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Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa
Polyphosphate (polyP) is a universally conserved molecule that plays critical roles in managing bacterial stress responses, in addition to biofilm formation and virulence. The enzymes that make polyphosphate molecules are called polyphosphate kinases (PPKs). Since these enzymes are not conserved in...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406150/ https://www.ncbi.nlm.nih.gov/pubmed/34340551 http://dx.doi.org/10.1128/mBio.01477-21 |
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author | Baijal, Kanchi Downey, Michael |
author_facet | Baijal, Kanchi Downey, Michael |
author_sort | Baijal, Kanchi |
collection | PubMed |
description | Polyphosphate (polyP) is a universally conserved molecule that plays critical roles in managing bacterial stress responses, in addition to biofilm formation and virulence. The enzymes that make polyphosphate molecules are called polyphosphate kinases (PPKs). Since these enzymes are not conserved in higher eukaryotes, PPKs make excellent therapeutic targets. In a recent paper in mBio, Neville and colleagues described gallein, a commercially available G-protein antagonist, as a novel dual-specificity inhibitor against two families of PPK enzymes in Pseudomonas aeruginosa. In this commentary, we discuss the impact of this discovery, outline potential challenges of implementing gallein use in the clinic, and describe how gallein will serve as a fantastic new tool to further fundamental PPK and polyP research in bacteria. |
format | Online Article Text |
id | pubmed-8406150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-84061502021-09-09 Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa Baijal, Kanchi Downey, Michael mBio Commentary Polyphosphate (polyP) is a universally conserved molecule that plays critical roles in managing bacterial stress responses, in addition to biofilm formation and virulence. The enzymes that make polyphosphate molecules are called polyphosphate kinases (PPKs). Since these enzymes are not conserved in higher eukaryotes, PPKs make excellent therapeutic targets. In a recent paper in mBio, Neville and colleagues described gallein, a commercially available G-protein antagonist, as a novel dual-specificity inhibitor against two families of PPK enzymes in Pseudomonas aeruginosa. In this commentary, we discuss the impact of this discovery, outline potential challenges of implementing gallein use in the clinic, and describe how gallein will serve as a fantastic new tool to further fundamental PPK and polyP research in bacteria. American Society for Microbiology 2021-08-03 /pmc/articles/PMC8406150/ /pubmed/34340551 http://dx.doi.org/10.1128/mBio.01477-21 Text en Copyright © 2021 Baijal and Downey. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Commentary Baijal, Kanchi Downey, Michael Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa |
title | Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa |
title_full | Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa |
title_fullStr | Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa |
title_full_unstemmed | Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa |
title_short | Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa |
title_sort | targeting polyphosphate kinases in the fight against pseudomonas aeruginosa |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406150/ https://www.ncbi.nlm.nih.gov/pubmed/34340551 http://dx.doi.org/10.1128/mBio.01477-21 |
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