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Fish-hunting cone snail venoms are a rich source of minimized ligands of the vertebrate insulin receptor

机译:猎鱼锥蜗牛毒是脊椎动物胰岛素受体最小化配体的丰富来源

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摘要

The fish-hunting marine cone snail Conus geographus uses a specialized venom insulin to induce hypoglycemic shock in its prey. We recently showed that this venom insulin, Con-Ins G1, has unique characteristics relevant to the design of new insulin therapeutics. Here, we show that fish-hunting cone snails provide a rich source of minimized ligands of the vertebrate insulin receptor. Insulins from C. geographus, Conus tulipa and Conus kinoshitai exhibit diverse sequences, yet all bind to and activate the human insulin receptor. Molecular dynamics reveal unique modes of action that are distinct from any other insulins known in nature. When tested in zebrafish and mice, venom insulins significantly lower blood glucose in the streptozotocin-induced model of diabetes. Our findings suggest that cone snails have evolved diverse strategies to activate the vertebrate insulin receptor and provide unique insight into the design of novel drugs for the treatment of diabetes.
机译:猎鱼海洋锥蜗牛Conus geographus使用特殊的毒液胰岛素在猎物中引起降血糖休克。我们最近显示,这种毒液胰岛素Con-Ins G1具有与新型胰岛素治疗药物设计相关的独特特征。在这里,我们表明,猎鱼锥蜗牛为脊椎动物胰岛素受体的最小配体提供了丰富的来源。来自地理隐孢子虫,郁金香圆锥体和粉角圆锥体的胰岛素具有多种序列,但都结合并激活人胰岛素受体。分子动力学揭示了独特的作用方式,与自然界已知的任何其他胰岛素不同。在斑马鱼和小鼠中进行测试时,在链脲佐菌素诱发的糖尿病模型中,毒液胰岛素可显着降低血糖。我们的发现表明,蜗牛蜗牛已经进化出多种策略来激活脊椎动物胰岛素受体,并为治疗糖尿病的新药设计提供了独特的见识。

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