Zhang Jing, Zheng Yujun George
Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy, The University of Georgia , Athens, Georgia 30602, United States.
ACS Chem Biol. 2016 Mar 18;11(3):583-97. doi: 10.1021/acschembio.5b00812. Epub 2015 Nov 16.
S-Adenosyl-L-methionine (SAM) is a sulfonium molecule with a structural hybrid of methionine and adenosine. As the second largest cofactor in the human body, its major function is to serve as methyl donor for SAM-dependent methyltransferases (MTases). The resultant transmethylation of biomolecules constitutes a significant biochemical mechanism in epigenetic regulation, cellular signaling, and metabolite degradation. Recently, numerous SAM analogs have been developed as synthetic cofactors to transfer the activated groups on MTase substrates for downstream ligation and identification. Meanwhile, new compounds built upon or derived from the SAM scaffold have been designed and tested as selective inhibitors for important MTase targets. Here, we summarized the recent development and application of SAM analogs as chemical biology tools for MTases.
S-腺苷-L-甲硫氨酸(SAM)是一种具有甲硫氨酸和腺苷结构杂合的锍分子。作为人体中第二大辅助因子,其主要功能是作为SAM依赖性甲基转移酶(MTases)的甲基供体。生物分子由此产生的甲基化是表观遗传调控、细胞信号传导和代谢物降解中的一种重要生化机制。最近,许多SAM类似物已被开发为合成辅助因子,用于在MTase底物上转移活化基团,以进行下游连接和鉴定。同时,基于SAM支架构建或衍生的新化合物已被设计并测试为重要MTase靶点的选择性抑制剂。在此,我们总结了SAM类似物作为MTases化学生物学工具的最新进展和应用。