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The mitochondrial permeability transition pore: a mystery solved?
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...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3650560/ https://www.ncbi.nlm.nih.gov/pubmed/23675351 http://dx.doi.org/10.3389/fphys.2013.00095 |
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author | Bernardi, Paolo |
author_facet | Bernardi, Paolo |
author_sort | Bernardi, Paolo |
collection | PubMed |
description | 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 F(O)F(1) 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. |
format | Online Article Text |
id | pubmed-3650560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-36505602013-05-14 The mitochondrial permeability transition pore: a mystery solved? Bernardi, Paolo Front Physiol Physiology 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 F(O)F(1) 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. Frontiers Media S.A. 2013-05-10 /pmc/articles/PMC3650560/ /pubmed/23675351 http://dx.doi.org/10.3389/fphys.2013.00095 Text en Copyright © 2013 Bernardi. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Physiology Bernardi, Paolo The mitochondrial permeability transition pore: a mystery solved? |
title | The mitochondrial permeability transition pore: a mystery solved? |
title_full | The mitochondrial permeability transition pore: a mystery solved? |
title_fullStr | The mitochondrial permeability transition pore: a mystery solved? |
title_full_unstemmed | The mitochondrial permeability transition pore: a mystery solved? |
title_short | The mitochondrial permeability transition pore: a mystery solved? |
title_sort | mitochondrial permeability transition pore: a mystery solved? |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3650560/ https://www.ncbi.nlm.nih.gov/pubmed/23675351 http://dx.doi.org/10.3389/fphys.2013.00095 |
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