Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
The Clive and Vera Ramaciotti Centre for Cryo-EM, Department of Biochemistry and Molecular Biology, Monash University, Victoria, 3800 Melbourne, Australia.
Nat Commun. 2017 Jun 30;8:16099. doi: 10.1038/ncomms16099.
With the advent of direct electron detectors, the perspectives of cryo-electron microscopy (cryo-EM) have changed in a profound way. These cameras are superior to previous detectors in coping with the intrinsically low contrast and beam-induced motion of radiation-sensitive organic materials embedded in amorphous ice, and hence they have enabled the structure determination of many macromolecular assemblies to atomic or near-atomic resolution. Nevertheless, there are still limitations and one of them is the size of the target structure. Here, we report the use of a Volta phase plate in determining the structure of human haemoglobin (64 kDa) at 3.2 Å. Our results demonstrate that this method can be applied to complexes that are significantly smaller than those previously studied by conventional defocus-based approaches. Cryo-EM is now close to becoming a fast and cost-effective alternative to crystallography for high-resolution protein structure determination.
随着直接电子探测器的出现,冷冻电子显微镜(cryo-EM)的前景发生了深刻的变化。与之前的探测器相比,这些相机在应对嵌入非晶态冰中的辐射敏感有机材料固有的低对比度和束致运动方面具有优势,因此它们已经能够将许多大分子组装体的结构确定到原子或近原子分辨率。然而,仍然存在一些限制,其中之一是目标结构的大小。在这里,我们报告了使用 Volta 相板在 3.2Å 下测定人血红蛋白(64kDa)结构的情况。我们的结果表明,该方法可应用于比以前使用传统基于离焦的方法研究的复合物小得多的复合物。冷冻电子显微镜现在接近于成为一种快速且具有成本效益的替代结晶学方法,用于高分辨率蛋白质结构测定。