Tissue Factor Pathway Inhibitor: The Carboxy-Terminus Is Required for Optimal Inhibition of Factor Xa

Tissue factor pathway inhibitor (TFPI) is a multivalent Kunitz-type protease inhibitor that binds to and inactivates factor Xa directly, and in a factor Xa-dependent fashion inhibits the factor Vila/tissue factor catalytic complex. TFPI is a slow, tight-binding, competitive, and reversible inhibitor...

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Veröffentlicht in:Blood 1992-04, Vol.79 (8), p.2004-2010
Hauptverfasser: Wesselschmidt, Robin, Likert, Karen, Girard, Thomas, Wun, Tze-Chein, Broze, George J.
Format: Artikel
Sprache:eng
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Zusammenfassung:Tissue factor pathway inhibitor (TFPI) is a multivalent Kunitz-type protease inhibitor that binds to and inactivates factor Xa directly, and in a factor Xa-dependent fashion inhibits the factor Vila/tissue factor catalytic complex. TFPI is a slow, tight-binding, competitive, and reversible inhibitor of factor Xa, in which the formation of an initial encounter complex between TFPI and factor Xa is followed by slow isomerization to a final, tightened complex. Wild-type recombinant TFPI (rTFPI), expressed in mouse C127 cells, separates into two forms on heparin-agarose chromatography that elute at 0.3 mol/L and 0.6 mol/L NaCl. Western blot analysis shows that both forms contain the N-terminus of full-length TFPI, but only rTFPI(0.6) is recognized by an antibody directed against the C-terminus. rTFPI(0.3) and rTFPI(0.6) inhibit factor Xa with 1:1 stoichiometry and inhibit factor Vlla/tissue factor equally in an endpoint-type assay. However, rTFPI(0.6) is a more potent inhibitor than rTFPI(0.3) of coagulation in normal plasma induced by either factor Xa or tissue factor.The initial inhibition of factor Xa (
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.V79.8.2004.2004