![]()
|
|
||||||||
J. Biol. Chem., Vol. 265, Issue 29, 17539-17544, 10, 1990
J Jesty
The activation of factor X in the presence of antithrombin has been studied
in order to determine the parameters that control the area under the
resulting factor Xa generation curve. Generation curves were analyzed using
a model containing three parameters: the total generation of factor Xa,
Emax; the rate of factor Xa generation, expressed as a first-order rate
constant, kappa 1; and the rate of inhibition, expressed as another
first-order rate constant, kappa 2. Using factor IXa-VIIIa to activate
factor X, we found the area under the generation curve to be proportional
to Emax, which was varied by varying the factor IXa concentration, and
inversely proportional to kappa 2, which was varied by varying the
antithrombin concentration. With this activator, however, kappa 1 varied in
parallel with Emax, resulting in a correlation between integrated area and
kappa 1. In order to determine whether Emax or kappa 1, or both, was a
controlling parameter, similar activations were done with varying
concentrations of the factor X-activating enzyme of Russell's viper venom.
With this activator it was possible to vary Emax and kappa 1 independently,
again at varying antithrombin concentrations. These results showed the
integrated area to be proportional to Emax and inversely proportional to
kappa 2, as before, but independent of the activation rate, kappa 1. In
this system, therefore, the area under the factor Xa generation curve is
controlled by the amount of factor Xa generated and its rate of inhibition
but is independent of the rate of factor Xa generation.
Analysis of the generation and inhibition of factor Xa. Area under generation curves is independent of enzyme generation rate
Department of Medicine, State University of New York, Stony Brook 11794.
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
V. B. Louvain-Quintard, E. P. Bianchini, C. Calmel-Tareau, M. Tagzirt, and B. F. Le Bonniec Thrombin-activable Factor X Re-establishes an Intrinsic Amplification in Tenase-deficient Plasmas J. Biol. Chem., December 16, 2005; 280(50): 41352 - 41359. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. S. Ahmad, J. M. Scandura, and P. N. Walsh Structural and Functional Characterization of Platelet Receptor-mediated Factor VIII Binding J. Biol. Chem., April 21, 2000; 275(17): 13071 - 13081. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. J. Fay and K. Koshibu The A2 Subunit of Factor VIIIa Modulates the Active Site of Factor IXa J. Biol. Chem., July 24, 1998; 273(30): 19049 - 19054. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. J. Fay, T. L. Beattie, L. M. Regan, L. M. O'Brien, and R. J. Kaufman Model for the Factor VIIIa-dependent Decay of the Intrinsic Factor Xase J. Biol. Chem., March 15, 1996; 271(11): 6027 - 6032. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. C. Underwood, D. Zhong, A. Mathur, T. Heyduk, and S. P. Bajaj Thermodynamic Linkage between the S1 Site, the Na+ Site, and the Ca2+ Site in the Protease Domain of Human Coagulation Factor Xa. STUDIES ON CATALYTIC EFFICIENCY AND INHIBITOR BINDING J. Biol. Chem., November 17, 2000; 275(47): 36876 - 36884. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Molecular and Cellular Proteomics |
| Journal of Lipid Research | ASBMB Today |