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20S 蛋白酶体对蛋白质稳态的贡献。

The Contribution of the 20S Proteasome to Proteostasis.

机构信息

Department of Biomolecular Sciences, Weizmann Institute of Science, Rehovot 7610001, Israel.

出版信息

Biomolecules. 2019 May 16;9(5):190. doi: 10.3390/biom9050190.

Abstract

The last decade has seen accumulating evidence of various proteins being degraded by the core 20S proteasome, without its regulatory particle(s). Here, we will describe recent advances in our knowledge of the functional aspects of the 20S proteasome, exploring several different systems and processes. These include neuronal communication, post-translational processing, oxidative stress, intrinsically disordered protein regulation, and extracellular proteasomes. Taken together, these findings suggest that the 20S proteasome, like the well-studied 26S proteasome, is involved in multiple biological processes. Clarifying our understanding of its workings calls for a transformation in our perception of 20S proteasome-mediated degradation-no longer as a passive and marginal path, but rather as an independent, coordinated biological process. Nevertheless, in spite of impressive progress made thus far, the field still lags far behind the front lines of 26S proteasome research. Therefore, we also touch on the gaps in our knowledge of the 20S proteasome that remain to be bridged in the future.

摘要

在过去的十年中,积累了越来越多的证据表明,各种蛋白质在没有其调节颗粒的情况下被核心 20S 蛋白酶体降解。在这里,我们将描述我们对 20S 蛋白酶体功能方面的最新认识,探索几种不同的系统和过程。这些过程包括神经元通讯、翻译后加工、氧化应激、无规卷曲蛋白调节和细胞外蛋白酶体。总之,这些发现表明,20S 蛋白酶体与研究充分的 26S 蛋白酶体一样,参与了多种生物学过程。为了澄清我们对其工作机制的理解,我们需要转变对 20S 蛋白酶体介导的降解的看法——不再将其视为一种被动和次要的途径,而是一种独立的、协调的生物学过程。然而,尽管迄今为止取得了令人印象深刻的进展,但该领域仍然远远落后于 26S 蛋白酶体研究的前沿。因此,我们还讨论了未来需要弥合的 20S 蛋白酶体知识空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fce/6571867/780935b2d85f/biomolecules-09-00190-g001.jpg

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