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Characterization of Plasmin-mediated Activation of Plasma Procarboxypeptidase B
Plasma carboxypeptidase B (PCB) is an exopeptidase that exerts an antifibrinolytic effect by releasing C-terminal Lys and Arg residues from partially degraded fibrin. PCB is produced in plasma via limited proteolysis of the zymogen, pro-PCB. In this report, we show that the K m (55 n m ) for plasmin...
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Published in: | The Journal of biological chemistry 1999-12, Vol.274 (49), p.35046-35052 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Plasma carboxypeptidase B (PCB) is an exopeptidase that exerts an antifibrinolytic effect by releasing C-terminal Lys and
Arg residues from partially degraded fibrin. PCB is produced in plasma via limited proteolysis of the zymogen, pro-PCB. In
this report, we show that the K
m (55 n m ) for plasmin-catalyzed activation of pro-PCB is similar to the plasma concentration of pro-PCB (50â70 n m ), whereas the K
m for the thrombin- or thrombin:thrombomodulin-catalyzed reaction is 10â40-fold higher than the pro-PCB level in plasma. Additionally,
tissue-type plasminogen activator triggers activation of pro-PCB in blood plasma in a reaction that is stimulated by a neutralizing
antibody versus α 2 -antiplasmin. Together, these results show that plasmin-mediated activation of pro-PCB can occur in blood plasma. Heparin
(UH) and other anionic glycosaminoglycans stimulate pro-PCB activation by plasmin but not by thrombin or thrombin:thrombomodulin.
Pro-PCB is a more favorable substrate for plasmin in the presence of UH (16-fold increase in k
cat / K
m ). UH also stabilizes PCB against spontaneous inactivation. The presence of UH in clots prepared with prothrombin-deficient
plasma delays tissue-type plasminogen activator-triggered lysis; this effect of UH on clot lysis is blocked by a PCB inhibitor
from potato tubers. These results show that UH accelerates plasmin-catalyzed activation of pro-PCB in plasma and PCB, in turn,
stabilizes fibrin against fibrinolysis. We propose that glycosaminoglycans in the subendothelial extracellular matrix serve
to augment the levels of PCB activity thereby stabilizing blood clots at sites where there is a breach in the integrity of
the vasculature. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.274.49.35046 |