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Carbonic anhydrase versatility: from pH regulation to CO(2) sensing and metabolism
While the carbonic anhydrase (CA, EC 4.2.1.1) superfamily of enzymes has been described primarily as involved only in pH regulation for decades, it also has many other important functions. CO(2), bicarbonate, and protons, the physiological substrates of CA, are indeed the main buffering system in or...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676200/ https://www.ncbi.nlm.nih.gov/pubmed/38028557 http://dx.doi.org/10.3389/fmolb.2023.1326633 |
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author | Supuran, Claudiu T. |
author_facet | Supuran, Claudiu T. |
author_sort | Supuran, Claudiu T. |
collection | PubMed |
description | While the carbonic anhydrase (CA, EC 4.2.1.1) superfamily of enzymes has been described primarily as involved only in pH regulation for decades, it also has many other important functions. CO(2), bicarbonate, and protons, the physiological substrates of CA, are indeed the main buffering system in organisms belonging to all life kingdoms; however, in the last period, relevant progress has been made in the direction of elucidating the involvement of the eight genetically distinct CA families in chemical sensing, metabolism, and several other crucial physiological processes. Interference with CA activity, both by inhibiting and activating these enzymes, has thus led to novel applications for CA inhibitors and activators in the field of innovative biomedicine and environment and health. In this perspective article, I will discuss the recent advances which have allowed for a deeper understanding of the biochemistry of these versatile enzymes and various applications of their modulators of activity. |
format | Online Article Text |
id | pubmed-10676200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106762002023-01-01 Carbonic anhydrase versatility: from pH regulation to CO(2) sensing and metabolism Supuran, Claudiu T. Front Mol Biosci Molecular Biosciences While the carbonic anhydrase (CA, EC 4.2.1.1) superfamily of enzymes has been described primarily as involved only in pH regulation for decades, it also has many other important functions. CO(2), bicarbonate, and protons, the physiological substrates of CA, are indeed the main buffering system in organisms belonging to all life kingdoms; however, in the last period, relevant progress has been made in the direction of elucidating the involvement of the eight genetically distinct CA families in chemical sensing, metabolism, and several other crucial physiological processes. Interference with CA activity, both by inhibiting and activating these enzymes, has thus led to novel applications for CA inhibitors and activators in the field of innovative biomedicine and environment and health. In this perspective article, I will discuss the recent advances which have allowed for a deeper understanding of the biochemistry of these versatile enzymes and various applications of their modulators of activity. Frontiers Media S.A. 2023-11-10 /pmc/articles/PMC10676200/ /pubmed/38028557 http://dx.doi.org/10.3389/fmolb.2023.1326633 Text en Copyright © 2023 Supuran. 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 | Molecular Biosciences Supuran, Claudiu T. Carbonic anhydrase versatility: from pH regulation to CO(2) sensing and metabolism |
title | Carbonic anhydrase versatility: from pH regulation to CO(2) sensing and metabolism |
title_full | Carbonic anhydrase versatility: from pH regulation to CO(2) sensing and metabolism |
title_fullStr | Carbonic anhydrase versatility: from pH regulation to CO(2) sensing and metabolism |
title_full_unstemmed | Carbonic anhydrase versatility: from pH regulation to CO(2) sensing and metabolism |
title_short | Carbonic anhydrase versatility: from pH regulation to CO(2) sensing and metabolism |
title_sort | carbonic anhydrase versatility: from ph regulation to co(2) sensing and metabolism |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676200/ https://www.ncbi.nlm.nih.gov/pubmed/38028557 http://dx.doi.org/10.3389/fmolb.2023.1326633 |
work_keys_str_mv | AT supuranclaudiut carbonicanhydraseversatilityfromphregulationtoco2sensingandmetabolism |