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Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope
Published on: March 24, 2017
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Structure-based Predictions of Conformational B Cell Epitopes by Protein Language Model and Deep Learning
Yuhao Zhang1, Zhaoqian Su1,2, Felipe Vilicich3
1Data Science Institute, Vanderbilt University, Nashville, 37212, TN, USA.
Biorxiv : the Preprint Server for Biology
|November 24, 2025
Summary
A new patch-centric framework accurately predicts B-cell epitopes on antigens using protein language models (PLMs). This method aids antibody discovery, engineering, and vaccine design by identifying critical binding regions on antigen structures.
Area of Science:
- Immunology
- Computational Biology
- Structural Biology
Background:
- Mapping B-cell epitopes is crucial for antibody discovery but remains challenging due to experimental costs and limitations of current computational tools.
- Existing computational methods often struggle with antibody-antigen recognition, performing poorly on specific interfaces.
- Accurate epitope prediction is vital for advancing antibody engineering and vaccine development.
Purpose of the Study:
- To introduce a novel patch-centric computational framework for predicting B-cell epitopes directly on antigen structures.
- To evaluate the performance of a protein language model (PLM) approach against a convolutional neural network (CNN) baseline for epitope prediction.
- To develop an interpretable method for identifying and prioritizing B-cell epitopes to aid in antibody discovery and vaccine design.
Main Methods:
- Developed a patch-centric framework defining epitopes as triads of neighboring residues capturing local shape and chemistry.
- Evaluated two classifiers: a PLM (ESM-2 embeddings) and a CNN using hand-crafted features.
- Trained and validated models on 1,151 antibody-antigen complexes from the AbDb database using five-fold cross-validation.
Main Results:
- The PLM classifier significantly outperformed the CNN at the patch level (F1 ≈ 0.986, ROC-AUC ≈ 0.998).
- Residue-wise performance aggregated from patch scores showed superior results for the PLM (ROC-AUC 0.689±0.072 vs. 0.548±0.018).
- The PLM achieved state-of-the-art performance on benchmark datasets and generalized well to external complexes (ROC-AUC 0.663).
Conclusions:
- The patch-centric PLM framework offers a robust and accurate method for B-cell epitope prediction.
- The model provides interpretable epitope likelihood maps, facilitating antigen prioritization and antibody engineering.
- This approach represents a practical advancement for antibody discovery, vaccine design, and related biotechnological applications.
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