Abstract
A key step in rational vaccine development is to understand how antigens are recognized by their receptors. Several crystal structures of MHC/HLA molecules are now available. We report a structural bioinformatics study of peptide-HLA complexes to derive features that generate recognition specificity, useful for guiding the design process.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Computational Biology / methods
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Databases, Protein
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Epitope Mapping / methods
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Epitopes, T-Lymphocyte / genetics
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Epitopes, T-Lymphocyte / immunology*
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Epitopes, T-Lymphocyte / metabolism
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Histocompatibility Antigens Class I / genetics
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Histocompatibility Antigens Class I / immunology*
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Histocompatibility Antigens Class I / metabolism
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Peptides / chemistry
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Peptides / immunology*
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Peptides / metabolism
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Protein Interaction Mapping
Substances
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Epitopes, T-Lymphocyte
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Histocompatibility Antigens Class I
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Peptides