Institute of Structural and Molecular Biology, Birkbeck College, London, UK.
Division of Biological Sciences, University of California San Diego, La Jolla, CA, USA.
Nat Commun. 2021 Apr 1;12(1):2034. doi: 10.1038/s41467-021-22110-6.
COPII mediates Endoplasmic Reticulum to Golgi trafficking of thousands of cargoes. Five essential proteins assemble into a two-layer architecture, with the inner layer thought to regulate coat assembly and cargo recruitment, and the outer coat forming cages assumed to scaffold membrane curvature. Here we visualise the complete, membrane-assembled COPII coat by cryo-electron tomography and subtomogram averaging, revealing the full network of interactions within and between coat layers. We demonstrate the physiological importance of these interactions using genetic and biochemical approaches. Mutagenesis reveals that the inner coat alone can provide membrane remodelling function, with organisational input from the outer coat. These functional roles for the inner and outer coats significantly move away from the current paradigm, which posits membrane curvature derives primarily from the outer coat. We suggest these interactions collectively contribute to coat organisation and membrane curvature, providing a structural framework to understand regulatory mechanisms of COPII trafficking and secretion.
COPII 介导内质网到高尔基体的数千种货物运输。五种必需的蛋白质组装成双层结构,内层被认为调节外壳组装和货物募集,而外层外壳形成假设支架膜曲率的笼子。在这里,我们通过冷冻电镜断层扫描和亚断层平均化来可视化完整的、膜组装的 COPII 外壳,揭示了壳层内部和之间相互作用的完整网络。我们使用遗传和生化方法证明了这些相互作用的生理重要性。突变分析表明,仅内层外壳就可以提供膜重塑功能,外层外壳提供组织输入。内层和外层外壳的这些功能作用显著偏离了当前的范式,该范式认为膜曲率主要来自于外层外壳。我们建议这些相互作用共同有助于外壳组织和膜曲率,为理解 COPII 运输和分泌的调节机制提供了一个结构框架。