Tsuchiya Yugo, Peak-Chew Sew Yeu, Newell Clare, Miller-Aidoo Sheritta, Mangal Sriyash, Zhyvoloup Alexander, Bakovic Jovana, Malanchuk Oksana, Pereira Gonçalo C, Kotiadis Vassilios, Szabadkai Gyorgy, Duchen Michael R, Campbell Mark, Cuenca Sergio Rodriguez, Vidal-Puig Antonio, James Andrew M, Murphy Michael P, Filonenko Valeriy, Skehel Mark, Gout Ivan
Department of Structural and Molecular Biology, University College London, London WC1E 6BT, U.K.
Biological Mass Spectrometry & Proteomics Cell Biology, MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, U.K.
Biochem J. 2017 Jul 11;474(14):2489-2508. doi: 10.1042/BCJ20170129.
Coenzyme A (CoA) is an obligatory cofactor in all branches of life. CoA and its derivatives are involved in major metabolic pathways, allosteric interactions and the regulation of gene expression. Abnormal biosynthesis and homeostasis of CoA and its derivatives have been associated with various human pathologies, including cancer, diabetes and neurodegeneration. Using an anti-CoA monoclonal antibody and mass spectrometry, we identified a wide range of cellular proteins which are modified by covalent attachment of CoA to cysteine thiols (CoAlation). We show that protein CoAlation is a reversible post-translational modification that is induced in mammalian cells and tissues by oxidising agents and metabolic stress. Many key cellular enzymes were found to be CoAlated and in ways that modified their activities. Our study reveals that protein CoAlation is a widespread post-translational modification which may play an important role in redox regulation under physiological and pathophysiological conditions.
辅酶A(CoA)是所有生命分支中必不可少的辅助因子。CoA及其衍生物参与主要代谢途径、变构相互作用和基因表达调控。CoA及其衍生物的生物合成异常和稳态失衡与多种人类疾病相关,包括癌症、糖尿病和神经退行性疾病。我们使用抗CoA单克隆抗体和质谱法,鉴定出了多种通过CoA与半胱氨酸硫醇共价连接修饰的细胞蛋白(CoAlation)。我们发现蛋白质CoAlation是一种可逆的翻译后修饰,在哺乳动物细胞和组织中由氧化剂和代谢应激诱导产生。许多关键细胞酶被发现发生了CoAlation,且其活性也因此发生了改变。我们的研究表明,蛋白质CoAlation是一种广泛存在的翻译后修饰,可能在生理和病理生理条件下的氧化还原调节中发挥重要作用。