蛇毒分解素:分类和治疗潜力。

O Kallech-Ziri, J Luis, M El Ayeb, N Marrakchi
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引用次数: 0

摘要

蛇毒的生物化学和药理学揭示了它们所含蛋白质的结构和功能多态性。这些酶通过其酶活性(蛋白酶、磷脂酶A2、l -氨基酸氧化酶等)或与膜受体结合来发挥作用。蛇毒崩解素通过结合整合素并阻断其功能,发挥细胞粘附和迁移的拮抗剂作用。从蛇毒中提取整合素拮抗剂的特性使我们能够了解某些整合素的功能,为开发新的治疗药物提供新的信息。在这篇综述中,我们报道了崩解素的分类和治疗意义。特别是lebestatin的结构和功能特征;从突尼斯大毒蛇毒液中分离的一种短崩解素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Snake venom disintegrins: classification and therapeutic potential].

Biochemistry and pharmacology of snake venoms reveal structural and functional polymorphisms of proteins they contain. These lead their effects by their enzymatic activities (proteases, phospholipases A2, L-amino acid oxydases...) or by binding to membrane receptors. Disintegrin from snake venoms play a role as antagonists of cell adhesion and migration by binding integrins and blocking their function. Characterization of integrin antagonists from snake venom allows us understanding the function of some integrins providing new information to develop new therapeutic agents. In this review, we report classification and therapeutic implications of disintegrins. In particular the structural and the functional characteristics of lebestatin; a short disintegrin isolated from Tunisian Macrovipera lebetina snake venom.

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