APTAnet: an atom-level peptide-TCR interaction affinity prediction model.

Peng Xiong, Anyi Liang, Xunhui Cai, Tian Xia
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Abstract

The prediction of affinity between TCRs and peptides is crucial for the further development of TIL (Tumor-Infiltrating Lymphocytes) immunotherapy. Inspired by the broader research of drug-protein interaction (DPI), we propose an atom-level peptide-TCR interaction (PTI) affinity prediction model APTAnet using natural language processing methods. APTAnet model achieved an average ROC-AUC and PR-AUC of 0.893 and 0.877, respectively, in ten-fold cross-validation on 25,675 pairs of PTI data. Furthermore, experimental results on an independent test set from the McPAS database showed that APTAnet outperformed the current mainstream models. Finally, through the validation on 11 cases of real tumor patient data, we found that the APTAnet model can effectively identify tumor peptides and screen tumor-specific TCRs.

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APTAnet:原子级多肽-TCR相互作用亲和力预测模型。
TCR与多肽之间的亲和力预测对于TIL(肿瘤浸润淋巴细胞)免疫疗法的进一步发展至关重要。受更广泛的药物-蛋白质相互作用(DPI)研究的启发,我们利用自然语言处理方法提出了原子级肽-TCR相互作用(PTI)亲和力预测模型APTAnet。在 25,675 对 PTI 数据的十倍交叉验证中,APTAnet 模型的平均 ROC-AUC 和 PR-AUC 分别达到了 0.893 和 0.877。此外,在 McPAS 数据库的独立测试集上的实验结果表明,APTAnet 的性能优于目前的主流模型。最后,通过对11例真实肿瘤患者数据的验证,我们发现APTAnet模型能有效识别肿瘤多肽和筛选肿瘤特异性TCR。
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