Sloan-Kettering Institute, Cell Biology Program, New York, NY 10065, USA.
Trends Biochem Sci. 2011 May;36(5):254-61. doi: 10.1016/j.tibs.2011.01.004. Epub 2011 Feb 25.
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.
线粒体功能障碍与衰老过程和许多疾病的发生长期相关。调节细胞器内复杂的蛋白质折叠环境对于维持高效的代谢输出至关重要。随着时间的推移,由于活性氧物种积累引起的应激和线粒体基因组在复制过程中引入的突变,导致蛋白质动态平衡失调。为了在生物发生、重塑和应激过程中维持细胞器功能,必须由驻留在细胞器四个隔室中的分子伴侣和蛋白酶来监测线粒体蛋白质的质量控制。在这里,我们重点讨论了细胞器生物发生和衰老过程中的线粒体蛋白质质量控制。