Antithrombin III, or heparin cofactor, is the major plasma inhibitor of the activated blood clotting proteases. Alone, antithrombin III reacts slowly with these enzymes to form a 1:1 inactive complex. Addition of heparin greatly accelerates the rate of protease inactivation without altering the stocichiometry of the reaction. This increase in reactivitiy appears to result from heparin-induced conformational changes in antithrombin and the coagulation proteases. We have shown that site-specific chemical modificaton of antithrombin blocks heparin binding but does not interfere with the formation of the protease inhibitor complex. The interaction of antithrombin with these proteases will be studied through the use of chromophoric """"""""reporter groups."""""""" Changes in protein conformation monitored with these chromophores will be correlated with the kinetics of protease inactivation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL024846-06
Application #
3337832
Study Section
Hematology Subcommittee 2 (HEM)
Project Start
1979-08-01
Project End
1988-03-31
Budget Start
1987-04-01
Budget End
1988-03-31
Support Year
6
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Louisiana State University Hsc Shreveport
Department
Type
Schools of Medicine
DUNS #
City
Shreveport
State
LA
Country
United States
Zip Code
71103
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Burch, M K; Blackburn, M N; Morgan, W T (1987) Further characterization of the interaction of histidine-rich glycoprotein with heparin: evidence for the binding of two molecules of histidine-rich glycoprotein by high molecular weight heparin and for the involvement of histidine residues in heparin bin Biochemistry 26:7477-82
Peterson, C B; Noyes, C M; Pecon, J M et al. (1987) Identification of a lysyl residue in antithrombin which is essential for heparin binding. J Biol Chem 262:8061-5
Peterson, C B; Blackburn, M N (1987) Antithrombin conformation and the catalytic role of heparin. I. Does cleavage by thrombin induce structural changes in the heparin-binding region of antithrombin? J Biol Chem 262:7552-8
Peterson, C B; Morgan, W T; Blackburn, M N (1987) Histidine-rich glycoprotein modulation of the anticoagulant activity of heparin. Evidence for a mechanism involving competition with both antithrombin and thrombin for heparin binding. J Biol Chem 262:7567-74
Peterson, C B; Blackburn, M N (1987) Antithrombin conformation and the catalytic role of heparin. II. Is the heparin-induced conformational change in antithrombin required for rapid inactivation of thrombin? J Biol Chem 262:7559-66
Peterson, C B; Blackburn, M N (1985) Isolation and characterization of an antithrombin III variant with reduced carbohydrate content and enhanced heparin binding. J Biol Chem 260:610-5