Literature DB >> 1070000

Rate of quaternary structure change in hemoglobin measured by modulated excitation.

F A Ferrone, J J Hopfield.   

Abstract

Using a novel technique of modulated photo-dissociation of carbon monoxide from hemoglobin, we have obtained the rates for conversion between the two quaternary states, R, and T, at 3-fold ligation. Our measurements at pH 7 and 22 degrees give rates of 780 +/- 40 sec-1 for going from R to T, and 2500 +/- 200 sec-1 from T to R. This yields an equilibrium constant of 0.31 +/- 0.04, which is in good agreement with previous estimates. The degree of agreement between this equilibrium constant and that predicted from the allosteric model provides a new, quantitative test of the allosteric description. A sequential model for the change in structure was found incompatible with the data, even if kinetic subunit inequivalence was assumed. The technique described here is quite general and can be used as long as the system under investigation can be repetitively excited in a regime in which it responds linearly to the excitation.

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Year:  1976        PMID: 1070000      PMCID: PMC431515          DOI: 10.1073/pnas.73.12.4497

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  11 in total

Review 1.  Allosteric interpretation of haemoglobin properties.

Authors:  R G Shulman; J J Hopfield; S Ogawa
Journal:  Q Rev Biophys       Date:  1975-07       Impact factor: 5.318

2.  Quaternary conformational changes in human hemoglobin studied by laser photolysis of carboxyhemoglobin.

Authors:  C A Sawicki; Q H Gibson
Journal:  J Biol Chem       Date:  1976-03-25       Impact factor: 5.157

3.  The photochemical formation of a quickly reacting form of haemoglobin.

Authors:  Q H GIBSON
Journal:  Biochem J       Date:  1959-02       Impact factor: 3.857

4.  Differences in spectra of alpha and beta chains of hemoglobin between isolated state and in tetramer.

Authors:  Y Sugita
Journal:  J Biol Chem       Date:  1975-02-25       Impact factor: 5.157

5.  Quaternary structure of partially liganded intermediates of sheep carbon monoxide hemoglobin at alkaline pH.

Authors:  R D Gray
Journal:  J Biol Chem       Date:  1975-01-25       Impact factor: 5.157

6.  Spectral differences between the alpha and beta heme groups within human deoxyhemoglobin.

Authors:  J S Olson
Journal:  Proc Natl Acad Sci U S A       Date:  1976-04       Impact factor: 11.205

7.  Influence of globin structure on the state of the heme. I. Human deoxyhemoglobin.

Authors:  M F Perutz; J E Ladner; S R Simon; C Ho
Journal:  Biochemistry       Date:  1974-05-07       Impact factor: 3.162

8.  Kinetics of oxygen binding to human hemoglobin. Temperature jump relaxation studies.

Authors:  G Ilgenfritz; T M Schuster
Journal:  J Biol Chem       Date:  1974-05-10       Impact factor: 5.157

9.  Extensions of the allosteric model for haemoglobin.

Authors:  S J Edelstein
Journal:  Nature       Date:  1971-03-26       Impact factor: 49.962

10.  The reaction of n-butyl isocyanide with human hemoglobin. I. Determination of the kinetic parameters involved in the last step in ligand binding.

Authors:  J S Olson; Q H Gibson
Journal:  J Biol Chem       Date:  1971-09-10       Impact factor: 5.157

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  6 in total

1.  Spectroscopic studies of oxy- and carbonmonoxyhemoglobin after pulsed optical excitation.

Authors:  B I Greene; R M Hochstrasser; R B Weisman; W A Eaton
Journal:  Proc Natl Acad Sci U S A       Date:  1978-11       Impact factor: 11.205

2.  Conformational kinetics of triligated hemoglobin.

Authors:  F A Ferrone; A J Martino; S Basak
Journal:  Biophys J       Date:  1985-08       Impact factor: 4.033

3.  Nanosecond absorption spectroscopy of hemoglobin: elementary processes in kinetic cooperativity.

Authors:  J Hofrichter; J H Sommer; E R Henry; W A Eaton
Journal:  Proc Natl Acad Sci U S A       Date:  1983-04       Impact factor: 11.205

4.  Allosteric kinetics and equilibria differ for carbon monoxide and oxygen binding to hemoglobin.

Authors:  N Q Zhang; F A Ferrone; A J Martino
Journal:  Biophys J       Date:  1990-08       Impact factor: 4.033

Review 5.  Kinetic mechanisms for O2 binding to myoglobins and hemoglobins.

Authors:  John S Olson
Journal:  Mol Aspects Med       Date:  2021-09-17

6.  Rate of allosteric change in hemoglobin measured by modulated excitation using fluorescence detection.

Authors:  A J Martino; F A Ferrone
Journal:  Biophys J       Date:  1989-10       Impact factor: 4.033

  6 in total

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