epiTCR-KDA: knowledge distillation model on dihedral angles for TCR-peptide prediction.

IF 2.8 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY Bioinformatics advances Pub Date : 2024-11-29 eCollection Date: 2024-01-01 DOI:10.1093/bioadv/vbae190
My-Diem Nguyen Pham, Chinh Tran-To Su, Thanh-Nhan Nguyen, Hoai-Nghia Nguyen, Dinh Duy An Nguyen, Hoa Giang, Dinh-Thuc Nguyen, Minh-Duy Phan, Vy Nguyen
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Abstract

Motivation: The prediction of the T-cell receptor (TCR) and antigen bindings is crucial for advancements in immunotherapy. However, most current TCR-peptide interaction predictors struggle to perform well on unseen data. This limitation may stem from the conventional use of TCR and/or peptide sequences as input, which may not adequately capture their structural characteristics. Therefore, incorporating the structural information of TCRs and peptides into the prediction model is necessary to improve its generalizability.

Results: We developed epiTCR-KDA (KDA stands for Knowledge Distillation model on Dihedral Angles), a new predictor of TCR-peptide binding that utilizes the dihedral angles between the residues of the peptide and the TCR as a structural descriptor. This structural information was integrated into a knowledge distillation model to enhance its generalizability. epiTCR-KDA demonstrated competitive prediction performance, with an area under the curve (AUC) of 1.00 for seen data and AUC of 0.91 for unseen data. On public datasets, epiTCR-KDA consistently outperformed other predictors, maintaining a median AUC of 0.93. Further analysis of epiTCR-KDA revealed that the cosine similarity of the dihedral angle vectors between the unseen testing data and training data is crucial for its stable performance. In conclusion, our epiTCR-KDA model represents a significant step forward in developing a highly effective pipeline for antigen-based immunotherapy.

Availability and implementation: epiTCR-KDA is available on GitHub (https://github.com/ddiem-ri-4D/epiTCR-KDA).

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epiTCR-KDA:用于 TCR 肽预测的二面角知识蒸馏模型。
动机:预测t细胞受体(TCR)和抗原结合对免疫治疗的进展至关重要。然而,目前大多数tcr -肽相互作用预测器在未知数据上表现不佳。这种限制可能源于常规使用TCR和/或肽序列作为输入,这可能无法充分捕获其结构特征。因此,在预测模型中加入tcr和多肽的结构信息,提高预测模型的通用性是必要的。结果:我们开发了epiTCR-KDA (KDA代表二面角知识蒸馏模型),这是一种新的TCR-肽结合预测器,利用肽残基与TCR之间的二面角作为结构描述符。将这些结构信息集成到一个知识蒸馏模型中,以提高其泛化能力。epiTCR-KDA显示出具有竞争力的预测性能,对已见数据的曲线下面积(AUC)为1.00,对未见数据的AUC为0.91。在公共数据集上,epiTCR-KDA始终优于其他预测因子,保持中位AUC为0.93。对epiTCR-KDA的进一步分析表明,未见过的测试数据和训练数据之间的二面角向量的余弦相似性对其稳定的性能至关重要。总之,我们的epiTCR-KDA模型代表了开发高效抗原免疫治疗管道的重要一步。可用性和实现:epiTCR-KDA可在GitHub (https://github.com/ddiem-ri-4D/epiTCR-KDA)上获得。
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