表位
T细胞受体
计算生物学
互补决定区
生物
免疫系统
T细胞
遗传学
抗原
基因
肽序列
作者
Emmi Jokinen,Jani Huuhtanen,Satu Mustjoki,Markus Heinonen,Harri Lähdesmäki
标识
DOI:10.1371/journal.pcbi.1008814
摘要
Adaptive immune system uses T cell receptors (TCRs) to recognize pathogens and to consequently initiate immune responses. TCRs can be sequenced from individuals and methods analyzing the specificity of the TCRs can help us better understand individuals’ immune status in different disorders. For this task, we have developed TCRGP, a novel Gaussian process method that predicts if TCRs recognize specified epitopes. TCRGP can utilize the amino acid sequences of the complementarity determining regions (CDRs) from TCR α and TCR β chains and learn which CDRs are important in recognizing different epitopes. Our comprehensive evaluation with epitope-specific TCR sequencing data shows that TCRGP achieves on average higher prediction accuracy in terms of AUROC score than existing state-of-the-art methods in epitope-specificity predictions. We also propose a novel analysis approach for combined single-cell RNA and TCR αβ (scRNA+TCR αβ ) sequencing data by quantifying epitope-specific TCRs with TCRGP and identify HBV-epitope specific T cells and their transcriptomic states in hepatocellular carcinoma patients.
科研通智能强力驱动
Strongly Powered by AbleSci AI