Lateral release of proteins from the TOM complex into the outer membrane of mitochondria

被引:52
作者
Harner, Max [1 ,2 ]
Neupert, Walter [1 ,2 ]
Deponte, Marcel [2 ,3 ]
机构
[1] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[2] Univ Munich, Inst Physiol Chem, D-8000 Munich, Germany
[3] Heidelberg Univ, Dept Parasitol, D-69120 Heidelberg, Germany
关键词
green fluorescent protein; lateral release; mitochondrial protein import; protein localization; protein translocase; TIM23; COMPLEX; TRANSLOCATION; IMPORT; INNER; PREPROTEINS; INSERTION; CHANNEL; BIOGENESIS; MACHINERY; PRECURSOR;
D O I
10.1038/emboj.2011.235
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The TOM complex of the outer membrane of mitochondria is the entry gate for the vast majority of precursor proteins that are imported into the mitochondria. It is made up by receptors and a protein conducting channel. Although precursor proteins of all subcompartments of mitochondria use the TOM complex, it is not known whether its channel can only mediate passage across the outer membrane or also lateral release into the outer membrane. To study this, we have generated fusion proteins of GFP and Tim23 which are inserted into the inner membrane and, at the same time, are spanning either the TOM complex or are integrated into the outer membrane. Our results demonstrate that the TOM complex, depending on sequence determinants in the precursors, can act both as a protein conducting pore and as an insertase mediating lateral release into the outer membrane. The EMBO Journal (2011) 30, 3232-3241. doi:10.1038/emboj.2011.235; Published online 15 July 2011
引用
收藏
页码:3232 / 3241
页数:10
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