Department of Agricultural Biotechnology, Center for Food Safety and Toxicology, Center for Food and Bioconvergence, and Research Institute for Agriculture and Life Sciences, CALS, Seoul National University, Seoul 08826, Korea.
Present address: KoBioLabs, Inc., Seoul 08826, Korea.
Mol Cells. 2020 Mar 31;43(3):298-303. doi: 10.14348/molcells.2020.2238.
Cryo-electron microscopy (cryo-EM) is now the first choice to determine the high-resolution structures of huge protein complexes. Grids with two-dimensional arrays of holes covered with a carbon film are typically used in cryo-EM. Although semi-automatic plungers are available, notable trial-and-error is still required to obtain a suitable grid specimen. Herein, we introduce a new method to obtain thin ice specimens using real-time measurement of the liquid amounts in cryo-EM grids. The grids for cryo-EM strongly diffracted laser light, and the diffraction intensity of each spot was measurable in real-time. The measured diffraction patterns represented the states of the liquid in the holes due to the curvature of the liquid around them. Using the diffraction patterns, the optimal time point for freezing the grids for cryo-EM was obtained in real-time. This development will help researchers rapidly determine highresolution protein structures using the limited resource of cryo-EM instrument access.
冷冻电子显微镜(cryo-EM)现在是确定大型蛋白质复合物高分辨率结构的首选方法。在 cryo-EM 中,通常使用具有覆盖有碳膜的二维孔阵列的网格。尽管有半自动的柱塞可供使用,但仍需要进行大量的反复试验才能获得合适的网格标本。在此,我们介绍了一种新方法,该方法使用 cryo-EM 网格中液体量的实时测量来获得薄冰标本。用于 cryo-EM 的网格强烈衍射激光,并且每个点的衍射强度都可以实时测量。由于周围液体的曲率,测量的衍射图案代表了孔中液体的状态。使用衍射图案,可以实时获得 cryo-EM 网格的最佳冻结时间点。这项开发将有助于研究人员利用 cryo-EM 仪器访问的有限资源快速确定高分辨率蛋白质结构。