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Fragment library screening identifies hits that bind to the non-catalytic surface of Pseudomonas aeruginosa DsbA1

At a time when the antibiotic drug discovery pipeline has stalled, antibiotic resistance is accelerating with catastrophic implications for our ability to treat bacterial infections. Globally we face the prospect of a future when common infections can once again kill. Anti-virulence approaches that...

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Autores principales: Mohanty, Biswaranjan, Rimmer, Kieran, McMahon, Róisín M., Headey, Stephen J., Vazirani, Mansha, Shouldice, Stephen R., Coinçon, Mathieu, Tay, Stephanie, Morton, Craig J., Simpson, Jamie S., Martin, Jennifer L., Scanlon, Martin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367682/
https://www.ncbi.nlm.nih.gov/pubmed/28346540
http://dx.doi.org/10.1371/journal.pone.0173436
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author Mohanty, Biswaranjan
Rimmer, Kieran
McMahon, Róisín M.
Headey, Stephen J.
Vazirani, Mansha
Shouldice, Stephen R.
Coinçon, Mathieu
Tay, Stephanie
Morton, Craig J.
Simpson, Jamie S.
Martin, Jennifer L.
Scanlon, Martin J.
author_facet Mohanty, Biswaranjan
Rimmer, Kieran
McMahon, Róisín M.
Headey, Stephen J.
Vazirani, Mansha
Shouldice, Stephen R.
Coinçon, Mathieu
Tay, Stephanie
Morton, Craig J.
Simpson, Jamie S.
Martin, Jennifer L.
Scanlon, Martin J.
author_sort Mohanty, Biswaranjan
collection PubMed
description At a time when the antibiotic drug discovery pipeline has stalled, antibiotic resistance is accelerating with catastrophic implications for our ability to treat bacterial infections. Globally we face the prospect of a future when common infections can once again kill. Anti-virulence approaches that target the capacity of the bacterium to cause disease rather than the growth or survival of the bacterium itself offer a tantalizing prospect of novel antimicrobials. They may also reduce the propensity to induce resistance by removing the strong selection pressure imparted by bactericidal or bacteriostatic agents. In the human pathogen Pseudomonas aeruginosa, disulfide bond protein A (PaDsbA1) plays a central role in the oxidative folding of virulence factors and is therefore an attractive target for the development of new anti-virulence antimicrobials. Using a fragment-based approach we have identified small molecules that bind to PaDsbA1. The fragment hits show selective binding to PaDsbA1 over the DsbA protein from Escherichia coli, suggesting that developing species-specific narrow-spectrum inhibitors of DsbA enzymes may be feasible. Structures of a co-complex of PaDsbA1 with the highest affinity fragment identified in the screen reveal that the fragment binds on the non-catalytic surface of the protein at a domain interface. This biophysical and structural data represent a starting point in the development of higher affinity compounds, which will be assessed for their potential as selective PaDsbA1 inhibitors.
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spelling pubmed-53676822017-04-06 Fragment library screening identifies hits that bind to the non-catalytic surface of Pseudomonas aeruginosa DsbA1 Mohanty, Biswaranjan Rimmer, Kieran McMahon, Róisín M. Headey, Stephen J. Vazirani, Mansha Shouldice, Stephen R. Coinçon, Mathieu Tay, Stephanie Morton, Craig J. Simpson, Jamie S. Martin, Jennifer L. Scanlon, Martin J. PLoS One Research Article At a time when the antibiotic drug discovery pipeline has stalled, antibiotic resistance is accelerating with catastrophic implications for our ability to treat bacterial infections. Globally we face the prospect of a future when common infections can once again kill. Anti-virulence approaches that target the capacity of the bacterium to cause disease rather than the growth or survival of the bacterium itself offer a tantalizing prospect of novel antimicrobials. They may also reduce the propensity to induce resistance by removing the strong selection pressure imparted by bactericidal or bacteriostatic agents. In the human pathogen Pseudomonas aeruginosa, disulfide bond protein A (PaDsbA1) plays a central role in the oxidative folding of virulence factors and is therefore an attractive target for the development of new anti-virulence antimicrobials. Using a fragment-based approach we have identified small molecules that bind to PaDsbA1. The fragment hits show selective binding to PaDsbA1 over the DsbA protein from Escherichia coli, suggesting that developing species-specific narrow-spectrum inhibitors of DsbA enzymes may be feasible. Structures of a co-complex of PaDsbA1 with the highest affinity fragment identified in the screen reveal that the fragment binds on the non-catalytic surface of the protein at a domain interface. This biophysical and structural data represent a starting point in the development of higher affinity compounds, which will be assessed for their potential as selective PaDsbA1 inhibitors. Public Library of Science 2017-03-27 /pmc/articles/PMC5367682/ /pubmed/28346540 http://dx.doi.org/10.1371/journal.pone.0173436 Text en © 2017 Mohanty et al http://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/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Mohanty, Biswaranjan
Rimmer, Kieran
McMahon, Róisín M.
Headey, Stephen J.
Vazirani, Mansha
Shouldice, Stephen R.
Coinçon, Mathieu
Tay, Stephanie
Morton, Craig J.
Simpson, Jamie S.
Martin, Jennifer L.
Scanlon, Martin J.
Fragment library screening identifies hits that bind to the non-catalytic surface of Pseudomonas aeruginosa DsbA1
title Fragment library screening identifies hits that bind to the non-catalytic surface of Pseudomonas aeruginosa DsbA1
title_full Fragment library screening identifies hits that bind to the non-catalytic surface of Pseudomonas aeruginosa DsbA1
title_fullStr Fragment library screening identifies hits that bind to the non-catalytic surface of Pseudomonas aeruginosa DsbA1
title_full_unstemmed Fragment library screening identifies hits that bind to the non-catalytic surface of Pseudomonas aeruginosa DsbA1
title_short Fragment library screening identifies hits that bind to the non-catalytic surface of Pseudomonas aeruginosa DsbA1
title_sort fragment library screening identifies hits that bind to the non-catalytic surface of pseudomonas aeruginosa dsba1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367682/
https://www.ncbi.nlm.nih.gov/pubmed/28346540
http://dx.doi.org/10.1371/journal.pone.0173436
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