Fujiyoshi Yoshinori
Department of Basic Biology, Cellular and Structural Physiology Institute, Nagoya University, Furo-cho, Chikusa, Nagoya, Japan.
Methods Mol Biol. 2013;955:103-18. doi: 10.1007/978-1-62703-176-9_6.
Our understanding of subcellular structures has been greatly increased owing to electron microscopy, even though radiation damage of biological samples by the electron beam demanded staining techniques. Technological and instrumental advances of electron microscopy have, however, established various highly sophisticated techniques to study biological systems in their native states without staining and thus facilitated comprehension of rather intact structures of biological components. Among these techniques, electron crystallography is a well-established one to analyze membrane protein structures within lipid bilayers, without staining at close-to-physiological conditions. Structures of membrane proteins could be analyzed at resolutions better than 3Å by electron crystallography due to techniques of low dose and cryo-electron microscopy (cryo-EM). Here, recent cryo-EM technological and instrumental advances crucial to optimal data collection in electron crystallography are summarized as well as examples of structures of membrane proteins analyzed with the help of this method.
尽管电子束对生物样品造成的辐射损伤需要染色技术,但由于电子显微镜的应用,我们对亚细胞结构的理解有了极大的提高。然而,电子显微镜的技术和仪器进步已经建立了各种高度复杂的技术,用于在不染色的天然状态下研究生物系统,从而有助于理解生物成分相当完整的结构。在这些技术中,电子晶体学是一种成熟的技术,可用于分析脂质双层中的膜蛋白结构,且在接近生理条件下无需染色。由于低剂量和冷冻电子显微镜(cryo-EM)技术,通过电子晶体学可以在优于3Å的分辨率下分析膜蛋白结构。在此,总结了最近对电子晶体学中最佳数据收集至关重要的冷冻电镜技术和仪器进展,以及借助该方法分析的膜蛋白结构实例。