Membrane potential stimulates ADP import and ATP export by the mitochondrial ADP/ATP carrier due to its positively charged binding site.


Journal

Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440

Informations de publication

Date de publication:
Nov 2024
Historique:
medline: 2 11 2024
pubmed: 2 11 2024
entrez: 1 11 2024
Statut: ppublish

Résumé

The mitochondrial adenosine 5'-diphosphate (ADP)/adenosine 5'-triphosphate (ATP) carrier imports ADP into the mitochondrion and exports ATP to the cell. Here, we demonstrate that 3.3 positive charges are translocated with the negatively charged substrate in each transport step. They can be assigned to three positively charged residues of the central substrate-binding site and two asparagine/arginine pairs. In this way, the membrane potential stimulates not only the ATP

Identifiants

pubmed: 39485853
doi: 10.1126/sciadv.adp7725
doi:

Substances chimiques

Adenosine Triphosphate 8L70Q75FXE
Adenosine Diphosphate 61D2G4IYVH
Mitochondrial ADP, ATP Translocases 9068-80-8
Saccharomyces cerevisiae Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

eadp7725

Auteurs

Vasiliki Mavridou (V)

MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge Biomedical Campus, Keith Peters Building, Cambridge CB2 0XY, UK.

Martin S King (MS)

MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge Biomedical Campus, Keith Peters Building, Cambridge CB2 0XY, UK.

Andre Bazzone (A)

Nanion Technologies GmbH, Ganghoferstrasse 70A, D-80339 Munich, Germany.

Roger Springett (R)

CellSpex, Kettering, Northamptonshire NN14 6GX, UK.

Edmund R S Kunji (ERS)

MRC Mitochondrial Biology Unit, University of Cambridge, Cambridge Biomedical Campus, Keith Peters Building, Cambridge CB2 0XY, UK.

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Classifications MeSH