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新型靶蛋白的鉴定及Herc5介导的ISGylation修饰

Identification and Herc5-mediated ISGylation of novel target proteins.

作者信息

Takeuchi Tomoharu, Inoue Satoshi, Yokosawa Hideyoshi

机构信息

Department of Biochemistry, Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan.

出版信息

Biochem Biophys Res Commun. 2006 Sep 22;348(2):473-7. doi: 10.1016/j.bbrc.2006.07.076. Epub 2006 Jul 28.

Abstract

ISG15, a protein containing two ubiquitin-like domains, is an interferon-stimulated gene product that functions in antiviral response and is conjugated to various cellular proteins (ISGylation) upon interferon stimulation. ISGylation occurs via a pathway similar to the pathway for ubiquitination that requires the sequential action of E1/E2/E3: the E1 (UBE1L), E2 (UbcH8), and E3 (Efp/Herc5) enzymes for ISGylation have been hitherto identified. In this study, we identified six novel candidate target proteins for ISGylation by a proteomic approach. Four candidate target proteins were demonstrated to be ISGylated in UBE1L- and UbcH8-dependent manners, and ISGylation of the respective target proteins was stimulated by Herc5. In addition, Herc5 was capable of binding with the respective target proteins. Thus, these results suggest that Herc5 functions as a general E3 ligase for protein ISGylation.

摘要

ISG15是一种含有两个类泛素结构域的蛋白质,是一种干扰素刺激基因产物,在抗病毒反应中发挥作用,并在干扰素刺激下与多种细胞蛋白结合(ISGylation)。ISGylation通过一条类似于泛素化的途径发生,该途径需要E1/E2/E3的顺序作用:迄今为止,已鉴定出用于ISGylation的E1(UBE1L)、E2(UbcH8)和E3(Efp/Herc5)酶。在本研究中,我们通过蛋白质组学方法鉴定了六种新的ISGylation候选靶蛋白。四种候选靶蛋白被证明以UBE1L和UbcH8依赖的方式发生ISGylation,并且各自靶蛋白的ISGylation受到Herc5的刺激。此外,Herc5能够与各自的靶蛋白结合。因此,这些结果表明Herc5作为蛋白质ISGylation的通用E3连接酶发挥作用。

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