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Covalent Lectin Inhibition and Application in Bacterial Biofilm Imaging

Biofilm formation by pathogenic bacteria is a hallmark of chronic infections. In many cases, lectins play key roles in establishing biofilms. The pathogen Pseudomonas aeruginosa often exhibiting various drug resistances employs its lectins LecA and LecB as virulence factors and biofilm building bloc...

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Autores principales: Wagner, Stefanie, Hauck, Dirk, Hoffmann, Michael, Sommer, Roman, Joachim, Ines, Müller, Rolf, Imberty, Anne, Varrot, Annabelle, Titz, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767747/
https://www.ncbi.nlm.nih.gov/pubmed/28960731
http://dx.doi.org/10.1002/anie.201709368
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author Wagner, Stefanie
Hauck, Dirk
Hoffmann, Michael
Sommer, Roman
Joachim, Ines
Müller, Rolf
Imberty, Anne
Varrot, Annabelle
Titz, Alexander
author_facet Wagner, Stefanie
Hauck, Dirk
Hoffmann, Michael
Sommer, Roman
Joachim, Ines
Müller, Rolf
Imberty, Anne
Varrot, Annabelle
Titz, Alexander
author_sort Wagner, Stefanie
collection PubMed
description Biofilm formation by pathogenic bacteria is a hallmark of chronic infections. In many cases, lectins play key roles in establishing biofilms. The pathogen Pseudomonas aeruginosa often exhibiting various drug resistances employs its lectins LecA and LecB as virulence factors and biofilm building blocks. Therefore, inhibition of the function of these proteins is thought to have potential in developing “pathoblockers” preventing biofilm formation and virulence. A covalent lectin inhibitor specific to a carbohydrate binding site is described for the first time. Its application in the LecA‐specific in vitro imaging of biofilms formed by P. aeruginosa is also reported.
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spelling pubmed-57677472018-02-01 Covalent Lectin Inhibition and Application in Bacterial Biofilm Imaging Wagner, Stefanie Hauck, Dirk Hoffmann, Michael Sommer, Roman Joachim, Ines Müller, Rolf Imberty, Anne Varrot, Annabelle Titz, Alexander Angew Chem Int Ed Engl Communications Biofilm formation by pathogenic bacteria is a hallmark of chronic infections. In many cases, lectins play key roles in establishing biofilms. The pathogen Pseudomonas aeruginosa often exhibiting various drug resistances employs its lectins LecA and LecB as virulence factors and biofilm building blocks. Therefore, inhibition of the function of these proteins is thought to have potential in developing “pathoblockers” preventing biofilm formation and virulence. A covalent lectin inhibitor specific to a carbohydrate binding site is described for the first time. Its application in the LecA‐specific in vitro imaging of biofilms formed by P. aeruginosa is also reported. John Wiley and Sons Inc. 2017-11-28 2017-12-22 /pmc/articles/PMC5767747/ /pubmed/28960731 http://dx.doi.org/10.1002/anie.201709368 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Communications
Wagner, Stefanie
Hauck, Dirk
Hoffmann, Michael
Sommer, Roman
Joachim, Ines
Müller, Rolf
Imberty, Anne
Varrot, Annabelle
Titz, Alexander
Covalent Lectin Inhibition and Application in Bacterial Biofilm Imaging
title Covalent Lectin Inhibition and Application in Bacterial Biofilm Imaging
title_full Covalent Lectin Inhibition and Application in Bacterial Biofilm Imaging
title_fullStr Covalent Lectin Inhibition and Application in Bacterial Biofilm Imaging
title_full_unstemmed Covalent Lectin Inhibition and Application in Bacterial Biofilm Imaging
title_short Covalent Lectin Inhibition and Application in Bacterial Biofilm Imaging
title_sort covalent lectin inhibition and application in bacterial biofilm imaging
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767747/
https://www.ncbi.nlm.nih.gov/pubmed/28960731
http://dx.doi.org/10.1002/anie.201709368
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