Challenges and opportunities in cryo-EM single-particle analysis
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[1] Justin M Kollman,et al. Vitrification after multiple rounds of sample application and blotting improves particle density on cryo-electron microscopy grids , 2016, bioRxiv.
[2] Peter B Rosenthal,et al. Validating maps from single particle electron cryomicroscopy. , 2015, Current opinion in structural biology.
[3] David Eisenberg,et al. Atomic resolution structures from fragmented protein crystals by the cryoEM method MicroED , 2017, Nature Methods.
[4] Anchi Cheng,et al. Automated molecular microscopy: the new Leginon system. , 2005, Journal of structural biology.
[5] Alan Brown,et al. Structure of the Yeast Mitochondrial Large Ribosomal Subunit , 2014, Science.
[6] Vincent B. Chen,et al. Correspondence e-mail: , 2000 .
[7] Christopher Irving,et al. Appion: an integrated, database-driven pipeline to facilitate EM image processing. , 2009, Journal of structural biology.
[8] Sriram Subramaniam,et al. Structure of trimeric HIV-1 envelope glycoproteins , 2013, Proceedings of the National Academy of Sciences.
[9] H. Padmore,et al. Design of an electron microscope phase plate using a focused continuous-wave laser , 2010, New journal of physics.
[10] A T Brünger,et al. Free R value: cross-validation in crystallography. , 1997, Methods in enzymology.
[11] W. O. Saxton. Observation of lens aberrations for very high‐resolution electron microscopy. I. Theory , 1995 .
[12] Dmitry Lyumkis,et al. Analysis of discrete local variability and structural covariance in macromolecular assemblies using Cryo-EM and focused classification. , 2019, Ultramicroscopy.
[13] K. Murata,et al. Cryo-electron microscopy for structural analysis of dynamic biological macromolecules. , 2018, Biochimica et biophysica acta. General subjects.
[14] J. Trinick,et al. A second generation apparatus for time-resolved electron cryo-microscopy using stepper motors and electrospray. , 2003, Journal of structural biology.
[15] E. Nogales. The development of cryo-EM into a mainstream structural biology technique , 2015, Nature Methods.
[16] Dmitry Lyumkis,et al. Likelihood-based classification of cryo-EM images using FREALIGN. , 2013, Journal of structural biology.
[17] Christopher J. Williams,et al. Model validation: local diagnosis, correction and when to quit , 2018, Acta crystallographica. Section D, Structural biology.
[18] David A Agard,et al. A simple and robust procedure for preparing graphene-oxide cryo-EM grids , 2018, bioRxiv.
[19] Andrej Bieri,et al. Miniaturized Sample Preparation for Transmission Electron Microscopy , 2018, Journal of visualized experiments : JoVE.
[20] Frank DiMaio,et al. RosettaES: a sampling strategy enabling automated interpretation of difficult cryo-EM maps , 2017, Nature Methods.
[21] David N Mastronarde,et al. Automated electron microscope tomography using robust prediction of specimen movements. , 2005, Journal of structural biology.
[22] Avinash Patel,et al. Structure of human TFIID and mechanism of TBP loading onto promoter DNA. , 2018 .
[23] N. Grigorieff,et al. Ensemble cryo-EM uncovers inchworm-like translocation of a viral IRES through the ribosome , 2016, eLife.
[24] Martin Grininger,et al. The deadly touch: protein denaturation at the water-air interface and how to prevent it , 2018, bioRxiv.
[25] R. Ghirlando,et al. Cryo-EM structures and atomic model of the HIV-1 strand transfer complex intasome , 2017, Science.
[26] C O S Sorzano,et al. Scipion: A software framework toward integration, reproducibility and validation in 3D electron microscopy. , 2016, Journal of structural biology.
[27] J. Dubochet,et al. Electron microscopy of frozen water and aqueous solutions , 1982 .
[28] Ahmed H. Zewail,et al. 4D cryo-electron microscopy of proteins. , 2013, Journal of the American Chemical Society.
[29] Randy J. Read,et al. Overview of the CCP4 suite and current developments , 2011, Acta crystallographica. Section D, Biological crystallography.
[30] Thomas C Terwilliger,et al. Automated map sharpening by maximization of detail and connectivity , 2018, bioRxiv.
[31] Tamir Gonen,et al. Analysis of global and site-specific radiation damage in cryo-EM , 2018, bioRxiv.
[32] Michael Levitt,et al. Architecture of an RNA Polymerase II Transcription Pre-Initiation Complex , 2013, Science.
[33] Zhenfeng Liu,et al. Structure of spinach photosystem II–LHCII supercomplex at 3.2 Å resolution , 2016, Nature.
[34] Alexis Rohou,et al. cisTEM: User-friendly software for single-particle image processing , 2017, bioRxiv.
[35] Dmitry Lyumkis,et al. Analysis of Local Variability and Allostery in Macromolecular Assemblies using Cryo-EM and Focused Classification , 2018, bioRxiv.
[36] S. Scheres,et al. Ribosome structures to near-atomic resolution from thirty thousand cryo-EM particles , 2013, eLife.
[37] Christopher Irving,et al. Automation in single-particle electron microscopy connecting the pieces. , 2010, Methods in enzymology.
[38] P. Penczek. Resolution measures in molecular electron microscopy. , 2010, Methods in enzymology.
[39] David Balchin,et al. Pathway of Actin Folding Directed by the Eukaryotic Chaperonin TRiC , 2018, Cell.
[40] F. Förster,et al. Subtomogram analysis using the Volta phase plate. , 2017, Journal of structural biology.
[41] Yifan Cheng,et al. Single-particle cryo-EM data acquisition by using direct electron detection camera. , 2016, Microscopy.
[42] Joachim Frank,et al. Single-Particle Reconstruction of Biological Molecules-Story in a Sample (Nobel Lecture). , 2018, Angewandte Chemie.
[43] Richard Henderson,et al. The energy dependence of contrast and damage in electron cryomicroscopy of biological molecules , 2019, Ultramicroscopy.
[44] B. Carragher,et al. Cryo-EM for Small Molecules Discovery, Design, Understanding, and Application. , 2018, Cell chemical biology.
[45] Alwyn Eades,et al. Obtaining TEM images with a uniform deviation parameter. , 2006, Ultramicroscopy.
[46] Sjors H. W. Scheres,et al. Unravelling biological macromolecules with cryo-electron microscopy , 2016, Nature.
[47] J Frank,et al. Three-dimensional reconstruction of the ribosome from Escherichia coli. , 1989, Biophysical journal.
[48] A. Steven,et al. One number does not fit all: mapping local variations in resolution in cryo-EM reconstructions. , 2013, Journal of structural biology.
[49] W. Baumeister,et al. Cryo-EM structure of haemoglobin at 3.2 Å determined with the Volta phase plate , 2016, Nature Communications.
[50] N. Unwin,et al. Analysis of transient structures by cryo-microscopy combined with rapid mixing of spray droplets. , 1994, Ultramicroscopy.
[51] Gabriel C Lander,et al. Site-specific labeling of proteins for electron microscopy. , 2015, Journal of structural biology.
[52] R. Glaeser,et al. Electron Diffraction of Frozen, Hydrated Protein Crystals , 1974, Science.
[53] Wolfgang Baumeister,et al. Graphene oxide: a substrate for optimizing preparations of frozen-hydrated samples. , 2010, Journal of structural biology.
[54] Dimitry Tegunov,et al. Real-time cryo–EM data pre-processing with Warp , 2018, Nature Methods.
[55] Alan Brown,et al. The structure of the human mitochondrial ribosome , 2015, Science.
[56] Xueming Li,et al. Fabs enable single particle cryoEM studies of small proteins. , 2012, Structure.
[57] R Henderson,et al. Electron-crystallographic refinement of the structure of bacteriorhodopsin. , 1996, Journal of molecular biology.
[58] Terrence Frey,et al. Faculty Opinions recommendation of TRPV1 structures in distinct conformations reveal activation mechanisms. , 2014 .
[59] Todd O. Yeates,et al. Near-atomic cryo-EM imaging of a small protein displayed on a designed scaffolding system , 2017, Proceedings of the National Academy of Sciences.
[60] J. Dubochet,et al. Cryo-electron microscopy of viruses , 1984, Nature.
[61] Yifan Cheng. Single-Particle Cryo-EM at Crystallographic Resolution , 2015, Cell.
[62] C. Oubridge,et al. CryoEM structure of the yeast U4/U6.U5 tri-snRNP at 3.7 Å resolution , 2016, Nature.
[63] José María Carazo,et al. Automatic local resolution-based sharpening of cryo-EM maps , 2018, bioRxiv.
[64] S H W Scheres,et al. Processing of Structurally Heterogeneous Cryo-EM Data in RELION. , 2016, Methods in enzymology.
[65] M Walker,et al. Millisecond time resolution electron cryo-microscopy of the M-ATP transient kinetic state of the acto-myosin ATPase. , 1995, Biophysical journal.
[66] Holger Stark,et al. GraFix: stabilization of fragile macromolecular complexes for single particle cryo-EM. , 2010, Methods in enzymology.
[67] Arthur Christopoulos,et al. Structural insights into G-protein-coupled receptor allostery , 2018, Nature.
[68] H. Stark,et al. Structure and Conformational Dynamics of the Human Spliceosomal Bact Complex , 2018, Cell.
[69] Gabriel C. Lander,et al. High-resolution structure determination of sub-100 kilodalton complexes using conventional cryo-EM , 2018, bioRxiv.
[70] E. Callaway. The revolution will not be crystallized: a new method sweeps through structural biology , 2015, Nature.
[71] V. Ramakrishnan,et al. Molecular Architecture of a Eukaryotic Translational Initiation Complex , 2013, Science.
[72] Edward M. Marcotte,et al. Classification of Single Particles from Human Cell Extract Reveals Distinct Structures , 2018, bioRxiv.
[73] Andreas Hierlemann,et al. Single-cell lysis for visual analysis by electron microscopy. , 2013, Journal of structural biology.
[74] S. Burgess,et al. Dynein structure and power stroke , 2003, Nature.
[75] G. Jensen,et al. Defocus-gradient corrected back-projection. , 2000, Ultramicroscopy.
[76] J. Dubochet,et al. Cryo-electron microscopy of vitrified specimens , 1988, Quarterly Reviews of Biophysics.
[77] H. Stahlberg,et al. Interaction of complexes I, III, and IV within the bovine respirasome by single particle cryoelectron tomography , 2011, Proceedings of the National Academy of Sciences.
[78] Jianlin Lei,et al. Single particle cryo-EM reconstruction of 52 kDa streptavidin at 3.2 Angstrom resolution , 2019, Nature communications.
[79] P. Penczek,et al. A Primer to Single-Particle Cryo-Electron Microscopy , 2015, Cell.
[80] D. J. De Rosier,et al. Reconstruction of Three Dimensional Structures from Electron Micrographs , 1968, Nature.
[81] D. Julius,et al. Structure of the TRPV1 ion channel determined by electron cryo-microscopy , 2013, Nature.
[82] R. Glaeser,et al. Opinion: hazards faced by macromolecules when confined to thin aqueous films , 2016, Biophysics reports.
[83] Qiyu Jin,et al. Iterative elastic 3D-to-2D alignment method using normal modes for studying structural dynamics of large macromolecular complexes. , 2014, Structure.
[84] B P Schoenborn,et al. Enhanced visibility of hydrogen atoms by neutron crystallography on fully deuterated myoglobin. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[85] Toh-Ming Lu,et al. Monolithic microfluidic mixing-spraying devices for time-resolved cryo-electron microscopy. , 2009, Journal of structural biology.
[86] Anchi Cheng,et al. Multiplexed TEM Specimen Preparation and Analysis of Plasmonic Nanoparticles , 2015, Microscopy and Microanalysis.
[87] Johannes Thomsen,et al. Conformational Activation Promotes CRISPR-Cas12a Catalysis and Resetting of the Endonuclease Activity , 2018, Cell.
[88] Koji Yonekura,et al. Electron crystallography of ultrathin 3D protein crystals: Atomic model with charges , 2015, Proceedings of the National Academy of Sciences.
[89] Gabriel C Lander,et al. Achieving better than 3 Å resolution by single particle cryo-EM at 200 keV , 2017, Nature Methods.
[90] Yuan He,et al. Near-atomic resolution visualization of human transcription promoter opening , 2017 .
[91] Guillermo Sapiro,et al. Atomic Resolution Cryo-EM Structure of β-Galactosidase. , 2018, Structure.
[92] J. Mahamid,et al. Unravelling molecular complexity in structural cell biology. , 2018, Current opinion in structural biology.
[93] José María Carazo,et al. MonoRes: Automatic and Accurate Estimation of Local Resolution for Electron Microscopy Maps. , 2018, Structure.
[94] David Baker,et al. Cryo‐EM model validation using independent map reconstructions , 2013, Protein science : a publication of the Protein Society.
[95] Pierre Stadelmann,et al. Effect of three-fold astigmatism on high resolution electron micrographs , 1995 .
[96] Anchi Cheng,et al. Automated data collection in single particle electron microscopy. , 2016, Microscopy.
[97] Frank DiMaio,et al. Automated structure refinement of macromolecular assemblies from cryo-EM maps using Rosetta , 2016, bioRxiv.
[98] Chuangye Yan,et al. Structural basis of pre-mRNA splicing , 2015, Science.
[99] D. Agard,et al. Electron counting and beam-induced motion correction enable near atomic resolution single particle cryoEM , 2013, Nature Methods.
[100] Yong Zi Tan,et al. Reducing effects of particle adsorption to the air-water interface in cryoEM , 2018, Nature Methods.
[101] L E Scriven,et al. Controlled environment vitrification system: an improved sample preparation technique. , 1988, Journal of electron microscopy technique.
[102] C. Russo,et al. Measuring the effects of particle orientation to improve the efficiency of electron cryomicroscopy , 2017, Nature Communications.
[103] Wah Chiu,et al. Structure of the AcrAB-TolC multidrug efflux pump , 2014, Nature.
[104] A. Cheng,et al. Beam-induced motion of vitrified specimen on holey carbon film. , 2012, Journal of structural biology.
[105] K. Nagayama,et al. Transmission electron microscopy with Zernike phase plate. , 2001, Ultramicroscopy.
[106] A. Kidera,et al. The structure of bacteriorhodopsin at 3.0 A resolution based on electron crystallography: implication of the charge distribution. , 1999, Journal of molecular biology.
[107] William J. Rice,et al. High Resolution Single Particle Cryo-Electron Microscopy using Beam-Image Shift , 2018, bioRxiv.
[108] Richard Henderson,et al. Avoiding the pitfalls of single particle cryo-electron microscopy: Einstein from noise , 2013, Proceedings of the National Academy of Sciences.
[109] J. Dubochet,et al. VITRIFICATION OF PURE WATER FOR ELECTRON MICROSCOPY , 1981 .
[110] J Pulokas,et al. Leginon: a system for fully automated acquisition of 1000 electron micrographs a day. , 1999, Ultramicroscopy.
[111] Z. Zhou,et al. 3.88 Å structure of cytoplasmic polyhedrosis virus by cryo-electron microscopy , 2008, Nature.
[112] Guanghui Yang,et al. Sampling the conformational space of the catalytic subunit of human γ-secretase , 2015, bioRxiv.
[113] W. O. Saxton,et al. The correlation averaging of a regularly arranged bacterial cell envelope protein , 1982, Journal of microscopy.
[114] Claudio Ciferri,et al. Cryo-EM in drug discovery: achievements, limitations and prospects , 2018, Nature Reviews Drug Discovery.
[115] Sjors H. W. Scheres,et al. The architecture of the spliceosomal U4/U6.U5 tri-snRNP , 2015, Nature.
[116] W. Baumeister,et al. Opening windows into the cell: focused-ion-beam milling for cryo-electron tomography. , 2013, Current opinion in structural biology.
[117] R. Egerton. Choice of operating voltage for a transmission electron microscope. , 2014, Ultramicroscopy.
[118] Markus Stabrin,et al. High-resolution Single Particle Analysis from Electron Cryo-microscopy Images Using SPHIRE , 2017, Journal of visualized experiments : JoVE.
[119] J Pulokas,et al. Leginon: an automated system for acquisition of images from vitreous ice specimens. , 2000, Journal of structural biology.
[120] Bo Liang,et al. Structure of the L Protein of Vesicular Stomatitis Virus from Electron Cryomicroscopy , 2015, Cell.
[121] Jimin Wang,et al. On the interpretation of electron microscopic maps of biological macromolecules , 2017, Protein science : a publication of the Protein Society.
[122] A. Cheng,et al. Movies of ice-embedded particles enhance resolution in electron cryo-microscopy. , 2012, Structure.
[123] Israel S. Fernández,et al. Molecular Architecture of a Eukaryotic Translational Initiation , 2014 .
[124] Alan Brown,et al. Tools for macromolecular model building and refinement into electron cryo-microscopy reconstructions , 2015, Acta crystallographica. Section D, Biological crystallography.
[125] Dmitry Lyumkis,et al. Modular Assembly of the Bacterial Large Ribosomal Subunit , 2016, Cell.
[126] Thomas Walz,et al. Negative Staining and Image Classification – Powerful Tools in Modern Electron Microscopy , 2004, Biological Procedures Online.
[127] Richard Henderson,et al. From Electron Crystallography to Single Particle CryoEM (Nobel Lecture). , 2018, Angewandte Chemie.
[128] Jimin Wang,et al. Experimental charge density from electron microscopic maps , 2017, Protein science : a publication of the Protein Society.
[129] J. Harris,et al. Negative staining and cryo-negative staining: applications in biology and medicine. , 2014, Methods in molecular biology.
[130] Bridget Carragher,et al. Software tools for molecular microscopy: an open-text Wikibook. , 2010, Methods in enzymology.
[131] Garib N Murshudov,et al. Current approaches for the fitting and refinement of atomic models into cryo-EM maps using CCP-EM , 2018, Acta crystallographica. Section D, Structural biology.
[132] Hemant D. Tagare,et al. The Local Resolution of Cryo-EM Density Maps , 2013, Nature Methods.
[133] R. Henderson. The potential and limitations of neutrons, electrons and X-rays for atomic resolution microscopy of unstained biological molecules , 1995, Quarterly Reviews of Biophysics.
[134] Zoya Ignatova,et al. Structure of a hibernating 100S ribosome reveals an inactive conformation of the ribosomal protein S1 , 2018, Nature Microbiology.
[135] S. Harrison,et al. Near-atomic resolution using electron cryomicroscopy and single-particle reconstruction , 2008, Proceedings of the National Academy of Sciences.
[136] Peter B. Rosenthal,et al. Cryomicroscopy of radiation sensitive specimens on unmodified graphene sheets: Reduction of electron-optical effects of charging☆ , 2013, Journal of structural biology.
[137] Priyanka D Abeyrathne,et al. The Affinity Grid: a pre-fabricated EM grid for monolayer purification. , 2008, Journal of molecular biology.
[138] Wen Jiang,et al. EMAN2: an extensible image processing suite for electron microscopy. , 2007, Journal of structural biology.
[139] Kathleen F Mittendorf,et al. While the revolution will not be crystallized, biochemistry reigns supreme , 2017, Protein science : a publication of the Protein Society.
[140] Prashant Rao,et al. Self-assembled monolayers improve protein distribution on holey carbon cryo-EM supports , 2014, Scientific Reports.
[141] M. van Heel,et al. Fourier shell correlation threshold criteria. , 2005, Journal of structural biology.
[142] David J. Fleet,et al. cryoSPARC: algorithms for rapid unsupervised cryo-EM structure determination , 2017, Nature Methods.
[143] Yong Zi Tan,et al. Routine single particle CryoEM sample and grid characterization by tomography , 2017, bioRxiv.
[144] R. Henderson,et al. Optimal determination of particle orientation, absolute hand, and contrast loss in single-particle electron cryomicroscopy. , 2003, Journal of molecular biology.
[145] Joachim Frank,et al. Time-resolved cryo-electron microscopy: Recent progress. , 2017, Journal of structural biology.
[146] Utz Fischer,et al. ProteoPlex: stability optimization of macromolecular complexes by sparse-matrix screening of chemical space , 2015, Nature Methods.
[147] Tanmay A M Bharat,et al. Design of a molecular support for cryo-EM structure determination , 2016, Proceedings of the National Academy of Sciences.
[148] Zbigniew Dauter,et al. High-Resolution Cryo-EM Maps and Models: A Crystallographer's Perspective. , 2017, Structure.
[149] Ruedi Aebersold,et al. The complete structure of the 55S mammalian mitochondrial ribosome , 2015, Science.
[150] Thomas Walz,et al. A practical guide to the use of monolayer purification and affinity grids. , 2010, Methods in enzymology.
[151] Erik Lindahl,et al. New tools for automated high-resolution cryo-EM structure determination in RELION-3 , 2018, eLife.
[152] J. Hirst,et al. Architecture of mammalian respiratory complex I , 2014, Nature.
[153] Tamir Gonen,et al. Three-dimensional electron crystallography of protein microcrystals , 2013, eLife.
[154] Sjors H.W. Scheres,et al. RELION: Implementation of a Bayesian approach to cryo-EM structure determination , 2012, Journal of structural biology.
[155] E. Lindahl,et al. Characterisation of molecular motions in cryo-EM single-particle data by multi-body refinement in RELION , 2018, bioRxiv.
[156] J Brink,et al. Evaluation of charging on macromolecules in electron cryomicroscopy. , 1998, Ultramicroscopy.
[157] Daniel E. Goldberg,et al. Malaria Parasite Translocon Structure and Mechanism of Effector Export , 2018, Nature.
[158] Daniel L. Minor,et al. Cryo-EM structures of the TMEM16A calcium-activated chloride channel , 2017, Nature.
[159] 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.
[160] Tamir Gonen,et al. Analysis of global and site-specific radiation damage in cryo-EM , 2018, bioRxiv.
[161] R. Henderson,et al. Detective quantum efficiency of electron area detectors in electron microscopy , 2009, Ultramicroscopy.
[162] Thomas Walz,et al. Single particle reconstructions of the transferrin-transferrin receptor complex obtained with different specimen preparation techniques. , 2006, Journal of molecular biology.
[163] Matthew L. Baker,et al. Backbone structure of the infectious ε15 virus capsid revealed by electron cryomicroscopy , 2008, Nature.
[164] R. Glaeser,et al. Near-concentric Fabry-Pérot cavity for continuous-wave laser control of electron waves. , 2017, Optics express.
[165] Jimin Wang,et al. On the appearance of carboxylates in electrostatic potential maps , 2017, Protein science : a publication of the Protein Society.
[166] Pawel A Penczek,et al. Three-dimensional spectral signal-to-noise ratio for a class of reconstruction algorithms. , 2002, Journal of structural biology.
[167] Thomas Walz,et al. Strategy for the use of affinity grids to prepare non-His-tagged macromolecular complexes for single-particle electron microscopy. , 2010, Journal of molecular biology.
[168] Carsten Sachse,et al. Thresholding of cryo-EM density maps by false discovery rate control , 2018, bioRxiv.
[169] R. Glaeser. PROTEINS, INTERFACES, AND CRYO-EM GRIDS. , 2017, Current opinion in colloid & interface science.
[170] Deborah F. Kelly,et al. Capturing Enveloped Viruses on Affinity Grids for Downstream Cryo-Electron Microscopy Applications , 2013, Microscopy and Microanalysis.
[171] J. C. Meyer,et al. The application of graphene as a sample support in transmission electron microscopy , 2012 .
[172] Robert M Glaeser,et al. Precise beam-tilt alignment and collimation are required to minimize the phase error associated with coma in high-resolution cryo-EM. , 2011, Journal of structural biology.
[173] A. Koster,et al. Conical Fourier shell correlation applied to electron tomograms. , 2015, Journal of structural biology.
[174] Rebecca F Thompson,et al. Approaches to altering particle distributions in cryo-electron microscopy sample preparation , 2018, Acta crystallographica. Section D, Structural biology.
[175] Richard Henderson,et al. Tilt-Pair Analysis of Images from a Range of Different Specimens in Single-Particle Electron Cryomicroscopy , 2011, Journal of molecular biology.
[176] N. Grigorieff,et al. Quantitative characterization of electron detectors for transmission electron microscopy. , 2013, Journal of structural biology.
[177] John P. Moore,et al. Cryo-EM Structure of a Fully Glycosylated Soluble Cleaved HIV-1 Envelope Trimer , 2013, Science.
[178] Wolfgang Baumeister,et al. Expanding the boundaries of cryo-EM with phase plates. , 2017, Current opinion in structural biology.
[179] R. Glaeser. Specimen Behavior in the Electron Beam. , 2016, Methods in enzymology.
[180] Wen Jiang,et al. Selective Capture of Histidine-tagged Proteins from Cell Lysates Using TEM grids Modified with NTA-Graphene Oxide , 2016, Scientific Reports.
[181] Yanyu Zhao,et al. Three-dimensional structure of human γ-secretase , 2014, Nature.
[182] D. DeRosier. Correction of high-resolution data for curvature of the Ewald sphere. , 2000, Ultramicroscopy.
[183] Marin van Heel,et al. Finding trimeric HIV-1 envelope glycoproteins in random noise , 2013 .
[184] A. Bartesaghi,et al. 2.2 Å resolution cryo-EM structure of β-galactosidase in complex with a cell-permeant inhibitor , 2015, Science.
[185] Deborah F. Kelly,et al. Preparation of Tunable Microchips to Visualize Native Protein Complexes for Single-Particle Electron Microscopy. , 2018, Methods in molecular biology.
[186] Henning Urlaub,et al. GraFix: sample preparation for single-particle electron cryomicroscopy , 2008, Nature Methods.
[187] Christopher J. Williams,et al. MolProbity: More and better reference data for improved all‐atom structure validation , 2018, Protein science : a publication of the Protein Society.
[188] M. Heel,et al. Exact filters for general geometry three dimensional reconstruction , 1986 .
[189] Henning Stahlberg,et al. Focus: The interface between data collection and data processing in cryo-EM. , 2017, Journal of structural biology.
[190] Yong Zi Tan,et al. Sub-2 Å Ewald curvature corrected structure of an AAV2 capsid variant , 2018, Nature Communications.
[191] Mikako Shirouzu,et al. Structural basis of the nucleosome transition during RNA polymerase II passage , 2018, Science.
[192] Yigong Shi,et al. Structure of a yeast spliceosome at 3.6-angstrom resolution , 2015, Science.
[193] Thomas C Terwilliger,et al. New tools for the analysis and validation of cryo-EM maps and atomic models , 2018, bioRxiv.
[194] Hstau Y Liao,et al. Trajectories of the ribosome as a Brownian nanomachine , 2014, Proceedings of the National Academy of Sciences.
[195] Joachim Frank,et al. Advances in the field of single-particle cryo-electron microscopy over the last decade , 2017, Nature Protocols.
[196] Joachim Frank,et al. A Fast and Effective Microfluidic Spraying-Plunging Method for High-Resolution Single-Particle Cryo-EM. , 2017, Structure.
[197] Joseph H. Davis,et al. Addressing preferred specimen orientation in single-particle cryo-EM through tilting , 2017, Nature Methods.
[198] Carsten Sachse,et al. Model-based local density sharpening of cryo-EM maps , 2017, eLife.
[199] Bijoya Paul,et al. Cryo-EM reconstruction of the chlororibosome to 3.2 Å resolution within 24 h , 2017, IUCrJ.
[200] C. Russo,et al. Progress towards an optimal specimen support for electron cryomicroscopy , 2016, Current opinion in structural biology.
[201] J. Dubochet,et al. A Reminiscence about Early Times of Vitreous Water in Electron Cryomicroscopy. , 2016, Biophysical journal.
[202] Bridget Carragher,et al. Structure of the Insulin Receptor-Insulin Complex by Single Particle CryoEM analysis , 2018, Nature.
[203] Mindy I. Davis,et al. Breaking Cryo-EM Resolution Barriers to Facilitate Drug Discovery , 2016, Cell.
[204] J. Dubochet,et al. On the Development of Electron Cryo-Microscopy (Nobel Lecture). , 2018, Angewandte Chemie.
[205] M. Baker,et al. Outcome of the First Electron Microscopy Validation Task Force Meeting , 2012, Structure.
[206] B. Carragher,et al. Spotiton: a prototype for an integrated inkjet dispense and vitrification system for cryo-TEM. , 2012, Journal of structural biology.
[207] Linquan Bai,et al. Genome engineering for microbial natural product discovery. , 2018, Current opinion in microbiology.
[208] Richard Henderson,et al. Single particle electron cryomicroscopy: trends, issues and future perspective , 2016, Quarterly Reviews of Biophysics.
[209] William J. Rice,et al. A new method for vitrifying samples for cryo-EM , 2017 .
[210] R. Turchetta,et al. Enhanced imaging in low dose electron microscopy using electron counting , 2009, Ultramicroscopy.
[211] John D. Westbrook,et al. EMDataBank.org: unified data resource for CryoEM , 2010, Nucleic Acids Res..