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蛋白酶体系统的组成部分及其在MHC I类抗原加工中的作用。

The components of the proteasome system and their role in MHC class I antigen processing.

作者信息

Krüger E, Kuckelkorn U, Sijts A, Kloetzel P-M

机构信息

Institut für Biochemie, Medizinische Fakultät, Humboldt-Universität zu Berlin, Charité, Monbijoust 2, 10117 Berlin, Germany.

出版信息

Rev Physiol Biochem Pharmacol. 2003;148:81-104. doi: 10.1007/s10254-003-0010-4. Epub 2003 Mar 25.

Abstract

By generating peptides from intracellular antigens which are then presented to T cells, the ubiquitin/26S proteasome system plays a central role in the cellular immune response. The proteolytic properties of the proteasome are adapted to the requirements of the immune system by proteasome components whose synthesis is under the control of interferon-gamma. Among these are three subunits with catalytic sites that are incorporated into the enzyme complex during its de novo synthesis. Thus, the proteasome assembly pathway and the formation of immunoproteasomes play a critical regulatory role in the regulation of the proteasome's catalytic properties. In addition, interferon-gamma also induces the synthesis of the proteasome activator PA28 which, as part of the so-called hybrid proteasome, exerts a more selective function in antigen presentation. Consequently, the combination of a number of regulatory events tunes the proteasome system to gain maximal efficiency in the generation of peptides with regard to their quality and quantity.

摘要

通过从细胞内抗原产生肽段,然后将其呈递给T细胞,泛素/26S蛋白酶体系统在细胞免疫反应中发挥核心作用。蛋白酶体的蛋白水解特性通过其合成受干扰素-γ控制的蛋白酶体成分来适应免疫系统的需求。其中有三个具有催化位点的亚基,在蛋白酶体从头合成过程中被整合到酶复合物中。因此,蛋白酶体组装途径和免疫蛋白酶体的形成在蛋白酶体催化特性的调节中起着关键的调节作用。此外,干扰素-γ还诱导蛋白酶体激活剂PA28的合成,PA28作为所谓混合蛋白酶体的一部分,在抗原呈递中发挥更具选择性的功能。因此,一系列调节事件的组合调整蛋白酶体系统,以便在肽段的质量和数量方面获得最大效率。

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