Milosevich Natalia, Hof Fraser
Department of Chemistry, University of Victoria , Victoria, British Columbia V8W 3V6, Canada.
Biochemistry. 2016 Mar 22;55(11):1570-83. doi: 10.1021/acs.biochem.5b01073. Epub 2015 Dec 28.
Protein methylation is a common post-translational modification with diverse biological functions. Methyllysine reader proteins are increasingly a focus of epigenetics research and play important roles in regulating many cellular processes. These reader proteins are vital players in development, cell cycle regulation, stress responses, oncogenesis, and other disease pathways. The recent emergence of a small number of chemical inhibitors for methyllysine reader proteins supports the viability of these proteins as targets for drug development. This article introduces the biochemistry and biology of methyllysine reader proteins, provides an overview of functions for those families of readers that have been targeted to date (MBT, PHD, tudor, and chromodomains), and reviews the development of synthetic agents that directly block their methyllysine reading functions.
蛋白质甲基化是一种常见的翻译后修饰,具有多种生物学功能。甲基赖氨酸识别蛋白越来越成为表观遗传学研究的焦点,并在调节许多细胞过程中发挥重要作用。这些识别蛋白在发育、细胞周期调控、应激反应、肿瘤发生及其他疾病途径中起着至关重要的作用。最近出现的少数几种针对甲基赖氨酸识别蛋白的化学抑制剂,证明了这些蛋白作为药物开发靶点的可行性。本文介绍了甲基赖氨酸识别蛋白的生物化学和生物学特性,概述了迄今为止已作为靶点的那些识别蛋白家族(MBT、PHD、tudor和染色质结构域)的功能,并综述了直接阻断其甲基赖氨酸识别功能的合成剂的研发情况。