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

Nitric Oxide. 2014 Nov 15:42:32-9. doi: 10.1016/j.niox.2014.08.007. Epub 2014 Aug 27.

Abstract

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.

Keywords: DFT; EPR; Hemoglobin; Myoglobin; Nitrite.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electron Spin Resonance Spectroscopy / methods*
  • Globins / metabolism*
  • Isomerism
  • Nitrites / metabolism*
  • Oxidation-Reduction
  • Spectrophotometry, Ultraviolet

Substances

  • Nitrites
  • Globins