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Target-Based Whole-Cell Screening by (1)H NMR Spectroscopy**

An NMR-based approach marries the two traditional screening technologies (phenotypic and target-based screening) to find compounds inhibiting a specific enzymatic reaction in bacterial cells. Building on a previous study in which it was demonstrated that hydrolytic decomposition of meropenem in livi...

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Autores principales: Ma, Junhe, Cao, Qing, McLeod, Sarah M, Ferguson, Keith, Gao, Ning, Breeze, Alexander L, Hu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471574/
https://www.ncbi.nlm.nih.gov/pubmed/25693499
http://dx.doi.org/10.1002/anie.201410701
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author Ma, Junhe
Cao, Qing
McLeod, Sarah M
Ferguson, Keith
Gao, Ning
Breeze, Alexander L
Hu, Jun
author_facet Ma, Junhe
Cao, Qing
McLeod, Sarah M
Ferguson, Keith
Gao, Ning
Breeze, Alexander L
Hu, Jun
author_sort Ma, Junhe
collection PubMed
description An NMR-based approach marries the two traditional screening technologies (phenotypic and target-based screening) to find compounds inhibiting a specific enzymatic reaction in bacterial cells. Building on a previous study in which it was demonstrated that hydrolytic decomposition of meropenem in living Escherichia coli cells carrying New Delhi metallo-β-lactamase subclass 1 (NDM-1) can be monitored in real time by NMR spectroscopy, we designed a cell-based NMR screening platform. A strong NDM-1 inhibitor was identified with cellular IC(50) of 0.51 μm, which is over 300-fold more potent than captopril, a known NDM-1 inhibitor. This new screening approach has great potential to be applied to targets in other cell types, such as mammalian cells, and to targets that are only stable or functionally competent in the cellular environment.
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spelling pubmed-44715742015-06-23 Target-Based Whole-Cell Screening by (1)H NMR Spectroscopy** Ma, Junhe Cao, Qing McLeod, Sarah M Ferguson, Keith Gao, Ning Breeze, Alexander L Hu, Jun Angew Chem Int Ed Engl Communications An NMR-based approach marries the two traditional screening technologies (phenotypic and target-based screening) to find compounds inhibiting a specific enzymatic reaction in bacterial cells. Building on a previous study in which it was demonstrated that hydrolytic decomposition of meropenem in living Escherichia coli cells carrying New Delhi metallo-β-lactamase subclass 1 (NDM-1) can be monitored in real time by NMR spectroscopy, we designed a cell-based NMR screening platform. A strong NDM-1 inhibitor was identified with cellular IC(50) of 0.51 μm, which is over 300-fold more potent than captopril, a known NDM-1 inhibitor. This new screening approach has great potential to be applied to targets in other cell types, such as mammalian cells, and to targets that are only stable or functionally competent in the cellular environment. WILEY-VCH Verlag 2015-04-13 2015-02-18 /pmc/articles/PMC4471574/ /pubmed/25693499 http://dx.doi.org/10.1002/anie.201410701 Text en © 2015 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution Non-Commercial NoDerivs 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
Ma, Junhe
Cao, Qing
McLeod, Sarah M
Ferguson, Keith
Gao, Ning
Breeze, Alexander L
Hu, Jun
Target-Based Whole-Cell Screening by (1)H NMR Spectroscopy**
title Target-Based Whole-Cell Screening by (1)H NMR Spectroscopy**
title_full Target-Based Whole-Cell Screening by (1)H NMR Spectroscopy**
title_fullStr Target-Based Whole-Cell Screening by (1)H NMR Spectroscopy**
title_full_unstemmed Target-Based Whole-Cell Screening by (1)H NMR Spectroscopy**
title_short Target-Based Whole-Cell Screening by (1)H NMR Spectroscopy**
title_sort target-based whole-cell screening by (1)h nmr spectroscopy**
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471574/
https://www.ncbi.nlm.nih.gov/pubmed/25693499
http://dx.doi.org/10.1002/anie.201410701
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