The first epidermal growth factor domain of human coagulation factor VII is essential for binding with tissue factor

FEBS Letters

Rickles, Frederick R.¹  Ofosu, Frederick A.²  Blajchman, Morris A.²  Clarke, Bryan J.²  Sridhara, Sampath²  Bona, Robert D.¹ 

[1] Department of Medicine, University of Connecticut, Farmington, CT and the VA Medical Center Newington, CT, USA;Departments of Pathology and Biomedical Sciences, McMaster University Medical Centre, McMaster University and the Canadian Red Cross Blood Transfusion Service, Hamilton, Ontario, Canada

关键词: Blood coagulation;    Extrinsic pathway;    Human factor VII;    tissue factor;   

DOI  :  10.1016/0014-5793(92)80058-O

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

The intrinsic pathway of coagulation is initiated when zymogen factor VII binds to its cell surface receptor tissue factor to form a catalytic binary complex. Both the activation of factor VII to factor VIIa and the expression of serine protease activity of factor VIIa are dependent on factor VII binding to tissue factor lipoprotein. To better understand the molecular basis of these rate-limiting events, the interaction of zymogen factor VII and tissue factor was investigated using as probes both a murine monoclonal antibody and a monospecific rabbit antiserum to human factor VII. To measure factor VIIa functional activity, a two-stage chromogenic assay was used; an assay which measures the factor Xa generated by the activation of factor VII to factor VIIa. Purified immunoglobulin from murine monoclonal antibody 231-7, which was shown to be reactive with amino acid residues 51–88 of the first epidermal growth factor-like (EGF) domain of human factor VII, inhibited the activation of factor VII to factor VIIa in a dose-dependent manner. The mechanism of this inhibition was demonstrated using a novel solid-phase ELISA which quantitatively measured the binding of purified factor VII zymogen to tissue factor adsorbed onto microtiter wells. Thus, the binding of factor VII zymogen to immobilized tissue factor was inhibited by antibody 231-7, again in a dose-dependent manner. Similar results were obtained using a monospecific rabbit antiserum to human factor VII which also reacted with the β-galactosidase fusion proteins containing amino acid residues 51–88 (exon 4) of human factor VII. We conclude therefore that the exon 4-encoded amino acids of the first EGF domain of human factor VII constitute an essential domain participating in the binding of factor VII to tissue factor.

【 授权许可】

Unknown