## Abstract We studied the kinetics of replacement of O~2~ by CO in hemoglobin in the presence and absence of organic cosolvents (methanol, ethanol, __iso__‐propanol, __n__‐propanol, formamide, acetamide, __N__‐methyl‐formamide) and at 10 and 25°C. Quantitative analysis of the results indicates tha
Effect of some organic cosolvents on the reaction of hemoglobin with oxygen
✍ Scribed by Lorenzo Cordone; Antonio Cupane; Pier L. San Biagio; Eugenio Vitrano
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1981
- Tongue
- English
- Weight
- 659 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
We studied the effects of some organic cosolvents (monohydric alcohols and amides) on the reaction of hemoglobin with oxygen. We present evidence showing that our data can be analyzed within the framework of the Monod‐Wyman‐Changeux model and that the main effect of cosolvents is to alter the T ⇄ R conformational equilibrium of hemoglobin, without significantly affecting the intrinsic oxygen dissociation constants. Following a previously described phenomenological approach, the overall effects have been separated into effects related to the variation of the bulk dielectric constant of the solvent and effects not related to the variation of this constant.
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## Abstract We studied the effect of methanol, ethanol, __iso__‐propanol, and __n__‐propanol on the reaction of hemoglobin with oxygen. The oxygen affinity was found to decrease with increasing alcohol concentration and alkyl group size; no detectable effect on Hill's constant was found. Difference