Thromb Haemost 2003; 89(05): 795-802
DOI: 10.1055/s-0037-1613464
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Contributions of Asn2198, Met2199, and Phe2200 in the factor VIII C2 domain to cofactor activity, phospholipid-binding, and von Willebrand factor-binding

Deborah A. Lewis
1   Department of Medicine, Division of Hematology, and the Department of Pathology, Duke University Medical Center, Durham, North Carolina, USA
,
Mary L. Pound
1   Department of Medicine, Division of Hematology, and the Department of Pathology, Duke University Medical Center, Durham, North Carolina, USA
,
Thomas L. Ortel
1   Department of Medicine, Division of Hematology, and the Department of Pathology, Duke University Medical Center, Durham, North Carolina, USA
› Author Affiliations
Financial support: Supported by a Research Grant from the March of Dimes (TLO).
Further Information

Publication History

Received 06 September 2002

Accepted after revision 10 February 2003

Publication Date:
09 December 2017 (online)

Summary

The crystal structure of the factor VIII C2 domain consists of a β-sandwich core from which β-hairpins and loops extend to form a hydrophobic surface. The hydrophobic surface includes M2199 and F2200 at the tip of the 1st β-hairpin. To determine the individual contributions of residues N2198, M2199, and F2200 to phospholipid and von Willebrand factor (vWF) binding properties of factor VIII, we prepared mutant proteins with single alanine substitutions. We found that single mutations at N2198 and M2199 had relatively little impact on cofactor activity, or phospholipid and vWF binding. However the F2200A mutant had slightly lower cofactor activity at subsaturating phospholipid concentrations. Competitive ELISAs suggested that F2200 plays a more important role in both phospholipid-binding and vWF-binding than N2198 and M2199. All mutant proteins were still recognized by a monoclonal antibody and two factor VIII inhibitors that neutralized cofactor activity and blocked factor VIII binding to phospholipids.

Presented in part at the XVIII Congress of the International Society on Thrombosis and Haemostasis, Paris, France, 6-12 July 2001, and the 43rd Annual Meeting of the American Society of Hematology, Orlando, Florida, 7-11 December 2001

 
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