预酸化
接合作用
相扑蛋白
翻译后修饰
琥珀酰化
化学
泛素
生物化学
赖氨酸
基因
泛素连接酶
氨基酸
酶
作者
Jinning Gao,Kai Shao,Xiatian Chen,Zhe Li,Ziqian Liu,Zhongjie Yu,Lynn Htet Htet Aung,Yin Wang,Peifeng Li
标识
DOI:10.1016/j.yjmcc.2019.11.146
摘要
Abstract
Cardiovascular disease (CVD) is one of the most threatening diseases to human health and life, and the number of patients is increasing year by year. Thus, it is of great significance to study the pathogenesis, prevention and treatment of CVDs. The occurrence and development of CVDs involve dynamic, complex and delicate intracellular processes and the pathogenesis is not entirely clear. In contrast to genetic mutations, most of the protein post-translational modifications (PTMs) are reversible, and can affect the activity, stability, subcellular localization, protein-protein interaction etc., of the substrate targets, emerging as key mediators of a number of CVD progression. Under pathological conditions, the PTMs undergo aberrant balances which cause changes of the substrate target proteins in expression level, localization and capacity to activate downstream signaling pathways. Therefore, new approaches can be created aiming to correct the abnormal PTM alterations in treating CVDs. This review summarizes some of the more recent advances in PTMs, focusing on SUMOylation, neddylation, succinylation, and prenylation, and the effect of these modifications on cardiovascular function and progression, which may provide potential targets for future therapeutics.
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