British Journal of Haematology · 1977 · 57 citations · 25 references
MedicineBiochemistryHematologyBiochemical GeneticsHematopathologyStructural BiologyAnemiaHematologic DisordersHemoglobin PhysiologyHemolytic DisordersRed Blood Cell DisordersBohr ModelHemoglobin FunctionHemoglobin StructureHemoglobin-oxygen AffinityOxygen Affinity RegulationOxygen Binding AffinityProtein Structure-function Relationships
Three members of an Oxfordshire family have polycythaemia. In each case their whole-blood oxygen affinity is increased. This is due to a previously undescribed haemoglobin variant which has been named haemoglobin Radcliffe (alpha2beta299(Gl)Ala). In addition to having a high oxygen affinity haemoglobin Radcliffe shows virtually no haem-haem interaction and a diminished Bohr effect. It is synthesized at the same rate and is as stable as haemoglobin A. X-ray analysis indicates that crystals of deoxyhaemoglobin Radcliffe are isomorphous with those of deoxyhaemoglobin A. Solutions of haemoglobin Radcliffe were also studied by high-resolution proton nuclear magnetic resonance spectroscopy. The structure/function relationships of haemoglobin Radcliffe are discussed in the light of these studies.
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J. B. Clegg, Michael A. Naughton, D. J. Weatherall · Journal of Molecular Biology · 1966 · 1.5K citations
Influence of globin structure on the state of the heme. I. Human deoxyhemoglobin
M. F. Perutz, Jane E. Ladner, Sanford R. Simon et al. · Biochemistry · 1974 · 291 citations
Preparation of Haemoglobin crystals
M. F. Perutz · Journal of Crystal Growth · 1968 · 266 citations