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Developing novel antifungals: lessons from G protein-coupled receptors

Up to 1.5 million people die yearly from fungal disease, but the repertoire of antifungal drug classes is minimal and the incidence of drug resistance is rising rapidly. This dilemma was recently declared by the World Health Organization as a global health emergency, but the discovery of new antifun...

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Autores principales: Velazhahan, Vaithish, McCann, Bethany L., Bignell, Elaine, Tate, Christopher G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614568/
https://www.ncbi.nlm.nih.gov/pubmed/36801017
http://dx.doi.org/10.1016/j.tips.2022.12.002
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author Velazhahan, Vaithish
McCann, Bethany L.
Bignell, Elaine
Tate, Christopher G.
author_facet Velazhahan, Vaithish
McCann, Bethany L.
Bignell, Elaine
Tate, Christopher G.
author_sort Velazhahan, Vaithish
collection PubMed
description Up to 1.5 million people die yearly from fungal disease, but the repertoire of antifungal drug classes is minimal and the incidence of drug resistance is rising rapidly. This dilemma was recently declared by the World Health Organization as a global health emergency, but the discovery of new antifungal drug classes remains excruciatingly slow. This process could be accelerated by focusing on novel targets, such as G protein-coupled receptor (GPCR)-like proteins, that have a high likelihood of being druggable and have well-defined biology and roles in disease. We discuss recent successes in understanding the biology of virulence and in structure determination of yeast GPCRs, and highlight new approaches that might pay significant dividends in the urgent search for novel antifungal drugs.
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spelling pubmed-76145682023-05-24 Developing novel antifungals: lessons from G protein-coupled receptors Velazhahan, Vaithish McCann, Bethany L. Bignell, Elaine Tate, Christopher G. Trends Pharmacol Sci Article Up to 1.5 million people die yearly from fungal disease, but the repertoire of antifungal drug classes is minimal and the incidence of drug resistance is rising rapidly. This dilemma was recently declared by the World Health Organization as a global health emergency, but the discovery of new antifungal drug classes remains excruciatingly slow. This process could be accelerated by focusing on novel targets, such as G protein-coupled receptor (GPCR)-like proteins, that have a high likelihood of being druggable and have well-defined biology and roles in disease. We discuss recent successes in understanding the biology of virulence and in structure determination of yeast GPCRs, and highlight new approaches that might pay significant dividends in the urgent search for novel antifungal drugs. 2023-03-01 /pmc/articles/PMC7614568/ /pubmed/36801017 http://dx.doi.org/10.1016/j.tips.2022.12.002 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/). https://creativecommons.org/licenses/by/4.0/This work is licensed under a CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) International license.
spellingShingle Article
Velazhahan, Vaithish
McCann, Bethany L.
Bignell, Elaine
Tate, Christopher G.
Developing novel antifungals: lessons from G protein-coupled receptors
title Developing novel antifungals: lessons from G protein-coupled receptors
title_full Developing novel antifungals: lessons from G protein-coupled receptors
title_fullStr Developing novel antifungals: lessons from G protein-coupled receptors
title_full_unstemmed Developing novel antifungals: lessons from G protein-coupled receptors
title_short Developing novel antifungals: lessons from G protein-coupled receptors
title_sort developing novel antifungals: lessons from g protein-coupled receptors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614568/
https://www.ncbi.nlm.nih.gov/pubmed/36801017
http://dx.doi.org/10.1016/j.tips.2022.12.002
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