Artículos de revistas
BepiPred-2.0: Improving sequence-based B-cell epitope prediction using conformational epitopes
Fecha
2017-07Registro en:
Jespersen, Martin Closter; Peters, Bjoern; Nielsen, Morten; Marcatili, Paolo; BepiPred-2.0: Improving sequence-based B-cell epitope prediction using conformational epitopes; Oxford University Press; Nucleic Acids Research; 45; W1; 7-2017; W24-W29
0305-1048
1362-4962
CONICET Digital
CONICET
Autor
Jespersen, Martin Closter
Peters, Bjoern
Nielsen, Morten
Marcatili, Paolo
Resumen
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.