| Literature DB >> 27761834 |
Mandy Beyer1, Nicole Kiweler1, Siavosh Mahboobi2, Oliver H Krämer3.
Abstract
Histone deacetylases (HDACs) catalyze the deacetylation of lysine residues in their target proteins. This biochemical modification can have profound effects on the functions of these proteins and a dysregulation of HDAC activity contributes to severe diseases, including neoplastic transformation. In the following chapter, we present a strategy that allows to distinguish between the inhibition of the class I HDACs HDAC1, 2, and 3 and of the class IIb HDAC HDAC6. This method is based on Western blot and relies on the detection of hyperacetylated substrates of class I or class IIb HDACs in lysates from cells that were treated with histone deacetylase inhibitors (HDACi).Entities:
Keywords: Acetylation; HDAC6; HDACi; HDACs; Histone; Tubulin
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Year: 2017 PMID: 27761834 DOI: 10.1007/978-1-4939-6527-4_26
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745