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      Single-particle cryo-EM structures from iDPC–STEM at near-atomic resolution

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          Abstract

          In electron cryomicroscopy (cryo-EM), molecular images of vitrified biological samples are obtained by conventional transmission microscopy (CTEM) using large underfocuses and subsequently computationally combined into a high-resolution three-dimensional structure. Here, we apply scanning transmission electron microscopy (STEM) using the integrated differential phase contrast mode also known as iDPC–STEM to two cryo-EM test specimens, keyhole limpet hemocyanin (KLH) and tobacco mosaic virus (TMV). The micrographs show complete contrast transfer to high resolution and enable the cryo-EM structure determination for KLH at 6.5 Å resolution, as well as for TMV at 3.5 Å resolution using single-particle reconstruction methods, which share identical features with maps obtained by CTEM of a previously acquired same-sized TMV data set. These data show that STEM imaging in general, and in particular the iDPC–STEM approach, can be applied to vitrified single-particle specimens to determine near-atomic resolution cryo-EM structures of biological macromolecules.

          Abstract

          This paper explores the use of scanning transmission electron microscopy (STEM) to vitrified biological samples for biomolecular structure elucidation. Integrated differential phase contrast (iDPC)–STEM imaging of keyhole limpet hemocyanin and tobacco mosaic virus enabled cryo-EM structure determination at 6.5 and 3.5 Å resolution, respectively.

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          Most cited references80

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          UCSF Chimera--a visualization system for exploratory research and analysis.

          The design, implementation, and capabilities of an extensible visualization system, UCSF Chimera, are discussed. Chimera is segmented into a core that provides basic services and visualization, and extensions that provide most higher level functionality. This architecture ensures that the extension mechanism satisfies the demands of outside developers who wish to incorporate new features. Two unusual extensions are presented: Multiscale, which adds the ability to visualize large-scale molecular assemblies such as viral coats, and Collaboratory, which allows researchers to share a Chimera session interactively despite being at separate locales. Other extensions include Multalign Viewer, for showing multiple sequence alignments and associated structures; ViewDock, for screening docked ligand orientations; Movie, for replaying molecular dynamics trajectories; and Volume Viewer, for display and analysis of volumetric data. A discussion of the usage of Chimera in real-world situations is given, along with anticipated future directions. Chimera includes full user documentation, is free to academic and nonprofit users, and is available for Microsoft Windows, Linux, Apple Mac OS X, SGI IRIX, and HP Tru64 Unix from http://www.cgl.ucsf.edu/chimera/. Copyright 2004 Wiley Periodicals, Inc.
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            cryoSPARC: algorithms for rapid unsupervised cryo-EM structure determination

            A software tool, cryoSPARC, addresses the speed bottleneck in cryo-EM image processing, enabling automated macromolecular structure determination in hours on a desktop computer without requiring a starting model.
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              UCSF ChimeraX : Structure visualization for researchers, educators, and developers

              UCSF ChimeraX is the next-generation interactive visualization program from the Resource for Biocomputing, Visualization, and Informatics (RBVI), following UCSF Chimera. ChimeraX brings (a) significant performance and graphics enhancements; (b) new implementations of Chimera's most highly used tools, many with further improvements; (c) several entirely new analysis features; (d) support for new areas such as virtual reality, light-sheet microscopy, and medical imaging data; (e) major ease-of-use advances, including toolbars with icons to perform actions with a single click, basic "undo" capabilities, and more logical and consistent commands; and (f) an app store for researchers to contribute new tools. ChimeraX includes full user documentation and is free for noncommercial use, with downloads available for Windows, Linux, and macOS from https://www.rbvi.ucsf.edu/chimerax.
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                Author and article information

                Contributors
                ivan.lazic@thermofisher.com
                c.sachse@fz-juelich.de
                Journal
                Nat Methods
                Nat Methods
                Nature Methods
                Nature Publishing Group US (New York )
                1548-7091
                1548-7105
                5 September 2022
                5 September 2022
                2022
                : 19
                : 9
                : 1126-1136
                Affiliations
                [1 ]GRID grid.433187.a, Materials and Structural Analysis Division, , Thermo Fisher Scientific, ; Eindhoven, Netherlands
                [2 ]GRID grid.483325.b, Ernst Ruska-Centre for Microscopy and Spectroscopy with Electrons (ER-C-3): Structural Biology, ; Jülich, Germany
                [3 ]GRID grid.5252.0, ISNI 0000 0004 1936 973X, Department of Chemistry and Centre for NanoScience, , Ludwig-Maximilians-University Munich, ; Munich, Germany
                [4 ]GRID grid.483325.b, Ernst Ruska-Centre for Microscopy and Spectroscopy with Electrons (ER-C-1): Physics of Nanoscale Systems, ; Jülich, Germany
                [5 ]Institute for Biological Information Processing (IBI-6): Cellular Structural Biology, Jülich, Germany
                [6 ]GRID grid.4709.a, ISNI 0000 0004 0495 846X, Structural and Computational Biology Unit, , European Molecular Biology Laboratory (EMBL), ; Heidelberg, Germany
                [7 ]GRID grid.411327.2, ISNI 0000 0001 2176 9917, Department of Biology, , Heinrich Heine University, ; Düsseldorf, Germany
                Author information
                http://orcid.org/0000-0001-5238-952X
                http://orcid.org/0000-0001-8896-1647
                http://orcid.org/0000-0002-9106-9358
                http://orcid.org/0000-0002-1168-5143
                Article
                1586
                10.1038/s41592-022-01586-0
                9467914
                36064775
                e3982808-1721-4b44-a818-e217fb9e45df
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 24 August 2021
                : 19 July 2022
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100009318, Helmholtz Association;
                Award ID: VH-NG-1317
                Award ID: ZT-I-0025
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s), under exclusive licence to Springer Nature America, Inc. 2022

                Life sciences
                cryoelectron microscopy,cryoelectron tomography
                Life sciences
                cryoelectron microscopy, cryoelectron tomography

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