Department of Medicinal Chemistry and Molecular Pharmacology, Purdue Institute for Drug Discovery, Purdue University Center for Cancer Research, Purdue University, 720 Clinic Drive, West Lafayette, IN, 47907, United States.
Department of Medicinal Chemistry and Molecular Pharmacology, Purdue Institute for Drug Discovery, Purdue University Center for Cancer Research, Purdue University, 720 Clinic Drive, West Lafayette, IN, 47907, United States.
Curr Opin Chem Biol. 2021 Aug;63:115-122. doi: 10.1016/j.cbpa.2021.02.017. Epub 2021 Apr 8.
The posttranslational methylation of the α-N-terminal amino group of proteins was first documented over 40 years ago, but the functional significance of this modification has been underexplored relative to lysine and arginine methylation. Increasing reports implicates α-N-terminal methylation as a widespread and critical regulator of mitosis, chromatin interactions, DNA repair, and translation fidelity. Here, we summarize advances in the current understanding of protein α-N-terminal methylation biological functions and mechanisms across eukaryotic organisms. Also, we describe the recent literature on substrate recognition and the discovery of potent and selective inhibitors for protein N-terminal methyltransferases. Finally, we summarize the emergent crosstalk between α-N-terminal methylation and other N-terminal modifications.
蛋白质α-N-端氨基的翻译后甲基化在 40 多年前就已被首次记录,但与赖氨酸和精氨酸甲基化相比,这种修饰的功能意义还没有得到充分的探索。越来越多的报道表明,α-N-端甲基化是有丝分裂、染色质相互作用、DNA 修复和翻译保真度的广泛而关键的调节剂。在这里,我们总结了当前对真核生物中蛋白质α-N-端甲基化生物学功能和机制的理解进展。此外,我们还描述了关于底物识别和发现有效且选择性的蛋白质 N-端甲基转移酶抑制剂的最新文献。最后,我们总结了α-N-端甲基化与其他 N-端修饰之间新兴的串扰。