The Heme and Sickle Cell Hemoglobin Polymerization
β Scribed by Vekilov, Peter G.; Uzunova, Veseilina; Pan, Weichun
- Book ID
- 119206178
- Publisher
- Biophysical Society
- Year
- 2010
- Tongue
- English
- Weight
- 32 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0006-3495
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π SIMILAR VOLUMES
## Abstract Under physiological conditions, sickle hemoglobin, a natural mutant of human hemoglobin A with a surface hydrophobic valine in place of a negatively charged glutamic acid, polymerizes at high volume occupancy. Equilibrium solubility of sickle hemoglobin entails activity coefficients tha
## Abstract We probe the role of free heme in the interactions between sickle cell hemoglobin (HbS) molecules in simulated physiological solutions: polymerization of deoxyβHbS is the primary pathogenic event of sickle cell anemia, and HbS releases heme after autoxidation more readily than normal ad