Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, United States.
Org Lett. 2023 Sep 15;25(36):6767-6772. doi: 10.1021/acs.orglett.3c02736. Epub 2023 Sep 5.
Prenylated proteins contain C or C isoprenoids linked to cysteine residues positioned near their C-termini. Here we describe the preparation of isoprenoid diphosphate analogues incorporating diazirine groups that can be used to probe interactions between prenylated proteins and other proteins that interact with them. Studies using synthetic peptides and whole proteins demonstrate that these diazirine analogues are efficient substrates for prenyltransferases. Photo-cross-linking experiments using peptides incorporating the diazirine-functionalized isoprenoids selectively cross-link to several different proteins. These new isoprenoid analogues should be broadly useful in the studies of protein prenylation.
被类异戊二烯基团修饰的蛋白质包含与靠近其 C 末端的半胱氨酸残基相连的 C 或 C 异戊二烯。在这里,我们描述了含有叠氮基团的异戊二烯二磷酸类似物的制备方法,这些类似物可用于探测被类异戊二烯基团修饰的蛋白质与其他与其相互作用的蛋白质之间的相互作用。使用合成肽和全蛋白的研究表明,这些叠氮类似物是有效的prenyltransferase 的底物。使用包含叠氮功能化异戊二烯的肽进行的光交联实验选择性地交联到几种不同的蛋白质上。这些新的异戊二烯类似物在蛋白质prenylation 的研究中应该具有广泛的用途。