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泛素结合酶在自噬依赖性降解途径的调控中

Ubiquitin conjugating enzymes in the regulation of the autophagy-dependent degradation pathway.

作者信息

Ikeda Fumiyo

机构信息

Medical Institute of Bioregulation (MIB), Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, Japan.

出版信息

Matrix Biol. 2021 Jun;100-101:23-29. doi: 10.1016/j.matbio.2020.11.004. Epub 2020 Dec 2.

Abstract

The ubiquitin-proteasomal system and the autophagy-lysosome system are two major degradation systems in mammalian cells. Ubiquitin not only regulates proteasomal degradation of substrates but also regulates the autophagy pathway. In one type of macroautophagy, called selective autophagy, cargos are recruited to phagophore in a ubiquitin-dependent manner. Ubiquitin can target autophagy regulators for proteasomal degradation, control protein conformation or change interacting partners of these regulators. To understand the regulatory mechanisms of these degradation pathways, it is critical to dissect how the ubiquitin system contributes to them. Since enzymes are key regulators of ubiquitination, in this review, such enzymes in autophagy regulation are discussed, with specific focus on ubiquitin conjugating enzyme E2s, of which roles in autophagy are emerging.

摘要

泛素-蛋白酶体系统和自噬-溶酶体系统是哺乳动物细胞中的两个主要降解系统。泛素不仅调节底物的蛋白酶体降解,还调节自噬途径。在一种称为选择性自噬的巨自噬类型中,货物以泛素依赖的方式被招募到吞噬泡中。泛素可以将自噬调节因子靶向蛋白酶体降解,控制蛋白质构象或改变这些调节因子的相互作用伙伴。为了理解这些降解途径的调节机制,剖析泛素系统如何对其产生作用至关重要。由于酶是泛素化的关键调节因子,在本综述中,将讨论自噬调节中的此类酶,特别关注泛素结合酶E2,其在自噬中的作用正在显现。

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