Articles |
From the Departments of Pathology (E.G.B., R.P.T., T.E.H., F.H.B.) and Biochemistry (R.J.J., K.G.M.), University of Vermont College of Medicine, Burlington.
Correspondence to Dr Edwin G. Bovill, Chairman, Department of Pathology, University of Vermont College of Medicine, Burlington, VT 05405.
Abstract Meizothrombin is an intermediate that is produced
during the conversion of prothrombin to thrombin in systems composed of
purified factor Xa and factor Va that are quantitatively assembled on
an anionic phospholipid surface. The biological significance of this
intermediate has recently been challenged by the apparent absence of
meizothrombin during clotting of sodium citrateanticoagulated plasma.
We analyzed the formation of thrombin during coagulation of
nonanticoagulated, unchilled, minimally manipulated whole blood in
glass tubes. The process was stopped at 0, 3, 5, and 7 minutes by the
addition of biotinylated peptidyl chloromethylketone active-site
labeling reagents. Plasma/serum was separated by centrifugation, and
labeled species were extracted by immunoadsorption with a polyclonal
anti-prothrombin antibody. The purified prothrombin-derived species
were separated by SDSpolyacrylamide gradient gel electrophoresis and
visualized on a chemiluminescent avidin blot. Meizothrombin appeared as
an intermediate product of this reaction and persisted with some
increase through the 7-minute time point. We also observed
incorporation of the active-site label into a species of lower
molecular weight consistent with the B1 chain of ß-
and/or
-thrombin. These degraded forms of thrombin have not been
previously demonstrated in a biologically relevant preparation. Our
data clearly establish the generation of meizothrombin as an
intermediate product of thrombin generation during whole-blood
clotting. The data also represent the first experimental
evidence for the generation of ß- and
-thrombin in a biologically
relevant environment and time scale.
Key Words: thrombosis meizothrombin coagulation whole blood
This article has been cited by other articles:
![]() |
R. A. Saad, G. M. Arepally, and T. L. Ortel Heparin-Induced Thrombocytopenia N. Engl. J. Med., December 14, 2006; 355(24): 2598 - 2599. [Full Text] [PDF] |
||||
![]() |
M. A. Bukys, T. Orban, P. Y. Kim, D. O. Beck, M. E. Nesheim, and M. Kalafatis The Structural Integrity of Anion Binding Exosite I of Thrombin Is Required and Sufficient for Timely Cleavage and Activation of Factor V and Factor VIII J. Biol. Chem., July 7, 2006; 281(27): 18569 - 18580. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Orfeo, N. Brufatto, M. E. Nesheim, H. Xu, S. Butenas, and K. G. Mann The Factor V Activation Paradox J. Biol. Chem., May 7, 2004; 279(19): 19580 - 19591. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Koike, D. Okuda, and T. Morita Mutations in Autolytic Loop-2 and at Asp554 of Human Prothrombin That Enhance Protein C Activation by Meizothrombin J. Biol. Chem., April 18, 2003; 278(17): 15015 - 15022. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Linder, J. Oldgren, N. Egberg, L. Grip, G. Larson, A. Siegbahn, and L. Wallentin The effect of a low molecular mass thrombin inhibitor, inogatran, and heparin on thrombin generation and fibrin turnover in patients with unstable coronary artery disease Eur. Heart J., April 1, 1999; 20(7): 506 - 518. [Abstract] [PDF] |
||||
![]() |
J.-H. Han, H. C. F. Cote, and D. M. Tollefsen Inhibition of Meizothrombin and Meizothrombin(desF1) by Heparin Cofactor II J. Biol. Chem., November 7, 1997; 272(45): 28660 - 28665. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. V. Byzova and E. F. Plow Networking in the Hemostatic System. INTEGRIN alpha IIbbeta 3 BINDS PROTHROMBIN AND INFLUENCES ITS ACTIVATION J. Biol. Chem., October 24, 1997; 272(43): 27183 - 27188. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. C.F. Cote, L. Bajzar, W. K. Stevens, J. A. Samis, J. Morser, R. T.A. MacGillivray, and M. E. Nesheim Functional Characterization of Recombinant Human Meizothrombin and Meizothrombin(desF1). THROMBOMODULIN-DEPENDENT ACTIVATION OF PROTEIN C AND THROMBIN-ACTIVATABLE FIBRINOLYSIS INHIBITOR (TAFI), PLATELET AGGREGATION, ANTITHROMBIN-III INHIBITION J. Biol. Chem., March 7, 1997; 272(10): 6194 - 6200. [Abstract] [Full Text] [PDF] |
||||
|
ATVB Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1995 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |