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Front Physiol. 2013 May 10;4:95. doi: 10.3389/fphys.2013.00095. eCollection 2013.

The mitochondrial permeability transition pore: a mystery solved?

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1
Department of Biomedical Sciences, University of Padova Padova, Italy.

Abstract

The permeability transition (PT) denotes an increase of the mitochondrial inner membrane permeability to solutes with molecular masses up to about 1500 Da. It is presumed to be mediated by opening of a channel, the permeability transition pore (PTP), whose molecular nature remains a mystery. Here I briefly review the history of the PTP, discuss existing models, and present our new results indicating that reconstituted dimers of the FOF1 ATP synthase form a channel with properties identical to those of the mitochondrial megachannel (MMC), the electrophysiological equivalent of the PTP. Open questions remain, but there is now promise that the PTP can be studied by genetic methods to solve the large number of outstanding problems.

KEYWORDS:

FOF1 ATP synthase; calcium; mitochondria; permeability transition

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