Snider Natasha T, Omary M Bishr
Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, North Carolina, USA.
Department of Molecular & Integrative Physiology, Department of Medicine, University of Michigan, Ann Arbor, Michigan, USA; VA Ann Arbor Healthcare System, Ann Arbor, Michigan, USA.
Methods Enzymol. 2016;568:113-38. doi: 10.1016/bs.mie.2015.09.005. Epub 2015 Nov 6.
Intermediate filament (IF) proteins are known to be regulated by a number of posttranslational modifications (PTMs). Phosphorylation is the best-studied IF PTM, whereas ubiquitination, sumoylation, acetylation, glycosylation, ADP-ribosylation, farnesylation, and transamidation are less understood in functional terms but are known to regulate specific IFs under various contexts. The number and diversity of IF PTMs is certain to grow along with rapid advances in proteomic technologies. Therefore, the need for a greater understanding of the implications of PTMs to the structure, organization, and function of the IF cytoskeleton has become more apparent with the increased availability of data from global profiling studies of normal and diseased specimens. This chapter will provide information on established methods for the isolation and monitoring of IF PTMs along with the key reagents that are necessary to carry out these experiments.
已知中间丝(IF)蛋白受多种翻译后修饰(PTM)调控。磷酸化是研究最为深入的中间丝翻译后修饰,而泛素化、SUMO化、乙酰化、糖基化、ADP-核糖基化、法尼基化和转酰胺化在功能方面的了解较少,但已知在各种情况下可调节特定的中间丝。随着蛋白质组学技术的快速发展,中间丝翻译后修饰的数量和多样性肯定会增加。因此,随着正常和患病标本的全球分析研究数据可用性的增加,更深入了解翻译后修饰对中间丝细胞骨架的结构、组织和功能的影响的需求变得更加明显。本章将提供有关分离和监测中间丝翻译后修饰的既定方法以及进行这些实验所需的关键试剂的信息。