Kus Bart, Gajadhar Aaron, Stanger Karen, Cho Rob, Sun Warren, Rouleau Nathalie, Lee Tammy, Chan Donovan, Wolting Cheryl, Edwards Aled, Bosse Roger, Rotin Daniela
Banting and Best Department of Medical Research, University of Toronto, Ontario, Canada.
J Biol Chem. 2005 Aug 19;280(33):29470-8. doi: 10.1074/jbc.M502197200. Epub 2005 Jun 13.
Ubiquitin-protein ligases (E3s) are implicated in various human disorders and are attractive targets for therapeutic intervention. Although most cellular proteins are ubiquitinated, ubiquitination cannot be linked directly to a specific E3 for a large fraction of these proteins, and the substrates of most E3 enzymes are unknown. We have developed a luminescent assay to detect ubiquitination in vitro, which is more quantitative, effective, and sensitive than conventional ubiquitination assays. By taking advantage of the abundance of purified proteins made available by genomic efforts, we screened hundreds of purified yeast proteins for ubiquitination, and we identified previously reported and novel substrates of the yeast E3 ligase Rsp5. The relevance of these substrates was confirmed in vivo by showing that a number of them interact genetically with Rsp5, and some were ubiquitinated by Rsp5 in vivo. The combination of this sensitive assay and the availability of purified substrates will enable the identification of substrates for any purified E3 enzyme.
泛素蛋白连接酶(E3s)与多种人类疾病有关,是治疗干预的有吸引力的靶点。尽管大多数细胞蛋白都会发生泛素化,但对于这些蛋白中的很大一部分,泛素化不能直接与特定的E3联系起来,而且大多数E3酶的底物尚不清楚。我们开发了一种发光测定法来体外检测泛素化,它比传统的泛素化测定法更具定量性、有效性和敏感性。利用基因组研究提供的大量纯化蛋白,我们筛选了数百种纯化的酵母蛋白以检测其泛素化情况,并鉴定出了酵母E3连接酶Rsp5先前报道的底物和新底物。通过证明其中一些底物在遗传上与Rsp5相互作用,并且一些在体内被Rsp5泛素化,这些底物在体内的相关性得到了证实。这种灵敏测定法与纯化底物的可得性相结合,将能够鉴定任何纯化的E3酶的底物。