刺鼠毒液中具有激肽释放和纤维蛋白原溶解活性的新型丝氨酸蛋白酶。

Yong-Hong Jia, Yang Jin, Qiu-Min Lü, Dong-Sheng Li, Wan-Yu Wang, Yu-Liang Xiong
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引用次数: 0

摘要

采用DEAE Sephadex A-50阴离子交换、Sephadex G-100(超细)凝胶过滤和反相高效液相色谱(RP-HPLC)技术,从刺眼Trimeresurus jerdonii毒液中纯化出一种新的激肽释放酶和纤维蛋白(原)裂解酶(jerdonase)。还原条件下Jerdonase的分子量约为55 kD,非还原条件下Jerdonase的分子量约为53 kD。该酶是一种含35.8%中性碳水化合物的糖蛋白。该酶n端氨基酸序列为IIGGDECNINEHPFLVALYDA,与其他蛇毒丝氨酸蛋白酶序列具有较高的同源性。Jerdonase对BAEE、S-2238和S-2302的水解作用受苯基甲基磺酰氟(PMSF)的抑制,而乙二胺四乙酸(EDTA)的影响较小。Jerdonase优先裂解人纤维蛋白原的A -链,对B -链的活性较低。此外,该酶还能水解牛低分子质量的激肽原,释放出缓激肽。综上所述,jerdonase是一种多功能蛇毒丝氨酸蛋白酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Jerdonase, a novel serine protease with kinin-releasing and fibrinogenolytic activity from Trimeresurus jerdonii venom.

A novel kinin-releasing and fibrin(ogen)olytic enzyme termed jerdonase was purified to homogeneity from the venom of Trimeresurus jerdonii by DEAE Sephadex A-50 anion exchange, Sephadex G-100 (superfine) gel filtration and reverse-phase high performance liquid chromatography (RP-HPLC). Jerdonase migrated as a single band with an approximate molecular weight of 55 kD under the reduced conditions and 53 kD under the non-reduced conditions. The enzyme was a glycoprotein containing 35.8% neutral carbohydrate. The N-terminal amino acid sequence of jerdonase was determined to be IIGGDECNINEHPFLVALYDA, which showed high sequence identity to other snake venom serine proteases. Jerdonase catalyzed the hydrolysis of BAEE, S-2238 and S-2302, which was inhibited by phenylmethylsulfonyl fluoride (PMSF), but not affected by ethylenediaminetetraacetic acid (EDTA). Jerdonase preferentially cleaved the A alpha-chain of human fibrinogen with lower activity towards B beta-chain. Moreover, the enzyme hydrolyzed bovine low-molecular-mass kininogen and releasing bradykinin. In conclusion, all results indicated that jerdonase was a multifunctional venom serine protease.

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