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单颗粒冷EM分析的胰岛素受体-胰岛素复合物的结构
Giovanna Scapin1, Venkata P Dandey2, Zhening Zhang2
1Merck & Co., Department of Biochemical Engineering & Structure, 2000 Galloping Hill Road, Kenilworth, New Jersey 07033, USA.
Nature
|March 8, 2018
概括
对胰岛素受体激活的结构洞察力揭示了胰岛素结合如何触发下游信号. 这些发现有助于我们更好地了解葡萄糖平衡和糖尿病等相关疾病.
科学领域:
- 生物化学
- 结构生物学
- 分子医学
背景情况:
- 胰岛素受体 (IR) 是一个关键的二元蛋白调节葡萄糖平衡和新陈代谢.
- 红外功能障碍与糖尿病,癌症和阿尔茨海默氏症等疾病有关.
- 之前的结构研究缺乏关于完全受体结合和信号传播的细节.
研究的目的:
- 阐明胰岛素与全胰岛素受体外膜 (ECD) 结合的结构基础.
- 了解由胰岛素结合启动的信号传播机制.
主要方法:
- 使用单粒子冷电子显微镜 (cryo-EM).
- 用胰岛素生成了4. 3 Å 和 7. 4 Å 分辨率的胰岛素受体ECD二元复合物的重建.
主要成果:
- 该4. 3 Å 结构显示了两个因分离体结合的胰岛素分子,与特定的子域 (L1,FnIII-1) 和α-CT螺旋相互作用.
- 7. 4 Å 结构显示每个二分体的胰岛素分子结合.
- 确定了S1和完整的S2胰岛素结合部位.
- 第一个胰岛素分子的结合似乎招募了α-CT螺旋,改变了子域的方向.
结论:
- 这项研究提供了与全胰岛素受体ECD结合的高分辨率结构.
- 这些结构揭示了S1和S2位点的胰岛素结合的分子细节.
- 这些发现表明信号启动的机制涉及α-CT螺旋在初始胰岛素结合时的招募,导致下游信号激活.
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