An attempt to define allergen-specific molecular surface features: a bioinformatic approach
Allergens are proteins that elicit T helper lymphocyte type 2 (Th2) responses culminating in IgE antibody production and allergic disease. However, we have no answer to the fundamental question of why certain proteins are allergens, while others are not. We hypothesized that analysis of the surface...
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Veröffentlicht in: | Bioinformatics 2005-12, Vol.21 (23), p.4201-4204 |
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description | Allergens are proteins that elicit T helper lymphocyte type 2 (Th2) responses culminating in IgE antibody production and allergic disease. However, we have no answer to the fundamental question of why certain proteins are allergens, while others are not. We hypothesized that analysis of the surface of diverse allergens may reveal common structural features which might enable them to be recognized as Th2-inducing antigens by cells of the innate immune system. We have therefore used the ConSurf server to search for allergen-specific motifs. This has enabled us to identify residue conservation patterns in the homologues of Ara t 8 (plant profilin), Act c 1 (actinidin), Bet v 1 (plant pathogenesis-related protein) and Ves v 5 (venom allergen). The results demonstrate the presence of allergen-specific patches consisting of an unusually high proportion of surface-exposed hydrophobic residues. The patches that have been identified may represent molecular patterns recognizable by cells of the innate immune system. Contact: farouk.shakib@nottingham.ac.uk Supplementary Information: |
doi_str_mv | 10.1093/bioinformatics/bti700 |
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However, we have no answer to the fundamental question of why certain proteins are allergens, while others are not. We hypothesized that analysis of the surface of diverse allergens may reveal common structural features which might enable them to be recognized as Th2-inducing antigens by cells of the innate immune system. We have therefore used the ConSurf server to search for allergen-specific motifs. This has enabled us to identify residue conservation patterns in the homologues of Ara t 8 (plant profilin), Act c 1 (actinidin), Bet v 1 (plant pathogenesis-related protein) and Ves v 5 (venom allergen). The results demonstrate the presence of allergen-specific patches consisting of an unusually high proportion of surface-exposed hydrophobic residues. The patches that have been identified may represent molecular patterns recognizable by cells of the innate immune system. Contact: farouk.shakib@nottingham.ac.uk Supplementary Information:</description><identifier>ISSN: 1367-4803</identifier><identifier>EISSN: 1460-2059</identifier><identifier>EISSN: 1367-4811</identifier><identifier>DOI: 10.1093/bioinformatics/bti700</identifier><identifier>PMID: 16204345</identifier><identifier>CODEN: BOINFP</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Algorithms ; Allergens - chemistry ; Amino Acid Motifs ; Amino Acid Sequence ; Biological and medical sciences ; Cell Membrane - metabolism ; Computational Biology - methods ; Crystallography, X-Ray ; Cysteine Endopeptidases - chemistry ; Desensitization, Immunologic ; Fundamental and applied biological sciences. Psychology ; General aspects ; Humans ; Hypersensitivity - immunology ; Immune System - immunology ; Immunoglobulin E - chemistry ; Mathematics in biology. Statistical analysis. Models. Metrology. 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However, we have no answer to the fundamental question of why certain proteins are allergens, while others are not. We hypothesized that analysis of the surface of diverse allergens may reveal common structural features which might enable them to be recognized as Th2-inducing antigens by cells of the innate immune system. We have therefore used the ConSurf server to search for allergen-specific motifs. This has enabled us to identify residue conservation patterns in the homologues of Ara t 8 (plant profilin), Act c 1 (actinidin), Bet v 1 (plant pathogenesis-related protein) and Ves v 5 (venom allergen). The results demonstrate the presence of allergen-specific patches consisting of an unusually high proportion of surface-exposed hydrophobic residues. The patches that have been identified may represent molecular patterns recognizable by cells of the innate immune system. Contact: farouk.shakib@nottingham.ac.uk Supplementary Information:</description><subject>Algorithms</subject><subject>Allergens - chemistry</subject><subject>Amino Acid Motifs</subject><subject>Amino Acid Sequence</subject><subject>Biological and medical sciences</subject><subject>Cell Membrane - metabolism</subject><subject>Computational Biology - methods</subject><subject>Crystallography, X-Ray</subject><subject>Cysteine Endopeptidases - chemistry</subject><subject>Desensitization, Immunologic</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects</subject><subject>Humans</subject><subject>Hypersensitivity - immunology</subject><subject>Immune System - immunology</subject><subject>Immunoglobulin E - chemistry</subject><subject>Mathematics in biology. Statistical analysis. Models. Metrology. 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However, we have no answer to the fundamental question of why certain proteins are allergens, while others are not. We hypothesized that analysis of the surface of diverse allergens may reveal common structural features which might enable them to be recognized as Th2-inducing antigens by cells of the innate immune system. We have therefore used the ConSurf server to search for allergen-specific motifs. This has enabled us to identify residue conservation patterns in the homologues of Ara t 8 (plant profilin), Act c 1 (actinidin), Bet v 1 (plant pathogenesis-related protein) and Ves v 5 (venom allergen). The results demonstrate the presence of allergen-specific patches consisting of an unusually high proportion of surface-exposed hydrophobic residues. The patches that have been identified may represent molecular patterns recognizable by cells of the innate immune system. Contact: farouk.shakib@nottingham.ac.uk Supplementary Information:</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>16204345</pmid><doi>10.1093/bioinformatics/bti700</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Algorithms Allergens - chemistry Amino Acid Motifs Amino Acid Sequence Biological and medical sciences Cell Membrane - metabolism Computational Biology - methods Crystallography, X-Ray Cysteine Endopeptidases - chemistry Desensitization, Immunologic Fundamental and applied biological sciences. Psychology General aspects Humans Hypersensitivity - immunology Immune System - immunology Immunoglobulin E - chemistry Mathematics in biology. Statistical analysis. Models. Metrology. Data processing in biology (general aspects) Molecular Sequence Data Plant Proteins - immunology Plants - chemistry Plants - immunology Profilins - chemistry Software T-Lymphocytes - immunology Th2 Cells - immunology |
title | An attempt to define allergen-specific molecular surface features: a bioinformatic approach |
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