Accurate modeling of single-particle cryo-EM images quantitates the benefits expected from using Zernike phase contrast
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作者:
Hall, R. J.
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Univ Calif Berkeley, Inst QB3, Berkeley, CA 94720 USAUniv Calif Berkeley, Inst QB3, Berkeley, CA 94720 USA
Hall, R. J.
[1
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Nogales, E.
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Univ Calif Berkeley, Inst QB3, Berkeley, CA 94720 USA
Univ Calif Berkeley, Howard Hughes Med Inst, Berkeley, CA 94720 USA
Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USAUniv Calif Berkeley, Inst QB3, Berkeley, CA 94720 USA
Nogales, E.
[1
,2
,3
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Glaeser, R. M.
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Univ Calif Berkeley, Inst QB3, Berkeley, CA 94720 USA
Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USAUniv Calif Berkeley, Inst QB3, Berkeley, CA 94720 USA
Glaeser, R. M.
[1
,3
]
机构:
[1] Univ Calif Berkeley, Inst QB3, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
The use of a Zernike-type phase plate in biological cryo-electron microscopy allows the imaging, without using defocus, of what are predominantly phase objects. It is thought that such phase-plate implementations might result in higher quality images, free from the problems of CTF correction that occur when images must be recorded at extremely high values of defocus. In single-particle cryo-electron microscopy it is hoped that these improvements in image quality will facilitate work on structures that have proved difficult to study, either because of their relatively small size or because the structures are not completely homogeneous. There is still a need, however, to quantitate how much improvement can be gained by using a phase plate for single-particle cryo-electron microscopy. We present a method for quantitatively modeling the images recorded with 200 keV electrons, for single particles embedded in vitreous ice. We then investigate what difference the use of a phase-plate device could have on the processing of single-particle data. We confirm that using a phase plate results in single-particle datasets in which smaller molecules can be detected, particles can be more accurately aligned and problems of heterogeneity can be more easily addressed. (C) 2011 Elsevier Inc. All rights reserved.
机构:
Department of Biochemistry and Molecular Biology and the Huck Institutes of the Life Sciences,Pennsylvania State UniversityDepartment of Biochemistry and Molecular Biology and the Huck Institutes of the Life Sciences,Pennsylvania State University
Jean-Paul Armache
Yifan Cheng
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Howard Hughes Medical Institute, University of California San Francisco
Department of Biochemistry and Biophysics,University of California San FranciscoDepartment of Biochemistry and Molecular Biology and the Huck Institutes of the Life Sciences,Pennsylvania State University
机构:
Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USAUniv Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
机构:
Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
Penn State Univ, Huck Inst Life Sci, University Pk, PA 16802 USAPenn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
Armache, Jean-Paul
Cheng, Yifan
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Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USAPenn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA