epitope3D: a machine learning method for conformational B-cell epitope prediction.


Journal

Briefings in bioinformatics
ISSN: 1477-4054
Titre abrégé: Brief Bioinform
Pays: England
ID NLM: 100912837

Informations de publication

Date de publication:
17 01 2022
Historique:
received: 07 06 2021
revised: 25 08 2021
accepted: 14 09 2021
pubmed: 23 10 2021
medline: 8 4 2022
entrez: 22 10 2021
Statut: ppublish

Résumé

The ability to identify antigenic determinants of pathogens, or epitopes, is fundamental to guide rational vaccine development and immunotherapies, which are particularly relevant for rapid pandemic response. A range of computational tools has been developed over the past two decades to assist in epitope prediction; however, they have presented limited performance and generalization, particularly for the identification of conformational B-cell epitopes. Here, we present epitope3D, a novel scalable machine learning method capable of accurately identifying conformational epitopes trained and evaluated on the largest curated epitope data set to date. Our method uses the concept of graph-based signatures to model epitope and non-epitope regions as graphs and extract distance patterns that are used as evidence to train and test predictive models. We show epitope3D outperforms available alternative approaches, achieving Mathew's Correlation Coefficient and F1-scores of 0.55 and 0.57 on cross-validation and 0.45 and 0.36 during independent blind tests, respectively.

Identifiants

pubmed: 34676398
pii: 6407730
doi: 10.1093/bib/bbab423
pii:
doi:

Substances chimiques

Epitopes, B-Lymphocyte 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Auteurs

Bruna Moreira da Silva (BM)

Structural Biology and Bioinformatics, Department of Biochemistry, University of Melbourne, Melbourne, Victoria, Australia.
Systems and Computational Biology, Bio21 Institute, University of Melbourne, Melbourne, Victoria, Australia.
Computational Biology and Clinical Informatics, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
School of Computing and Information Systems, University of Melbourne, Melbourne, Victoria, Australia.

YooChan Myung (Y)

Structural Biology and Bioinformatics, Department of Biochemistry, University of Melbourne, Melbourne, Victoria, Australia.
Systems and Computational Biology, Bio21 Institute, University of Melbourne, Melbourne, Victoria, Australia.
Computational Biology and Clinical Informatics, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Baker Department of Cardiometabolic Health, University of Melbourne, Melbourne, Victoria, Australia.

David B Ascher (DB)

Structural Biology and Bioinformatics, Department of Biochemistry, University of Melbourne, Melbourne, Victoria, Australia.
Systems and Computational Biology, Bio21 Institute, University of Melbourne, Melbourne, Victoria, Australia.
Computational Biology and Clinical Informatics, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Baker Department of Cardiometabolic Health, University of Melbourne, Melbourne, Victoria, Australia.
Department of Biochemistry, University of Cambridge, 80 Tennis Ct Rd, Cambridge CB2 1GA, UK.

Douglas E V Pires (DEV)

Structural Biology and Bioinformatics, Department of Biochemistry, University of Melbourne, Melbourne, Victoria, Australia.
Systems and Computational Biology, Bio21 Institute, University of Melbourne, Melbourne, Victoria, Australia.
Computational Biology and Clinical Informatics, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
School of Computing and Information Systems, University of Melbourne, Melbourne, Victoria, Australia.

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Classifications MeSH