z-logo
open-access-imgOpen Access
The Mitochondrial Permeability Transition Pore and ATP Synthase
Author(s) -
Gisela Beutner,
Kambiz N. Alavian,
Elizabeth A. Jonas,
George A. Porter
Publication year - 2016
Publication title -
handbook of experimental pharmacology
Language(s) - English
Resource type - Book series
SCImago Journal Rank - 1.605
H-Index - 90
eISSN - 1865-0325
pISSN - 0171-2004
DOI - 10.1007/164_2016_5
Subject(s) - atp synthase , mitochondrial permeability transition pore , mitochondrion , oxidative phosphorylation , microbiology and biotechnology , biology , protein subunit , biochemistry , chemistry , programmed cell death , enzyme , apoptosis , gene
Mitochondrial ATP generation by oxidative phosphorylation combines the stepwise oxidation by the electron transport chain (ETC) of the reducing equivalents NADH and FADH 2 with the generation of ATP by the ATP synthase. Recent studies show that the ATP synthase is not only essential for the generation of ATP but may also contribute to the formation of the mitochondrial permeability transition pore (PTP). We present a model, in which the PTP is located within the c-subunit ring in the F o subunit of the ATP synthase. Opening of the PTP was long associated with uncoupling of the ETC and the initiation of programmed cell death. More recently, it was shown that PTP opening may serve a physiologic role: it can transiently open to regulate mitochondrial signaling in mature cells, and it is open in the embryonic mouse heart. This review will discuss how the ATP synthase paradoxically lies at the center of both ATP generation and cell death.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom