主要组织相容性复合体
表位
肽
人类白细胞抗原
MHC限制
人类白细胞抗原-DR
计算生物学
MHC II级
MHC I级
生物
免疫系统
抗原
免疫学
生物化学
作者
Kamilla Kjærgaard Jensen,Massimo Andreatta,Paolo Marcatili,Søren Buus,Jason Greenbaum,Yan Zhen,Alessandro Sette,Bjoern Peters,Morten Nielsen
出处
期刊:Immunology
[Wiley]
日期:2018-01-10
卷期号:154 (3): 394-406
被引量:642
摘要
Summary Major histocompatibility complex class II ( MHC ‐ II ) molecules are expressed on the surface of professional antigen‐presenting cells where they display peptides to T helper cells, which orchestrate the onset and outcome of many host immune responses. Understanding which peptides will be presented by the MHC ‐ II molecule is therefore important for understanding the activation of T helper cells and can be used to identify T‐cell epitopes. We here present updated versions of two MHC – II –peptide binding affinity prediction methods, Net MHCII and Net MHCII pan. These were constructed using an extended data set of quantitative MHC –peptide binding affinity data obtained from the Immune Epitope Database covering HLA ‐ DR , HLA ‐ DQ , HLA ‐ DP and H‐2 mouse molecules. We show that training with this extended data set improved the performance for peptide binding predictions for both methods. Both methods are publicly available at www.cbs.dtu.dk/services/NetMHCII-2.3 and www.cbs.dtu.dk/services/NetMHCIIpan-3.2 .
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