用于发现抑制剂的基于细胞的共价捕获去泛素酶测定法

IF 4.9 Q1 CHEMISTRY, MEDICINAL
Megan N. Doleschal, Jenna Miller, Sankalp Jain, Alexey V. Zakharov, Ganesha Rai, Anton Simeonov, Bolormaa Baljinnyam* and Zhihao Zhuang*, 
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引用次数: 0

摘要

泛素化是一种翻译后修饰,可引起多种细胞反应。去泛素化酶(DUBs)可清除蛋白质中的泛素分子,并通过抵消泛素连接酶的活性来调节细胞过程。泛素化和去泛素化过程受到不同机制的严格调控,它们的失调与许多疾病相关。发现 DUB 抑制剂不仅能开发治疗药物,还能促进对泛素化/去泛素化过程及其调控机制的了解。为了能够发现针对 DUB 的抑制剂,我们开发了一种基于细胞的 DUB 检测方法,利用细胞渗透性泛素探针 Biotin-cR10-Ub-PA,共价标记原生细胞环境中的 DUB。放大发光接近均相分析法(Alpha,特别是 AlphaLISA)用于定量评估 Biotin-cR10-Ub-PA 探针捕获目标 DUB 的情况。我们证明了这种新的基于细胞的 DUB 检测方法是可靠的,适合高通量筛选。作为概念验证,我们选择了人类 USP15 作为感兴趣的 DUB,并对照蛋白酶抑制剂库进行了筛选。除了被广泛采用的泛 DUB 抑制剂 PR-619 外,该库中的其他几种 DUB 抑制剂也被确定为命中物。这种新的 DUB 检测方法可随时用于发现针对许多其他人类 DUB 的抑制剂,从而鉴定出强效的细胞渗透性抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cell-Based Covalent-Capture Deubiquitinase Assay for Inhibitor Discovery

Cell-Based Covalent-Capture Deubiquitinase Assay for Inhibitor Discovery

Ubiquitination is a post-translational modification that elicits a variety of cellular responses. Deubiquitinases (DUBs) remove ubiquitin moieties from proteins and modulate cellular processes by counteracting the ubiquitin ligase activities. Ubiquitination and deubiquitination processes are tightly regulated by different mechanisms and their dysregulation is associated with many diseases. Discovery of DUB inhibitors could not only lead to therapeutics but also facilitate the understanding of ubiquitination/deubiquitination processes and their regulatory mechanisms. To enable the inhibitor discovery against DUBs, we developed a cell-based DUB assay that utilizes a cell-permeable ubiquitin probe, Biotin-cR10-Ub-PA, to covalently label DUBs in their native cellular environment. Amplified luminescent proximity homogeneous assay (Alpha, specifically AlphaLISA) is utilized to quantitatively assess the capture of the target DUB by the Biotin-cR10-Ub-PA probe. We demonstrated that this new cell-based DUB assay is robust and amenable to high-throughput screening. Human USP15 was selected as a DUB of interest and screened against a library of protease inhibitors as a proof of concept. In addition to the widely adopted pan-DUB inhibitor PR-619, several other DUB inhibitors from the library were also identified as hits. This new DUB assay can be readily adapted for inhibitor discovery against many other human DUBs to identify potent and cell-permeable inhibitors.

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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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