Seeing tobacco mosaic virus through direct electron detectors

With the introduction of direct electron detectors (DED) to the field of electron cryo-microscopy, a wave of atomic-resolution structures has become available. As the new detectors still require comparative characterization, we have used tobacco mosaic virus (TMV) as a test specimen to study the quality of 3D image reconstructions from data recorded on the two direct electron detector cameras, K2 Summit and Falcon II. Using DED movie frames, we explored related image-processing aspects and compared the performance of micrograph-based and segment-based motion correction approaches. In addition, we investigated the effect of dose deposition on the atomic-resolution structure of TMV and show that radiation damage affects negative carboxyl chains first in a side-chain specific manner. Finally, using 450,000 asymmetric units and limiting the effects of radiation damage, we determined a high-resolution cryo-EM map at 3.35 Å resolution. Here, we provide a comparative case study of highly ordered TMV recorded on different direct electron detectors to establish recording and processing conditions that enable structure determination up to 3.2 Å in resolution using cryo-EM.

[1]  W. Kühlbrandt,et al.  Atomic model of the F420-reducing [NiFe] hydrogenase by electron cryo-microscopy using a direct electron detector , 2014, eLife.

[2]  R. Ravelli,et al.  Radiation damage in macromolecular cryocrystallography. , 2006, Current opinion in structural biology.

[3]  A. Cheng,et al.  Beam-induced motion of vitrified specimen on holey carbon film. , 2012, Journal of structural biology.

[4]  D. Agard,et al.  Electron counting and beam-induced motion correction enable near atomic resolution single particle cryoEM , 2013, Nature Methods.

[5]  Hemant D. Tagare,et al.  The Local Resolution of Cryo-EM Density Maps , 2013, Nature Methods.

[6]  Z. Zhou,et al.  3.88 Å structure of cytoplasmic polyhedrosis virus by cryo-electron microscopy , 2008, Nature.

[7]  J. Dubochet,et al.  Cryo-electron microscopy of viruses , 1984, Nature.

[8]  S. Scheres Beam-induced motion correction for sub-megadalton cryo-EM particles , 2014, eLife.

[9]  David A Agard,et al.  Influence of electron dose rate on electron counting images recorded with the K2 camera. , 2013, Journal of structural biology.

[10]  Yanyu Zhao,et al.  Three-dimensional structure of human γ-secretase , 2014, Nature.

[11]  S. Scheres,et al.  Ribosome structures to near-atomic resolution from thirty thousand cryo-EM particles , 2013, eLife.

[12]  Elspeth F Garman,et al.  Experimental determination of the radiation dose limit for cryocooled protein crystals. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[13]  W. Kühlbrandt,et al.  High-resolution electron microscopy of biological specimens in cubic ice. , 1994, Ultramicroscopy.

[14]  Shaoxia Chen,et al.  Prevention of overfitting in cryo-EM structure determination , 2012, Nature Methods.

[15]  R. K. Bull,et al.  Stopping powers for electrons and positrons: ICRU Report 37; 271 pp.; 24 figures; U.S. $24.00. , 1986 .

[16]  A. Cheng,et al.  Movies of ice-embedded particles enhance resolution in electron cryo-microscopy. , 2012, Structure.

[17]  David N Mastronarde,et al.  Automated electron microscope tomography using robust prediction of specimen movements. , 2005, Journal of structural biology.

[18]  Randy J. Read,et al.  Overview of the CCP4 suite and current developments , 2011, Acta crystallographica. Section D, Biological crystallography.

[19]  Israel S. Fernández,et al.  Structure of the Mammalian Ribosome-Sec61 Complex to 3.4 Å Resolution , 2014, Cell.

[20]  N. Grigorieff Direct detection pays off for electron cryo-microscopy , 2013, eLife.

[21]  Z. Zhou,et al.  Limiting factors in atomic resolution cryo electron microscopy: no simple tricks. , 2011, Journal of structural biology.

[22]  Richard Henderson,et al.  Cryo-protection of protein crystals against radiation damage in electron and X-ray diffraction , 1990, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[23]  Sriram Subramaniam,et al.  Structure of β-galactosidase at 3.2-Å resolution obtained by cryo-electron microscopy , 2014, Proceedings of the National Academy of Sciences.

[24]  N. Grigorieff,et al.  High-resolution electron microscopy of helical specimens: a fresh look at tobacco mosaic virus. , 2007, Journal of molecular biology.

[25]  J. D. Bernal,et al.  X-RAY AND CRYSTALLOGRAPHIC STUDIES OF PLANT VIRUS PREPARATIONS , 1941, The Journal of general physiology.

[26]  J L Sussman,et al.  Specific chemical and structural damage to proteins produced by synchrotron radiation. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[27]  N. Unwin,et al.  Refined structure of the nicotinic acetylcholine receptor at 4A resolution. , 2005, Journal of molecular biology.

[28]  V. Ramakrishnan,et al.  Molecular Architecture of a Eukaryotic Translational Initiation Complex , 2013, Science.

[29]  J. D. Bernal,et al.  X-RAY AND CRYSTALLOGRAPHIC STUDIES OF PLANT VIRUS PREPARATIONS. III , 1941, The Journal of general physiology.

[30]  Kevin Cowtan,et al.  research papers Acta Crystallographica Section D Biological , 2005 .

[31]  R. Henderson,et al.  High-resolution noise substitution to measure overfitting and validate resolution in 3D structure determination by single particle electron cryomicroscopy☆ , 2013, Ultramicroscopy.

[32]  R. Henderson,et al.  Model for the structure of bacteriorhodopsin based on high-resolution electron cryo-microscopy. , 1990, Journal of molecular biology.

[33]  R Henderson,et al.  Electron-crystallographic refinement of the structure of bacteriorhodopsin. , 1996, Journal of molecular biology.

[34]  R. Henderson,et al.  Comparison of optimal performance at 300 keV of three direct electron detectors for use in low dose electron microscopy , 2014, Ultramicroscopy.

[35]  N. Grigorieff,et al.  Accurate determination of local defocus and specimen tilt in electron microscopy. , 2003, Journal of structural biology.

[36]  Daniel K. Clare,et al.  4.6 Å Cryo-EM reconstruction of tobacco mosaic virus from images recorded at 300 keV on a 4k × 4k CCD camera , 2010, Journal of structural biology.

[37]  Irina Gutsche,et al.  SPRING - an image processing package for single-particle based helical reconstruction from electron cryomicrographs. , 2014, Journal of structural biology.

[38]  N. Grigorieff,et al.  Quantitative characterization of electron detectors for transmission electron microscopy. , 2013, Journal of structural biology.

[39]  D. Julius,et al.  Structure of the TRPV1 ion channel determined by electron cryo-microscopy , 2013, Nature.

[40]  R Henderson,et al.  Electronic detectors for electron microscopy. , 2007, Current opinion in structural biology.

[41]  F J Sigworth,et al.  Noise models and cryo-EM drift correction with a direct-electron camera. , 2013, Ultramicroscopy.

[42]  Alan Brown,et al.  Structure of the Yeast Mitochondrial Large Ribosomal Subunit , 2014, Science.

[43]  E. Egelman A robust algorithm for the reconstruction of helical filaments using single-particle methods. , 2000, Ultramicroscopy.

[44]  Richard Henderson,et al.  Molecular Mechanism of Antibody-Mediated Activation of β-galactosidase , 2014, Structure.

[45]  Randy J. Read,et al.  Acta Crystallographica Section D Biological , 2003 .

[46]  R. Henderson,et al.  Optimal determination of particle orientation, absolute hand, and contrast loss in single-particle electron cryomicroscopy. , 2003, Journal of molecular biology.

[47]  Matthew L. Baker,et al.  An atomic model of brome mosaic virus using direct electron detection and real-space optimization , 2014, Nature Communications.

[48]  Z. Zhou,et al.  Hydrogen-bonding networks and RNA bases revealed by cryo electron microscopy suggest a triggering mechanism for calcium switches , 2011, Proceedings of the National Academy of Sciences.

[49]  S. Harrison,et al.  Near-atomic resolution using electron cryomicroscopy and single-particle reconstruction , 2008, Proceedings of the National Academy of Sciences.

[50]  Wen Jiang,et al.  EMAN2: an extensible image processing suite for electron microscopy. , 2007, Journal of structural biology.

[51]  F. Karimi Nejadasl,et al.  Radiation damage in single-particle cryo-electron microscopy: effects of dose and dose rate , 2011, Journal of synchrotron radiation.

[52]  Conrad C. Huang,et al.  UCSF Chimera—A visualization system for exploratory research and analysis , 2004, J. Comput. Chem..