Undariase, a Direct-Acting Fibrin(ogen)olytic Enzyme from Undaria pinnatifida, Inhibits Thrombosis In Vivo and Exhibits In Vitro Thrombolytic Properties

作者：Choi Jun Hui; Sapkota Kumar; Kim Myung Kon; Kim Seung; Kim Sung Jun

来源：Applied Biochemistry and Biotechnology, 2014, 173(8): 1985-2004.

DOI：10.1007/s12010-014-0981-4

• Undaria pinnatifida
• Fibrinolysis
• Antithrombotic
• In vivo
• In vitro

A direct-acting fibrinolytic serine protease named undariase possessing anticoagulant and antiplatelet properties was purified from Undaria pinnatifida. Undariase showed a molecular weight of 50 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and mass spectrometry. It displayed a strong fibrin zymogram lysis band corresponding to the same molecular mass. The N-terminal sequence of undariase, LTATTCEELAAAPTD, does not match with any known fibrinolytic enzyme. The enzyme was stable and active at high temperatures (35-70 A degrees C). The fibrinolytic activity of undariase was strongly inhibited by phenylmethylsulfonyl fluoride (PMSF) and 4-(amidinophenyl) methanesulfonyl fluoride (APMSF). The K (m) and V (max) values for substrate S-2251 were determined as 6.15 mM and 90.91 mM/min/ml, respectively. Undariase resulted in clot lysis by directly cleaving alpha and beta chains of fibrin. Similarly, it preferentially acted on the A alpha chain of fibrinogen followed by cleavage of the B beta chain. It significantly prolonged the PFA-100 closure times of citrated whole human blood. In addition, undariase delayed the coagulation time and increased activated partial thromboplastin time (APTT), prothrombin time (PT), and thrombin time (TT). Undariase exerted a significant protective effect against collagen plus epinephrine-induced pulmonary thromboembolism in mice. It prevented carrageenan-induced thrombus formation in the tail of mice. It also resulted in prolongation of APTT ex vivo. In conclusion, these results suggested a therapeutic potential of undariase for thrombosis.

• 出版日期2014-8