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The F1Fo-ATPase inhibitor protein IF1 in pathophysiology
The endogenous inhibitor of ATP synthase is a protein of about 10 kDa, known as IF1 which binds to the catalytic domain of the enzyme during ATP hydrolysis. The main role of IF1 consists of limiting ATP dissipation under condition of severe oxygen deprivation or in the presence of dysfunctions of mi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389554/ https://www.ncbi.nlm.nih.gov/pubmed/35991181 http://dx.doi.org/10.3389/fphys.2022.917203 |
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author | Gatto, Cristina Grandi, Martina Solaini, Giancarlo Baracca, Alessandra Giorgio, Valentina |
author_facet | Gatto, Cristina Grandi, Martina Solaini, Giancarlo Baracca, Alessandra Giorgio, Valentina |
author_sort | Gatto, Cristina |
collection | PubMed |
description | The endogenous inhibitor of ATP synthase is a protein of about 10 kDa, known as IF1 which binds to the catalytic domain of the enzyme during ATP hydrolysis. The main role of IF1 consists of limiting ATP dissipation under condition of severe oxygen deprivation or in the presence of dysfunctions of mitochondrial respiratory complexes, causing a collapse in mitochondrial membrane potential and therefore ATP hydrolysis. New roles of IF1 are emerging in the fields of cancer and neurodegeneration. Its high expression levels in tumor tissues have been associated with different roles favouring tumor formation, progression and evasion. Since discordant mechanisms of action have been proposed for IF1 in tumors, it is of the utmost importance to clarify them in the prospective of defining novel approaches for cancer therapy. Other IF1 functions, including its involvement in mitophagy, may be protective for neurodegenerative and aging-related diseases. In the present review we aim to clarify and discuss the emerging mechanisms in which IF1 is involved, providing a critical view of the discordant findings in the literature. |
format | Online Article Text |
id | pubmed-9389554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93895542022-08-20 The F1Fo-ATPase inhibitor protein IF1 in pathophysiology Gatto, Cristina Grandi, Martina Solaini, Giancarlo Baracca, Alessandra Giorgio, Valentina Front Physiol Physiology The endogenous inhibitor of ATP synthase is a protein of about 10 kDa, known as IF1 which binds to the catalytic domain of the enzyme during ATP hydrolysis. The main role of IF1 consists of limiting ATP dissipation under condition of severe oxygen deprivation or in the presence of dysfunctions of mitochondrial respiratory complexes, causing a collapse in mitochondrial membrane potential and therefore ATP hydrolysis. New roles of IF1 are emerging in the fields of cancer and neurodegeneration. Its high expression levels in tumor tissues have been associated with different roles favouring tumor formation, progression and evasion. Since discordant mechanisms of action have been proposed for IF1 in tumors, it is of the utmost importance to clarify them in the prospective of defining novel approaches for cancer therapy. Other IF1 functions, including its involvement in mitophagy, may be protective for neurodegenerative and aging-related diseases. In the present review we aim to clarify and discuss the emerging mechanisms in which IF1 is involved, providing a critical view of the discordant findings in the literature. Frontiers Media S.A. 2022-08-04 /pmc/articles/PMC9389554/ /pubmed/35991181 http://dx.doi.org/10.3389/fphys.2022.917203 Text en Copyright © 2022 Gatto, Grandi, Solaini, Baracca and Giorgio. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Gatto, Cristina Grandi, Martina Solaini, Giancarlo Baracca, Alessandra Giorgio, Valentina The F1Fo-ATPase inhibitor protein IF1 in pathophysiology |
title | The F1Fo-ATPase inhibitor protein IF1 in pathophysiology |
title_full | The F1Fo-ATPase inhibitor protein IF1 in pathophysiology |
title_fullStr | The F1Fo-ATPase inhibitor protein IF1 in pathophysiology |
title_full_unstemmed | The F1Fo-ATPase inhibitor protein IF1 in pathophysiology |
title_short | The F1Fo-ATPase inhibitor protein IF1 in pathophysiology |
title_sort | f1fo-atpase inhibitor protein if1 in pathophysiology |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389554/ https://www.ncbi.nlm.nih.gov/pubmed/35991181 http://dx.doi.org/10.3389/fphys.2022.917203 |
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