Fritz Kristofer S
Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Division of Cardiology, School of Medicine, University of Colorado Denver Anschutz Medical Center, Aurora, CO, USA.
Methods Mol Biol. 2013;1077:191-201. doi: 10.1007/978-1-62703-637-5_13.
Lysine acetylation is an important posttranslational modification known to alter protein structure and function. Understanding the mechanisms involved in regulating protein acetylation remains a key factor in elucidating what role this modification plays in numerous disease pathologies. Here, we describe an in vitro strategy to examine the site-specific deacetylation of proteins utilizing the chemical acetylation of protein lysine residues via acetic anhydride. The impact of chemical acetylation on protein lysine residues is characterized by native gel electrophoresis and Western blotting. Acetyl-Lys modifications are then examined for deacetylation using a SIRT3 deacetylase activity assay and followed by stable isotope dilution mass spectrometry.
赖氨酸乙酰化是一种重要的翻译后修饰,已知其可改变蛋白质的结构和功能。了解调节蛋白质乙酰化的机制仍然是阐明这种修饰在众多疾病病理过程中所起作用的关键因素。在此,我们描述了一种体外策略,通过利用乙酸酐对蛋白质赖氨酸残基进行化学乙酰化来检测蛋白质的位点特异性去乙酰化。化学乙酰化对蛋白质赖氨酸残基的影响通过非变性凝胶电泳和蛋白质免疫印迹进行表征。然后使用SIRT3去乙酰化酶活性测定法检测乙酰赖氨酸修饰的去乙酰化情况,随后进行稳定同位素稀释质谱分析。