Kanaseki Takayuki, Shastri Nilabh
Department of Pathology, Sapporo Medical University, Sapporo, Japan.
Division of Immunology and Pathogenesis, Department of Molecular and Cell Biology, University of California, Berkeley, CA, USA.
Methods Mol Biol. 2013;960:179-185. doi: 10.1007/978-1-62703-218-6_15.
Immune surveillance of infected or tumor cells by CD8(+) T cells requires that MHC class I molecules present a diverse repertoire of peptides on the cell surface. Even a few copies of individual peptides among this mixture are sufficient for recognition by the antigen receptors of appropriate CD8(+) T cells. Here we describe a method for biochemical analysis of the naturally processed peptides in living cells. The peptide mixture in cell extracts is fractionated using reverse phase high performance liquid chromatography and detected by the activation of CD8(+) T cell hybridomas. The results provide information on the structure and amount of the peptides and yield insights into the mechanisms that generate the naturally processed peptides.
CD8(+) T细胞对感染细胞或肿瘤细胞的免疫监视要求MHC I类分子在细胞表面呈现多样化的肽库。即使在这种混合物中个别肽只有几份拷贝,也足以被合适的CD8(+) T细胞的抗原受体识别。在此,我们描述了一种对活细胞中天然加工肽进行生化分析的方法。使用反相高效液相色谱法对细胞提取物中的肽混合物进行分离,并通过CD8(+) T细胞杂交瘤的激活进行检测。结果提供了有关肽的结构和数量的信息,并深入了解了产生天然加工肽的机制。