Kühlbrandt Werner
Max-Planck-Institute of Biophysics, Frankfurt, Germany.
Methods Mol Biol. 2013;955:1-16. doi: 10.1007/978-1-62703-176-9_1.
From the earliest work on regular arrays in negative stain, electron crystallography has contributed greatly to our understanding of the structure and function of biological macromolecules. The development of electron cryo-microscopy (cryo-EM) then lead to the first groundbreaking atomic models of the membrane proteins bacteriorhodopsin and light harvesting complex II within lipid bilayers. Key contributions towards cryo-EM and electron crystallography methods included specimen preparation and vitrification, liquid-helium cooling, data collection, and image processing. These methods are now applied almost routinely to both membrane and soluble proteins. Here we outline the advances and the breakthroughs that paved the way towards high-resolution structures by electron crystallography, both in terms of methods development and biological milestones.
从最早关于负染中规则阵列的研究工作开始,电子晶体学就为我们理解生物大分子的结构和功能做出了巨大贡献。随后,电子冷冻显微镜(cryo-EM)的发展带来了脂质双层中膜蛋白细菌视紫红质和光捕获复合物II的首个具有开创性的原子模型。对cryo-EM和电子晶体学方法的关键贡献包括样品制备和玻璃化、液氦冷却、数据收集以及图像处理。这些方法现在几乎已常规应用于膜蛋白和可溶性蛋白。在这里,我们概述了在方法开发和生物学里程碑方面为通过电子晶体学获得高分辨率结构铺平道路的进展和突破。