Literature DB >> 3838826

A kinetic model describing the interaction of bovine prothrombin fragment 1 with calcium ions.

C W Kabis, M M Sarasua, K E Gottschalk, C D Bourne, L G Pedersen, C M Jackson, R G Hiskey, K A Koehler.   

Abstract

A kinetic model is derived for the interaction of bovine prothrombin fragment 1 with calcium ions. The model requires binding of a minimum of two calcium ions for induction of the observed biphasic fluorescence decrease as a function of time. The model is shown to be consistent with experimental kinetic and equilibrium data by fitting theoretical curves for the biphasic fluorescence change to the data through exact solution of the nonlinear differential rate equations derived from the model. The rate constants for the binding of these two required calcium ions are calculated from the solutions as best fit parameters. The thermodynamic equilibrium constants, K1 and K2, for the binding of these two calcium ions are calculated from ratios of the forward and reverse rate constants as 0.6 X 10(4) and 5.4 X 10(4), respectively. Thus, the model correctly predicts positively cooperative calcium ion binding for at least the two calcium ions required to induce fluorescence quenching.

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Year:  1985        PMID: 3838826

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  1 in total

1.  Cooperativity in the calcium ion-induced quenching of the intrinsic fluorescence of a series of normal and GLA-deficient bovine prothrombin fragment 1 molecules.

Authors:  O P Malhotra; F Valencic; E T Fossel; K A Koehler
Journal:  J Protein Chem       Date:  1991-02
  1 in total

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