Experimental evaluation of super-resolution imaging and magnification choice in single-particle cryo-EM

IF 3.5 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Structural Biology: X Pub Date : 2021-01-01 DOI:10.1016/j.yjsbx.2021.100047
J. Ryan Feathers , Katherine A. Spoth , J. Christopher Fromme
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引用次数: 8

Abstract

The resolution of cryo-EM reconstructions is fundamentally limited by the Nyquist frequency, which is half the sampling frequency of the detector and depends upon the magnification used. In principle, super-resolution imaging should enable reconstructions to surpass the physical Nyquist limit by increasing sampling frequency, yet there are few reports of reconstructions that do so. Here we directly examine the contribution of super-resolution information, obtained with the K3 direct electron detector using a 2-condenser microscope, to single-particle cryo-EM reconstructions surpassing the physical Nyquist limit. We also present a comparative analysis of a sample imaged at four different magnifications. This analysis demonstrates that lower magnifications can be beneficial, despite the loss of higher resolution signal, due to the increased number of particle images obtained. To highlight the potential utility of lower magnification data collection, we produced a 3.5 Å reconstruction of jack bean urease with particles from a single micrograph.

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单粒子低温电镜超分辨成像及放大倍率选择的实验评价
低温电镜重建的分辨率基本上受到奈奎斯特频率的限制,奈奎斯特频率是探测器采样频率的一半,并取决于所使用的放大倍率。原则上,通过增加采样频率,超分辨率成像应该能够使重建超越物理奈奎斯特极限,然而,很少有报道这样做的重建。在这里,我们直接研究了使用双电容显微镜的K3直接电子探测器获得的超分辨率信息对超越物理奈奎斯特极限的单粒子低温电镜重建的贡献。我们还提出了在四种不同的放大率下成像的样品的比较分析。这一分析表明,较低的放大倍率可以是有益的,尽管高分辨率信号的损失,由于获得的粒子图像的数量增加。为了强调低倍率数据收集的潜在效用,我们用单个显微照片中的颗粒重建了3.5 Å豆角脲酶。
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来源期刊
Journal of Structural Biology: X
Journal of Structural Biology: X Biochemistry, Genetics and Molecular Biology-Structural Biology
CiteScore
6.50
自引率
0.00%
发文量
20
审稿时长
62 days
期刊最新文献
Corrigendum to “Minimizing ice contamination during specimen preparation for cryo-soft X-ray tomography and cryo-electron tomography” [J. Struct. Biol.: X 10(2024) 100113] Editorial by Natalie Reznikov [for Buss et al., “Hierarchical organization of bone in three dimensions: A twist of twists” (2022)] Structural analysis of the stable form of fibroblast growth factor 2 – FGF2-STAB Localization of albumin with correlative super resolution light- and electron microscopy in the kidney Minimizing ice contamination during specimen preparation for cryo-soft X-ray tomography and cryo-electron tomography
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