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BepiPred-2.0: improving sequence-based B-cell epitope prediction using conformational epitopes
Antibodies have become an indispensable tool for many biotechnological and clinical applications. They bind their molecular target (antigen) by recognizing a portion of its structure (epitope) in a highly specific manner. The ability to predict epitopes from antigen sequences alone is a complex task...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570230/ https://www.ncbi.nlm.nih.gov/pubmed/28472356 http://dx.doi.org/10.1093/nar/gkx346 |
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author | Jespersen, Martin Closter Peters, Bjoern Nielsen, Morten Marcatili, Paolo |
author_facet | Jespersen, Martin Closter Peters, Bjoern Nielsen, Morten Marcatili, Paolo |
author_sort | Jespersen, Martin Closter |
collection | PubMed |
description | Antibodies have become an indispensable tool for many biotechnological and clinical applications. They bind their molecular target (antigen) by recognizing a portion of its structure (epitope) in a highly specific manner. The ability to predict epitopes from antigen sequences alone is a complex task. Despite substantial effort, limited advancement has been achieved over the last decade in the accuracy of epitope prediction methods, especially for those that rely on the sequence of the antigen only. Here, we present BepiPred-2.0 (http://www.cbs.dtu.dk/services/BepiPred/), a web server for predicting B-cell epitopes from antigen sequences. BepiPred-2.0 is based on a random forest algorithm trained on epitopes annotated from antibody-antigen protein structures. This new method was found to outperform other available tools for sequence-based epitope prediction both on epitope data derived from solved 3D structures, and on a large collection of linear epitopes downloaded from the IEDB database. The method displays results in a user-friendly and informative way, both for computer-savvy and non-expert users. We believe that BepiPred-2.0 will be a valuable tool for the bioinformatics and immunology community. |
format | Online Article Text |
id | pubmed-5570230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55702302017-08-29 BepiPred-2.0: improving sequence-based B-cell epitope prediction using conformational epitopes Jespersen, Martin Closter Peters, Bjoern Nielsen, Morten Marcatili, Paolo Nucleic Acids Res Web Server Issue Antibodies have become an indispensable tool for many biotechnological and clinical applications. They bind their molecular target (antigen) by recognizing a portion of its structure (epitope) in a highly specific manner. The ability to predict epitopes from antigen sequences alone is a complex task. Despite substantial effort, limited advancement has been achieved over the last decade in the accuracy of epitope prediction methods, especially for those that rely on the sequence of the antigen only. Here, we present BepiPred-2.0 (http://www.cbs.dtu.dk/services/BepiPred/), a web server for predicting B-cell epitopes from antigen sequences. BepiPred-2.0 is based on a random forest algorithm trained on epitopes annotated from antibody-antigen protein structures. This new method was found to outperform other available tools for sequence-based epitope prediction both on epitope data derived from solved 3D structures, and on a large collection of linear epitopes downloaded from the IEDB database. The method displays results in a user-friendly and informative way, both for computer-savvy and non-expert users. We believe that BepiPred-2.0 will be a valuable tool for the bioinformatics and immunology community. Oxford University Press 2017-07-03 2017-05-02 /pmc/articles/PMC5570230/ /pubmed/28472356 http://dx.doi.org/10.1093/nar/gkx346 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Web Server Issue Jespersen, Martin Closter Peters, Bjoern Nielsen, Morten Marcatili, Paolo BepiPred-2.0: improving sequence-based B-cell epitope prediction using conformational epitopes |
title | BepiPred-2.0: improving sequence-based B-cell epitope prediction using conformational epitopes |
title_full | BepiPred-2.0: improving sequence-based B-cell epitope prediction using conformational epitopes |
title_fullStr | BepiPred-2.0: improving sequence-based B-cell epitope prediction using conformational epitopes |
title_full_unstemmed | BepiPred-2.0: improving sequence-based B-cell epitope prediction using conformational epitopes |
title_short | BepiPred-2.0: improving sequence-based B-cell epitope prediction using conformational epitopes |
title_sort | bepipred-2.0: improving sequence-based b-cell epitope prediction using conformational epitopes |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570230/ https://www.ncbi.nlm.nih.gov/pubmed/28472356 http://dx.doi.org/10.1093/nar/gkx346 |
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