Rexach Jessica E, Clark Peter M, Hsieh-Wilson Linda C
Division of Chemistry and Chemical Engineering, and Howard Hughes Medical Institute, California Institute of Technology, Pasadena, California 91125, USA.
Nat Chem Biol. 2008 Feb;4(2):97-106. doi: 10.1038/nchembio.68.
O-GlcNAc glycosylation is a unique, dynamic form of glycosylation found on intracellular proteins of all multicellular organisms. Studies suggest that O-GlcNAc represents a key regulatory modification in the brain, contributing to transcriptional regulation, neuronal communication and neurodegenerative disease. Recently, several new chemical tools have been developed to detect and study the modification, including chemoenzymatic tagging methods, quantitative proteomics strategies and small-molecule inhibitors of O-GlcNAc enzymes. Here we highlight some of the emerging roles for O-GlcNAc in the nervous system and describe how chemical tools have significantly advanced our understanding of the scope, functional significance and cellular dynamics of this modification.
O-连接的N-乙酰葡糖胺糖基化是一种独特的、动态的糖基化形式,存在于所有多细胞生物的细胞内蛋白质上。研究表明,O-连接的N-乙酰葡糖胺是大脑中的一种关键调节修饰,有助于转录调控、神经元通讯和神经退行性疾病。最近,已经开发了几种新的化学工具来检测和研究这种修饰,包括化学酶标记方法、定量蛋白质组学策略和O-连接的N-乙酰葡糖胺酶的小分子抑制剂。在这里,我们重点介绍O-连接的N-乙酰葡糖胺在神经系统中的一些新出现的作用,并描述化学工具如何显著推进了我们对这种修饰的范围、功能意义和细胞动力学的理解。