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Cephalosporins inhibit human metallo β-lactamase fold DNA repair nucleases SNM1A and SNM1B/apollo

Bacterial metallo-β-lactamases (MBLs) are involved in resistance to β-lactam antibiotics including cephalosporins. Human SNM1A and SNM1B are MBL superfamily exonucleases that play a key role in the repair of DNA interstrand cross-links, which are induced by antitumour chemotherapeutics, and are ther...

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Autores principales: Lee, Sook Y., Brem, Jürgen, Pettinati, Ilaria, Claridge, Timothy D. W., Gileadi, Opher, Schofield, Christopher J., McHugh, Peter J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063058/
https://www.ncbi.nlm.nih.gov/pubmed/27121860
http://dx.doi.org/10.1039/c6cc00529b
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author Lee, Sook Y.
Brem, Jürgen
Pettinati, Ilaria
Claridge, Timothy D. W.
Gileadi, Opher
Schofield, Christopher J.
McHugh, Peter J.
author_facet Lee, Sook Y.
Brem, Jürgen
Pettinati, Ilaria
Claridge, Timothy D. W.
Gileadi, Opher
Schofield, Christopher J.
McHugh, Peter J.
author_sort Lee, Sook Y.
collection PubMed
description Bacterial metallo-β-lactamases (MBLs) are involved in resistance to β-lactam antibiotics including cephalosporins. Human SNM1A and SNM1B are MBL superfamily exonucleases that play a key role in the repair of DNA interstrand cross-links, which are induced by antitumour chemotherapeutics, and are therefore targets for cancer chemosensitization. We report that cephalosporins are competitive inhibitors of SNM1A and SNM1B exonuclease activity; both the intact β-lactam and their hydrolysed products are active. This discovery provides a lead for the development of potent and selective SNM1A and SNM1B inhibitors.
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spelling pubmed-50630582016-10-19 Cephalosporins inhibit human metallo β-lactamase fold DNA repair nucleases SNM1A and SNM1B/apollo Lee, Sook Y. Brem, Jürgen Pettinati, Ilaria Claridge, Timothy D. W. Gileadi, Opher Schofield, Christopher J. McHugh, Peter J. Chem Commun (Camb) Chemistry Bacterial metallo-β-lactamases (MBLs) are involved in resistance to β-lactam antibiotics including cephalosporins. Human SNM1A and SNM1B are MBL superfamily exonucleases that play a key role in the repair of DNA interstrand cross-links, which are induced by antitumour chemotherapeutics, and are therefore targets for cancer chemosensitization. We report that cephalosporins are competitive inhibitors of SNM1A and SNM1B exonuclease activity; both the intact β-lactam and their hydrolysed products are active. This discovery provides a lead for the development of potent and selective SNM1A and SNM1B inhibitors. Royal Society of Chemistry 2016-05-18 2016-04-18 /pmc/articles/PMC5063058/ /pubmed/27121860 http://dx.doi.org/10.1039/c6cc00529b Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Lee, Sook Y.
Brem, Jürgen
Pettinati, Ilaria
Claridge, Timothy D. W.
Gileadi, Opher
Schofield, Christopher J.
McHugh, Peter J.
Cephalosporins inhibit human metallo β-lactamase fold DNA repair nucleases SNM1A and SNM1B/apollo
title Cephalosporins inhibit human metallo β-lactamase fold DNA repair nucleases SNM1A and SNM1B/apollo
title_full Cephalosporins inhibit human metallo β-lactamase fold DNA repair nucleases SNM1A and SNM1B/apollo
title_fullStr Cephalosporins inhibit human metallo β-lactamase fold DNA repair nucleases SNM1A and SNM1B/apollo
title_full_unstemmed Cephalosporins inhibit human metallo β-lactamase fold DNA repair nucleases SNM1A and SNM1B/apollo
title_short Cephalosporins inhibit human metallo β-lactamase fold DNA repair nucleases SNM1A and SNM1B/apollo
title_sort cephalosporins inhibit human metallo β-lactamase fold dna repair nucleases snm1a and snm1b/apollo
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063058/
https://www.ncbi.nlm.nih.gov/pubmed/27121860
http://dx.doi.org/10.1039/c6cc00529b
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