Demonstrates enhanced accuracy and diversity of antibody-antigen structures using B-cell epitope predictions, suggesting improved therapeutic applications.
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.
No takes yet. Share an insight, caveat, or question.
Clifford et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: