BConformeR: A Conformer Based on Mutual Sampling for Unified Prediction of Continuous and Discontinuous Antibody Binding Sites
- URL: http://arxiv.org/abs/2508.12029v2
- Date: Mon, 01 Sep 2025 08:40:36 GMT
- Title: BConformeR: A Conformer Based on Mutual Sampling for Unified Prediction of Continuous and Discontinuous Antibody Binding Sites
- Authors: Zhangyu You, Jiahao Ma, Hongzong Li, Ye-Fan Hu, Jian-Dong Huang,
- Abstract summary: In this work, we propose a conformer-based model trained on antigen sequences derived from 1,080 antigen-antibody complexes.<n>CNN enhances the prediction of linears, and the Transformer module improves the prediction of conformationals.<n> Experimental results show that our model outperforms existing baselines in terms of PCC, ROC-AUC, PR-AUC, and F1 scores on both linear and conformationals.
- Score: 3.947298454012977
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Accurate prediction of antibody-binding sites (epitopes) on antigens is crucial for vaccine design, immunodiagnostics, therapeutic antibody development, antibody engineering, research into autoimmune and allergic diseases, and for advancing our understanding of immune responses. Despite in silico methods that have been proposed to predict both linear (continuous) and conformational (discontinuous) epitopes, they consistently underperform in predicting conformational epitopes. In this work, we propose a conformer-based model trained on antigen sequences derived from 1,080 antigen-antibody complexes, leveraging convolutional neural networks (CNNs) to extract local features and Transformers to capture long-range dependencies within antigen sequences. Ablation studies demonstrate that CNN enhances the prediction of linear epitopes, and the Transformer module improves the prediction of conformational epitopes. Experimental results show that our model outperforms existing baselines in terms of PCC, ROC-AUC, PR-AUC, and F1 scores on both linear and conformational epitopes.
Related papers
- ABConformer: Physics-inspired Sliding Attention for Antibody-Antigen Interface Prediction [3.947298454012977]
We present ABCONFORMER, a model based on the Conformer backbone that captures both local and global features of a biosequence.<n>ABCONFORMER can accurately predict paratopes and antigens given the antibody and sequence, and predict pan-epitopes on the antigen without antibody information.
arXiv Detail & Related papers (2025-09-27T11:12:04Z) - ImmunoDiff: A Diffusion Model for Immunotherapy Response Prediction in Lung Cancer [10.797150801746957]
Accurately predicting immunotherapy response in Non-Small Cell Lung Cancer (NSCLC) remains a critical unmet need.<n>Existing radiomics and deep learning-based predictive models rely primarily on pre-treatment imaging to predict categorical response outcomes.<n>This study introduces ImmunoDiff, an anatomy-aware diffusion model designed to synthesize post-treatment CT scans from baseline imaging while incorporating clinically relevant constraints.
arXiv Detail & Related papers (2025-05-29T17:19:40Z) - dyAb: Flow Matching for Flexible Antibody Design with AlphaFold-driven Pre-binding Antigen [52.809470467635194]
Development of therapeutic antibodies heavily relies on accurate predictions of how antigens will interact with antibodies.<n>Existing computational methods in antibody design often overlook crucial conformational changes that antigens undergo during the binding process.<n>We introduce dyAb, a flexible framework that incorporates AlphaFold2-driven predictions to model pre-binding antigen structures.
arXiv Detail & Related papers (2025-03-01T03:53:18Z) - Relation-Aware Equivariant Graph Networks for Epitope-Unknown Antibody Design and Specificity Optimization [61.06622479173572]
We propose a novel Relation-Aware Design (RAAD) framework, which models antigen-antibody interactions for co-designing sequences and structures of antigen-specific CDRs.<n> Furthermore, we propose a new evaluation metric to better measure antibody specificity and develop a contrasting specificity-enhancing constraint to optimize the specificity of antibodies.
arXiv Detail & Related papers (2024-12-14T03:00:44Z) - DapPep: Domain Adaptive Peptide-agnostic Learning for Universal T-cell Receptor-antigen Binding Affinity Prediction [38.358558338444624]
We introduce a domain-adaptive peptide-agnostic learning framework DapPep for universal TCR-antigen binding affinity prediction.<n>DapPep consistently outperforms existing tools, showcasing robust generalization capability.<n>It proves effective in challenging clinical tasks such as sorting reactive T cells in tumor neoantigen therapy and identifying key positions in 3D structures.
arXiv Detail & Related papers (2024-11-26T18:06:42Z) - A Hierarchical Training Paradigm for Antibody Structure-sequence
Co-design [54.30457372514873]
We propose a hierarchical training paradigm (HTP) for the antibody sequence-structure co-design.
HTP consists of four levels of training stages, each corresponding to a specific protein modality.
Empirical experiments show that HTP sets the new state-of-the-art performance in the co-design problem.
arXiv Detail & Related papers (2023-10-30T02:39:15Z) - BeeTLe: A Framework for Linear B-Cell Epitope Prediction and
Classification [0.43512163406551996]
This paper presents a new deep learning-based framework for linear B-cell prediction as well as antibody type-specific classification.
We propose an amino acid encoding method based on eigen decomposition to help the model learn the representations of antibodies.
Experimental results on data curated from the largest public database demonstrate the validity of the proposed methods.
arXiv Detail & Related papers (2023-09-05T09:18:29Z) - AI driven B-cell Immunotherapy Design [0.0]
The effectiveness of antigen neutralisation and elimination hinges upon the strength, sensitivity, and specificity of the paratope-epitope interaction.
In recent years, artificial intelligence and machine learning methods have made significant strides, revolutionising the prediction of protein structures and their complexes.
This review focuses on the progress of machine learning-based tools and their frameworks in the domain of B-cell immunotherapy design.
arXiv Detail & Related papers (2023-09-03T09:14:10Z) - xTrimoABFold: De novo Antibody Structure Prediction without MSA [77.47606749555686]
We develop a novel model named xTrimoABFold to predict antibody structure from antibody sequence.
The model was trained end-to-end on the antibody structures in PDB by minimizing the ensemble loss of domain-specific focal loss on CDR and the frame-aligned point loss.
arXiv Detail & Related papers (2022-11-30T09:26:08Z) - Incorporating Pre-training Paradigm for Antibody Sequence-Structure
Co-design [134.65287929316673]
Deep learning-based computational antibody design has attracted popular attention since it automatically mines the antibody patterns from data that could be complementary to human experiences.
The computational methods heavily rely on high-quality antibody structure data, which is quite limited.
Fortunately, there exists a large amount of sequence data of antibodies that can help model the CDR and alleviate the reliance on structure data.
arXiv Detail & Related papers (2022-10-26T15:31:36Z) - Reprogramming Pretrained Language Models for Antibody Sequence Infilling [72.13295049594585]
Computational design of antibodies involves generating novel and diverse sequences, while maintaining structural consistency.
Recent deep learning models have shown impressive results, however the limited number of known antibody sequence/structure pairs frequently leads to degraded performance.
In our work we address this challenge by leveraging Model Reprogramming (MR), which repurposes pretrained models on a source language to adapt to the tasks that are in a different language and have scarce data.
arXiv Detail & Related papers (2022-10-05T20:44:55Z) - Neural message passing for joint paratope-epitope prediction [0.0]
Antibodies are proteins in the immune system which bind to antigens to detect and neutralise them.
Prediction of binding sites in an antibody-antigen interaction are known as the paratope and, respectively, and are key to vaccine and synthetic antibody development.
arXiv Detail & Related papers (2021-05-31T16:37:55Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.