Pocket restraints guided by B‐cell epitope prediction improve Chai‐1 antibody–antigen structure modeling

The accurate prediction of antibody-antigen (AbAg) complexes is a key challenge for computational immunology, with applications in therapeutic antibody design and diagnostics. Current deep learning methods have the potential to generate high-confidence AbAg structures. However, these methods often fail to predict the correct AbAg structure, placing the antibody incorrectly on the antigen and converge on repeatedly predicting the same redundant binding mode. Here, we present BepiPocket and DiscoPocket, two simple approaches that integrate B-cell epitope prediction tools to guide antibody-epitope restraints during Chai-1 structure prediction. On a dataset of 1628 AbAg complexes, we demonstrate that using the sequence-based predictor BepiPred-3.0 (BepiPocket) and the structure-based predictor DiscoTope-3.0 (DiscoPocket) substantially improved both the accuracy and diversity of predicted AbAg complexes compared to standard Chai-1 modeling with random seed variation. The software for both BepiPocket and DiscoPocket algorithms is freely available at https://github.com/mnielLab/BepiPocket.

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Publication Details

Journal
Protein Science
Published
2026-07-23
DOI
https://doi.org/10.1002/pro.70730
Primary Topic
vaccines and immunoinformatics approaches
Type
article
Field-Weighted Citation Impact
0.00

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article

Pocket restraints guided by B‐cell epitope prediction improve Chai‐1 antibody–antigen structure modeling

Joakim Nøddeskov Clifford, Morten Nielsen
Protein Science
vaccines and immunoinformatics approaches
article

Pocket restraints guided by B‐cell epitope prediction improve Chai‐1 antibody–antigen structure modeling

Joakim Nøddeskov Clifford, Morten Nielsen
article en

Abstract

The accurate prediction of antibody-antigen (AbAg) complexes is a key challenge for computational immunology, with applications in therapeutic antibody design and diagnostics. Current deep learning methods have the potential to generate high-confidence AbAg structures. However, these methods often fail to predict the correct AbAg structure, placing the antibody incorrectly on the antigen and converge on repeatedly predicting the same redundant binding mode. Here, we present BepiPocket and DiscoPocket, two simple approaches that integrate B-cell epitope prediction tools to guide antibody-epitope restraints during Chai-1 structure prediction. On a dataset of 1628 AbAg complexes, we demonstrate that using the sequence-based predictor BepiPred-3.0 (BepiPocket) and the structure-based predictor DiscoTope-3.0 (DiscoPocket) substantially improved both the accuracy and diversity of predicted AbAg complexes compared to standard Chai-1 modeling with random seed variation. The software for both BepiPocket and DiscoPocket algorithms is freely available at https://github.com/mnielLab/BepiPocket.

Protein ScienceVol. 35(8)
Technical University of Denmark (DK)
National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 14%
vaccines and immunoinformatics approaches
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Pocket restraints guided by B‐cell epitope prediction improve Chai‐1 antibody–antigen structure modeling — Joakim Nøddeskov Clifford, Morten Nielsen · Protein Science (2026) | TGRS Research Map | TGRS