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一种来自红口蝮蛇毒的新型α型纤维蛋白原酶。

A novel alpha-type fibrinogenase from Agkistrodon rhodostoma snake venom.

作者信息

Huang T F, Chang M C, Peng H C, Teng C M

机构信息

Pharmacological Institute, College of Medicine, National Taiwan University, Taipei.

出版信息

Biochim Biophys Acta. 1992 Dec 28;1160(3):262-8. doi: 10.1016/0167-4838(92)90086-s.

Abstract

By means of CM-Sephadex C-50 column chromatography, gel-filtration on sephadex G-75 and Sephacryl S-200 columns, a purified fibrinogenase, kistomin, was obtained from venom of Agkistrodon rhodostoma. It was a single peptide-chain with a molecular mass of about 21,800 Da containing about 202 amino-acid residues as revealed by amino acid analysis. Kistomin preferentially cleaved A alpha- and subsequently the gamma-chain of fibrinogen, leaving the B beta-chain unaffected. Its fibrinogenolytic activity was estimated to be 36.6 +/- 4.5 mg/min per mg protein and was inhibited by the pretreatment of EDTA, suggesting that it is a metalloproteinase. Its fibrinogenolytic activity in platelet-poor plasma is much less potent as compared to that in purified fibrinogen solution. It inhibited ristocetin-induced aggregation of human platelets in a dose-dependent manner in the presence of von Willebrand factor.

摘要

通过CM - Sephadex C - 50柱色谱法、在sephadex G - 75和Sephacryl S - 200柱上进行凝胶过滤,从红口蝮蛇毒中获得了一种纯化的纤维蛋白原酶——基斯托明。氨基酸分析表明,它是一条单肽链,分子量约为21,800道尔顿,含有约202个氨基酸残基。基斯托明优先切割纤维蛋白原的Aα链,随后切割γ链,而Bβ链不受影响。其纤维蛋白原水解活性估计为每毫克蛋白质36.6±4.5毫克/分钟,并受到EDTA预处理的抑制,表明它是一种金属蛋白酶。与在纯化纤维蛋白原溶液中的情况相比,它在乏血小板血浆中的纤维蛋白原水解活性要低得多。在存在血管性血友病因子的情况下,它以剂量依赖性方式抑制瑞斯托霉素诱导的人血小板聚集。

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