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蛋白酶体降解蛋白质的模式。

Paradigms of protein degradation by the proteasome.

机构信息

Frontier Research Core for Life Sciences, University of Toyama, Toyama 930-8555, Japan.

Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712, USA.

出版信息

Curr Opin Struct Biol. 2014 Feb;24:156-64. doi: 10.1016/j.sbi.2014.02.002. Epub 2014 Mar 14.

Abstract

The proteasome is the main proteolytic machine in the cytosol and nucleus of eukaryotic cells where it degrades hundreds of regulatory proteins, removes damaged proteins, and produces peptides that are presented by MHC complexes. New structures of the proteasome particle show how its subunits are arranged and provide insights into how the proteasome is regulated. Proteins are targeted to the proteasome by tags composed of several ubiquitin moieties. The structure of the tags tunes the order in which proteins are degraded. The proteasome itself edits the ubiquitin tags and drugs that interfere in this process can enhance the clearance of toxic proteins from cells. Finally, the proteasome initiates degradation at unstructured regions within its substrates and this step contributes to substrate selection.

摘要

蛋白酶体是真核细胞细胞质和细胞核中主要的蛋白水解机器,它可以降解数百种调节蛋白,清除受损蛋白,并产生由 MHC 复合物呈递的肽段。蛋白酶体颗粒的新结构显示了其亚基的排列方式,并提供了关于蛋白酶体如何被调节的见解。蛋白质通过由几个泛素单位组成的标签靶向蛋白酶体。标签的结构调节了蛋白质降解的顺序。蛋白酶体本身编辑泛素标签,干扰这个过程的药物可以增强有毒蛋白从细胞中的清除。最后,蛋白酶体在其底物的无结构区域启动降解,这一步骤有助于底物选择。

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