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MHC I类限制性肽的产生、转运及呈递。

Generation, translocation, and presentation of MHC class I-restricted peptides.

作者信息

Heemels M T, Ploegh H

机构信息

Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139, USA.

出版信息

Annu Rev Biochem. 1995;64:463-91. doi: 10.1146/annurev.bi.64.070195.002335.

Abstract

The T lymphocytes of the vertebrate immune system look for changes that take place within the organism by examining a display of peptides at the cell surface. These peptides are presented by the products of the major histocompatibility complex (MHC). MHC class I products present peptides derived by proteolysis of cytosolic proteins by the multicatalytic protease, the proteasome. These peptides are translocated from the cytosol into the endoplasmic reticulum by a dedicated peptide transporter, the transporter associated with antigen presentation (TAP). TAP consists of two subunits, and translocates peptides that are approximately 8-12 residues in length. The COOH terminal residue of the peptide is a major determinant in the specificity of translocation. Following translocation, peptides bind to MHC class I molecules, which depend on the peptide ligand as well as on interactions with chaperonins for proper folding. These complexes then egress from the ER and are transported to their final destination, the cell surface.

摘要

脊椎动物免疫系统的T淋巴细胞通过检查细胞表面的肽展示来寻找生物体内发生的变化。这些肽由主要组织相容性复合体(MHC)的产物呈递。MHC I类产物呈递由多催化蛋白酶(蛋白酶体)对胞质蛋白进行蛋白水解产生的肽。这些肽通过一种专门的肽转运体——与抗原呈递相关的转运体(TAP)从胞质溶胶转运到内质网。TAP由两个亚基组成,转运长度约为8 - 12个残基的肽。肽的COOH末端残基是转运特异性的主要决定因素。转运后,肽与MHC I类分子结合,MHC I类分子依赖于肽配体以及与伴侣蛋白的相互作用来正确折叠。这些复合物然后从内质网排出并被运输到它们的最终目的地——细胞表面。

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