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一种基于体外荧光共振能量转移的高通量筛选测定法,用于筛选SUMO化途径中蛋白质-蛋白质相互作用的抑制剂。

An in vitro Förster resonance energy transfer-based high-throughput screening assay for inhibitors of protein-protein interactions in SUMOylation pathway.

作者信息

Song Yang, Liao Jiayu

机构信息

Department of Bioengineering, University of California, Riverside, California 92521, USA.

出版信息

Assay Drug Dev Technol. 2012 Aug;10(4):336-43. doi: 10.1089/adt.2011.0394. Epub 2011 Dec 22.

Abstract

Förster resonance energy transfer (FRET) is a powerful tool in biological research and has been widely used in the study of biomolecular interactions. SUMOylation is an important post-translational modification that is involved in many key biological processes. As a multi-step cascade reaction, SUMOylation involves multiple enzymes and protein-protein interactions. Here, we report the development of an in vitro FRET-based high-throughput screening (HTS) assay in SUMOylation. This assay is based on steady state and high efficiency of the fluorescent energy transfer between CyPet and YPet fused to SUMO1 and Ubc9, respectively. We optimized the assay and performed a small-scale pilot study to validate the screening platform. Carried out in 384-well plate format, our FRET-based HTS provides a powerful tool for large-scale and high-throughput applications.

摘要

荧光共振能量转移(FRET)是生物学研究中的一种强大工具,已广泛应用于生物分子相互作用的研究。小泛素样修饰(SUMOylation)是一种重要的翻译后修饰,参与许多关键的生物学过程。作为一个多步骤的级联反应,SUMOylation涉及多种酶和蛋白质-蛋白质相互作用。在此,我们报告了一种基于体外FRET的SUMOylation高通量筛选(HTS)检测方法的开发。该检测方法基于分别与SUMO1和Ubc9融合的CyPet和YPet之间荧光能量转移的稳态和高效率。我们优化了该检测方法,并进行了小规模的初步研究以验证筛选平台。以384孔板形式进行,我们基于FRET的HTS为大规模和高通量应用提供了一个强大的工具。

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