Hemoglobin conformation couples erythrocyte S-nitrosothiol content to O2 gradients

Allan Doctor, Ruth Platt, Mary Lynn Sheram, Anne Eischeid, Timothy McMahon, Thomas Maxey, Joseph Doherty, Mark Axelrod, Jaclyn Kline, Matthew Gurka, Andrew Gow, Benjamin Gaston

Research output: Contribution to journalArticle

149 Scopus citations

Abstract

It is proposed that the bond between nitric oxide (NO) and the Hb thiol Cys-β93 (SNOHb) is favored when hemoglobin (Hb) is in the relaxed (R, oxygenated) conformation, and that deoxygenation to tense (T) state destabilizes the SNOHb bond, allowing transfer of NO from Hb to form other (vasoactive) S-nitrosothiols (SNOs). However, it has not previously been possible to measure SNOHb without extensive Hb preparation, altering its allostery and SNO distribution. Here, we have validated an assay for SNOHb that uses carbon monoxide (CO) and cuprous chloride (CuCl)-saturated Cys. This assay is specific for SNOs and sensitive to 2-5 pmol. Uniquely, it measures the total SNO content of unmodified erythrocytes (RBCs) (SNORBC), preserving Hb allostery. In room air, the ratio of SNORBC to Hb in intact RBCs is stable over time, but there is a logarithmic loss of SNORBC with oxyHb desaturation (slope, 0.043). This decay is accelerated by extraerythrocytic thiol (slope, 0.089; P < 0.001). SNORBC stability is uncoupled from O2 tension when Hb is locked in the R state by CO pretreatment. Also, SNORBC is increased ≈20-fold in human septic shock (P = 0.002) and the O2-dependent vasoactivity of RBCs is affected profoundly by SNO content in a murine lung bioassay. These data demonstrate that SNO content and O2 saturation are tightly coupled in intact RBCs and that this coupling is likely to be of pathophysiological significance.

Original languageEnglish (US)
Pages (from-to)5709-5714
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume102
Issue number16
DOIs
StatePublished - Apr 19 2005
Externally publishedYes

Keywords

  • Nitric oxide
  • Sepsis
  • Vascular physiology

ASJC Scopus subject areas

  • General

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    Doctor, A., Platt, R., Sheram, M. L., Eischeid, A., McMahon, T., Maxey, T., Doherty, J., Axelrod, M., Kline, J., Gurka, M., Gow, A., & Gaston, B. (2005). Hemoglobin conformation couples erythrocyte S-nitrosothiol content to O2 gradients. Proceedings of the National Academy of Sciences of the United States of America, 102(16), 5709-5714. https://doi.org/10.1073/pnas.0407490102