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  Tilt-Pair Analysis of Images from a Range of Different Specimens in Single-Particle Electron Cryomicroscopy

Henderson, R., Chen, S., Chen, J. Z., Grigorieff, N., Passmore, L. A., Ciccarelli, L., et al. (2011). Tilt-Pair Analysis of Images from a Range of Different Specimens in Single-Particle Electron Cryomicroscopy. Journal of Molecular Biology (London), 413(5), 1028-1046. doi:10.1016/j.jmb.2011.09.008.

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 Creators:
Henderson, Richard1, Author
Chen, Shaoxia1, Author
Chen, James Z.2, Author
Grigorieff, Nikolaus2, Author
Passmore, Lori A.1, Author
Ciccarelli, Luciano3, Author           
Rubinstein, John L.4, Author
Crowther, R. Anthony1, Author
Stewart, Phoebe L.5, Author
Rosenthal, Peter B.6, Author
Affiliations:
1MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK, ou_persistent22              
2Rosenstiel Basic Medical Science Research Center, Howard Hughes Medical Institute, Brandeis University, Waltham, MA 02154, USA, ou_persistent22              
3Department of Structural Biology, Max Planck Institute of Biophysics, Max Planck Society, ou_2068291              
4Molecular Structure and Function Program, The Hospital for Sick Children Research Institute, Toronto, ON, Canada M5G 1X8, ou_persistent22              
5Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, TN 37232, USA, ou_persistent22              
6Division of Physical Biochemistry, MRC National Institute for Medical Research, London NW7 1AA, UK, ou_persistent22              

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Free keywords: electron microscopy; structure validation; particle orientation; beam-induced specimen motion; radiation damage
 Abstract: The comparison of a pair of electron microscope images recorded at different specimen tilt angles provides a powerful approach for evaluating the quality of images, image-processing procedures, or three-dimensional structures. Here, we analyze tilt-pair images recorded from a range of specimens with different symmetries and molecular masses and show how the analysis can produce valuable information not easily obtained otherwise. We show that the accuracy of orientation determination of individual single particles depends on molecular mass, as expected theoretically since the information in each particle image increases with molecular mass. The angular uncertainty is less than 1° for particles of high molecular mass (∼ 50 MDa), several degrees for particles in the range 1–5 MDa, and tens of degrees for particles below 1 MDa. Orientational uncertainty may be the major contributor to the effective temperature factor (B-factor) describing contrast loss and therefore the maximum resolution of a structure determination. We also made two unexpected observations. Single particles that are known to be flexible showed a wider spread in orientation accuracy, and the orientations of the largest particles examined changed by several degrees during typical low-dose exposures. Smaller particles presumably also reorient during the exposure; hence, specimen movement is a second major factor that limits resolution. Tilt pairs thus enable assessment of orientation accuracy, map quality, specimen motion, and conformational heterogeneity. A convincing tilt-pair parameter plot, where 60% of the particles show a single cluster around the expected tilt axis and tilt angle, provides confidence in a structure determined using electron cryomicroscopy.

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Language(s): eng - English
 Dates: 2011-08-302011-06-162011-09-052011-09-122011-11-11
 Publication Status: Issued
 Pages: 19
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.jmb.2011.09.008
PMID: 21939668
PMC: PMC3220764
 Degree: -

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Title: Journal of Molecular Biology (London)
  Other : J Mol Biol
Source Genre: Journal
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Publ. Info: London : Academic Press
Pages: - Volume / Issue: 413 (5) Sequence Number: - Start / End Page: 1028 - 1046 Identifier: ISSN: 0022-2836
CoNE: https://pure.mpg.de/cone/journals/resource/954922646042