+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-2782 | |||||||||
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Title | Cryo-electron microscopy of Rice dwarf virus virion | |||||||||
Map data | 3D reconstruction of Rice dwarf virus virion | |||||||||
Sample |
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Keywords | Rice dwarf virus / Phytoreovirus / Reoviridae family / Virus particle | |||||||||
Biological species | Rice dwarf virus | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 13.0 Å | |||||||||
Authors | Miyazaki N / Higashiura A / Higashiura T / Akita F / Hibino H / Omura T / Nakagawa A / Iwasaki K | |||||||||
Citation | Journal: J Biochem / Year: 2016 Title: Electron microscopic imaging revealed the flexible filamentous structure of the cell attachment protein P2 of Rice dwarf virus located around the icosahedral 5-fold axes. Authors: Naoyuki Miyazaki / Akifumi Higashiura / Tomoko Higashiura / Fusamichi Akita / Hiroyuki Hibino / Toshihiro Omura / Atsushi Nakagawa / Kenji Iwasaki / Abstract: The minor outer capsid protein P2 of Rice dwarf virus (RDV), a member of the genus Phytoreovirus in the family Reoviridae, is essential for viral cell entry. Here, we clarified the structure of P2 ...The minor outer capsid protein P2 of Rice dwarf virus (RDV), a member of the genus Phytoreovirus in the family Reoviridae, is essential for viral cell entry. Here, we clarified the structure of P2 and the interactions to host insect cells. Negative stain electron microscopy (EM) showed that P2 proteins are monomeric and flexible L-shaped filamentous structures of ∼20 nm in length. Cryo-EM structure revealed the spatial arrangement of P2 in the capsid, which was prescribed by the characteristic virion structure. The P2 proteins were visualized as partial rod-shaped structures of ∼10 nm in length in the cryo-EM map and accommodated in crevasses on the viral surface around icosahedral 5-fold axes with hydrophobic interactions. The remaining disordered region of P2 assumed to be extended to the radial direction towards exterior. Electron tomography clearly showed that RDV particles were away from the cellular membrane at a uniform distance and several spike-like densities, probably corresponding to P2, connecting a viral particle to the host cellular membrane during cell entry. By combining the in vitro and in vivo structural information, we could gain new insights into the detailed mechanism of the cell entry of RDV. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_2782.map.gz | 193.6 MB | EMDB map data format | |
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Header (meta data) | emd-2782-v30.xml emd-2782.xml | 7.8 KB 7.8 KB | Display Display | EMDB header |
Images | emd_2782.png | 279.4 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-2782 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-2782 | HTTPS FTP |
-Validation report
Summary document | emd_2782_validation.pdf.gz | 221.8 KB | Display | EMDB validaton report |
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Full document | emd_2782_full_validation.pdf.gz | 220.9 KB | Display | |
Data in XML | emd_2782_validation.xml.gz | 7.6 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-2782 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-2782 | HTTPS FTP |
-Related structure data
Similar structure data |
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-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_2782.map.gz / Format: CCP4 / Size: 238.4 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | 3D reconstruction of Rice dwarf virus virion | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 2.93 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Sample components
-Entire : Rice dwarf virus virion
Entire | Name: Rice dwarf virus virion |
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Components |
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-Supramolecule #1000: Rice dwarf virus virion
Supramolecule | Name: Rice dwarf virus virion / type: sample / ID: 1000 / Oligomeric state: Icosahedral particle / Number unique components: 1 |
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Molecular weight | Experimental: 75 MDa / Theoretical: 75 MDa |
-Supramolecule #1: Rice dwarf virus
Supramolecule | Name: Rice dwarf virus / type: virus / ID: 1 / NCBI-ID: 10991 / Sci species name: Rice dwarf virus / Virus type: VIRION / Virus isolate: SPECIES / Virus enveloped: No / Virus empty: No |
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Host (natural) | Organism: Oryza sativa (Asian cultivated rice) / synonym: PLANTAE(HIGHER PLANTS) |
Molecular weight | Experimental: 75 MDa / Theoretical: 75 MDa |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 6.2 / Details: 100mM Histidine, 10mM MgCl2 |
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Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 120 K / Instrument: FEI VITROBOT MARK III |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Date | Mar 23, 2011 |
Image recording | Category: CCD / Film or detector model: GATAN ULTRASCAN 4000 (4k x 4k) |
Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
CTF correction | Details: Each particle |
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Final reconstruction | Applied symmetry - Point group: I (icosahedral) / Resolution.type: BY AUTHOR / Resolution: 13.0 Å / Resolution method: OTHER / Software - Name: EMAN2 / Number images used: 1034 |