线粒体
粒体自噬
细胞生物学
转运蛋白
蛋白质靶向
胞浆
蛋白质降解
蛋白质稳态
生物
线粒体膜转运蛋白
生物化学
膜蛋白
线粒体内膜
自噬
酶
细胞凋亡
膜
作者
Fabian den Brave,Jeannine Engelke,Thomas Becker
摘要
Mitochondria import about 1000 proteins that are produced as precursors on cytosolic ribosomes. Defects in mitochondrial protein import result in the accumulation of non-imported precursor proteins and proteotoxic stress. The cell is equipped with different quality control mechanisms to monitor protein transport into mitochondria. First, molecular chaperones guide unfolded proteins to mitochondria and deliver non-imported proteins to proteasomal degradation. Second, quality control factors remove translocation stalled precursor proteins from protein translocases. Third, protein translocases monitor protein sorting to mitochondrial subcompartments. Fourth, AAA proteases of the mitochondrial subcompartments remove mislocalized or unassembled proteins. Finally, impaired efficiency of protein transport is an important sensor for mitochondrial dysfunction and causes the induction of cellular stress responses, which could eventually result in the removal of the defective mitochondria by mitophagy. In this review, we summarize our current understanding of quality control mechanisms that govern mitochondrial protein transport.
科研通智能强力驱动
Strongly Powered by AbleSci AI