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用于研究SUMO E3连接酶活性的体外SUMO化测定

In Vitro SUMOylation Assay to Study SUMO E3 Ligase Activity.

作者信息

Yang Wan-Shan, Campbell Mel, Kung Hsing-Jien, Chang Pei-Ching

机构信息

Institute of Microbiology and Immunology, National Yang-Ming University.

UC Davis Cancer Center, University of California, Davis.

出版信息

J Vis Exp. 2018 Jan 29(131):56629. doi: 10.3791/56629.

Abstract

Small ubiquitin-like modifier (SUMO) modification is an important post-translational modification (PTM) that mediates signal transduction primarily through modulating protein-protein interactions. Similar to ubiquitin modification, SUMOylation is directed by a sequential enzyme cascade including E1-activating enzyme (SAE1/SAE2), E2-conjugation enzyme (Ubc9), and E3-ligase (i.e., PIAS family, RanBP2, and Pc2). However, different from ubiquitination, an E3 ligase is non-essential for the reaction but does provide precision and efficacy for SUMO conjugation. Proteins modified by SUMOylation can be identified by in vivo assay via immunoprecipitation with substrate-specific antibodies and immunoblotting with SUMO-specific antibodies. However, the demonstration of protein SUMO E3 ligase activity requires in vitro reconstitution of SUMOylation assays using purified enzymes, substrate, and SUMO proteins. Since in the in vitro reactions, usually SAE1/SAE2 and Ubc9, alone are sufficient for SUMO conjugation, enhancement of SUMOylation by a putative E3 ligase is not always easy to detect. Here, we describe a modified in vitro SUMOylation protocol that consistently identifies SUMO modification using an in vitro reconstituted system. A step-by-step protocol to purify catalytically active K-bZIP, a viral SUMO-2/3 E3 ligase, is also presented. The SUMOylation activities of the purified K-bZIP are shown on p53, a well-known target of SUMO. This protocol can not only be employed for elucidating novel SUMO E3 ligases, but also for revealing their SUMO paralog specificity.

摘要

小泛素样修饰物(SUMO)修饰是一种重要的翻译后修饰(PTM),主要通过调节蛋白质-蛋白质相互作用来介导信号转导。与泛素修饰类似,SUMO化由一个顺序酶级联反应指导,该级联反应包括E1激活酶(SAE1/SAE2)、E2缀合酶(Ubc9)和E3连接酶(即PIAS家族、RanBP2和Pc2)。然而,与泛素化不同的是,E3连接酶对于该反应并非必不可少,但它确实为SUMO缀合提供了精确性和有效性。通过用底物特异性抗体进行免疫沉淀并使用SUMO特异性抗体进行免疫印迹的体内试验,可以鉴定出被SUMO化修饰的蛋白质。然而,蛋白质SUMO E3连接酶活性的证明需要使用纯化的酶、底物和SUMO蛋白在体外重建SUMO化试验。由于在体外反应中,通常单独的SAE1/SAE2和Ubc9就足以进行SUMO缀合,因此推定的E3连接酶对SUMO化的增强并不总是容易检测到。在这里,我们描述了一种改良的体外SUMO化方案,该方案使用体外重建系统一致地鉴定SUMO修饰。还介绍了一种纯化具有催化活性的K-bZIP(一种病毒SUMO-2/3 E3连接酶)的分步方案。纯化的K-bZIP的SUMO化活性在p53(一种众所周知的SUMO靶标)上得到了展示。该方案不仅可用于阐明新型SUMO E3连接酶,还可用于揭示它们的SUMO旁系同源物特异性。

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