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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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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2009
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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. |
format | Text |
id | pubmed-2753772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
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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