EpiDope: a deep neural network for linear B-cell epitope prediction

Bioinformatics. 2021 May 1;37(4):448-455. doi: 10.1093/bioinformatics/btaa773.

Abstract

Motivation: By binding to specific structures on antigenic proteins, the so-called epitopes, B-cell antibodies can neutralize pathogens. The identification of B-cell epitopes is of great value for the development of specific serodiagnostic assays and the optimization of medical therapy. However, identifying diagnostically or therapeutically relevant epitopes is a challenging task that usually involves extensive laboratory work. In this study, we show that the time, cost and labor-intensive process of epitope detection in the lab can be significantly reduced using in silico prediction.

Results: Here, we present EpiDope, a python tool which uses a deep neural network to detect linear B-cell epitope regions on individual protein sequences. With an area under the curve between 0.67 ± 0.07 in the receiver operating characteristic curve, EpiDope exceeds all other currently used linear B-cell epitope prediction tools. Our software is shown to reliably predict linear B-cell epitopes of a given protein sequence, thus contributing to a significant reduction of laboratory experiments and costs required for the conventional approach.

Availabilityand implementation: EpiDope is available on GitHub (http://github.com/mcollatz/EpiDope).

Supplementary information: Supplementary data are available at Bioinformatics online.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Computer Simulation
  • Epitope Mapping
  • Epitopes, B-Lymphocyte*
  • Neural Networks, Computer
  • Software*

Substances

  • Epitopes, B-Lymphocyte