Hemoglobin Roanne [alpha 94(G1) Asp-->Glu]: a variant of the alpha 1 beta 2 interface with an unexpected high oxygen affinity

Biochim Biophys Acta. 1995 Jan 5;1246(1):34-8. doi: 10.1016/0167-4838(94)00190-r.

Abstract

In hemoglobin (Hb) Roanne, the aspartate residue alpha 94(G1) is replaced by a glutamic acid. This residue plays a key role in the structural changes affecting the alpha 1 beta 2 contact area during the deoxy- to oxy-state transition in the hemoglobin molecule. Aspartate alpha 94(G1) is involved in several contacts both in the deoxy- and oxy-structures. The most important of those is a hydrogen bond with asparagine beta 102 (G4), stabilizing the oxygenated structure. Alteration of this contact usually leads to a decrease in oxygen affinity. Hb Roanne is the first example in which an increased oxygen affinity was found as a result of a structural modification at this position. Functional data suggested that the mechanisms responsible for this altered property are a destabilisation of the T-structure and a modification of the allosteric equilibrium.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Aspartic Acid*
  • Binding Sites
  • Carbon Monoxide / metabolism
  • Female
  • Glutamic Acid*
  • Hemoglobins, Abnormal / chemistry*
  • Hemoglobins, Abnormal / genetics
  • Hemoglobins, Abnormal / metabolism
  • Humans
  • Hydrogen Bonding
  • Isoelectric Focusing
  • Kinetics
  • Mass Spectrometry
  • Molecular Structure
  • Oxygen / blood*
  • Structure-Activity Relationship

Substances

  • Hemoglobins, Abnormal
  • hemoglobin Roanne
  • Aspartic Acid
  • Glutamic Acid
  • Carbon Monoxide
  • Oxygen