Literature DB >> 3804994

Oxygen binding and subunit interaction of hemoglobin in relation to the two-state model.

Q H Gibson, S J Edelstein.   

Abstract

Mills and Ackers (Mills, F.C., and Ackers, G.K. (1979) J. Biol. Chem. 254, 2881-2887) have reported the subunit interactions of hemoglobin to decrease on binding of the fourth molecule of oxygen to hemoglobin. This effect, which they called quaternary enhancement, is incompatible with the two-state Monod, Wyman, and Changeux allosteric model. Their free energy of binding of the fourth molecule (-9.3 kcal/mol) has been compared with independent kinetic estimates which give -8.6 kcal/mol. This smaller value is consistent with literature values and allows reasonable representation of the equilibrium curve using the two-state model without invoking quaternary enhancement.

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Year:  1987        PMID: 3804994

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  2 in total

1.  Resolvability of free energy changes for oxygen binding and subunit association by human hemoglobin.

Authors:  M Straume; M L Johnson
Journal:  Biophys J       Date:  1989-07       Impact factor: 4.033

2.  Symmetric allosteric mechanism of hexameric Escherichia coli arginine repressor exploits competition between L-arginine ligands and resident arginine residues.

Authors:  Rebecca Strawn; Milan Melichercik; Michael Green; Thomas Stockner; Jannette Carey; Rüdiger Ettrich
Journal:  PLoS Comput Biol       Date:  2010-06-03       Impact factor: 4.475

  2 in total

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