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Thromb Haemost 1996; 75(02): 275-282
DOI: 10.1055/s-0038-1650260
Original Article
Schattauer GmbH Stuttgart

The Gla26 Residue of Protein C Is Required for the Binding of Protein C to Thrombomodulin and Endothelial Cell Protein C Receptor, but not to Protein S and Factor Va

Junji Nishioka
The Department of Molecular Pathobiology, Mie University School of Medicine, Mie, Japan
,
Masaru Ido
The Department of Molecular Pathobiology, Mie University School of Medicine, Mie, Japan
,
Tatsuya Hayashi
The Department of Molecular Pathobiology, Mie University School of Medicine, Mie, Japan
,
Koji Suzuki
The Department of Molecular Pathobiology, Mie University School of Medicine, Mie, Japan
› Author Affiliations
Further Information

Publication History

Received: 14 June 1995

Accepted after resubmission13 November 1995

Publication Date:
26 July 2018 (online)

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Summary

A functionally defective protein C (PC)-Mie, detected in the plasma of a patient with hereditary thrombophilia, has Lys substituted for γ-carboxyglutamic acid (Gla)26 residue. The activation rate of PC-Mie by Protac or thrombin in the absence of Ca2+ and that by thrombin with native thrombomodulin (TM), recombinant soluble truncated TM or on cultured endothelial cells in the presence of Ca2+ were all apparently lower than that of normal PC. The anticoagulant activity of Protac-activated PC (APC)-Mie on the plasma clotting time and the rate of inactivation of factor Va by APC-Mie in the presence of phospholipids were lower than those seen with normal APC. APC-Mie and normal APC bound equally to protein S and to biotinyl-factor Va. However, neither PC-Mie nor APC-Mie bound to phospholipids and to cultured human endothelial cells. It was similar to that observed with Gla-domainless PC/APC, but different from that seen with normal PC/APC. These results suggest that Gla26-dependent conformation is required for the binding of PC/APC to phospholipids, TM and the surface of endothelial cell PC/APC receptor, but not to protein S and factor Va.

 

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