Measuring the effects of ice thickness on resolution in single particle cryo-EM

被引:23
|
作者
Neselu, Kasahun [1 ]
Wang, Bing [2 ]
Rice, William J. [2 ,3 ]
Potter, Clinton S. [1 ]
Carragher, Bridget [1 ]
Chua, Eugene Y. D. [1 ]
机构
[1] New York Struct Biol Ctr, Simons Electron Microscopy Ctr, New York, NY 60131 USA
[2] NYU, Grossman Sch Med, Cryo Electron Microscopy Core, New York, NY USA
[3] NYU, Grossman Sch Med, Dept Cell Biol, New York, NY USA
来源
JOURNAL OF STRUCTURAL BIOLOGY-X | 2023年 / 7卷
关键词
Cryo-EM; Ice thickness; Single particle analysis; Energy filter; High tension; Resolution; BEAM-INDUCED MOTION; DATA-ACQUISITION; MICROSCOPY;
D O I
10.1016/j.yjsbx.2023.100085
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ice thickness is a critical parameter in single particle cryo-EM - too thin ice can break during imaging or exclude the sample of interest, while ice that is too thick contributes to more inelastic scattering that precludes obtaining high resolution reconstructions. Here we present the practical effects of ice thickness on resolution, and the influence of energy filters, accelerating voltage, or detector mode. We collected apoferritin data with a wide range of ice thicknesses on three microscopes with different instrumentation and settings. We show that on a 300 kV microscope, using a 20 eV energy filter slit has a greater effect on improving resolution in thicker ice; that operating at 300 kV instead of 200 kV accelerating voltage provides significant resolution improvements at an ice thickness above 150 nm; and that on a 200 kV microscope using a detector operating in super resolution mode enables good reconstructions for up to 200 nm ice thickness, while collecting in counting instead of linear mode leads to improvements in resolution for ice of 50-150 nm thickness. Our findings can serve as a guide for users seeking to optimize data collection or sample preparation routines for both single particle and in situ cryo-EM. We note that most in situ data collection is done on samples in a range of ice thickness above 150 nm so these results may be especially relevant to that community.
引用
收藏
页数:7
相关论文
共 50 条
  • [31] Single-particle Cryo-EM of calcium release channels: structural validation
    Ludtke, Steven J.
    Serysheva, Irina I.
    CURRENT OPINION IN STRUCTURAL BIOLOGY, 2013, 23 (05) : 755 - 762
  • [32] High-resolution cryo-EM reconstructions in the presence of substantial aberrations
    Bromberg, Raquel
    Guo, Yirui
    Borek, Dominika
    Otwinowski, Zbyszek
    IUCRJ, 2020, 7 : 445 - 452
  • [33] Benchmarking the ideal sample thickness in cryo-EM
    Martynowycz, Michael W.
    Clabbers, Max T. B.
    Unge, Johan
    Hattne, Johan
    Gonen, Tamir
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2021, 118 (49)
  • [34] Achieving better-than-3-Å resolution by single-particle cryo-EM at 200 keV
    Herzik, Mark A., Jr.
    Wu, Mengyu
    Lander, Gabriel C.
    NATURE METHODS, 2017, 14 (11) : 1075 - +
  • [35] A Bayesian approach to beam-induced motion correction in cryo-EM single-particle analysis
    Zivanov, Jasenko
    Nakane, Takanori
    Scheres, Sjors H. W.
    IUCRJ, 2019, 6 : 5 - 17
  • [36] Membrane protein structural biology in the era of single particle cryo-EM
    Cheng, Yifan
    CURRENT OPINION IN STRUCTURAL BIOLOGY, 2018, 52 : 58 - 63
  • [37] GRAFIX: STABILIZATION OF FRAGILE MACROMOLECULAR COMPLEXES FOR SINGLE PARTICLE CRYO-EM
    Stark, Holger
    METHODS IN ENZYMOLOGY, VOL 481: CRYO-EM, PART A - SAMPLE PREPARATION AND DATA COLLECTION, 2010, 481 : 109 - 126
  • [38] Single-Particle Cryo-EM Data Collection with Stage Tilt using Leginon
    Aiyer, Sriram
    Strutzenberg, Timothy S.
    Bowman, Marianne E.
    Noel, Joseph P.
    Lyumkis, Dmitry
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2022, (185):
  • [39] Joint Angular Refinement and Reconstruction for Single-Particle Cryo-EM
    Zehni, Mona
    Donati, Laurene
    Soubies, Emmanuel
    Zhao, Zhizhen
    Unser, Michael
    IEEE TRANSACTIONS ON IMAGE PROCESSING, 2020, 29 : 6151 - 6163
  • [40] Cryo-EM single-particle structure refinement and map calculation using Servalcat
    Yamashita, Keitaro
    Palmer, Colin M.
    Burnley, Tom
    Murshudov, Garib N.
    ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2021, 77 : 1282 - 1291