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A Novel Antithrombotic Protease from Marine Worm Sipunculus Nudus

机译:一种新型的抗海洋蠕虫Sipunculus Nudus的抗血栓蛋白酶

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摘要

Sipunculus nudus, an old marine species, has great potential for use as functional seafood due to its various bioactivities. Its potential antithrombotic activity pushed us to isolate the bio-active components bio-guided by tracking fibrinolytic activity. As a result, a novel protease named as SK (the kinase obtained from S. nudus) was obtained, which possessed a molecular weight of 28,003.67 Da and 15 N-terminal amino acid sequences of PFPVPDPFVWDTSFQ. SK exerted inhibitory effects on thrombus formation through improving the coagulation system with dose-effect relationship within a certain range. Furthermore, in most cases SK got obviously better effect than that of urokinase. With the help of untargeted mass spectrometry-based metabolomics profiling, arachidonic acid, sphingolipid, and nicotinate and nicotinamide mechanism pathways were found to be important pathways. They revealed that the effect mechanism of SK on common carotid arterial thrombosis induced by FeCl3 was achieved by inhibiting vessel contraction, platelet aggregation, adhesion, and release, correcting endothelial cell dysfunction and retarding process of thrombus formation. This study demonstrated SK was a promising thrombolytic agent on the basis of its comprehensive activities on thrombosis, and it should get further exploitation and utilization.
机译:Sipunculus nudus是一种古老的海洋物种,由于其多种生物活性,具有用作功能性海鲜的巨大潜力。它潜在的抗血栓形成活性促使我们通过追踪纤维蛋白溶解活性来分离生物引导的生物活性成分。结果,获得了新的蛋白酶,称为SK(得自葡萄球菌的激酶),其分子量为28,003.67 Da,并且具有PFPVPDPFVVWDTSFQ的15个N末端氨基酸序列。 SK通过在一定范围内以剂量-效应关系改善凝血系统,对血栓形成产生抑制作用。此外,在大多数情况下,SK的疗效明显优于尿激酶。借助基于非靶向质谱的代谢组学分析,发现花生四烯酸,鞘脂以及烟酸和烟酰胺的机制途径是重要的途径。他们发现,SK通过抑制血管收缩,血小板聚集,粘附和释放,纠正内皮细胞功能障碍和延迟血栓形成过程来实现FeCl3诱导的颈总动脉血栓形成的作用机制。这项研究表明,基于其对血栓形成的全面活性,SK是一种很有前途的溶栓剂,应进一步开发和利用。

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