn Gly Lys Glu Thr Le - #u Gln Arg Thr Asp Ala 170 - # 175 - # 180 - - Pro Lys Thr His Met Thr His His Ala Val Se - #r Asp His Glu Ala Thr 185 1 - #90 1 - #95 2 -#00 - - Leu Arg Cys Trp Ala Leu Ser Phe Tyr Pro Al - #a Glu Ile Thr LeuThr 205 - # 210 - # 215 - - Trp Gln Arg Asp Gly Glu Asp Gln Thr Gln As - #p Thr Glu Leu Val Glu 220 - # 225 - # 230 - - Thr Arg Pro Ala Gly Asp Gly Thr Phe Gln Ly - #s Trp Val Ala Val Val 235 - # 240 - # 245 - - Val Pro Ser Gly Gln Glu Gln Arg Tyr Thr Cy - #s His Val Gln His Glu 250 - # 255 - # 260 - - Gly Leu Pro Lys Pro Leu Thr Leu Pro Trp Gl - #u Pro Ser Ser Gln Pro 265 2 - #70 2 - #75 2 -#80 - - Thr Ile Pro Ile Val Gly Ile Ile Ala Gly Le - #u Val Leu Phe GlyAla 285 - # 290 - # 295 - - Val Ile Thr Gly Ala Val Val Ala Ala Val Me - #t Trp Arg Arg Lys Ser 300 - # 305 - # 310 - - Ser Asp Arg Lys Gly Gly Ser Tyr Ser Gln Al - #a Ala Ser Ser Asp Ser 315 - # 320 - # 325 - - Ala Gln Gly Ser Asp Val Ser Leu Thr Ala Cy - #s Lys Val 330 - # 335 - # 340 - - - - (2) INFORMATION FOR SEQ ID NO:103: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 365 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:103: - - Met Ala Val Met Ala Pro Arg Thr Leu Val Le - #u Leu Leu Ser Gly Ala24 -20 - # -15 - # -10 - - Leu Ala Leu Thr Gln Thr Trp Ala Gly Ser Hi - #s Ser Met Arg Tyr Phe -5 - # 1 - # 5 - - Tyr Thr Ser Met Ser Arg Pro Gly Arg Gly Gl - #u Pro Arg Phe Ile Ala 10 - # 15 - # 20 - - Val Gly Tyr Val Asp Asp Thr Gln Phe Val Ar - #g Phe Asp Ser Asp Ala 25 - #30 - #35 - #40 - - Ala Ser Gln Arg Met Glu Pro Arg Ala Pro Tr - #p Ile Glu Gln Glu Gly 45 - # 50 - # 55 - - Pro Glu Tyr Trp Asp Arg Asn Thr Arg Asn Va - #l Lys Ala Gln Ser Gln 60 - # 65 - # 70 - - Thr Asp Arg Val Asp Leu Ser Thr Leu Arg Gl - #y Tyr Tyr Asn Gln Ser 75 - # 80 - # 85 - - Glu Ala Gly Ser His Thr Ile Gln Arg Met Ty - #r Gly Cys Asp Val Gly 90 - # 95 - # 100 - - Phe Asp Gly Arg Phe Leu Arg Gly Tyr Arg Gl - #n Asp Ala Tyr Asp Gly 105 1 - #10 1 - #15 1 -#20 - - Lys Asp Tyr Ile Ala Leu Lys Glu Asp Leu Ar - #g Ser Trp Thr AlaAla 125 - # 130 - # 135 - - Asp Met Ala Ala Gln Thr Thr Lys His Lys Tr - #p Glu Ala Ala His Val 140 - # 145 - # 150 - - Ala Glu Gln Trp Arg Ala Tyr Leu Glu Gly Th - #r Cys Val Glu Trp Leu 155 - # 160 - # 165 - - Arg Arg Tyr Leu Glu Asn Gly Lys Glu Thr Le - #u Gln Arg Thr Asp Ala 170 - # 175 - # 180 - - Pro Lys Thr His Met Thr His His Ala Val Se - #r Asp His Glu Ala Thr 185 1 - #90 1 - #95 2 -#00 - - Leu Arg Cys Trp Ala Leu Ser Phe Tyr Pro Al - #a Glu Ile Thr LeuThr 205 - # 210 - # 215 - - Trp Gln Arg Asp Gly Glu Asp Gln Thr Gln As - #p Thr Glu Leu Val Glu 220 - # 225 - # 230 - - Thr Arg Pro Ala Gly Asp Gly Thr Phe Gln Ly - #s Trp Val Ala Val Val 235 - # 240 - # 245 - - Val Pro Ser Gly Gln Glu Gln Arg Tyr Thr Cy - #s His Val Gln His Glu 250 - # 255 - # 260 - - Gly Leu Pro Lys Pro Leu Thr Leu Pro Trp Gl - #u Pro Ser Ser Gln Pro 265 2 - #70 2 - #75 2 -#80 - - Thr Ile Pro Ile Val Gly Ile Ile Ala Gly Le - #u Val Leu Phe GlyAla 285 - # 290 - # 295 - - Val Ile Thr Gly Ala Val Val Ala Ala Val Me - #t Trp Arg Arg Lys Ser 300 - # 305 - # 310 - - Ser Asp Arg Lys Gly Gly Ser Tyr Ser Gln Al - #a Ala Ser Ser Asp Ser 315 - # 320 - # 325 - - Ala Gln Gly Ser Asp Val Ser Leu Thr Ala Cy - #s Lys Val 330 - # 335 - # 340 - - - - (2) INFORMATION FOR SEQ ID NO:104: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 365 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:104: - - Met Ala Val Met Ala Pro Arg Thr Leu Val Le - #u Leu Leu Ser Gly Ala24 -20 - # -15 - # -10 - - Leu Ala Leu Thr Gln Thr Trp Ala Gly Ser Hi - #s Ser Met Arg Tyr Phe -5 - # 1 - # 5 - - Tyr Thr Ser Val Ser Arg Pro Gly Arg Gly Gl - #u Pro Arg Phe Ile Ala 10 - # 15 - # 20 - - Val Gly Tyr Val Asp Asp Thr Gln Phe Val Ar - #g Phe Asp Ser Asp Ala 25 - #30 - #35 - #40 - - Ala Ser Gln Arg Met Glu Pro Arg Ala Pro Tr - #p Ile Glu Gln Glu Gly 45 - # 50 - # 55 - - Pro Glu Tyr Trp Asp Phe Asn Thr Arg Asn Va - #l Lys Ala Gln Ser Gln 60 - # 65 - # 70 - - Thr Asp Arg Val Asp Leu Ser Thr Leu Arg Gl - #y Tyr Tyr Asn Gln Ser 75 - # 80 - # 85 - - Glu Ala Gly Ser His Thr Ile Gln Met Met Ty - #r Gly Cys Asp Val Gly 90 - # 95 - # 100 - - Ser Asp Gly Arg Phe Leu Arg Gly Tyr Arg Gl - #n Asp Ala Tyr Asp Gly 105 1 - #10 1 - #15 1 -#20 - - Lys Asp Tyr Ile Ala Leu Lys Glu Asp Leu Ar - #g Ser Trp Thr AlaAla 125 - # 130 - # 135 - - Asp Met Ala Ala Gln Thr Thr Lys His Lys Tr - #p Glu Ala Ala His Val 140 - # 145 - # 150 - - Ala Glu Gln Trp Arg Ala Tyr Leu Glu Gly Th - #r Cys Val Glu Trp Leu 155 - # 160 - # 165 - - Arg Arg Tyr Leu Glu Asn Gly Lys Glu Thr Le - #u Gln Arg Thr Asp Ala 170 - # 175 - # 180 - - Pro Lys Thr His Met Thr His His Ala Val Se - #r Asp His Glu Ala Thr 185 1 - #90 1 - #95 2 -#00 - - Leu Arg Cys Trp Ala Leu Ser Phe Tyr Pro Al - #a Glu Ile Thr LeuThr 205 - # 210 - # 215 - - Trp Gln Arg Asp Gly Glu Asp Gln Thr Gln As - #p Thr Glu Leu Val Glu 220 - # 225 - # 230 - - Thr Arg Pro Ala Gly Asp Gly Thr Phe Gln Ly - #s Trp Val Ala Val Val 235 - # 240 - # 245 - - Val Pro Ser Gly Gln Glu Gln Arg Tyr Thr Cy - #s His Val Gln His Glu 250 - # 255 - # 260 - - Gly Leu Pro Lys Pro Leu Thr Leu Pro Trp Gl - #u Pro Ser Ser Gln Pro 265 2 - #70 2 - #75 2 -#80 - - Thr Ile Pro Ile Val Gly Ile Ile Ala Gly Le - #u Val Leu Phe GlyAla 285 - # 290 - # 295 - - Val Ile Thr Gly Ala Val Val Ala Ala Val Me - #t Trp Arg Arg Lys Ser 300 - # 305 - # 310 - - Ser Asp Arg Lys Gly Gly Ser Tyr Ser Gln Al - #a Ala Ser Ser Asp Ser 315 - # 320 - # 325 - - Ala Gln Gly Ser Asp Val Ser Leu Thr Ala Cy - #s Lys Val 330 - # 335 - # 340 - - - - (2) INFORMATION FOR SEQ ID NO:105: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 274 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:105: - - Gly Ser His Ser Met Arg Tyr Phe Phe Thr Se - #r Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Arg Gly Glu Pro Arg Phe Ile Ala Val Gly Ty - #r Val Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Ala Ser Gl - #n Arg Met Glu Pro Arg 35 - # 40 - # 45 - - Ala Pro Trp Ile Glu Gln Glu Gly Pro Glu Ty - #r Trp Asp Gly Glu Thr 50 - # 55 - # 60 - - Arg Lys Val Lys Ala His Ser Gln Thr His Ar - #g Val Asp Leu Ser Thr 65 - #70 - #75 - #80 - - Leu Arg Gly Tyr Tyr Asn Gln Ser Glu Ala Gl - #y Ser His Thr Val Gln 85 - # 90 - # 95 - - Arg Met Cys Gly Cys Asp Val Gly Ser Asp Tr - #p Arg Phe Leu Arg Gly 100 - # 105 - # 110 - - Tyr His Gln Tyr Ala Tyr Asp Gly Lys Asp Ty - #r Ile Ala Leu Lys Glu 115 - # 120 - # 125 - - Asp Leu Arg Ser Trp Thr Ala Ala Asp Met Al - #a Ala Gln Thr Thr Lys 130 - # 135 - # 140 - - His Lys Trp Glu Ala Ala His Val Ala Glu Gl - #n Leu Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Thr Cys Val Glu Trp Leu Arg Arg Ty - #r Leu Glu Asn GlyLys 165 - # 170 - # 175 - - Glu Thr Leu Gln Arg Thr Asp Ala Pro Lys Th - #r His Met Thr His His 180 - # 185 - # 190 - - Ala Val Ser Asp His Glu Ala Thr Leu Arg Cy - #s Trp Ala Leu Ser Phe 195 - # 200 - # 205 - - Tyr Pro Ala Glu Ile Thr Leu Thr Trp Gln Ar - #g Asp Gly Glu Asp Gln 210 - # 215 - # 220 - - Thr Gln Asp Thr Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ala Val Val Val Pro Se - #r Gly Gln Glu GlnArg 245 - # 250 - # 255 - - Tyr Thr Cys His Val Gln His Glu Gly Leu Pr - #o Lys Pro Leu Thr Leu 260 - # 265 - # 270 - - Pro Trp - - - - (2) INFORMATION FOR SEQ ID NO:106: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 274 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:106: - - Gly Ser His Ser Met Arg Tyr Phe Phe Thr Se - #r Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Arg Gly Glu Pro Arg Phe Ile Ala Val Gly Ty - #r Val Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Ala Ser Gl - #n Arg Met Glu Pro Arg 35 - # 40 - # 45 - - Ala Pro Trp Ile Glu Gln Glu Gly Pro Glu Ty - #r Trp Asp Gly Glu Thr 50 - # 55 - # 60 - - Arg Lys Val Lys Ala His Ser Gln Thr His Ar - #g Val Asp Leu Ser Thr 65 - #70 - #75 - #80 - - Leu Arg Gly Tyr Tyr Asn Gln Ser Glu Ala Gl - #y Ser His Thr Val Gln 85 - # 90 - # 95 - - Arg Met Tyr Gly Cys Asp Val Gly Ser Asp Tr - #p Arg Phe Leu Arg Gly 100 - # 105 - # 110 - - Tyr His Gln Tyr Ala Tyr Asp Gly Lys Asp Ty - #r Ile Ala Leu Lys Glu 115 - # 120 - # 125 - - Asp Leu Arg Ser Trp Thr Ala Ala Asp Met Al - #a Ala Gln Thr Thr Lys 130 - # 135 - # 140 - - His Lys Trp Glu Ala Ala His Val Ala Glu Gl - #n Leu Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Thr Cys Val Glu Trp Leu Arg Arg Ty - #r Leu Glu Asn GlyLys 165 - # 170 - # 175 - - Glu Thr Leu Gln Arg Thr Asp Ala Pro Lys Th - #r His Met Thr His His 180 - # 185 - # 190 - - Ala Val Ser Asp His Glu Ala Thr Leu Arg Cy - #s Trp Ala Leu Ser Phe 195 - # 200 - # 205 - - Tyr Pro Ala Glu Ile Thr Leu Thr Trp Gln Ar - #g Asp Gly Glu Asp Gln 210 - # 215 - # 220 - - Thr Gln Asp Thr Glu Leu Val Glu Thr Arg Pr - #o Glu Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ala Val Val Val Pro Se - #r Gly Gln Glu GlnArg 245 - # 250 - # 255 - - Tyr Thr Cys His Val Gln His Glu Gly Leu Pr - #o Lys Pro Leu Thr Leu 260 - # 265 - # 270 - - Pro Trp - - - - (2) INFORMATION FOR SEQ ID NO:107: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 274 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:107: - - Gly Ser His Ser Met Arg Tyr Phe Phe Thr Se - #r Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Arg Gly Glu Pro Arg Phe Ile Ala Val Gly Ty - #r Val Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Ala Ser Ar - #g Arg Met Glu Pro Arg 35 - # 40 - # 45 - - Ala Pro Trp Ile Glu Gln Glu Gly Pro Glu Ty - #r Trp Asp Gly Glu Thr 50 - # 55 - # 60 - - Arg Lys Val Lys Ala His Ser Gln Thr His Ar - #g Val Asp Leu Ser Thr 65 - #70 - #75 - #80 - - Leu Arg Gly Tyr Tyr Asn Gln Ser Glu Ala Gl - #y Ser His Thr Leu Gln 85 - # 90 - # 95 - - Arg Met Tyr Gly Cys Asp Val Gly Ser Asp Tr - #p Arg Phe Leu Arg Gly 100 - # 105 - # 110 - - Tyr His Gln Tyr Ala Tyr Asp Gly Lys Asp Ty - #r Ile Ala Leu Lys Glu 115 - # 120 - # 125 - - Asp Leu Arg Ser Trp Thr Ala Ala Asp Met Al - #a Ala Gln Thr Thr Lys 130 - # 135 - # 140 - - His Lys Trp Glu Ala Ala His Val Ala Glu Gl - #n Trp Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Thr Cys Val Glu Trp Leu Arg Arg Ty - #r Leu Glu Asn GlyLys 165 - # 170 - # 175 - - Glu Thr Leu Gln Arg Thr Asp Ala Pro Lys Th - #r His Met Thr His His 180 - # 185 - # 190 - - Ala Val Ser Asp His Glu Ala Thr Leu Arg Cy - #s Trp Ala Leu Ser Phe 195 - # 200 - # 205 - - Tyr Pro Ala Glu Ile Thr Leu Thr Trp Gln Ar - #g Asp Gly Glu Asp Gln 210 - # 215 - # 220 - - Thr Gln Asp Thr Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ala Val Val Val Pro Se - #r Gly Gln Glu GlnArg 245 - # 250 - # 255 - - Tyr Thr Cys His Val Gln His Glu Gly Leu Pr - #o Lys Pro Leu Thr Leu 260 - # 265 - # 270 - - Pro Trp - - - - (2) INFORMATION FOR SEQ ID NO:108: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 274 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:108: - - Gly Ser His Ser Met Arg Tyr Phe Tyr Thr Se - #r Val Ser Arg Pro Gly 1 5 - # 10 - # 15 - - Arg Gly Glu Pro Arg Phe Ile Ala Val Gly Ty - #r Val Asp Asp Thr Gln 20 - # 25 - # 30 - - Phe Val Arg Phe Asp Ser Asp Ala Ala Ser Ar - #g Arg Met Glu Pro Arg 35 - # 40 - # 45 - - Ala Pro Trp Ile Glu Gln Glu Gly Pro Glu Ty - #r Trp Asp Gly Glu Thr 50 - # 55 - # 60 - - Arg Asn Val Lys Ala His Ser Gln Thr His Ar - #g Val Asp Leu Ser Thr 65 - #70 - #75 - #80 - - Leu Arg Gly Tyr Tyr Asn Gln Ser Glu Ala Gl - #y Ser His Thr Leu Gln 85 - # 90 - # 95 - - Arg Met Tyr Gly Cys Asp Val Gly Ser Asp Tr - #p Arg Phe Leu Arg Gly 100 - # 105 - # 110 - - Tyr His Gln Tyr Ala Tyr Asp Gly Lys Asp Ty - #r Ile Ala Leu Lys Glu 115 - # 120 - # 125 - - Asp Leu Arg Ser Trp Thr Ala Ala Asp Met Al - #a Ala Gln Thr Thr Lys 130 - # 135 - # 140 - - His Lys Trp Glu Ala Ala His Val Ala Glu Gl - #n Trp Arg Ala Tyr Leu 145 1 - #50 1 - #55 1 -#60 - - Glu Gly Thr Cys Val Glu Trp Leu Arg Arg Ty - #r Leu Glu Asn GlyLys 165 - # 170 - # 175 - - Glu Thr Leu Gln Arg Thr Asp Ala Pro Lys Th - #r His Met Thr His His 180 - # 185 - # 190 - - Ala Val Ser Asp His Glu Ala Thr Leu Arg Cy - #s Trp Ala Leu Ser Phe 195 - # 200 - # 205 - - Tyr Pro Ala Glu Ile Thr Leu Thr Trp Gln Ar - #g Asp Gly Glu Asp Gln 210 - # 215 - # 220 - - Thr Gln Asp Thr Glu Leu Val Glu Thr Arg Pr - #o Ala Gly Asp Gly Thr 225 2 - #30 2 - #35 2 -#40 - - Phe Gln Lys Trp Ala Ala Val Val Val Pro Se - #r Gly Gln Glu GlnArg 245 - # 250 - # 255 - - Tyr Thr Cys His Val Gln His Glu Gly Leu Pr - #o Lys Pro Leu Thr Leu 260 - # 265 - # 270 - - Pro Trp - - - - (2) INFORMATION FOR SEQ ID NO:109: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 253 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 7 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:109: - - Met Ala Ile Ser Gly Val Pro Val Leu Gly Ph - #e Phe Ile Ile Ala Val25 - - #20 - - #15 - -#10 - - Leu Met Ser Ala Gln Glu Ser Trp Ala Ile Ly - #s Glu Glu His ValXaa -5 - # 1 - # 5 - - Ile Ile Gln Ala Glu Phe Tyr Leu Asn Pro As - #p Gln Ser Gly GluPhe 10 - # 15 - # 20 - - Met Phe Asp Phe Asp Gly Asp Glu Ile Phe Hi - #s Val Asp Met AlaLys 25 - # 30 - # 35 - - Lys Glu Thr Val Trp Arg Leu Glu Glu Phe Gl - #y Arg Phe Ala SerPhe 40 - #45 - #50 - #55 - - Glu Ala Gln Gly Ala Leu Ala Asn Ile Ala Va - #l Asp Lys Ala Asn Leu 60 - # 65 - # 70 - - Glu Ile Met Thr Lys Arg Ser Asn Tyr Thr Pr - #o Ile Thr Asn Val Pro 75 - # 80 - # 85 - - Pro Glu Val Thr Val Leu Thr Asn Ser Pro Va - #l Glu Leu Arg Glu Pro 90 - # 95 - # 100 - - Asn Val Leu Ile Cys Phe Ile Asp Lys Phe Th - #r Pro Pro Val Val Asn 105 - # 110 - # 115 - - Val Thr Trp Leu Arg Asn Gly Lys Pro Val Th - #r Thr Gly Val Ser Glu 120 1 - #25 1 - #30 1 -#35 - - Thr Val Phe Leu Pro Arg Glu Asp His Leu Ph - #e Arg Lys Phe HisTyr 140 - # 145 - # 150 - - Leu Pro Phe Leu Pro Ser Thr Glu Asp Val Ty - #r Asp Cys Arg Val Glu 155 - # 160 - # 165 - - His Trp Gly Leu Asp Glu Pro Leu Leu Lys Hi - #s Trp Glu Phe Asp Ala 170 - # 175 - # 180 - - Pro Ser Pro Leu Pro Glu Thr Thr Glu Asn Va - #l Val Cys Ala Leu Thr 185 - # 190 - # 195 - - Val Gly Leu Val Gly Ile Ile Ile Gly Thr Il - #e Phe Ile Ile Lys Gly 200 2 - #05 2 - #10 2 -#15 - - Leu Arg Lys Ser Asn Ala Ala Glu Arg Arg Gl - #y Pro Leu 220 - # 225 - - - - (2) INFORMATION FOR SEQ ID NO:110: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 255 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:110: - - Met Ile Leu Asn Lys Ala Leu Leu Leu Gly Al - #a Leu Ala Leu ThrThr 25 - - #20 - - #15 - -#10 - - Val Met Ser Pro Cys Gly Gly Glu Asp Ile Va - #l Ala Asp His ValAla -5 - # 1 - # 5 - - Ser Cys Gly Val Asn Leu Tyr Gln Phe Tyr Gl - #y Pro Ser Gly GlnTyr 10 - # 15 - # 20 - - Thr His Glu Phe Asp Gly Asp Glu Gln Phe Ty - #r Val Asp Leu GluArg 25 - # 30 - # 35 - - Lys Glu Thr Ala Trp Arg Trp Pro Glu Phe Se - #r Lys Phe Gly GlyPhe 40 - #45 - #50 - #55 - - Asp Pro Gln Gly Ala Leu Arg Asn Met Ala Va - #l Ala Lys His Asn Leu 60 - # 65 - # 70 - - Asn Ile Met Ile Lys Arg Tyr Asn Ser Thr Al - #a Ala Thr Asn Glu Val 75 - # 80 - # 85 - - Pro Glu Val Thr Val Phe Ser Lys Ser Pro Va - #l Thr Leu Gly Gln Pro 90 - # 95 - # 100 - - Asn Thr Leu Ile Cys Leu Val Asp Asn Ile Ph - #e Pro Pro Val Val Asn 105 - # 110 - # 115 - - Ile Thr Trp Leu Ser Asn Gly Gln Ser Val Th - #r Glu Asp Val Ser Glu 120 1 - #25 1 - #30 1 -#35 - - Thr Ser Phe Leu Ser Lys Ser Asp His Ser Ph - #e Phe Lys Ile SerTyr 140 - # 145 - # 150 - - Leu Thr Phe Leu Pro Ser Ala Asp Glu Ile Ty - #r Asp Cys Lys Val Glu 155 - # 160 - # 165 - - His Trp Gly Leu Asp Gln Pro Leu Leu Lys Hi - #s Trp Glu Pro Glu Ile 170 - # 175 - # 180 - - Pro Ala Pro Met Ser Glu Leu Thr Glu Thr Va - #l Val Cys Ala Leu Gly 185 - # 190 - # 195 - - Leu Ser Val Gly Leu Met Gly Ile Val Val Gl - #y Thr Val Phe Ile Ile 200 2 - #05 2 - #10 2 -#15 - - Gln Gly Leu Arg Ser Val Gly Ala Ser Arg Hi - #s Gln Gly Pro Leu 220 - # 225 - # 230 - - - - (2) INFORMATION FOR SEQ ID NO:111: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 261 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 7 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:111: - - Met Arg Pro Glu Asp Arg Met Phe His Ile Ar - #g Ala Val Ile Leu Arg -30 - # -25 - # -20 - - Ala Leu Ser Leu Ala Phe Leu Leu Ser Leu Ar - #g Gly Ala Gly Ala Ile15 - - #10 - - #5 - #1 - - Lys Ala Asp His Val Xaa Ser Thr Tyr Ala Al - #a Phe Val Gln Thr His 5 - # 10 - # 15 - - Arg Pro Thr Gly Glu Phe Met Phe Glu Phe As - #p Glu Asp Glu Met Phe 20 - # 25 - # 30 - - Tyr Val Asp Leu Asp Lys Lys Glu Thr Val Tr - #p His Leu Glu Glu Phe 35 - # 40 - # 45 - - Gly Gln Ala Phe Ser Phe Glu Ala Gln Gly Gl - #y Leu Ala Asn Ile Ala 50 - #55 - #60 - #65 - - Ile Leu Asn Asn Asn Leu Asn Thr Leu Ile Gl - #n Arg Ser Asn His Thr 70 - # 75 - # 80 - - Gln Ala Thr Asn Asp Pro Pro Glu Val Thr Va - #l Phe Pro Lys Glu Pro 85 - # 90 - # 95 - - Val Glu Leu Gly Gln Pro Asn Thr Leu Ile Cy - #s His Ile Asp Lys Phe 100 - # 105 - # 110 - - Phe Pro Pro Val Leu Asn Val Thr Trp Leu Cy - #s Asn Gly Glu Leu Val 115 - # 120 - # 125 - - Thr Glu Gly Val Ala Glu Ser Leu Phe Leu Pr - #o Arg Thr Asp Tyr Ser 130 1 - #35 1 - #40 1 -#45 - - Phe His Lys Phe His Tyr Leu Thr Phe Val Pr - #o Ser Ala Glu AspPhe 150 - # 155 - # 160 - - Tyr Asp Cys Arg Val Glu His Trp Gly Leu As - #p Gln Pro Leu Leu Lys 165 - # 170 - # 175 - - His Trp Glu Ala Gln Glu Pro Ile Gln Met Pr - #o Glu Thr Thr Glu Thr 180 - # 185 - # 190 - - Val Leu Cys Ala Leu Gly Leu Val Leu Gly Le - #u Val Gly Phe Ile Val 195 - # 200 - # 205 - - Gly Thr Val Leu Ile Ile Lys Ser Leu Arg Se - #r Gly His Asp Pro Arg 210 2 - #15 2 - #20 2 -#25 - - Ala Gln Gly Thr Leu 230 - - - - (2) INFORMATION FOR SEQ ID NO:112: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 250 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:112: - - Met Ala Leu Arg Ala Gly Leu Val Leu Gly Ph - #e His Thr Leu MetThr 25 - - #20 - - #15 - -#10 - - Leu Leu Ser Pro Gln Glu Ala Gly Ala Thr Ly - #s Ala Asp His MetGly -5 - # 1 - # 5 - - Ser Tyr Gly Pro Ala Phe Tyr Gln Ser Tyr Gl - #y Ala Ser Gly GlnPhe 10 - # 15 - # 20 - - Thr His Glu Phe Asp Glu Glu Gln Leu Phe Se - #r Val Asp Leu LysLys 25 - # 30 - # 35 - - Ser Glu Ala Val Trp Arg Leu Pro Glu Phe Gl - #y Asp Phe Ala ArgPhe 40 - #45 - #50 - #55 - - Asp Pro Gln Gly Gly Leu Ala Gly Ile Ala Al - #a Ile Lys Ala His Leu 60 - # 65 - # 70 - - Asp Ile Leu Val Glu Arg Ser Asn Arg Ser Ar - #g Ala Ile Asn Val Pro 75 - # 80 - # 85 - - Pro Arg Val Thr Val Leu Pro Lys Ser Arg Va - #l Glu Leu Gly Gln Pro 90 - # 95 - # 100 - - Asn Ile Leu Ile Cys Ile Val Asp Asn Ile Ph - #e Pro Pro Val Ile Asn 105 - # 110 - # 115 - - Ile Thr Trp Leu Arg Asn Gly Gln Thr Val Th - #r Glu Gly Val Ala Gln 120 1 - #25 1 - #30 1 -#35 - - Thr Ser Phe Tyr Ser Gln Pro Asp His Leu Ph - #e Arg Lys Phe HisTyr 140 - # 145 - # 150 - - Leu Pro Phe Val Pro Ser Ala Glu Asp Val Ty - #r Asp Cys Gln Val Glu 155 - # 160 - # 165 - - His Trp Gly Leu Asp Ala Pro Leu Leu Arg Hi - #s Trp Glu Leu Gln Val 170 - # 175 - # 180 - - Pro Ile Pro Pro Pro Asp Ala Met Glu Thr Le - #u Val Cys Ala Leu Gly 185 - # 190 - # 195 - - Leu Ala Ile Gly Leu Val Gly Phe Leu Val Gl - #y Thr Val Leu Ile Ile 200 2 - #05 2 - #10 2 -#15 - - Met Gly Thr Tyr Val Ser Ser Val Pro Arg 220 - # 225 - - - - (2) INFORMATION FOR SEQ ID NO:113: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 256 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:113: - - Met Pro Arg Ser Arg Ala Leu Ile Leu Gly Va - #l Leu Ala Leu ThrThr 25 -20 - # -15 - # -10 - - Met Leu Ser Leu Cys Gly Gly Glu Asp Asp Il - #e Glu Ala Asp His Val -5 - # 1 - # 5 - - Gly Ser Tyr Gly Ile Thr Phe Tyr Gln Ser Pr - #o Gly Asp Ile Gly Gln 10 - # 15 - # 20 - - Tyr Thr Phe Glu Phe Asp Gly Asp Glu Leu Ph - #e Tyr Val Asp Leu Asp 25 - # 30 - # 35 - - Lys Lys Glu Thr Val Trp Met Leu Pro Glu Ph - #e Ala Gln Leu Arg Arg 40 - #45 - #50 - #55 - - Phe Glu Pro Gln Gly Gly Leu Gln Asn Ile Al - #a Thr Gly Lys His Asn 60 - # 65 - # 70 - - Leu Glu Ile Leu Thr Lys Arg Ser Asn Ser Th - #r Pro Ala Thr Asn Glu 75 - # 80 - # 85 - - Ala Pro Gln Ala Thr Val Phe Pro Lys Ser Pr - #o Val Leu Leu Gly Gln 90 - # 95 - # 100 - - Pro Asn Thr Leu Ile Cys Phe Val Asp Asn Il - #e Phe Pro Pro Val Ile 105 - # 110 - # 115 - - Asn Ile Thr Trp Leu Arg Asn Ser Lys Ser Va - #l Thr Asp Gly Val Tyr 120 1 - #25 1 - #30 1 -#35 - - Glu Thr Ser Phe Phe Val Asn Arg Asp Tyr Se - #r Phe His Lys LeuSer 140 - # 145 - # 150 - - Tyr Leu Thr Phe Ile Pro Ser Asp Asp Asp Il - #e Tyr Asp Cys Lys Val 155 - # 160 - # 165 - - Glu His Trp Gly Leu Glu Glu Pro Val Leu Ly - #s His Trp Glu Pro Glu 170 - # 175 - # 180 - - Ile Pro Ala Pro Met Ser Glu Leu Thr Glu Th - #r Val Val Cys Ala Leu 185 - # 190 - # 195 - - Gly Leu Ser Val Gly Leu Val Gly Ile Val Va - #l Gly Thr Ile Phe Ile 200 2 - #05 2 - #10 2 -#15 - - Ile Gln Gly Leu Arg Ser Gly Gly Thr Ser Ar - #g His Pro Gly ProLeu 220 - # 225 - # 230 - - - - (2) INFORMATION FOR SEQ ID NO:114: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 256 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 7 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:114: - - Met Ala Thr Ile Gly Ala Leu Val Leu Arg Ph - #e Phe Phe Ile Ala Val25 -20 - # -15 - # -10 - - Leu Met Ser Ser Gln Lys Ser Trp Ala Ile Ly - #s Glu Glu His Thr Xaa -5 - # 1 - # 5 - - Ile Ile Gln Ala Glu Phe Tyr Leu Leu Pro As - #p Lys Arg Gly Glu Phe 10 - # 15 - # 20 - - Met Phe Asp Phe Asp Gly Asp Glu Ile Phe Hi - #s Val Asp Ile Glu Lys 25 - # 30 - # 35 - - Ser Glu Thr Ile Trp Arg Leu Glu Glu Phe Al - #a Lys Phe Ala Ser Phe 40 - #45 - #50 - #55 - - Glu Ala Gln Gly Ala Leu Ala Asn Ile Ala Va - #l Asp Lys Ala Asn Leu 60 - # 65 - # 70 - - Asp Val Met Lys Glu Arg Ser Asn Asn Thr Pr - #o Ser Ala Asn Val Ala 75 - # 80 - # 85 - - Pro Glu Val Thr Val Leu Ser Arg Ser Pro Va - #l Asn Leu Gly Glu Pro 90 - # 95 - # 100 - - Asn Ile Leu Ile Cys Phe Ile Asp Lys Phe Se - #r Pro Pro Val Val Asn 105 - # 110 - # 115 - - Val Thr Trp Leu Arg Asn Gly Arg Pro Val Th - #r Glu Gly Val Ser Glu 120 1 - #25 1 - #30 1 -#35 - - Thr Val Phe Leu Pro Arg Asp Asp His Leu Ph - #e Arg Lys Phe HisTyr 140 - # 145 - # 150 - - Leu Thr Phe Leu Pro Ser Thr Asp Asp Phe Ty - #r Asp Cys Glu Val Asp 155 - # 160 - # 165 - - His Trp Gly Leu Glu Glu Pro Leu Arg Lys Al - #a Trp Glu Phe Glu Glu 170 - # 175 - # 180 - - Lys Thr Leu Leu Pro Glu Thr Lys Glu Asn Va - #l Val Cys Ala Leu Gly 185 - # 190 - # 195 - - Leu Phe Val Gly Leu Val Gly Ile Val Val Gl - #y Ile Ile Leu Ile Met 200 2 - #05 2 - #10 2 -#15 - - Lys Gly Ile Lys Lys Arg Asn Val Val Glu Ar - #g Arg Gln Gly AlaLeu 220 - # 225 - # 230 - - - - (2) INFORMATION FOR SEQ ID NO:115: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 266 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:115: - - Met Val Cys Leu Lys Leu Pro Gly Gly Ser Cy - #s Met Thr Ala Leu Thr29 -25 - # -20 - # -15 - - Val Thr Leu Met Val Leu Ser Ser Pro Leu Al - #a Leu Ala Gly Asp Thr -10 - # -5 - # 1 - - Arg Pro Arg Phe Leu Trp Gln Leu Lys Phe Gl - #u Cys His Phe Phe Asn 5 - # 10 - # 15 - - Gly Thr Glu Arg Val Arg Leu Leu Glu Arg Cy - #s Ile Tyr Asn Gln Glu 20 - # 25 - # 30 - - Glu Ser Val Arg Phe Asp Ser Asp Val Gly Gl - #u Tyr Arg Ala Val Thr 35 - #40 - #45 - #50 - - Glu Leu Gly Arg Pro Asp Ala Glu Tyr Trp As - #n Ser Gln Lys Asp Leu 55 - # 60 - # 65 - - Leu Glu Gln Arg Arg Ala Ala Val Asp Thr Ty - #r Cys Arg His Asn Tyr 70 - # 75 - # 80 - - Gly Val Gly Glu Ser Phe Thr Val Gln Arg Ar - #g Val Glu Pro Lys Val 85 - # 90 - # 95 - - Thr Val Tyr Pro Ser Lys Thr Gln Pro Leu Gl - #n His His Asn Leu Leu 100 - # 105 - # 110 - - Val Cys Ser Val Ser Gly Phe Tyr Pro Gly Se - #r Ile Glu Val Arg Trp 115 1 - #20 1 - #25 1 -#30 - - Phe Arg Asn Gly Gln Glu Glu Lys Ala Gly Va - #l Val Ser Thr GlyLeu 135 - # 140 - # 145 - - Ile Gln Asn Gly Asp Trp Thr Phe Gln Thr Le - #u Val Met Leu Glu Thr 150 - # 155 - # 160 - - Val Pro Arg Ser Gly Glu Val Tyr Thr Cys Gl - #n Val Glu His Pro Ser 165 - # 170 - # 175 - - Val Thr Ser Pro Leu Thr Val Glu Trp Arg Al - #a Arg Ser Glu Ser Ala 180 - # 185 - # 190 - - Gln Ser Lys Met Leu Ser Gly Val Gly Gly Ph - #e Val Leu Gly Leu Leu 195 2 - #00 2 - #05 2 -#10 - - Phe Leu Gly Ala Gly Leu Phe Ile Tyr Phe Ar - #g Asn Gln Lys GlyHis 215 - # 220 - # 225 - - Ser Gly Leu Gln Pro Thr Gly Phe Leu Ser 230 - # 235 - - - - (2) INFORMATION FOR SEQ ID NO:116: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 269 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 226..233 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:116: - - Met Ser Trp Lys Lys Ser Leu Arg Ile Pro Gl - #y Asp Leu Arg Val Ala -30 - # -25 - # -20 - - Thr Val Thr Leu Met Leu Ala Ile Leu Ser Se - #r Ser Leu Ala Glu Gly -15 - # -10 - # -5 - - Arg Asp Ser Pro Glu Asp Phe Val Tyr Gln Ph - #e Lys Gly Leu Cys Tyr 1 5 - # 10 - # 15 - - Phe Thr Asn Gly Thr Glu Arg Val Arg Gly Va - #l Thr Arg His Ile Tyr 20 - # 25 - # 30 - - Asn Arg Glu Glu Tyr Val Arg Phe Asp Ser As - #p Val Gly Val Tyr Arg 35 - # 40 - # 45 - - Ala Val Thr Pro Gln Gly Arg Pro Val Ala Gl - #u Tyr Trp Asn Ser Gln 50 - # 55 - # 60 - - Lys Glu Val Leu Glu Gly Ala Arg Ala Ser Va - #l Asp Arg Val Cys Arg 65 - #70 - #75 - #80 - - His Asn Tyr Glu Val Ala Tyr Arg Gly Ile Le - #u Gln Arg Arg Val Glu 85 - # 90 - # 95 - - Pro Thr Val Thr Ile Ser Pro Ser Arg Thr Gl - #u Ala Leu Asn His His 100 - # 105 - # 110 - - Asn Leu Leu Ile Cys Ser Val Thr Asp Phe Ty - #r Pro Ser Gln Ile Lys 115 - # 120 - # 125 - - Val Arg Trp Phe Arg Asn Asp Gln Glu Glu Th - #r Ala Gly Val Val Ser 130 - # 135 - # 140 - - Thr Pro Leu Ile Arg Asn Gly Asp Trp Thr Ph - #e Gln Ile Leu Val Met 145 1 - #50 1 - #55 1 -#60 - - Leu Glu Met Thr Pro Gln Arg Gly Asp Val Ty - #r Thr Cys His ValGlu 165 - # 170 - # 175 - - His Pro Ser Leu Gln Ser Pro Ile Thr Val Gl - #u Trp Arg Ala Gln Ser 180 - # 185 - # 190 - - Glu Ser Ala Gln Ser Lys Met Leu Ser Gly Va - #l Gly Gly Phe Val Leu 195 - # 200 - # 205 - - Gly Leu Ile Phe Leu Gly Leu Gly Leu Ile Il - #e Arg Gln Arg Ser Arg 210 - # 215 - # 220 - - Lys Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Gly Le - #u Leu His 225 2 - #30 2 - #35 - - - - (2) INFORMATION FOR SEQ ID NO:117: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 259 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (ix) FEATURE: (A) NAME/KEY: Region (B) LOCATION: 24..25 (D) OTHER INFORMATION: - #/note= "Xaa is an unidentified amino aci - #d residue." - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:117: - - Met Val Leu Gln Val Ser Ala Ala Pro Arg Th - #r Val Ala Leu Thr Ala28 -25 - # -20 - # -15 - - Leu Leu Met Val Leu Leu Thr Ser Val Val Gl - #n Gly Arg Ala Thr Pro -10 - # -5 - # 1 - - Glu Asn Tyr Leu Phe Gln Gly Arg Gln Glu Cy - #s Tyr Ala Phe Asn Gly 5 - # 10 - # 15 - # 20 - - Thr Gln Arg Xaa Xaa Phe Leu Glu Arg Tyr Il - #e Tyr Asn Arg Glu Glu 25 - # 30 - # 35 - - Phe Val Arg Phe Asp Ser Asp Val Gly Glu Ph - #e Arg Ala Val Thr Glu 40 - # 45 - # 50 - - Leu Gly Arg Pro Asp Glu Glu Tyr Trp Asn Se - #r Gln Lys Asp Ile Leu 55 - # 60 - # 65 - - Glu Glu Glu Arg Ala Val Pro Asp Arg Met Cy - #s Arg His Asn Tyr Glu 70 - # 75 - # 80 - - Leu Gly Gly Pro Met Thr Leu Gln Arg Arg Va - #l Gln Pro Arg Val Asn 85 - #90 - #95 - #100 - - Val Ser Pro Ser Lys Lys Gly Pro Leu Gln Hi - #s His Asn Leu Leu Val 105 - # 110 - # 115 - - Cys His Val Thr Asp Phe Tyr Pro Gly Ser Il - #e Gln Val Arg Trp Phe 120 - # 125 - # 130 - - Leu Asn Gly Gln Glu Glu Thr Ala Gly Val Va - #l Ser Thr Asn Leu Ile 135 - # 140 - # 145 - - Arg Asn Gly Asp Trp Thr Phe Gln Ile Leu Va - #l Met Leu Glu Met Thr 150 - # 155 - # 160 - - Pro Gln Gln Gly Asp Val Tyr Thr Cys Gln Va - #l Glu His Thr Ser Leu 165 1 - #70 1 - #75 1 -#80 - - Asp Ser Pro Val Thr Val Glu Trp Lys Ala Gl - #n Ser Asp Ser AlaArg 185 - # 190 - # 195 - - Ser Lys Thr Leu Thr Gly Ala Gly Gly Phe Va - #l Leu Gly Leu Ile Ile 200 - # 205 - # 210 - - Cys Gly Val Gly Ile Phe Met His Arg Arg Se - #r Lys Lys Val Gln Arg 215 - # 220 - # 225 - - Gly Ser Ala 230 - - - - (2) INFORMATION FOR SEQ ID NO:118: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 273 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:118: - - Met Gly Ser Gly Trp Val Pro Trp Val Val Al - #a Leu Leu Val Asn Leu -25 - # -20 - # -15 - - Thr Arg Leu Asp Ser Ser Met Thr Gln Gly Th - #r Asp Ser Pro Glu Asp10 - - #5 - #1 5 - - Phe Val Ile Gln Ala Lys Ala Asp Cys Tyr Ph - #e Thr Asn Gly Thr Glu 10 - # 15 - # 20 - - Lys Val Gln Phe Val Val Arg Phe Ile Phe As - #n Leu Glu Glu Tyr Val 25 - # 30 - # 35 - - Arg Phe Asp Ser Asp Val Gly Met Phe Val Al - #a Leu Thr Lys Leu Gly 40 - # 45 - # 50 - - Gln Pro Asp Ala Glu Gln Trp Asn Ser Arg Le - #u Asp Leu Leu Glu Arg 55 - #60 - #65 - #70 - - Ser Arg Gln Ala Val Asp Gly Val Cys Arg Hi - #s Asn Tyr Arg Leu Gly 75 - # 80 - # 85 - - Ala Pro Phe Thr Val Gly Arg Lys Val Gln Pr - #o Glu Val Thr Val Tyr 90 - # 95 - # 100 - - Pro Glu Arg Thr Pro Leu Leu His Gln His As - #n Leu Leu His Cys Ser 105 - # 110 - # 115 - - Val Thr Gly Phe Tyr Pro Gly Asp Ile Lys Il - #e Lys Trp Phe Leu Asn 120 - # 125 - # 130 - - Gly Gln Glu Glu Arg Ala Gly Val Met Ser Th - #r Gly Pro Ile Arg Asn 135 1 - #40 1 - #45 1 -#50 - - Gly Asp Trp Thr Phe Gln Thr Val Val Met Le - #u Glu Met Thr ProGlu 155 - # 160 - # 165 - - Leu Gly His Val Tyr Thr Cys Leu Val Asp Hi - #s Ser Ser Leu Leu Ser 170 - # 175 - # 180 - - Pro Val Ser Val Glu Trp Arg Ala Gln Ser Gl - #u Tyr Ser Trp Arg Lys 185 - # 190 - # 195 - - Met Leu Ser Gly Ile Ala Ala Phe Leu Leu Gl - #y Leu Ile Phe Leu Leu 200 - # 205 - # 210 - - Val Gly Ile Val Ile Gln Leu Arg Ala Gln Ly - #s Gly Tyr Val Arg Thr 215 2 - #20 2 - #25 2 -#30 - - Gln Met Ser Gly Asn Glu Val Ser Arg Ala Va - #l Leu Leu Pro GlnSer 235 - # 240 - # 245 - - Gln - - - - (2) INFORMATION FOR SEQ ID NO:119: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 265 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:119: - - Met Ala Leu Gln Ile Pro Ser Leu Leu Leu Se - #r Ala Ala Val Val Val -25 - # -20 - # -15 - - Leu Met Val Leu Ser Ser Pro Arg Thr Glu Gl - #y Gly Asn Ser Glu Arg -10 - # -5 - # 1 - #5 - - His Phe Val Ala Gln Leu Lys Gly Glu Cys Ty - #r Phe Thr Asn Gly Thr 10 - # 15 - # 20 - - Gln Arg Ile Arg Ser Val Asn Arg Tyr Ile Ty - #r Asn Arg Glu Glu Trp 25 - # 30 - # 35 - - Val Arg Phe Asp Ser Asp Val Gly Glu Tyr Ar - #g Ala Val Thr Glu Leu 40 - # 45 - # 50 - - Gly Arg Pro Asp Ala Glu Tyr Trp Asn Ser Gl - #n Pro Glu Ile Leu Glu 55 - # 60 - # 65 - - Arg Thr Arg Ala Glu Val Asp Thr Val Cys Ar - #g His Asn Tyr Glu Gly 70 - #75 - #80 - #85 - - Val Glu Thr His Thr Ser Leu Arg Arg Leu Gl - #u Gln Pro Asn Val Ala 90 - # 95 - # 100 - - Ile Ser Leu Ser Arg Thr Glu Ala Leu Asn Hi - #s His Asn Thr Leu Val 105 - # 110 - # 115 - - Cys Ser Val Thr Asp Phe Tyr Pro Ala Lys Il - #e Lys Val Arg Trp Phe 120 - # 125 - # 130 - - Arg Asn Gly Gln Glu Glu Thr Val Gly Val Se - #r Ser Thr Gln Leu Ile 135 - # 140 - # 145 - - Arg Asn Gly Asp Trp Thr Phe Gln Val Leu Va - #l Met Leu Glu Met Thr 150 1 - #55 1 - #60 1 -#65 - - Pro His Gln Gly Glu Val Tyr Thr Cys His Va - #l Glu His Pro SerLeu 170 - # 175 - # 180 - - Lys Ser Pro Ile Thr Val Glu Trp Arg Ala Gl - #n Ser Glu Ser Ala Arg 185 - # 190 - # 195 - - Ser Lys Met Leu Ser Gly Ile Gly Gly Cys Va - #l Leu Gly Val Ile Phe 200 - # 205 - # 210 - - Leu Gly Leu Gly Leu Phe Ile Arg His Arg Se - #r Gln Lys Gly Pro Arg 215 - # 220 - # 225 - - Gly Pro Pro Pro Ala Gly Leu Leu Gln 230 2 - #35 - - - - (2) INFORMATION FOR SEQ ID NO:120: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 264 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:120: - - Met Val Trp Leu Pro Arg Val Pro Cys Val Al - #a Ala Val Ile Leu Leu -25 - # -20 - # -15 - - Leu Thr Val Leu Ser Pro Pro Val Ala Leu Va - #l Arg Asp Thr Pro Pro -10 - - #5 - # 1 - # 5 - - Arg Phe Leu Glu Tyr Val Thr Ser Glu Cys Hi - #s Phe Tyr Asn Gly Thr 10 - # 15 - # 20 - - Gln His Val Arg Phe Leu Glu Arg Phe Ile Ty - #r Asn Arg Glu Glu Asn 25 - # 30 - # 35 - - Leu Arg Phe Asp Ser Asp Val Gly Glu Tyr Ar - #g Ala Val Thr Glu Leu 40 - # 45 - # 50 - - Gly Arg Pro Asp Ala Glu Asn Trp Asn Ser Gl - #n Pro Glu Ile Leu Glu 55 - # 60 - # 65 - - Asp Ala Arg Ala Ser Val Asp Thr Tyr Cys Ar - #g His Asn Tyr Glu Ile 70 - #75 - #80 - #85 - - Ser Asp Lys Phe Leu Val Arg Arg Arg Val Gl - #u Pro Thr Val Thr Val 90 - # 95 - # 100 - - Tyr Pro Thr Lys Thr Gln Pro Leu Glu His Hi - #s Asn Leu Leu Val Cys 105 - # 110 - # 115 - - Ser Val Ser Asp Phe Tyr Pro Gly Asn Ile Gl - #u Val Arg Trp Phe Arg 120 - # 125 - # 130 - - Asn Gly Lys Glu Glu Glu Thr Gly Ile Val Se - #r Thr Gly Leu Val Arg 135 - # 140 - # 145 - - Asn Gly Asp Trp Thr Phe Gln Thr Leu Val Me - #t Leu Glu Trp Val Pro 150 1 - #55 1 - #60 1 -#65 - - Gln Ser Gly Glu Val Tyr Thr Cys Gln Val Gl - #u His Pro Ser LeuThr 170 - # 175 - # 180 - - Asp Pro Val Thr Val Glu Trp Lys Ala Gln Se - #r Thr Ser Ala Gln Asn 185 - # 190 - # 195 - - Lys Met Leu Ser Gly Val Gly Gly Phe Val Le - #u Gly Leu Leu Phe Leu 200 - # 205 - # 210 - - Gly Ala Gly Leu Phe Ile Tyr Phe Arg Asn Gl - #n Lys Gly Gln Ser Glu 215 - # 220 - # 225 - - Leu Gln Pro Thr Gly Leu Leu Ser 230 2 - #35 - - - - (2) INFORMATION FOR SEQ ID NO:121: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 6 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:121: - - Glu Phe Ser Lys Phe Gly 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:122: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 5 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:122: - - Val Leu Arg Gln Arg 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:123: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 6 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:123: - - Leu Phe Arg Arg Arg Arg 1 5 - - - - (2) INFORMATION FOR SEQ ID NO:124: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 4 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:124: - - Glu Val Ala Tyr 1 - - - - (2) INFORMATION FOR SEQ ID NO:125: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 4 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:125: - - Glu Val Ala Phe 1 - - - - (2) INFORMATION FOR SEQ ID NO:126: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 4 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:126: - - Glu Val Ala Gly 1 - - - - (2) INFORMATION FOR SEQ ID NO:127: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 4 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:127: - - Gln Leu Glu Leu__________________________________________________________________________

Number	Name	Date
4478823	Sanderson	Oct 1984
4946778	Ladner	Aug 1990
5242687	Tykocinski et al.	Sep 1993
5260422	Clark et al.	Nov 1993
5528498	Huston et al.	Jun 1996
5583031	Stern	Dec 1996

	Number	Date	Country
Parent	117575	Sep 1993
Parent	792473	Nov 1991

	Number	Date	Country
Parent	072787	Jun 1993
Parent	801818	Dec 1991

Altered major histocompatibility complex (MHC) determinant and methods of using the determinant

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Inventors

Original Assignees

Examiners

Agents

CPC

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US

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Abstract

Description

Claims

CROSS-REFERENCE TO RELATED APPLICATION

US Referenced Citations (6)

Foreign Referenced Citations (1)

Non-Patent Literature Citations (22)

Continuations (2)

Continuation in Parts (2)

Entry
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Rock et al., "Dissociation of beta2-microglobulin leads to the accumulation of a substantial pool of inactive class I MHC heavy chains on the cell surface", Cell 65: 611-620 (1991).
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Huston et al., "Protein engineering of antibody binding sites: Recovery of specific activity in an anti-digoxin single-chain Fv analogue produced in Escherichia coli", Proc. Natl. Acad. Sci. USA 85: 5879-5883 (1988).
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