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Title: Probing the hemoglobin central cavity by direct quantification of effector binding using fluorescence lifetime methods. Author: Gottfried DS, Juszczak LJ, Fataliev NA, Acharya AS, Hirsch RE, Friedman JM. Journal: J Biol Chem; 1997 Jan 17; 272(3):1571-8. PubMed ID: 8999830. Abstract: Time-resolved fluorescence methods have been used to show that 8-hydroxy-1,3,6-pyrenetrisulfonate (HPT), a fluorescent analog of 2,3-diphosphoglycerate, binds to the central cavity of carboxyhemoglobin A (HbACO) at pH 6.35. A direct quantitative approach, based on the distinctive free and bound HPT fluorescent lifetimes of 5.6 ns and approximately 27 ps, respectively, was developed to measure the binding affinity of this probe. HPT binds to a single site and is displaced by inositol hexaphosphate at a 1:1 mol ratio, indicating that binding occurs at the 2,3-diphosphoglycerate site in the central cavity. Furthermore, the results imply that low pH HbACO exists as an altered R state and not an equilibrium mixture of R and T states. The probe was also used to monitor competitive effector binding and to compare the affinity of the binding site in several cross-bridged HbA derivatives.[Abstract] [Full Text] [Related] [New Search]