Wieferig Jan-Philip, Mills Deryck J, Kühlbrandt Werner
Department of Structural Biology, Max Planck Institute of Biophysics, Frankfurt, Germany.
IUCrJ. 2021 Mar 1;8(Pt 2):186-194. doi: 10.1107/S2052252520016243.
As cryo-EM approaches the physical resolution limits imposed by electron optics and radiation damage, it becomes increasingly urgent to address the issues that impede high-resolution structure determination of biological specimens. One of the persistent problems has been beam-induced movement, which occurs when the specimen is irradiated with high-energy electrons. Beam-induced movement results in image blurring and loss of high-resolution information. It is particularly severe for biological samples in unsupported thin films of vitreous water. By controlled devitrification of conventionally plunge-frozen samples, the suspended film of vitrified water was converted into cubic ice, a polycrystalline, mechanically stable solid. It is shown that compared with vitrified samples, devitrification reduces beam-induced movement in the first 5 e Å of an exposure by a factor of ∼4, substantially enhancing the contribution of the initial, minimally damaged frames to a structure. A 3D apoferritin map reconstructed from the first frames of 20 000 particle images of devitrified samples resolved undamaged side chains. Devitrification of frozen-hydrated specimens helps to overcome beam-induced specimen motion in single-particle cryo-EM, as a further step towards realizing the full potential of cryo-EM for high-resolution structure determination.
随着冷冻电镜接近电子光学和辐射损伤所施加的物理分辨率极限,解决阻碍生物标本高分辨率结构测定的问题变得越来越紧迫。一直存在的问题之一是束流诱导运动,当标本用高能电子照射时就会发生这种情况。束流诱导运动会导致图像模糊和高分辨率信息丢失。对于处于玻璃态水的无支撑薄膜中的生物样品来说,这种情况尤为严重。通过对传统 plunge 冷冻样品进行可控脱玻化处理,玻璃态水的悬浮膜被转化为立方冰,一种多晶的、机械稳定的固体。结果表明,与玻璃化样品相比,脱玻化处理使曝光前 5 e Å 内的束流诱导运动减少了约 4 倍,显著增强了初始的、损伤最小的帧对结构的贡献。从 20000 个脱玻化样品的粒子图像的第一帧重建的三维脱铁铁蛋白图谱解析出了未受损的侧链。冷冻水合标本的脱玻化有助于克服单粒子冷冻电镜中束流诱导的标本运动,这是朝着实现冷冻电镜在高分辨率结构测定方面的全部潜力迈出的又一步。