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Two novel dermonecrotic toxins LiRecDT4 and LiRecDT5 from Brown spider (Loxosceles intermedia) venom: From cloning to functional characterization

机译:棕蜘蛛毒的两种新型皮肤坏死毒素LiRecDT4和LiRecDT5:从克隆到功能鉴定

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摘要

Loxoscelism (the condition produced by the bite of brown spiders) has been reported worldwide, but especially in warmer regions. Clinical manifestations include skin necrosis with gravitational spreading while systemic loxoscelism may include renal failure, hemolysis and throm-bocytopenia. The venom contains several toxins, of which the best biochemically and biologically studied is the dermonecrotic toxin, a phos-pholipase-D. Purified toxin induces cutaneous and systemic loxoscelism, especially necrotic lesions, hematological disturbances and renal failure. Herein, we describe cloning, heterologous expression and purification of two novel dermonecrotic toxins: LiRecDT4 and LiRecDT5. The recombinant proteins stably expressed in Escherichia coli cells were purified from culture supernatants in a single step using Ni~(2+)-chelating chromatography producing soluble proteins of 34 kDa (LiRecDT4) and 37 kDa (LiRecDT5). Circular dichroism analysis evidenced correctly folding for toxins but differences in secondary structures. Both proteins were recognized by whole venom serum antibodies and by a specific antibody to dermonecrotic toxin. Also, recombinant toxins with phospholipase activity induced experimental skin lesions and caused a massive inflammatory response in rabbit skin dermis. Nevertheless, toxins displayed different effects upon platelet aggregation, increase in vascular permeability and not caused death in mice. These characteristics in combination with functional studies illustrates that a family of dermonecrotic toxins exists, and includes two novel members that are useful for future structural and functional studies. They will also be useful in biotech-nological ends, for example, as inflammatory and platelet aggregating studies, as antigens for serum therapy source and for lipids biochemical research.
机译:在世界范围内,特别是在较温暖的地区,已经报道了低氧症(由棕色蜘蛛咬伤产生的状况)。临床表现包括皮肤坏死并引力扩散,而系统性骨质疏松症可能包括肾功能衰竭,溶血和血小板减少症。毒液中含有几种毒素,其中生化和生物学方面研究得最好的是皮肤坏死毒素,一种磷酸酶-D。纯化的毒素会引起皮肤和系统性氧囊肿,特别是坏死性病变,血液学紊乱和肾衰竭。在这里,我们描述了两种新型皮肤坏死毒素:LiRecDT4和LiRecDT5的克隆,异源表达和纯化。使用Ni〜(2 +)-螯合色谱法从培养上清液中一步纯化纯化于大肠杆菌细胞中稳定表达的重组蛋白,产生34 kDa(LiRecDT4)和37 kDa(LiRecDT5)的可溶性蛋白。圆二色性分析证明正确折叠了毒素,但二级结构存在差异。两种蛋白均被全毒血清抗体和抗皮肤坏死毒素的特异性抗体识别。同样,具有磷脂酶活性的重组毒素诱导实验性皮肤损伤,并在兔皮肤真皮中引起大量的炎症反应。然而,毒素对血小板聚集显示出不同的作用,增加了血管通透性,并没有引起小鼠死亡。这些特征与功能研究相结合,说明存在皮肤坏死性毒素家族,并且包括两个对将来的结构和功能研究有用的新颖成员。它们还将在生物技术方面有用,例如作为炎症和血小板聚集研究,作为血清治疗来源的抗原和脂质生化研究的抗原。

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