Genome biology unit, European Molecular Biology Laboratory, Heidelberg, Germany.
Angew Chem Int Ed Engl. 2013 Jan 2;52(1):254-69. doi: 10.1002/anie.201205674. Epub 2012 Nov 19.
N-Methylation is one of the simplest chemical modifications often occurring in peptides and proteins of prokaryotes and higher eukaryotes. Over years of evolution, nature has employed N-methylation of peptides as an ingenious technique to modulate biological function, often as a mode of survival through the production of antibiotics. This small structural change can not only mobilize large protein complexes (as in the histone methylation), but also inhibits the action of enzymes by selective recognition of protein-protein interaction surfaces. In recent years through the advancement in synthetic approaches, the potential of N-methylation has begun to be revealed, not only in modulating biological activity and selectivity as well as pharmacokinetic properties of peptides, but also in delivering novel drugs. Herein, we summarize the current knowledge of the versatility of N-methylation in modulating biological, structural, and pharmacokinetic properties of peptides.
N-甲基化是原核生物和高等真核生物中多肽和蛋白质中最常见的简单化学修饰之一。经过多年的进化,自然界已经将肽的 N-甲基化作为一种巧妙的技术来调节生物功能,通常作为产生抗生素的生存模式。这种小的结构变化不仅可以动员大的蛋白质复合物(如组蛋白甲基化),而且还可以通过选择性识别蛋白质-蛋白质相互作用表面来抑制酶的作用。近年来,通过合成方法的进步,N-甲基化的潜力开始显现,不仅可以调节肽的生物活性和选择性以及药代动力学特性,还可以用于递送新型药物。在此,我们总结了 N-甲基化在调节肽的生物学、结构和药代动力学特性方面的多功能性的现有知识。