Borchani L, Stankiewicz M, Kopeyan C, Mansuelle P, Kharrat R, Cestèle S, Karoui H, Rochat H, Pelhate M, el Ayeb M
Laboratoire des Venins et Toxines, Institut Pasteur de Tunis, Belvédère, Tunisia.
Toxicon. 1997 Mar;35(3):365-82. doi: 10.1016/s0041-0101(96)00173-0.
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.
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%)。