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Nitrite binding to globins: linkage isomerism, EPR silence and reductive chemistry

The nitrite adducts of globins can potentially bind via O- or N- linkage to the heme iron. We have used EPR (electron paramagnetic resonance) and DFT (density functional theory) to explore these binding modes to myoglobin and hemoglobin. We demonstrate that the nitrite adducts of both globins have d...

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Autores principales: Silaghi-Dumitrescu, Radu, Svistunenko, Dimitri A., Cioloboc, Daniela, Bischin, Cristina, Scurtu, Florina, Cooper, Chris E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256065/
https://www.ncbi.nlm.nih.gov/pubmed/25172022
http://dx.doi.org/10.1016/j.niox.2014.08.007
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author Silaghi-Dumitrescu, Radu
Svistunenko, Dimitri A.
Cioloboc, Daniela
Bischin, Cristina
Scurtu, Florina
Cooper, Chris E.
author_facet Silaghi-Dumitrescu, Radu
Svistunenko, Dimitri A.
Cioloboc, Daniela
Bischin, Cristina
Scurtu, Florina
Cooper, Chris E.
author_sort Silaghi-Dumitrescu, Radu
collection PubMed
description The nitrite adducts of globins can potentially bind via O- or N- linkage to the heme iron. We have used EPR (electron paramagnetic resonance) and DFT (density functional theory) to explore these binding modes to myoglobin and hemoglobin. We demonstrate that the nitrite adducts of both globins have detectable EPR signals; we provide an explanation for the difficulty in detecting these EPR features, based on uniaxial state considerations. The EPR and DFT data show that both nitrite linkage isomers can be present at the same time and that the two isomers are readily interconvertible in solution. The millisecond-scale process of nitrite reduction by Hb is investigated in search of the elusive Fe(II)-nitrite adduct.
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spelling pubmed-42560652014-12-09 Nitrite binding to globins: linkage isomerism, EPR silence and reductive chemistry Silaghi-Dumitrescu, Radu Svistunenko, Dimitri A. Cioloboc, Daniela Bischin, Cristina Scurtu, Florina Cooper, Chris E. Nitric Oxide Article The nitrite adducts of globins can potentially bind via O- or N- linkage to the heme iron. We have used EPR (electron paramagnetic resonance) and DFT (density functional theory) to explore these binding modes to myoglobin and hemoglobin. We demonstrate that the nitrite adducts of both globins have detectable EPR signals; we provide an explanation for the difficulty in detecting these EPR features, based on uniaxial state considerations. The EPR and DFT data show that both nitrite linkage isomers can be present at the same time and that the two isomers are readily interconvertible in solution. The millisecond-scale process of nitrite reduction by Hb is investigated in search of the elusive Fe(II)-nitrite adduct. Elsevier 2014-11-15 /pmc/articles/PMC4256065/ /pubmed/25172022 http://dx.doi.org/10.1016/j.niox.2014.08.007 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Article
Silaghi-Dumitrescu, Radu
Svistunenko, Dimitri A.
Cioloboc, Daniela
Bischin, Cristina
Scurtu, Florina
Cooper, Chris E.
Nitrite binding to globins: linkage isomerism, EPR silence and reductive chemistry
title Nitrite binding to globins: linkage isomerism, EPR silence and reductive chemistry
title_full Nitrite binding to globins: linkage isomerism, EPR silence and reductive chemistry
title_fullStr Nitrite binding to globins: linkage isomerism, EPR silence and reductive chemistry
title_full_unstemmed Nitrite binding to globins: linkage isomerism, EPR silence and reductive chemistry
title_short Nitrite binding to globins: linkage isomerism, EPR silence and reductive chemistry
title_sort nitrite binding to globins: linkage isomerism, epr silence and reductive chemistry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256065/
https://www.ncbi.nlm.nih.gov/pubmed/25172022
http://dx.doi.org/10.1016/j.niox.2014.08.007
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