Institute of Molecular Medicine, Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119992 Moscow, Russia.
Biomolecules. 2020 Apr 23;10(4):650. doi: 10.3390/biom10040650.
Proteolytic enzymes play a crucial role in metabolic processes, providing the cell with amino acids through the hydrolysis of multiple endogenous and exogenous proteins. In addition to this function, proteases are involved in numerous protein cascades to maintain cellular and extracellular homeostasis. The redox regulation of proteolysis provides a flexible dose-dependent mechanism for proteolytic activity control. The excessive reactive oxygen species (ROS) and reactive nitrogen species (RNS) in living organisms indicate pathological conditions, so redox-sensitive proteases can swiftly induce pro-survival responses or regulated cell death (RCD). At the same time, severe protein oxidation can lead to the dysregulation of proteolysis, which induces either protein aggregation or superfluous protein hydrolysis. Therefore, oxidative stress contributes to the onset of age-related dysfunction. In the present review, we consider the post-translational modifications (PTMs) of proteolytic enzymes and their impact on homeostasis.
蛋白酶在代谢过程中发挥着关键作用,通过水解多种内源性和外源性蛋白质为细胞提供氨基酸。除了这种功能外,蛋白酶还参与了许多蛋白质级联反应,以维持细胞内和细胞外的稳态。蛋白水解的氧化还原调节为蛋白酶活性的控制提供了一种灵活的、依赖剂量的机制。生物体内过多的活性氧(ROS)和活性氮(RNS)表明存在病理状况,因此氧化还原敏感的蛋白酶可以迅速诱导生存相关反应或调节细胞死亡(RCD)。同时,严重的蛋白质氧化会导致蛋白水解的失调,从而导致蛋白质聚集或过多的蛋白质水解。因此,氧化应激会导致与年龄相关的功能障碍的发生。在本综述中,我们考虑了蛋白水解酶的翻译后修饰(PTMs)及其对稳态的影响。