主要组织相容性复合体
抗原呈递
MHC I级
表位
获得性免疫系统
抗原处理
生物
细胞毒性T细胞
内质网
细胞生物学
免疫系统
蛋白质组
交叉展示
蛋白酵素
与抗原处理相关的转运体
人类多任务处理
计算生物学
抗原
T细胞
免疫学
遗传学
神经科学
生物化学
酶
体外
作者
Sabine Hulpke,Robert Tampé
标识
DOI:10.1016/j.tibs.2013.06.003
摘要
Recognition and elimination of virally or malignantly transformed cells are pivotal tasks of the adaptive immune system. For efficient immune detection, snapshots of the cellular proteome are presented as epitopes on major histocompatibility complex class I (MHC I) molecules for recognition by cytotoxic T cells. Knowledge about the track from the equivocal protein to the presentation of antigenic peptides has greatly expanded, leading to an astonishingly elaborate understanding of the MHC I peptide loading pathway. Here, we summarize the current view on this complex process, which involves ABC transporters, proteases, chaperones, and endoplasmic reticulum (ER) quality control. The contribution of individual proteins and subcomplexes is discussed, with a focus on the architecture and dynamics of the key player in the pathway, the peptide-loading complex (PLC).
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