粒体自噬
蛋白酵素
生物
线粒体
线粒体生物发生
细胞生物学
功能(生物学)
自噬
DNAJA3公司
粒线体疾病
线粒体融合
生物发生
线粒体DNA
蛋白水解酶
遗传学
计算生物学
生物化学
酶
细胞凋亡
基因
作者
Pedro M. Quirós,Thomas Langer,Carlos López‐Otín
摘要
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'.
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