DeMars R, Spies T
Laboratory of Genetics, University of Wisconsin, Madison, WI 53706, USA.
Trends Cell Biol. 1992 Mar;2(3):81-6. doi: 10.1016/0962-8924(92)90077-z.
Most cells process proteins into short peptides that are displayed on the cell surface bound to class I or class II proteins encoded by the major histocompatibility complex (MHC). These protein-peptide complexes can then be recognized by the circulating lymphocytes of the immune system. Several genes found recently in the MHC encode proteins with possible roles in the supply of peptides to class I molecules. The results imply that the peptides are produced in the cytoplasm by proteasomes and are translocated into the endoplasmic reticulum by 'peptide transporters' related to the multidrug resistance proteins. While there is little biochemical evidence to validate these ideas, Robert DeMars and Thomas Spies discuss here the arguments supporting this view. New data indicate that there may also be factors for class II peptide-processing hidden in the MHC.
大多数细胞将蛋白质加工成短肽,这些短肽会与主要组织相容性复合体(MHC)编码的I类或II类蛋白质结合,展示在细胞表面。然后,这些蛋白质 - 肽复合物可被免疫系统的循环淋巴细胞识别。最近在MHC中发现的几个基因编码的蛋白质可能在向I类分子供应肽方面发挥作用。结果表明,肽是由蛋白酶体在细胞质中产生的,并通过与多药耐药蛋白相关的“肽转运体”转运到内质网中。虽然几乎没有生化证据来证实这些观点,但罗伯特·德马斯和托马斯·斯皮斯在此讨论支持这一观点的论据。新数据表明,MHC中可能还隐藏着参与II类肽加工的因子。