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Oximetry with the NMR signals of hemoglobin Val E11 and Tyr C7

The NMR visibility of the signals from erythrocyte hemoglobin (Hb) presents an opportunity to assess the vascular PO(2) (partial pressure of oxygen) in vivo to gather insight into the regulation of O(2) transport, especially in contracting muscle tissue. Some concerns, however, have arisen about the...

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Autores principales: Xie, Hongtao, Kreutzer, Ulrike, Jue, Thomas
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2753772/
https://www.ncbi.nlm.nih.gov/pubmed/19621237
http://dx.doi.org/10.1007/s00421-009-1125-3
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author Xie, Hongtao
Kreutzer, Ulrike
Jue, Thomas
author_facet Xie, Hongtao
Kreutzer, Ulrike
Jue, Thomas
author_sort Xie, Hongtao
collection PubMed
description The NMR visibility of the signals from erythrocyte hemoglobin (Hb) presents an opportunity to assess the vascular PO(2) (partial pressure of oxygen) in vivo to gather insight into the regulation of O(2) transport, especially in contracting muscle tissue. Some concerns, however, have arisen about the validity of using the Val E11 signal as an indicator of PO(2), since its intensity depends on tertiary structural changes, in contrast to the quaternary structure changes associated with relaxed (R) and tense (T) transition during O(2) binding. We have examined the Val E11 and Tyr C7 signal intensity as a function of Hb saturation by developing an oximetry system, which permits the comparative analysis of the NMR and spectrophotometric measurements. The spectrophotometric assay defines the Hb saturation level at a given PO(2) and yields standard oxygen-binding curves. Under defined PO(2) and Hb saturation values, the NMR measurements have determined that the Val E11 signal, as well as the Tyr C7 signal, tracks closely Hb saturation and can therefore serve as a vascular oxygen biomarker.
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spelling pubmed-27537722009-10-02 Oximetry with the NMR signals of hemoglobin Val E11 and Tyr C7 Xie, Hongtao Kreutzer, Ulrike Jue, Thomas Eur J Appl Physiol Original Article The NMR visibility of the signals from erythrocyte hemoglobin (Hb) presents an opportunity to assess the vascular PO(2) (partial pressure of oxygen) in vivo to gather insight into the regulation of O(2) transport, especially in contracting muscle tissue. Some concerns, however, have arisen about the validity of using the Val E11 signal as an indicator of PO(2), since its intensity depends on tertiary structural changes, in contrast to the quaternary structure changes associated with relaxed (R) and tense (T) transition during O(2) binding. We have examined the Val E11 and Tyr C7 signal intensity as a function of Hb saturation by developing an oximetry system, which permits the comparative analysis of the NMR and spectrophotometric measurements. The spectrophotometric assay defines the Hb saturation level at a given PO(2) and yields standard oxygen-binding curves. Under defined PO(2) and Hb saturation values, the NMR measurements have determined that the Val E11 signal, as well as the Tyr C7 signal, tracks closely Hb saturation and can therefore serve as a vascular oxygen biomarker. Springer-Verlag 2009-07-21 2009-10 /pmc/articles/PMC2753772/ /pubmed/19621237 http://dx.doi.org/10.1007/s00421-009-1125-3 Text en © The Author(s) 2009
spellingShingle Original Article
Xie, Hongtao
Kreutzer, Ulrike
Jue, Thomas
Oximetry with the NMR signals of hemoglobin Val E11 and Tyr C7
title Oximetry with the NMR signals of hemoglobin Val E11 and Tyr C7
title_full Oximetry with the NMR signals of hemoglobin Val E11 and Tyr C7
title_fullStr Oximetry with the NMR signals of hemoglobin Val E11 and Tyr C7
title_full_unstemmed Oximetry with the NMR signals of hemoglobin Val E11 and Tyr C7
title_short Oximetry with the NMR signals of hemoglobin Val E11 and Tyr C7
title_sort oximetry with the nmr signals of hemoglobin val e11 and tyr c7
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2753772/
https://www.ncbi.nlm.nih.gov/pubmed/19621237
http://dx.doi.org/10.1007/s00421-009-1125-3
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