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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...

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Detalles Bibliográficos
Autores principales: Jespersen, Martin Closter, Peters, Bjoern, Nielsen, Morten, Marcatili, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
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.
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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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