Department of Biology, University of Utah School of Medicine, Salt Lake City, United States.
Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, United States.
Elife. 2019 Feb 12;8:e41574. doi: 10.7554/eLife.41574.
The fish-hunting marine cone snail 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 , and 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.
捕食鱼类的海洋芋螺利用一种特殊的毒液胰岛素来诱导猎物发生低血糖休克。我们最近发现,这种毒液胰岛素 Con-Ins G1 具有独特的特性,与新型胰岛素治疗药物的设计相关。在这里,我们展示了捕食鱼类的芋螺为脊椎动物胰岛素受体的最小化配体提供了丰富的来源。来自 、 和 的胰岛素具有不同的序列,但都能与人和胰岛素受体结合并激活它。分子动力学揭示了独特的作用模式,与自然界中已知的任何其他胰岛素都不同。在斑马鱼和小鼠中进行测试时,毒液胰岛素可显著降低链脲佐菌素诱导的糖尿病模型中的血糖。我们的研究结果表明,芋螺已经进化出多种激活脊椎动物胰岛素受体的策略,并为治疗糖尿病的新型药物设计提供了独特的见解。