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来自突尼斯金蝎毒液的三种昆虫毒素的纯化、结构与活性

Purification, structure and activity of three insect toxins from Buthus occitanus tunetanus venom.

作者信息

Borchani L, Stankiewicz M, Kopeyan C, Mansuelle P, Kharrat R, Cestèle S, Karoui H, Rochat H, Pelhate M, el Ayeb M

机构信息

Laboratoire des Venins et Toxines, Institut Pasteur de Tunis, Belvédère, Tunisia.

出版信息

Toxicon. 1997 Mar;35(3):365-82. doi: 10.1016/s0041-0101(96)00173-0.

Abstract

One contractive and two depressant toxins active on insect were purified by high-performance liquid chromatography from the venom of Buthus occitanus tunetanus (Bot). The two depressant toxins, BotIT4 and BotIT5, differ only at position 6 (Arg for Lys) and are equally toxic to insects (LD50 to Blatella germanica = 110 ng/100 mg body weight). They show a strong antigenic cross-reaction with a depressive toxin from Leiurus quinquestriatus quinquestriatus (LqqIT2). The two toxins are able to inhibit with high affinity (K0.5 between 2 and 3 nM) the specific binding of the radioiodinated excitatory insect toxin (125I-AaHIT) on its receptor site on Periplaneta americana synaptosomal membranes. These toxins depolarize the cockroach axon, irreversibly block the action potential, and slow down and very progressively block the transmembrane transient Na+ current. The contracturant toxin BotIT1 is highly toxic to B. germanica (LD50 = 60 ng/ 100 mg body weight) and barely toxic to mice (LD50 = 1 microgram/20 g body weight) when injected intracerebroventricularly. It does not compete with 125I-AaHIT for its receptor site on P. americana synaptosomal membranes. On cockroach axon, BotIT1 develops plateau potentials and slows down the inactivation mechanism of the Na+ channels. Thus, BotIT1 belongs to the group of alpha insect-selective toxins and shows a strong sequence identity (> 90%) with Lqh alpha IT and LqqIII, two insect alpha-toxins previously purified from the venom of L. q. hebraeus and L. q. quinquestriatus. respectively.

摘要

通过高效液相色谱法从突尼斯金蝎(Buthus occitanus tunetanus,Bot)的毒液中纯化出一种对昆虫有活性的收缩毒素和两种抑制毒素。这两种抑制毒素,即BotIT4和BotIT5,仅在第6位不同(BotIT4的第6位是精氨酸,BotIT5的第6位是赖氨酸),对昆虫的毒性相同(对德国小蠊的半数致死量LD50 = 110 ng/100 mg体重)。它们与来自以色列金蝎(Leiurus quinquestriatus quinquestriatus,Lqq)的一种抑制毒素(LqqIT2)表现出强烈的抗原交叉反应。这两种毒素能够以高亲和力(半数抑制浓度K0.5在2至3 nM之间)抑制放射性碘化兴奋性昆虫毒素(125I - AaHIT)在美洲大蠊突触体膜上其受体位点的特异性结合。这些毒素使蟑螂轴突去极化,不可逆地阻断动作电位,并减缓并逐渐完全阻断跨膜瞬时钠电流。收缩毒素BotIT1对德国小蠊毒性极高(LD50 = 60 ng/100 mg体重),脑室内注射时对小鼠毒性极小(LD50 = 1微克/20 g体重)。它不与125I - AaHIT竞争其在美洲大蠊突触体膜上的受体位点。在蟑螂轴突上,BotIT1产生平台电位并减缓钠通道的失活机制。因此,BotIT1属于α型昆虫选择性毒素组,与先前分别从以色列金蝎(L. q. hebraeus)和以色列金蝎(L. q. quinquestriatus)毒液中纯化出的两种昆虫α毒素LqhαIT和LqqIII具有高度的序列同一性(> 90%)。

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