人类白细胞抗原
肽
表位
主要组织相容性复合体
T细胞
T细胞受体
MHC限制
免疫突触
MHC I级
生物
细胞生物学
分子生物学
计算生物学
抗原
免疫学
免疫系统
生物化学
作者
Paula Ruibal,Kees L. M. C. Franken,Krista E. van Meijgaarden,Lucy C. Walters,Andrew J. McMichael,Geraldine M. Gillespie,Simone A. Joosten,Tom H. M. Ottenhoff
出处
期刊:Methods in molecular biology
日期:2022-01-01
卷期号:: 15-30
被引量:7
标识
DOI:10.1007/978-1-0716-2712-9_2
摘要
Understanding the interactions involved during the immunological synapse between peptide, HLA-E molecules, and TCR is crucial to effectively target protective HLA-E-restricted T-cell responses in humans. Here we describe three techniques based on the generation of MHC-E/peptide complexes (MHC-E generically includes HLA-E-like molecules in human and nonhuman species, while HLA-E specifically refers to human molecules), which allow to investigate MHC-E/peptide binding at the molecular level through binding assays and by using peptide loaded HLA-E tetramers, to detect, isolate, and study peptide-specific HLA-E-restricted human T-cells.
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