首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Blarina toxin, a mammalian lethal venom from the short-tailed shrew Blarina brevicauda: Isolation and characterization.
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Blarina toxin, a mammalian lethal venom from the short-tailed shrew Blarina brevicauda: Isolation and characterization.

机译:Blarina毒素,短尾the Blarina brevicauda的哺乳动物致死性毒液:分离和鉴定。

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摘要

Venomous mammals are rare, and their venoms have not been characterized. We have purified and characterized the blarina toxin (BLTX), a lethal mammalian venom with a tissue kallikrein-like activity from the submaxillary and sublingual glands of the short-tailed shrew Blarina brevicauda. Mice administered BLTX i.p. developed irregular respiration, paralysis, and convulsions before dying. Based on the amino acid sequence of purified protein, we cloned the BLTX cDNA. It consists of a prosequence and an active form of 253 aa with a typical catalytic triad of serine proteases, with a high identity with tissue kallikreins. BLTX is an N-linked microheterogeneous glycoprotein with a unique insertion of 10 residues, L(106)TFFYKTFLG(115). BLTX converted kininogens to kinins, which may be one of the toxic pathogens, and had dilatory effects on the blood vessel walls. The acute toxicity and proteolytic activity of BLTX were strongly inhibited by aprotinin, a kallikrein inhibitor, suggesting that its toxicity is due to a kallikrein-like activity of the venom.
机译:有毒的哺乳动物很少见,其毒液尚未鉴定。我们已经从短尾shBlarina brevicauda的上颌下和舌下腺中纯化并鉴定了白粉虱毒素(BLTX),这是一种致命的哺乳动物毒液,具有组织激肽释放酶样活性。小鼠经BLTX i.p.死亡前出现不规则的呼吸,麻痹和抽搐。根据纯化蛋白的氨基酸序列,我们克隆了BLTX cDNA。它由253 aa的前序列和活性形式组成,具有典型的丝氨酸蛋白酶催化三联体,与激肽释放酶具有高度的同一性。 BLTX是具有10个残基(L(106)TFFYKTFLG(115))的独特插入的N-连接微异源糖蛋白。 BLTX将激肽原转化为激肽,激肽可能是有毒的病原体之一,并且对血管壁有扩张作用。抑肽酶(一种激肽释放酶抑制剂)强烈抑制了BLTX的急性毒性和蛋白水解活性,这表明它的毒性归因于毒液的激肽释放酶样活性。

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