Abstract
We have investigated the energy requirement of mitochondrial protein import with a simplified system containing only isolated yeast mitochondria, energy sources and a purified precursor protein. This precursor was a fusion protein composed of 22 residues of the cytochrome oxidase subunit IV pre-sequence fused to mouse dihydrofolate reductase. Import of this protein required not only an energized inner membrane, but also ATP. ATP could be replaced by GTP, but not by CTP, TTP or non-hydrolyzable ATP analogs. Added ATP did not increase the membrane potential of respiring mitochondria; it supported import even if the proton-translocating mitochondrial ATPase and the entry of ATP into the matrix were blocked. We conclude that ATP exerts its effect on mitochondrial protein import outside the inner membrane.
MeSH Terms
Adenosine Triphosphate/metabolism
Biological Transport
Electron Transport Complex IV/genetics,metabolism
Intracellular Membranes/metabolism
Macromolecular Substances
Membrane Potentials
Mitochondria/metabolism
Recombinant Fusion Proteins/metabolism
Recombinant Proteins/metabolism
Ribonucleotides/metabolism
Saccharomyces cerevisiae/metabolism
Tetrahydrofolate Dehydrogenase/genetics,metabolism
Chemicals
Macromolecular Substances
Recombinant Fusion Proteins
Recombinant Proteins
Ribonucleotides
Adenosine Triphosphate
Tetrahydrofolate Dehydrogenase
Electron Transport Complex IV
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Eilers M
Oppliger W
Schatz G
References (27)
27 references, click to expand
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