From TOM to the TIM23 complex - handing over of a precursor

被引:38
作者
Callegari, Sylvie [1 ]
Cruz-Zaragoza, Luis Daniel [1 ]
Rehling, Peter [1 ,2 ]
机构
[1] Univ Med Ctr Gottingen, Dept Cellular Biochem, D-37073 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
关键词
membrane translocation; mitochondria; presequence pathway; protein translocation; TIM23; complex; TIM50; MITOCHONDRIAL PROTEIN IMPORT; OUTER-MEMBRANE PROTEIN; CYTOPLASMICALLY SYNTHESIZED PROTEINS; INTERMEMBRANE SPACE DOMAIN; ACIDIC RECEPTOR DOMAINS; ADP-ATP CARRIER; INNER MEMBRANE; PRESEQUENCE TRANSLOCASE; PREPROTEIN TRANSLOCATION; TERMINAL REGION;
D O I
10.1515/hsz-2020-0101
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondrial precursor proteins with aminoterminal presequences are imported via the presequence pathway, utilizing the TIM23 complex for inner membrane translocation. Initially, the precursors pass the outer membrane through the TOM complex and are handed over to the TIM23 complex where they are sorted into the inner membrane or translocated into the matrix. This handover process depends on the receptor proteins at the inner membrane, Tim50 and Tim23, which are critical for efficient import. In this review, we summarize key findings that shaped the current concepts of protein translocation along the presequence import pathway, with a particular focus on the precursor handover process from TOM to the TIM23 complex. In addition, we discuss functions of the human TIM23 pathway and the recently uncovered-pathogenic mutations in TIM50.
引用
收藏
页码:709 / 721
页数:13
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