首页> 外文期刊>The biochemical journal >Ubiquitin C-terminal hydrolases cleave isopeptide- and peptide-linked ubiquitin from structured proteins but do not edit ubiquitin homopolymers
【24h】

Ubiquitin C-terminal hydrolases cleave isopeptide- and peptide-linked ubiquitin from structured proteins but do not edit ubiquitin homopolymers

机译:泛素C末端水解酶从结构化蛋白质上切割异肽和肽连接的泛素,但不编辑泛素均聚物

获取原文
           

摘要

Modification of proteins with ubiquitin (Ub) occurs through a variety of topologically distinct Ub linkages, including Ube2W-mediated monoubiquitylation of N-terminal alpha amines to generate peptide-linked linear mono-Ub fusions. Protein ubiquitylation can be reversed by the action of deubiquitylating enzymes (DUBs), many of which show striking preference for particular Ub linkage types. Here, we have screened for DUBs that preferentially cleave N-terminal Ub from protein substrates but do not act on Ub homopolymers. We show that members of the Ub C-terminal hydrolase (UCH) family of DUBs demonstrate this preference for N-terminal deubiquitylating activity as they are capable of cleaving N-terminal Ub from SUMO2 and Ube2W, while displaying no activity against any of the eight Ub linkage types. Surprisingly, this ability to cleave Ub from SUMO2 was 100?times more efficient for UCH-L3 when we deleted the unstructured N-terminus of SUMO2, demonstrating that UCH enzymes can cleave Ub from structured proteins. However, UCH-L3 could also cleave chemically synthesized isopeptide-linked Ub from lysine 11 (K11) of SUMO2 with similar efficiency, demonstrating that UCH DUB activity is not limited to peptide-linked Ub. These findings advance our understanding of the specificity of the UCH family of DUBs, which are strongly implicated in cancer and neurodegeneration but whose substrate preference has remained unclear. In addition, our findings suggest that the reversal of Ube2W-mediated N-terminal ubiquitylation may be one physiological role of UCH DUBs in?vivo .Abbreviations: DUB, deubiquitylating enzyme; Ni-NTA, Ni2+-nitrilotriacetate; OTU, ovarian tumour; SENP, SUMO protease; Ub, ubiquitin; UCH, ubiquitin C-terminal hydrolase; USP, ubiquitin-specific protease
机译:蛋白质通过泛素(Ub)修饰的过程是通过多种拓扑学上独特的Ub键进行的,包括Ube2W介导的N末端α胺的单泛素化,以生成肽连接的线性单Ub融合物。蛋白质泛素化作用可以通过去泛素化酶(DUBs)的作用逆转,其中许多都显示出对特定Ub连锁类型的强烈偏好。在这里,我们筛选了优先从蛋白质底物上切割N末端Ub但不作用于Ub均聚物的DUB。我们显示DUBs的Ub C末端水解酶(UCH)家族成员展示了对N末端去泛素化活性的这种偏爱,因为它们能够从SUMO2和Ube2W裂解N末端Ub,而对任何八个都没有活性Ub链接类型。令人惊讶的是,当我们删除SUMO2的非结构化N末端时,这种从SUMO2切割Ub的能力比UCH-L3高100倍,表明UCH酶可以从结构蛋白切割Ub。但是,UCH-L3还可以类似的效率从SUMO2的赖氨酸11(K11)裂解化学合成的异肽连接的Ub,这表明UCH DUB活性不限于肽连接的Ub。这些发现使我们对UCH系列DUBs的特异性有了更深入的了解,这些DUBs与癌症和神经退行性疾病密切相关,但其底物偏好仍不清楚。此外,我们的发现表明,Ube2W介导的N末端泛素化的逆转可能是UCH DUBs在体内的一种生理作用。 Ni-NTA,Ni2 +-亚硝酸三乙酸酯; OTU,卵巢肿瘤; SENP,SUMO蛋白酶; UB,泛素; UCH,泛素C末端水解酶; USP,泛素特异性蛋白酶

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号