Sun Willy W, Michalak Dennis J, Sochacki Kem A, Kunamaneni Prasanthi, Alfonzo-Méndez Marco A, Arnold Andreas M, Strub Marie-Paule, Hinshaw Jenny E, Taraska Justin W
National Heart, Lung, and Blood Institute, US National Institutes of Health, Bethesda, MD, USA.
National Institute of Diabetes and Digestive and Kidney Diseases, US National Institutes of Health, Bethesda, MD, USA.
Nat Commun. 2025 Jan 20;16(1):855. doi: 10.1038/s41467-025-56045-z.
Cryo-electron tomography (cryoET) provides sub-nanometer protein structure within the dense cellular environment. Existing sample preparation methods are insufficient at accessing the plasma membrane and its associated proteins. Here, we present a correlative cryo-electron tomography pipeline optimally suited to image large ultra-thin areas of isolated basal and apical plasma membranes. The pipeline allows for angstrom-scale structure determination with subtomogram averaging and employs a genetically encodable rapid chemically-induced electron microscopy visible tag for marking specific proteins within the complex cellular environment. The pipeline provides efficient, distributable, low-cost sample preparation and enables targeted structural studies of identified proteins at the plasma membrane of mammalian cells.
冷冻电子断层扫描(cryoET)可在致密的细胞环境中提供亚纳米级的蛋白质结构。现有的样品制备方法在获取质膜及其相关蛋白质方面存在不足。在此,我们展示了一种相关冷冻电子断层扫描流程,该流程最适合对分离的基底和顶端质膜的大面积超薄区域进行成像。该流程通过亚断层平均实现埃级结构测定,并采用一种可遗传编码的快速化学诱导电子显微镜可见标签,用于在复杂的细胞环境中标记特定蛋白质。该流程提供了高效、可分发、低成本的样品制备方法,并能够对哺乳动物细胞质膜上已鉴定的蛋白质进行靶向结构研究。