Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases (NIAID), Bethesda, MD 20892, USA.
Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases (NIAID), Bethesda, MD 20892, USA.
Trends Cell Biol. 2019 Dec;29(12):929-939. doi: 10.1016/j.tcb.2019.09.004. Epub 2019 Oct 29.
MHC class I presentation of short peptides enables CD8 T cell (T) immunosurveillance of tumors and intracellular pathogens. A key feature of the class I pathway is that the immunopeptidome is highly skewed from the cellular degradome, indicating high selectivity of the access of protease-generated peptides to class I molecules. Similarly, in professional antigen-presenting cells, peptides from minute amounts of proteins introduced into the cytosol outcompete an overwhelming supply of constitutively generated peptides. Here, we propose that antigen processing is based on substrate channeling and review recent studies from the antigen processing and cell biology fields that provide a starting point for testing this hypothesis.
MHC I 类分子呈递短肽使 CD8 T 细胞(T)对肿瘤和细胞内病原体具有免疫监视作用。该途径的一个关键特征是免疫肽组与细胞内肽组高度偏倚,表明蛋白酶生成的肽进入 I 类分子具有很高的选择性。同样,在专业抗原呈递细胞中,从细胞质中引入的极少量蛋白质产生的肽会与大量组成性产生的肽竞争。在这里,我们提出抗原加工基于底物通道化,并回顾了来自抗原加工和细胞生物学领域的最新研究,为测试这一假设提供了起点。