Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Instituto Universitario de Oncología, Universidad de Oviedo, 33006 Oviedo, Spain.
Cologne Cluster of Excellence in Cellular Stress Responses in Aging-associated Diseases, Institute for Genetics, University of Cologne, Joseph-Stelzmann-Str. 26, 50931 Cologne, Germany.
Nat Rev Mol Cell Biol. 2015 Jun;16(6):345-59. doi: 10.1038/nrm3984. Epub 2015 May 13.
Recent advances in mitochondrial biology have revealed the high diversity and complexity of proteolytic enzymes that regulate mitochondrial function. We have classified mitochondrial proteases, or mitoproteases, on the basis of their function and location, and defined the human mitochondrial degradome as the complete set of mitoproteases that are encoded by the human genome. In addition to their nonspecific degradative functions, mitoproteases perform highly regulated proteolytic reactions that are important in mitochondrial function, integrity and homeostasis. These include protein synthesis, quality control, mitochondrial biogenesis and dynamics, mitophagy and apoptosis. Impaired or dysregulated function of mitoproteases is associated with ageing and with many pathological conditions such as neurodegenerative disorders, metabolic syndromes and cancer. A better understanding of the mitochondrial proteolytic landscape and its modulation may contribute to improving human lifespan and 'healthspan'.
线粒体生物学的最新进展揭示了调节线粒体功能的蛋白酶具有高度的多样性和复杂性。我们根据功能和位置对线粒体蛋白酶(mitoproteases)进行了分类,并将人类线粒体降解组定义为人类基因组编码的完整的线粒体蛋白酶组。除了具有非特异性的降解功能外,线粒体蛋白酶还执行高度调控的蛋白水解反应,这些反应对线粒体功能、完整性和动态平衡至关重要。这些反应包括蛋白质合成、质量控制、线粒体生物发生和动力学、线粒体自噬和细胞凋亡。线粒体蛋白酶功能受损或失调与衰老以及许多病理状况有关,如神经退行性疾病、代谢综合征和癌症。更好地了解线粒体蛋白水解景观及其调节可能有助于提高人类的寿命和“健康寿命”。