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泛素C末端水解酶L1(UCHL1),超越水解作用。

Ubiquitin C-Terminal Hydrolase L1 (UCHL1), Beyond Hydrolysis.

作者信息

Bdarneh Anwar, Maniv Inbal, Glickman Michael H

机构信息

Faculty of Biology, Technion-IIT, Haifa, Israel.

出版信息

Bioessays. 2025 Aug;47(8):e70028. doi: 10.1002/bies.70028. Epub 2025 Jun 9.

Abstract

Ubiquitin C-terminal hydrolase L1 (UCHL1) is a component of the ubiquitin-proteasome system (UPS) linked to neurodegeneration. Despite its exceptionally high abundance in neurons, UCHL1's precise role remains unclear. This review critically examines the proposed functions of UCHL1 and the challenges to understanding its role in neuronal cells. While UCHL1 hydrolyzes small adducts from the C-terminus of ubiquitin, its occluded active site limits the range of possible substrates and restricts its activity as an efficient deubiquitinase (DUB). These constraints, alongside the paucity of identified substrates, challenge the centrality of this proposed role. We also explore the potential of UCHL1 acting as a ubiquitin ligase and its nonenzymatic role in stabilizing mono-ubiquitin by preventing its lysosomal degradation. By highlighting the unresolved complexities surrounding UCHL1, this perspective proposes several approaches to elucidate UCHL1's significance in the brain.

摘要

泛素C末端水解酶L1(UCHL1)是与神经退行性变相关的泛素-蛋白酶体系统(UPS)的一个组成部分。尽管UCHL1在神经元中含量异常高,但其确切作用仍不清楚。这篇综述批判性地审视了UCHL1的假定功能以及理解其在神经元细胞中作用所面临的挑战。虽然UCHL1能从泛素的C末端水解小的加合物,但其封闭的活性位点限制了可能的底物范围,并限制了其作为高效去泛素酶(DUB)的活性。这些限制,连同已鉴定底物的匮乏,对这一假定作用的核心地位提出了挑战。我们还探讨了UCHL1作为泛素连接酶的潜力及其通过防止单泛素的溶酶体降解来稳定单泛素的非酶作用。通过强调围绕UCHL1的未解决的复杂性,这一观点提出了几种阐明UCHL1在大脑中重要性的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4a0/12278803/3223ec5fec89/BIES-47-e70028-g002.jpg

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