人类白细胞抗原
计算生物学
抗原呈递
肽
稳健性(进化)
抗原
人工智能
计算机科学
免疫疗法
机器学习
抗原处理
磷酸化
免疫系统
班级(哲学)
生物
免疫学
生物信息学
训练集
鉴定(生物学)
介绍(产科)
癌症免疫疗法
支持向量机
数据挖掘
作者
Heli M. Garcia Alvarez,Saghar Kaabinejadian,Hooman Yari,Chloe M. Shepherd,William H. Hildebrand,Alessandro Sette,Bjoern Peters,Robert Parker,Nicola Ternette,Morten Nielsen
标识
DOI:10.1021/acs.jproteome.5c01284
摘要
Phosphorylated peptides presented by human leukocyte antigen (HLA) class II molecules play pivotal roles in immune regulation, yet their characterization and prediction remain challenging due to data noise and limited HLA coverage. Here, we introduce NetMHCIIphosPan, a prediction method for HLA-II antigen presentation of phosphorylated peptides, developed using mass spectrometry (MS)-based immunopeptidomics data sets. Employing a refined peptide identification workflow, we reanalyzed earlier HLA-II phospholigand data sets and trained predictive models, achieving superior performance compared to models trained on the original data. Binding motif analysis revealed that HLA-specific preferences for phospholigands closely aligned with those of unmodified ligands. Incorporating unmodified ligands into training further enhanced predictive accuracy, particularly for HLA-DP and HLA-DQ molecules. NetMHCIIphosPan outperformed existing tools, such as NetMHCIIpan-4.3 and MixMHC2pred-1.3, for prediction of HLA antigen presentation of phosphorylated peptides, demonstrating robustness and utility. This work establishes NetMHCIIphosPan as a state-of-the-art tool for understanding the HLA-II phospholigandome, with potential applications in immunotherapy and vaccine design.
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