articleProceedings of the National Academy of SciencesJun 16, 2014BRONZE OA

An uncoupling channel within the c-subunit ring of the F 1 F O ATP synthase is the mitochondrial permeability transition pore

Yale University · Imperial College London · +2 more institutions

PubMed
Indexed incrossrefpubmed

Abstract

Mitochondria maintain tight regulation of inner mitochondrial membrane (IMM) permeability to sustain ATP production. Stressful events cause cellular calcium (Ca(2+)) dysregulation followed by rapid loss of IMM potential known as permeability transition (PT), which produces osmotic shifts, metabolic dysfunction, and cell death. The molecular identity of the mitochondrial PT pore (mPTP) was previously unknown. We show that the purified reconstituted c-subunit ring of the FO of the F1FO ATP synthase forms a voltage-sensitive channel, the persistent opening of which leads to rapid and uncontrolled depolarization of the IMM in cells. Prolonged high matrix Ca(2+) enlarges the c-subunit ring and unhooks it from…

Citation impact

576
total citations
FWCI
30.30
Percentile
100%
References
33
Citations per year

Authors

12

Topics & keywords

Keywords
  • ATP synthase
  • Protein subunit
  • Mitochondrial permeability transition pore
  • Intracellular
  • Mitochondrion
  • Cell biology
  • Biology
  • Programmed cell death
UN Sustainable Development Goals
  • Affordable and clean energy
No related works found for this paper.