蛋白质稳态
转位酶
细胞生物学
胞浆
线粒体
生物
膜间隙
蛋白酶体
内膜转移酶
转运蛋白
AAA蛋白
线粒体载体
生物化学
线粒体膜转运蛋白
染色体易位
线粒体内膜
ATP酶
细菌外膜
酶
大肠杆菌
基因
作者
Magda Krakowczyk,Anna Lenkiewicz,Tomasz Sitarz,Dominika Malińska,Mayra Borrero,Ben Hur Marins Mussulini,Vanessa Linke,Andrzej A. Szczepankiewicz,Joanna Biazik,Agata Wydrych,Hanna Nieznańska,Remigiusz A. Serwa,Agnieszka Chacińska,Piotr Brągoszewski
标识
DOI:10.1083/jcb.202306051
摘要
Most mitochondrial proteins originate from the cytosol and require transport into the organelle. Such precursor proteins must be unfolded to pass through translocation channels in mitochondrial membranes. Misfolding of transported proteins can result in their arrest and translocation failure. Arrested proteins block further import, disturbing mitochondrial functions and cellular proteostasis. Cellular responses to translocation failure have been defined in yeast. We developed the cell line-based translocase clogging model to discover molecular mechanisms that resolve failed import events in humans. The mechanism we uncover differs significantly from these described in fungi, where ATPase-driven extraction of blocked protein is directly coupled with proteasomal processing. We found human cells to rely primarily on mitochondrial factors to clear translocation channel blockage. The mitochondrial membrane depolarization triggered proteolytic cleavage of the stalled protein, which involved mitochondrial protease OMA1. The cleavage allowed releasing the protein fragment that blocked the translocase. The released fragment was further cleared in the cytosol by VCP/p97 and the proteasome.
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