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从日本蝮蛇蛇毒中纯化出的卤丝氨酸蛋白酶的纯化及氨基酸序列,该酶可特异性切割纤维蛋白原和激肽原。

Purification and amino acid sequence of halystase from snake venom of Agkistrodon halys blomhoffii, a serine protease that cleaves specifically fibrinogen and kininogen.

作者信息

Matsui T, Sakurai Y, Fujimura Y, Hayashi I, Oh-Ishi S, Suzuki M, Hamako J, Yamamoto Y, Yamazaki J, Kinoshita M, Titani K

机构信息

Division of Biomedical Polymer Science, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Aichi, Japan.

出版信息

Eur J Biochem. 1998 Mar 15;252(3):569-75. doi: 10.1046/j.1432-1327.1998.2520569.x.

Abstract

We have isolated a serine protease, halystase, from Agkistrodon halys blomhoffii venom by chromatography on DEAE-Sepharose, heparin-Sepharose and Q-Sepharose columns, and have determined the complete amino acid sequence by Edman degradation and by mass spectral analysis of peptides generated by enzymatic and chemical cleavage. The 238-residue sequence of halystase, containing N-linked carbohydrates (about 13%) at two sites showed significant similarity to other thrombin-like snake venom serine proteases (66-72%), mammalian tissue kallikrein (42%) and thrombin (26%). Halystase contained the tentative catalytic triad of His43, Asp88 and Ser184 common to all serine proteases and Asp178 in the primary substrate-binding site. Although halystase contained an RGD sequence at residues 181-183, it did not inhibit platelet aggregation induced by ADP or collagen. It hydrolyzed most efficiently a tissue-kallikrein substrate, prolylphenylalanylarginyl-4-methyl-coumaryl-7-amide, and released bradykinin from bovine kininogen. Halystase did not coagulate human plasma, but it cleaved the fibrinogen B beta chain at the carboxyl side of Arg42 and cleaved slowly the fibrogen A alpha chain. Fibrinogen thus treated gradually became insensitive to thrombin. The proteolytic activity was inhibited with diisopropyl fluorophosphate, phenylmethylsulfonyl fluoride or leupeptin. These results indicate that halystase is a serine protease structurally similar to coagulating thrombin-like snake venom proteases, but it specifically cleaves fibrinogen at sites different from thrombin without inducing fibrin clotting, and hydrolyzes kininogen to produce bradykinin, resulting in the reduction of blood pressure.

摘要

我们通过在DEAE-琼脂糖、肝素-琼脂糖和Q-琼脂糖柱上进行色谱分离,从蝮蛇毒中分离出一种丝氨酸蛋白酶——海蛇毒酶,并通过埃德曼降解法以及对酶解和化学裂解产生的肽段进行质谱分析,确定了其完整的氨基酸序列。海蛇毒酶由238个氨基酸残基组成,在两个位点含有N-连接碳水化合物(约13%),与其他凝血酶样蛇毒丝氨酸蛋白酶(66 - 72%)、哺乳动物组织激肽释放酶(42%)和凝血酶(26%)具有显著相似性。海蛇毒酶含有所有丝氨酸蛋白酶共有的His43、Asp88和Ser184组成的暂定催化三联体以及位于主要底物结合位点的Asp178。尽管海蛇毒酶在181 - 183位残基处含有RGD序列,但它并不抑制ADP或胶原诱导的血小板聚集。它最有效地水解一种组织激肽释放酶底物——脯氨酰苯丙氨酰精氨酰-4-甲基-香豆素-7-酰胺,并从牛激肽原中释放出缓激肽。海蛇毒酶不会使人体血浆凝固,但它在Arg42的羧基侧切割纤维蛋白原Bβ链,并缓慢切割纤维蛋白原Aα链。如此处理后的纤维蛋白原逐渐对凝血酶不敏感。其蛋白水解活性被二异丙基氟磷酸、苯甲基磺酰氟或亮抑酶肽抑制。这些结果表明,海蛇毒酶是一种结构上与凝血的凝血酶样蛇毒蛋白酶相似的丝氨酸蛋白酶,但它在与凝血酶不同的位点特异性切割纤维蛋白原,且不诱导纤维蛋白凝块形成,并水解激肽原产生缓激肽,从而导致血压降低。

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