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破解赖氨酸巴豆酰化(Kcr):揭示一种有前景的翻译后修饰

Cracking Lysine Crotonylation (Kcr): Enlightening a Promising Post-Translational Modification.

作者信息

Westerveld Marinda, Besermenji Kosta, Aidukas David, Ostrovitsa Nikita, Petracca Rita

机构信息

Department of Pharmaceutical Sciences, Faculty of Science, Utrecht University, David De Wied Building, Universiteitsweg 99, 3584 CG, Utrecht, NL.

Trinity Biomedical Sciences Institute (TBSI), Trinity College Dublin (TCD), 152-160 Pearse St., Dublin, D02 R590, Ireland.

出版信息

Chembiochem. 2025 Jan 14;26(2):e202400639. doi: 10.1002/cbic.202400639. Epub 2024 Oct 27.

Abstract

Lysine crotonylation (Kcr) is a recently discovered post-translational modification (PTM). Both histone and non-histone Kcr-proteins have been associated with numerous diseases including cancer, acute kidney injury, HIV latency, and cardiovascular disease. Histone Kcr enhances gene expression to a larger extend than the extensively studied lysine acetylation (Kac), suggesting Kcr as a novel potential therapeutic target. Although numerous scientific reports on crotonylation were published in the last years, relevant knowledge gaps concerning this PTM and its regulation still remain. To date, only few selective Kcr-interacting proteins have been identified and selective methods for the enrichment of Kcr-proteins in chemical proteomics analysis are still lacking. The development of new techniques to study this underexplored PTM could then clarify its function in health and disease and hopefully accelerate the development of new therapeutics for Kcr-related disease. Herein we briefly review what is known about the regulation mechanisms of Kcr and the current methods used to identify Kcr-proteins and their interacting partners. This report aims to highlight the significant potential of Kcr as a therapeutic target and to identify the existing scientific gaps that new research must address.

摘要

赖氨酸巴豆酰化(Kcr)是一种最近发现的翻译后修饰(PTM)。组蛋白和非组蛋白Kcr修饰的蛋白质都与多种疾病有关,包括癌症、急性肾损伤、HIV潜伏感染和心血管疾病。与广泛研究的赖氨酸乙酰化(Kac)相比,组蛋白Kcr能更大程度地增强基因表达,这表明Kcr是一种新的潜在治疗靶点。尽管近年来发表了许多关于巴豆酰化的科学报告,但关于这种翻译后修饰及其调控的相关知识空白仍然存在。迄今为止,仅鉴定出少数几种选择性与Kcr相互作用的蛋白质,在化学蛋白质组学分析中仍缺乏富集Kcr修饰蛋白质的选择性方法。因此,开发新技术来研究这种尚未充分探索的翻译后修饰,可能会阐明其在健康和疾病中的功能,并有望加速Kcr相关疾病新疗法的开发。在此,我们简要回顾一下已知的Kcr调控机制以及目前用于鉴定Kcr修饰蛋白质及其相互作用伴侣的方法。本报告旨在突出Kcr作为治疗靶点的巨大潜力,并确定新研究必须解决的现有科学空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e750/11776371/ac68ecc39adb/CBIC-26-e202400639-g010.jpg

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