The goals of the research proposed are first, to characterize the effect of plasma on factor VIII binding to von Willebrand factor (vWF) and identify a vWF-binding protein that inhibits factor VIII binding. Aspects such as affinity and stoichiometry for the interaction of factor VIII with pure vWF vs. vWF reconstituted in plasma will be studied. It will also be determined whether the putative plasma vWF-binding protein decreases the rate of factor VIII association with vWF or increases the rate of dissociation from vWF. The importance of these findings relates to a better understanding of modulation of factor VIII levels in pregnancy, inflammation and DDAVP therapy, as well as secondary factor VIII deficiency. Until now, the explanation of secondary factor VIII deficiency is limited to a """"""""decreased binding"""""""" of factor VIII to vWF due to specific mutations in the factor VIII binding region of vWF. Understanding binding kinetics of the association of another protein with vWF will help to better characterize secondary factor VIII deficiency. The second goal of this proposal is to identify structural features of vWF that influence the interaction with factor VIII. To accomplish this aim, we will focus on studies to characterize the role of inter and intrasubunit vWF disulfide bonds on factor VIII binding. We will conduct equilibrium and kinetics studies that will compare binding of factor VIII to multimeric vWF and mutant vWF incapable of multimer formation. In addition, we will construct vWF mutants based on mutations found in a patient with secondary factor VIII deficiency (R9lQ and C268S), and investigate what is the role of vWF Cys 268 on factor VIII binding. vWF regulates the levels of factor VIII, which has been shown to increase its plasma levels in deep venous thrombosis (DVT). Our results may alter the understanding of pathogenesis of DVT.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32HL009506-02
Application #
2459907
Study Section
Hematology Subcommittee 2 (HEM)
Project Start
1997-08-01
Project End
Budget Start
1997-08-01
Budget End
1997-10-18
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02115
Fresco, Victor M; Kern, Christine B; Mohammadi, Moosa et al. (2016) Fibulin-1 Binds to Fibroblast Growth Factor 8 with High Affinity: EFFECTS ON EMBRYO SURVIVAL. J Biol Chem 291:18730-9
Twal, Waleed O; Hammad, Samar M; Guffy, Sharon L et al. (2015) A novel intracellular fibulin-1D variant binds to the cytoplasmic domain of integrin beta 1 subunit. Matrix Biol 43:97-108