Suppr超能文献

一种神秘的蛋白酶将去泛素化与蛋白酶体介导的降解偶联起来。

A cryptic protease couples deubiquitination and degradation by the proteasome.

作者信息

Yao Tingting, Cohen Robert E

机构信息

Department of Biochemistry, University of Iowa, 51 Newton Road, Iowa City, Iowa 52242, USA.

出版信息

Nature. 2002 Sep 26;419(6905):403-7. doi: 10.1038/nature01071. Epub 2002 Sep 1.

Abstract

The 26S proteasome is responsible for most intracellular proteolysis in eukaryotes. Efficient substrate recognition relies on conjugation of substrates with multiple ubiquitin molecules and recognition of the polyubiquitin moiety by the 19S regulatory complex--a multisubunit assembly that is bound to either end of the cylindrical 20S proteasome core. Only unfolded proteins can pass through narrow axial channels into the central proteolytic chamber of the 20S core, so the attached polyubiquitin chain must be released to allow full translocation of the substrate polypeptide. Whereas unfolding is rate-limiting for the degradation of some substrates and appears to involve chaperone-like activities associated with the proteasome, the importance and mechanism of degradation-associated deubiquitination has remained unclear. Here we report that the POH1 (also known as Rpn11 in yeast) subunit of the 19S complex is responsible for substrate deubiquitination during proteasomal degradation. The inability to remove ubiquitin can be rate-limiting for degradation in vitro and is lethal to yeast. Unlike all other known deubiquitinating enzymes (DUBs) that are cysteine proteases, POH1 appears to be a Zn(2+)-dependent protease.

摘要

26S蛋白酶体负责真核生物中大多数的细胞内蛋白质水解。高效的底物识别依赖于底物与多个泛素分子的缀合以及19S调节复合物对多聚泛素部分的识别,19S调节复合物是一种多亚基组装体,与圆柱形20S蛋白酶体核心的两端相连。只有未折叠的蛋白质才能通过狭窄的轴向通道进入20S核心的中央蛋白水解腔,因此附着的多聚泛素链必须被释放,以使底物多肽能够完全转运。虽然对于某些底物的降解来说,去折叠是限速步骤,并且似乎涉及与蛋白酶体相关的类似伴侣的活性,但降解相关的去泛素化的重要性和机制仍不清楚。在这里,我们报告19S复合物的POH1(在酵母中也称为Rpn11)亚基在蛋白酶体降解过程中负责底物去泛素化。无法去除泛素在体外可能是降解的限速因素,并且对酵母是致命的。与所有其他已知的作为半胱氨酸蛋白酶的去泛素化酶(DUB)不同,POH1似乎是一种依赖锌离子的蛋白酶。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验