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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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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. |
format | Online Article Text |
id | pubmed-4256065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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