Assays for Posttranslational Modifications of Intermediate Filament Proteins

被引:18
|
作者
Snider, Natasha T. [1 ]
Omary, M. Bishr [2 ,3 ]
机构
[1] Univ N Carolina, Dept Cell Biol & Physiol, Chapel Hill, NC USA
[2] Univ Michigan, Dept Med, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[3] VA Ann Arbor Healthcare Syst, Ann Arbor, MI USA
来源
关键词
MASS-SPECTROMETRY; KERATIN FUNCTION; PHOSPHORYLATION; CELLS; DISEASE; GLYCOSYLATION; MECHANISMS; STRESS; SITES; IDENTIFICATION;
D O I
10.1016/bs.mie.2015.09.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:113 / 138
页数:26
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