细胞器生物发生
生物发生
细胞器
蛋白质稳态
线粒体生物发生
细胞生物学
线粒体
DNAJA3公司
粒体自噬
生物
伴侣(临床)
蛋白质折叠
线粒体DNA
线粒体融合
遗传学
基因
自噬
医学
病理
细胞凋亡
作者
Brooke Baker,Cole M. Haynes
标识
DOI:10.1016/j.tibs.2011.01.004
摘要
Mitochondrial dysfunction has long been associated with the aging process and the onset of numerous diseases. Regulation of the complex protein-folding environment within the organelle is essential for maintaining efficient metabolic output. Over time, dysregulation of protein homeostasis arises through stress induced by the accumulation of reactive oxygen species and mutations in the mitochondrial genome introduced during replication. To preserve organelle function during biogenesis, remodeling and stress, quality control of mitochondrial proteins must be monitored by molecular chaperones and proteases stationed in the four compartments of the organelle. Here, we review mitochondrial protein quality control with a focus on organelle biogenesis and aging.
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