bioRxiv · 10.1101/2022.06.20.496780
SEMA: Antigen B-cell conformational epitope prediction using deep transfer learning
Abstract
One of the primary tasks in vaccine design and development of immunotherapeutic drugs is to predict conformational B-cell epitopes corresponding to primary antibody binding sites within the antigen tertiary structure. To date, multiple approaches have been developed to address this issue. However, for a wide range of antigens their accuracy is limited. In this paper, we applied the transfer learning approach using pretrained deep learning models to develop a model that predicts conformational B-cell epitopes based on the primary antigen sequence and tertiary structure. A pretrained protein language model, ESM-1b, and an inverse folding model, ESM-IF1, were fine-tuned to quantitatively predict antibody-antigen interaction features and distinguish between epitope and non-epitope residues. The resulting model called SEMA demonstrated the best performance on an independent test set with ROC AUC of 0.76 compared to peer-reviewed tools. We show that SEMA can quantitatively rank the immunodominant regions within the RBD domain of SARS-CoV-2. SEMA is available at https://github.com/AIRI-Institute/SEMAi and the web-interface http://sema.airi.net.
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Shashkova, T. I., Umerenkov, D., Salnikov, M., Strashnov, P. V., Konstantinova, A. V., Lebed, I., Shcherbinin, D. N., Asatryan, M. N., Kardymon, O. L., Ivanisenko, N. V.. 2022-06-21. SEMA: Antigen B-cell conformational epitope prediction using deep transfer learning. https://doi.org/10.1101/2022.06.20.496780
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