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Mol Cell Biol. 2014 Sep 15;34(18):3473-85. doi: 10.1128/MCB.00433-14. Epub 2014 Jul 7.

Presequence recognition by the tom40 channel contributes to precursor translocation into the mitochondrial matrix.

Author information

1
Institute of Cellular Biochemistry, University Medical Center Göttingen, Göttingen, Germany.
2
International Institute of Molecular and Cell Biology, Warsaw, Poland.
3
Proteomics Group, Max Planck Institute for Experimental Medicine, Göttingen, Germany.
4
Institute of Cellular Biochemistry, University Medical Center Göttingen, Göttingen, Germany Max Planck Institute for Biophysical Chemistry, Göttingen, Germany Peter.Rehling@medizin.uni-goettingen.de.

Abstract

More than 70% of mitochondrial proteins utilize N-terminal presequences as targeting signals. Presequence interactions with redundant cytosolic receptor domains of the translocase of the outer mitochondrial membrane (TOM) are well established. However, after the presequence enters the protein-conducting Tom40 channel, the recognition events that occur at the trans side leading up to the engagement of the presequence with inner membrane-bound receptors are less well defined. Using a photoaffinity-labeling approach with modified presequence peptides, we identified Tom40 as a presequence interactor of the TOM complex. Utilizing mass spectrometry, we mapped Tom40's presequence-interacting regions to both sides of the β-barrel. Analysis of a phosphorylation site within one of the presequence-interacting regions revealed altered translocation kinetics along the presequence pathway. Our analyses assess the relation between the identified presequence-binding region of Tom40 and the intermembrane space domain of Tom22. The identified presequence-interacting region of Tom40 is capable of functioning independently of the established trans-acting TOM presequence-binding domain during matrix import.

PMID:
25002531
PMCID:
PMC4135617
DOI:
10.1128/MCB.00433-14
[Indexed for MEDLINE]
Free PMC Article

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