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Intra-site differential inhibition of multi-specific enzymes

The ability to catalyse a reaction acting on different substrates, known as “broad-specificity” or “multi-specificity”, and to catalyse different reactions at the same active site (“promiscuity”) are common features among the enzymes. These properties appear to go against the concept of extreme spec...

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Autores principales: Cappiello, Mario, Balestri, Francesco, Moschini, Roberta, Mura, Umberto, Del-Corso, Antonella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144184/
https://www.ncbi.nlm.nih.gov/pubmed/32208768
http://dx.doi.org/10.1080/14756366.2020.1743988
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author Cappiello, Mario
Balestri, Francesco
Moschini, Roberta
Mura, Umberto
Del-Corso, Antonella
author_facet Cappiello, Mario
Balestri, Francesco
Moschini, Roberta
Mura, Umberto
Del-Corso, Antonella
author_sort Cappiello, Mario
collection PubMed
description The ability to catalyse a reaction acting on different substrates, known as “broad-specificity” or “multi-specificity”, and to catalyse different reactions at the same active site (“promiscuity”) are common features among the enzymes. These properties appear to go against the concept of extreme specificity of the catalytic action of enzymes and have been re-evaluated in terms of evolution and metabolic adaptation. This paper examines the potential usefulness of a differential inhibitory action in the study of the susceptibility to inhibition of multi-specific or promiscuous enzymes acting on different substrates. Aldose reductase is a multi-specific enzyme that catalyses the reduction of both aldoses and hydrophobic cytotoxic aldehydes and is used here as a concrete case to deal with the differential inhibition approach.
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spelling pubmed-71441842020-04-13 Intra-site differential inhibition of multi-specific enzymes Cappiello, Mario Balestri, Francesco Moschini, Roberta Mura, Umberto Del-Corso, Antonella J Enzyme Inhib Med Chem Review Article The ability to catalyse a reaction acting on different substrates, known as “broad-specificity” or “multi-specificity”, and to catalyse different reactions at the same active site (“promiscuity”) are common features among the enzymes. These properties appear to go against the concept of extreme specificity of the catalytic action of enzymes and have been re-evaluated in terms of evolution and metabolic adaptation. This paper examines the potential usefulness of a differential inhibitory action in the study of the susceptibility to inhibition of multi-specific or promiscuous enzymes acting on different substrates. Aldose reductase is a multi-specific enzyme that catalyses the reduction of both aldoses and hydrophobic cytotoxic aldehydes and is used here as a concrete case to deal with the differential inhibition approach. Taylor & Francis 2020-03-25 /pmc/articles/PMC7144184/ /pubmed/32208768 http://dx.doi.org/10.1080/14756366.2020.1743988 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Cappiello, Mario
Balestri, Francesco
Moschini, Roberta
Mura, Umberto
Del-Corso, Antonella
Intra-site differential inhibition of multi-specific enzymes
title Intra-site differential inhibition of multi-specific enzymes
title_full Intra-site differential inhibition of multi-specific enzymes
title_fullStr Intra-site differential inhibition of multi-specific enzymes
title_full_unstemmed Intra-site differential inhibition of multi-specific enzymes
title_short Intra-site differential inhibition of multi-specific enzymes
title_sort intra-site differential inhibition of multi-specific enzymes
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144184/
https://www.ncbi.nlm.nih.gov/pubmed/32208768
http://dx.doi.org/10.1080/14756366.2020.1743988
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