Thromb Haemost 1995; 74(04): 1079-1087
DOI: 10.1055/s-0038-1649885
Original Article
Coagulation
Schattauer GmbH Stuttgart

Characterization of a cDNA for Rhesus Monkey Protein C Inhibitor – Evidence for N-Terminal Involvement in Heparin Stimulation

Klaus-P Radtke
Department of Molecular and Experimental Medicine, Department of Vascular Biology, The Scrlpps Research Institute, La Jolla, California, CA, USA
,
José A Fernández
Department of Molecular and Experimental Medicine, Department of Vascular Biology, The Scrlpps Research Institute, La Jolla, California, CA, USA
,
Bruno O Villoutreix
Department of Molecular and Experimental Medicine, Department of Vascular Biology, The Scrlpps Research Institute, La Jolla, California, CA, USA
,
Judith S Greengard
Department of Molecular and Experimental Medicine, Department of Vascular Biology, The Scrlpps Research Institute, La Jolla, California, CA, USA
,
John H Griffin
Department of Molecular and Experimental Medicine, Department of Vascular Biology, The Scrlpps Research Institute, La Jolla, California, CA, USA
› Author Affiliations
Further Information

Publication History

Received 14 July 1994

Accepted 29 June 1995

Publication Date:
09 July 2018 (online)

Summary

cDNAs for protein C inhibitor (PCI) were cloned from human and rhesus monkey[ 1 ] liver RNAs by reverse transcription and polymerase chain reaction (PCR) amplification. Sequencing showed that rhesus monkey and human PCI cDNAs were 93% identical. Predicted amino acid sequences differed at 26 of 387 residues. Pour of these differences (T352M, N359S, R362K, L3631) were in the reactive center loop that is important for inhibitory specificity, and two were in the N-terminal helix (M8T, E13K) that is implicated in glycosaminoglycan binding. PCI in human or rhesus monkey plasma showed comparable inhibitory activity towards human activated protein C in the presence of 10 U/ml heparin. However, maximal acceleration of the inhibition of activated protein C required 5-fold lower heparin concentration for rhesus monkey than for human plasma, consistent with the interpretation that the additional positive charge (E13K) in a putative-heparin binding region increased the affinity for heparin.

1 The nucleotide sequence(s) reported in this paper has been submitted to the GenBank/EMBL Data Bank with accession number(s) U224117


 
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