使用UbFluor高通量筛选HECT E3泛素连接酶。

Q3 Biochemistry, Genetics and Molecular Biology
Peter K Foote, David T Krist, Alexander V Statsyuk
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引用次数: 7

摘要

HECT E3泛素连接酶与许多人类疾病表型有关,是有希望的药物靶点;然而,HECT E3抑制剂的筛选试验本身就很复杂,需要上游E1和E2酶以及泛素、ATP和检测试剂。中间泛素硫酯和多泛素产物的复杂混合物为脱靶抑制提供了进一步的机会,并增加了测定的复杂性。UbFluor是一种新型泛素硫酯,绕过E1和E2酶,通过HECT E3连接酶直接转硫代化。转硫代化后荧光团的释放使HECT E3活性的荧光偏振检测成为可能。在抑制剂存在的情况下,HECT E3的活性被抑制,因此没有反应,FP也没有变化。该方法已适用于针对HECT E3连接酶的小分子高通量筛选,其效用已在发现HECT E3连接酶抑制剂中得到证实。©2017 by John Wiley & Sons, Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-Throughput Screening of HECT E3 Ubiquitin Ligases Using UbFluor.

High-Throughput Screening of HECT E3 Ubiquitin Ligases Using UbFluor.

HECT E3 ubiquitin ligases are responsible for many human disease phenotypes and are promising drug targets; however, screening assays for HECT E3 inhibitors are inherently complex, requiring upstream E1 and E2 enzymes as well as ubiquitin, ATP, and detection reagents. Intermediate ubiquitin thioesters and a complex mixture of polyubiquitin products provide further opportunities for off-target inhibition and increase the complexity of the assay. UbFluor is a novel ubiquitin thioester that bypasses the E1 and E2 enzymes and undergoes direct transthiolation with HECT E3 ligases. The release of fluorophore upon transthiolation allows fluorescence polarization detection of HECT E3 activity. In the presence of inhibitors, HECT E3 activity is ablated, and thus no reaction and no change in FP are observed. This assay has been adapted for high-throughput screening of small molecules against HECT E3 ligases, and its utility has been proven in the discovery of HECT E3 ligase inhibitors. © 2017 by John Wiley & Sons, Inc.

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来源期刊
Current protocols in chemical biology
Current protocols in chemical biology Biochemistry, Genetics and Molecular Biology-Biophysics
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