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Ubc13的ISG15修饰抑制其泛素结合活性。

ISG15 modification of Ubc13 suppresses its ubiquitin-conjugating activity.

作者信息

Takeuchi Tomoharu, 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. 2005 Oct 14;336(1):9-13. doi: 10.1016/j.bbrc.2005.08.034.

Abstract

ISG15 is one of the interferon-stimulated genes and is classified as a ubiquitin-like protein. Upon interferon stimuli, ISG15 is upregulated and becomes conjugated to various cellular proteins (ISGylation). Several target proteins for ISGylation have recently been identified, but the biological consequence of protein ISGylation remains unclear. In the course of our study to identify components of the ISGylation system, we found that Ubc13, an E2 enzyme for ubiquitin conjugation, is covalently modified with ISG15. To determine the meaning of ISGylation of Ubc13, we isolated ISG15-modified Ubc13 protein and compared its ubiquitin-conjugating activity with that of an unmodified one. We found that ISGylation of Ubc13 suppresses its ability to form a thioester intermediate with ubiquitin.

摘要

ISG15是一种干扰素刺激基因,被归类为类泛素蛋白。在干扰素刺激下,ISG15上调并与各种细胞蛋白结合(ISGylation修饰)。最近已鉴定出几种ISGylation修饰的靶蛋白,但蛋白ISGylation修饰的生物学后果仍不清楚。在我们鉴定ISGylation修饰系统成分的研究过程中,我们发现泛素结合的E2酶Ubc13被ISG15共价修饰。为了确定Ubc13的ISGylation修饰的意义,我们分离了ISG15修饰的Ubc13蛋白,并将其泛素结合活性与未修饰的Ubc13蛋白进行比较。我们发现Ubc13的ISGylation修饰抑制了其与泛素形成硫酯中间体的能力。

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