High-resolution low-dose scanning transmission electron microscopy

被引:98
作者
Buban, James P. [1 ]
Ramasse, Quentin [2 ]
Gipson, Bryant [1 ]
Browning, Nigel D. [3 ,4 ,5 ]
Stahlberg, Henning [1 ]
机构
[1] Univ Calif Davis, Coll Biol Sci, Dept Mol & Cellular Biol, Davis, CA 95616 USA
[2] Lawrence Berkeley Natl Lab, Berkeley, CA USA
[3] Univ Calif Davis, Dept Chem & Mat Sci, Davis, CA 95616 USA
[4] Lawrence Livermore Natl Lab, Div Mat Sci & Technol, Livermore, CA 94550 USA
[5] Lawrence Livermore Natl Lab, Chem Mat Earth & Life Sci Directorate, Livermore, CA 94550 USA
来源
JOURNAL OF ELECTRON MICROSCOPY | 2010年 / 59卷 / 02期
关键词
STEM; low-dose; aberration correction; CRYOELECTRON MICROSCOPY; MEMBRANE-PROTEINS; LIMITATIONS; CRITERION; MODEL;
D O I
10.1093/jmicro/dfp052
中图分类号
TH742 [显微镜];
学科分类号
摘要
During the past two decades instrumentation in scanning transmission electron microscopy (STEM) has pushed toward higher intensity electron probes to increase the signal-to-noise ratio of recorded images. While this is suitable for robust specimens, biological specimens require a much reduced electron dose for high-resolution imaging. We describe here protocols for low-dose STEM image recording with a conventional field-emission gun STEM, while maintaining the high-resolution capability of the instrument. Our findings show that a combination of reduced pixel dwell time and reduced gun current can achieve radiation doses comparable to low-dose TEM.
引用
收藏
页码:103 / 112
页数:10
相关论文
共 31 条
[1]   Sub-angstrom resolution using aberration corrected electron optics [J].
Batson, PE ;
Dellby, N ;
Krivanek, OL .
NATURE, 2002, 418 (6898) :617-620
[2]   MRC image processing programs [J].
Crowther, RA ;
Henderson, R ;
Smith, JM .
JOURNAL OF STRUCTURAL BIOLOGY, 1996, 116 (01) :9-16
[3]   Low-dose aberration corrected cryo-electron microscopy of organic specimens [J].
Evans, James E. ;
Hetherington, Crispin ;
Kirkland, Angus ;
Chang, Lan-Yun ;
Stahlberg, Henning ;
Browning, Nigel .
ULTRAMICROSCOPY, 2008, 108 (12) :1636-1644
[4]   SPIDER and WEB: Processing and visualization of images in 3D electron microscopy and related fields [J].
Frank, J ;
Radermacher, M ;
Penczek, P ;
Zhu, J ;
Li, YH ;
Ladjadj, M ;
Leith, A .
JOURNAL OF STRUCTURAL BIOLOGY, 1996, 116 (01) :190-199
[5]   The structural study of membrane proteins by electron crystallography [J].
Fujiyoshi, Y .
ADVANCES IN BIOPHYSICS, VOL 35 1998, 1998, 35 :25-80
[6]   2dx_merge:: Data management and merging for 2D crystal images [J].
Gipson, Bryant ;
Zeng, Xiangyan ;
Stahlberg, Henning .
JOURNAL OF STRUCTURAL BIOLOGY, 2007, 160 (03) :375-384
[7]   2dx -: User-friendly image processing for 2D crystals [J].
Gipson, Bryant ;
Zeng, Xiangyan ;
Zhang, Zi Yan ;
Stahlberg, Henning .
JOURNAL OF STRUCTURAL BIOLOGY, 2007, 157 (01) :64-72
[8]   LIMITATIONS TO SIGNIFICANT INFORMATION IN BIOLOGICAL ELECTRON MICROSCOPY AS A RESULT OF RADIATION DAMAGE [J].
GLAESER, RM .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1971, 36 (3-4) :466-&
[9]   Lipid-protein interactions in double-layered two-dimensional AQPO crystals [J].
Gonen, T ;
Cheng, YF ;
Sliz, P ;
Hiroaki, Y ;
Fujiyoshi, Y ;
Harrison, SC ;
Walz, T .
NATURE, 2005, 438 (7068) :633-638
[10]   Improved specimen preparation for cryo-electron microscopy using a symmetric carbon sandwich technique [J].
Gyobu, N ;
Tani, K ;
Hiroaki, Y ;
Kamegawa, A ;
Mitsuoka, K ;
Fujiyoshi, Y .
JOURNAL OF STRUCTURAL BIOLOGY, 2004, 146 (03) :325-333