My long-term goals are to define the interactions between the gamma variant form of fibrinogen and thrombin.
The specific aims of this proposal are to: I- Map the Ca2+ binding site(s) on the gamma chain. The hypothesis to be tested is that the gamma chain provides an additional Ca2+ binding site(s) in f?brinogen.II - Determine the effect of the gamma chain on thrombin's enzymatic activity towards protein substrates. The hypothesis to be tested is that the gamma chain modulates thrombin cleavage of substrates by binding to exosite II. III- Determine the effect of the gamma chain on thrombin inhibition by protease inhibitors. The hypothesis to be tested is that a plasmin cleavage product of the gamma chain catalyzes thrombin inhibition by heparin-dependent inhibitors, and that the gamma chain binds to heparin-dependent inhibitors. IV- Determine the effect of the gamma chain on thrombin's procoagulant activity and platelet aggregating activity in whole plasma. The hypothesis to be tested is that a plasmin cleavage product of the gamma chain acts as an anticoagulant in plasma.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32HL071463-03
Application #
6740144
Study Section
Special Emphasis Panel (ZRG1-F10 (20))
Program Officer
Mondoro, Traci
Project Start
2002-06-01
Project End
2005-05-31
Budget Start
2004-06-01
Budget End
2005-05-31
Support Year
3
Fiscal Year
2004
Total Cost
$60,736
Indirect Cost
Name
Oregon Health and Science University
Department
Pathology
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Lovely, Rehana S; Rein, Chantelle M; White, Tara C et al. (2008) gammaA/gamma'fibrinogen inhibits thrombin-induced platelet aggregation. Thromb Haemost 100:837-46
Lovely, Rehana S; Boshkov, Lynn K; Marzec, Ulla M et al. (2007) Fibrinogen gamma'chain carboxy terminal peptide selectively inhibits the intrinsic coagulation pathway. Br J Haematol 139:494-503
Buccellato, Leonard J; Tso, May; Akinci, Ozkan I et al. (2004) Reactive oxygen species are required for hyperoxia-induced Bax activation and cell death in alveolar epithelial cells. J Biol Chem 279:6753-60