Determination of the ribosome structure to a resolution of 2.5 Å by single‐particle cryo‐EM

With the advance of new instruments and algorithms, and the accumulation of experience over decades, single‐particle cryo‐EM has become a pivotal part of structural biology. Recently, we determined the structure of a eukaryotic ribosome at 2.5 Å for the large subunit. The ribosome was derived from Trypanosoma cruzi, the protozoan pathogen of Chagas disease. The high‐resolution density map allowed us to discern a large number of unprecedented details including rRNA modifications, water molecules, and ions such as Mg2+ and Zn2+. In this paper, we focus on the procedures for data collection, image processing, and modeling, with particular emphasis on factors that contributed to the attainment of high resolution. The methods described here are readily applicable to other macromolecules for high‐resolution reconstruction by single‐particle cryo‐EM.

[1]  J. Frank,et al.  Structure and assembly model for the Trypanosoma cruzi 60S ribosomal subunit , 2016, Proceedings of the National Academy of Sciences.

[2]  J. Frank,et al.  Structural Basis for Gating and Activation of RyR1 , 2016, Cell.

[3]  Yigong Shi,et al.  Structure of a yeast activated spliceosome at 3.5 Å resolution , 2016, Science.

[4]  G. Skiniotis,et al.  2.8-Å Cryo-EM Structure of the Large Ribosomal Subunit from the Eukaryotic Parasite Leishmania. , 2016, Cell reports.

[5]  C O S Sorzano,et al.  Scipion: A software framework toward integration, reproducibility and validation in 3D electron microscopy. , 2016, Journal of structural biology.

[6]  Mindy I. Davis,et al.  Breaking Cryo-EM Resolution Barriers to Facilitate Drug Discovery , 2016, Cell.

[7]  W. Baumeister,et al.  Cryo-EM single particle analysis with the Volta phase plate , 2016, eLife.

[8]  Wen Jiang,et al.  2.9 Å Resolution Cryo-EM 3D Reconstruction of Close-Packed Virus Particles. , 2016, Structure.

[9]  Dmitry Lyumkis,et al.  Single-particle cryoEM analysis at near-atomic resolution from several thousand asymmetric subunits. , 2015, Journal of structural biology.

[10]  David A Agard,et al.  Asynchronous data acquisition and on-the-fly analysis of dose fractionated cryoEM images by UCSFImage. , 2015, Journal of structural biology.

[11]  Joachim Frank,et al.  Dynamical features of the Plasmodium falciparum ribosome during translation , 2015, Nucleic acids research.

[12]  Guanghui Yang,et al.  Sampling the conformational space of the catalytic subunit of human γ-secretase , 2015, bioRxiv.

[13]  Nikolaus Grigorieff,et al.  Measuring the optimal exposure for single particle cryo-EM using a 2.6 Å reconstruction of rotavirus VP6 , 2015, eLife.

[14]  J. Frank,et al.  Activation of GTP hydrolysis in mRNA-tRNA translocation by elongation factor G , 2015, Science Advances.

[15]  Xueming Li,et al.  Alignment of direct detection device micrographs using a robust Optical Flow approach. , 2015, Journal of structural biology.

[16]  Marina V. Rodnina,et al.  Structure of the E. coli ribosome–EF-Tu complex at <3 Å resolution by Cs-corrected cryo-EM , 2015, Nature.

[17]  Alan Brown,et al.  Tools for macromolecular model building and refinement into electron cryo-microscopy reconstructions , 2015, Acta crystallographica. Section D, Biological crystallography.

[18]  Alan Brown,et al.  Structure of the large ribosomal subunit from human mitochondria , 2014, Science.

[19]  J. Frank,et al.  Structure of a mammalian ryanodine receptor , 2014, Nature.

[20]  W. Chiu,et al.  Capsid expansion mechanism of bacteriophage T7 revealed by multistate atomic models derived from cryo-EM reconstructions , 2014, Proceedings of the National Academy of Sciences.

[21]  Marcus A. Brubaker,et al.  Alignment of cryo-EM movies of individual particles by optimization of image translations. , 2014, Journal of structural biology.

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

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

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

[25]  J. Frank,et al.  High-resolution cryo-electron microscopy structure of the Trypanosoma brucei ribosome , 2013, Nature.

[26]  Zheng Liu,et al.  A graph theory method for determination of cryo-EM image focuses. , 2012, Journal of structural biology.

[27]  Henning Stahlberg,et al.  Limiting factors in single particle cryo electron tomography , 2012, Computational and structural biotechnology journal.

[28]  M. Baker,et al.  Outcome of the First Electron Microscopy Validation Task Force Meeting , 2012, Structure.

[29]  Sjors H.W. Scheres,et al.  A Bayesian View on Cryo-EM Structure Determination , 2012, 2012 9th IEEE International Symposium on Biomedical Imaging (ISBI).

[30]  Sergey Melnikov,et al.  The Structure of the Eukaryotic Ribosome at 3.0 Å Resolution , 2011, Science.

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

[32]  Nikolaus Grigorieff,et al.  Near-atomic resolution reconstructions of icosahedral viruses from electron cryo-microscopy. , 2011, Current opinion in structural biology.

[33]  Johannes Söding,et al.  Cryo-EM structure and rRNA model of a translating eukaryotic 80S ribosome at 5.5-Å resolution , 2010, Proceedings of the National Academy of Sciences.

[34]  Eileen Kraemer,et al.  TriTrypDB: a functional genomic resource for the Trypanosomatidae , 2009, Nucleic Acids Res..

[35]  J. Frank Single-particle reconstruction of biological macromolecules in electron microscopy – 30 years , 2009, Quarterly Reviews of Biophysics.

[36]  Christian Suloway,et al.  Fully automated, sequential tilt-series acquisition with Leginon. , 2009, Journal of structural biology.

[37]  Christopher Irving,et al.  Appion: an integrated, database-driven pipeline to facilitate EM image processing. , 2009, Journal of structural biology.

[38]  Joachim Frank,et al.  Exploration of parameters in cryo-EM leading to an improved density map of the E. coli ribosome. , 2008, Journal of structural biology.

[39]  David A Agard,et al.  Electron energy filtering significantly improves amplitude contrast of frozen-hydrated protein at 300kV. , 2006, Journal of structural biology.

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

[41]  Joachim Frank,et al.  Automated acquisition of cryo-electron micrographs for single particle reconstruction on an FEI Tecnai electron microscope. , 2005, Journal of structural biology.

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

[43]  J M Carazo,et al.  XMIPP: a new generation of an open-source image processing package for electron microscopy. , 2004, Journal of structural biology.

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

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

[46]  Randy J Read,et al.  Electronic Reprint Biological Crystallography Phenix: Building New Software for Automated Crystallographic Structure Determination Biological Crystallography Phenix: Building New Software for Automated Crystallographic Structure Determination , 2022 .

[47]  Heymann Jb,et al.  Bsoft: Image and Molecular Processing in Electron Microscopy , 2001 .

[48]  Liu Zhen Revolutionary Breakthrough of Structure Determination——Recent Advances of Electron Direct Detection Device Application in Cryo-EM , 2014 .

[49]  Sergey V. Melnikov,et al.  The structure of the eukaryotic ribosome at 3.0 angstrom resolution. , 2011 .

[50]  Wah Chiu,et al.  JADAS: a customizable automated data acquisition system and its application to ice-embedded single particles. , 2009, Journal of structural biology.

[51]  Nikolaus Grigorieff,et al.  FREALIGN: high-resolution refinement of single particle structures. , 2007, Journal of structural biology.

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

[53]  Chao Yang,et al.  SPARX, a new environment for Cryo-EM image processing. , 2007, Journal of structural biology.

[54]  J B Heymann,et al.  Bsoft: image and molecular processing in electron microscopy. , 2001, Journal of structural biology.

[55]  A Leith,et al.  SPIDER and WEB: processing and visualization of images in 3D electron microscopy and related fields. , 1996, Journal of structural biology.

[56]  M van Heel,et al.  A new generation of the IMAGIC image processing system. , 1996, Journal of structural biology.

[57]  R. Wade,et al.  Electron microscope transfer functions for partially coherent axial illumination and chromatic defocus spread , 1977 .