Tom40 forms the hydrophilic channel of the mitochondrial import pore for preproteins

被引:406
作者
Hill, K
Model, K
Ryan, MT
Dietmeier, K
Martin, F
Wagner, R
Pfanner, N
机构
[1] Univ Freiburg, Inst Biochem & Mol Biol, D-79104 Freiburg, Germany
[2] Univ Osnabruck, Fachbereich Biol Chem, D-49034 Osnabruck, Germany
[3] Univ Freiburg, Fak Biol, D-79104 Freiburg, Germany
关键词
D O I
10.1038/26780
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mitochondrial outer membrane contains machinery for the import of preproteins encoded by nuclear genes(1-3). Eight different Tom (translocase of outer membrane) proteins have been identified that function as receptors and/or are related to a hypothetical general import pore. Many mitochondrial membrane channel activities have been described(4-7), including one related to Tim23 of the inner-membrane protein-import system(5); however, the pore-forming subunit(s) of the Tom machinery have not been identified until now. Here we describe the expression and functional reconstitution of Tom40, an integral membrane protein with mainly beta-sheet structure. Tom40 forms a cation-selective high-conductance channel that specifically binds to and transports mitochondrial-targeting sequences added to the cis side of the membrane. We conclude that Tom40 is the pore-forming subunit of the mitochondrial general import pore and that it constitutes a hydrophilic, similar to 22 Angstrom wide channel for the import of preproteins.
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页码:516 / 521
页数:6
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