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Revealing the Membrane-Bound Catalytic Oxidation of NADH by the Drug Target Type-II NADH Dehydrogenase
[Image: see text] Type-II NADH:quinone oxidoreductases (NDH-2s) are an important element of microbial pathogen electron transport chains and an attractive drug target. Despite being widely studied, its mechanism and catalysis are still poorly understood in a hydrophobic membrane environment. A recen...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812066/ https://www.ncbi.nlm.nih.gov/pubmed/31592658 http://dx.doi.org/10.1021/acs.biochem.9b00752 |
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author | Godoy-Hernandez, Albert Tate, Daniel J. McMillan, Duncan G. G. |
author_facet | Godoy-Hernandez, Albert Tate, Daniel J. McMillan, Duncan G. G. |
author_sort | Godoy-Hernandez, Albert |
collection | PubMed |
description | [Image: see text] Type-II NADH:quinone oxidoreductases (NDH-2s) are an important element of microbial pathogen electron transport chains and an attractive drug target. Despite being widely studied, its mechanism and catalysis are still poorly understood in a hydrophobic membrane environment. A recent report for the Escherichia coli NDH-2 showed NADH oxidation in a solution-based assay but apparently showed the reverse reaction in electrochemical studies, calling into question the validity of the electrochemical approach. Here we report electrochemical catalysis in the well-studied NDH-2 from Caldalkalibacillus thermarum (CthNDH-2). In agreement with previous reports, we demonstrated CthNDH-2 NADH oxidation in a solution assay and electrochemical assays revealed a system artifact in the absence of quinone that was absent in a membrane system. However, in the presence of either immobilized quinone or mobile quinone in a membrane, NADH oxidation was observed as in solution-phase assays. This conclusively establishes surface-based electrochemistry as a viable approach for interrogating electron transfer chain drug targets. |
format | Online Article Text |
id | pubmed-6812066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-68120662019-10-25 Revealing the Membrane-Bound Catalytic Oxidation of NADH by the Drug Target Type-II NADH Dehydrogenase Godoy-Hernandez, Albert Tate, Daniel J. McMillan, Duncan G. G. Biochemistry [Image: see text] Type-II NADH:quinone oxidoreductases (NDH-2s) are an important element of microbial pathogen electron transport chains and an attractive drug target. Despite being widely studied, its mechanism and catalysis are still poorly understood in a hydrophobic membrane environment. A recent report for the Escherichia coli NDH-2 showed NADH oxidation in a solution-based assay but apparently showed the reverse reaction in electrochemical studies, calling into question the validity of the electrochemical approach. Here we report electrochemical catalysis in the well-studied NDH-2 from Caldalkalibacillus thermarum (CthNDH-2). In agreement with previous reports, we demonstrated CthNDH-2 NADH oxidation in a solution assay and electrochemical assays revealed a system artifact in the absence of quinone that was absent in a membrane system. However, in the presence of either immobilized quinone or mobile quinone in a membrane, NADH oxidation was observed as in solution-phase assays. This conclusively establishes surface-based electrochemistry as a viable approach for interrogating electron transfer chain drug targets. American Chemical Society 2019-10-08 2019-10-22 /pmc/articles/PMC6812066/ /pubmed/31592658 http://dx.doi.org/10.1021/acs.biochem.9b00752 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Godoy-Hernandez, Albert Tate, Daniel J. McMillan, Duncan G. G. Revealing the Membrane-Bound Catalytic Oxidation of NADH by the Drug Target Type-II NADH Dehydrogenase |
title | Revealing the Membrane-Bound Catalytic Oxidation of
NADH by the Drug Target Type-II NADH Dehydrogenase |
title_full | Revealing the Membrane-Bound Catalytic Oxidation of
NADH by the Drug Target Type-II NADH Dehydrogenase |
title_fullStr | Revealing the Membrane-Bound Catalytic Oxidation of
NADH by the Drug Target Type-II NADH Dehydrogenase |
title_full_unstemmed | Revealing the Membrane-Bound Catalytic Oxidation of
NADH by the Drug Target Type-II NADH Dehydrogenase |
title_short | Revealing the Membrane-Bound Catalytic Oxidation of
NADH by the Drug Target Type-II NADH Dehydrogenase |
title_sort | revealing the membrane-bound catalytic oxidation of
nadh by the drug target type-ii nadh dehydrogenase |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812066/ https://www.ncbi.nlm.nih.gov/pubmed/31592658 http://dx.doi.org/10.1021/acs.biochem.9b00752 |
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