首页> 外文期刊>Biochimica et Biophysica Acta. General Subjects >Identification, cloning and functional characterization of a novel dermonecrotic toxin (phospholipase D) from brown spider (Loxosceles intermedia) venom
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Identification, cloning and functional characterization of a novel dermonecrotic toxin (phospholipase D) from brown spider (Loxosceles intermedia) venom

机译:鉴定,克隆和功能性表征从棕色蜘蛛(中间Loxosceles中间)的新型皮肤坏死毒素(磷脂酶D)。

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摘要

Brown spider bites are associated with lesions including dermonecrosis, gravitational spreading and a massive inflammatory response, along with systemic problems that may include hematological disturbances and renal failure. The mechanisms by which the venom exerts its noxious effects are currently under investigation. It is known that the venom contains a major toxin (dermonecrotic toxin, biochemically a phospholipase D) that can experimentally induce dermonecrosis, inflammatory response, animal mortality and platelet aggregation. Herein, we describe cloning, heterologous expression, purification and functionality of a novel isoform of the 33 kDa dermonecrotic toxin. Circular dichroism analysis evidenced correct folding for the toxin. The recombinant toxin was recognized by whole venom serum antibodies and by a specific antibody to a previously described dermonecrotic toxin. The identified toxin was found to display phospholipase activity and dermonecrotic properties. Additionally, the toxin caused a massive inflammatory response in rabbit skin dermis, evoked platelet aggregation, increased vascular permeability, caused edema and death in mice. These characteristics in combination with functional studies for other dermonecrotic toxins illustrate that a family of dermonecrotic toxins exists, and includes a novel member with high activity that may be useful for future structural and functional studies. (C) 2007 Elsevier B.V. All rights reserved.
机译:棕色蜘蛛咬伤与包括皮肤坏死,引力扩散和大量炎症反应在内的病变有关,还可能伴有全身问题,包括血液系统疾病和肾功能衰竭。毒液发挥其有害作用的机制目前正在研究中。已知毒液中含有一种主要毒素(皮肤坏死毒素,生化磷脂酶D),该毒素可通过实验诱导皮肤坏死,炎症反应,动物死亡和血小板聚集。在本文中,我们描述了33 kDa皮肤坏死毒素的新型同工型的克隆,异源表达,纯化和功能。圆二色性分析证明该毒素正确折叠。重组毒素被全毒血清抗体和针对先前描述的皮肤坏死毒素的特异性抗体识别。发现鉴定出的毒素显示磷脂酶活性和皮肤坏死性。此外,该毒素在兔皮肤真皮中引起大量炎症反应,引起血小板聚集,血管通透性增加,在小鼠中引起水肿和死亡。这些特征与对其他皮肤坏死毒素的功能研究相结合,说明存在皮肤坏死毒素家族,并且包括具有高活性的新成员,可能对将来的结构和功能研究有用。 (C)2007 Elsevier B.V.保留所有权利。

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