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Yorodumi- EMDB-42515: Intracellular Ebola nucleocapsid-like structure obtained from cel... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-42515 | |||||||||
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Title | Intracellular Ebola nucleocapsid-like structure obtained from cells expressing NP, VP24 and VP35 at 17.6 angstrom | |||||||||
Map data | intracellular Ebola virus nucelocapsid from cells expressing NP, VP24 and VP35 | |||||||||
Sample |
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Keywords | VIRAL PROTEIN / nucleoprotein / nucleocapsid / Ebola virus / EBOV / filovirus / subtomogram averaging / cryo-ET / FIB / intracellular / in situ | |||||||||
Biological species | Ebola virus - Mayinga, Zaire, 1976 | |||||||||
Method | subtomogram averaging / cryo EM / Resolution: 17.57 Å | |||||||||
Authors | Watanabe R / Zyla D / Saphire EO | |||||||||
Funding support | 1 items
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Citation | Journal: Cell / Year: 2024 Title: Intracellular Ebola virus nucleocapsid assembly revealed by in situ cryo-electron tomography. Authors: Reika Watanabe / Dawid Zyla / Diptiben Parekh / Connor Hong / Ying Jones / Sharon L Schendel / William Wan / Guillaume Castillon / Erica Ollmann Saphire / Abstract: Filoviruses, including the Ebola and Marburg viruses, cause hemorrhagic fevers with up to 90% lethality. The viral nucleocapsid is assembled by polymerization of the nucleoprotein (NP) along the ...Filoviruses, including the Ebola and Marburg viruses, cause hemorrhagic fevers with up to 90% lethality. The viral nucleocapsid is assembled by polymerization of the nucleoprotein (NP) along the viral genome, together with the viral proteins VP24 and VP35. We employed cryo-electron tomography of cells transfected with viral proteins and infected with model Ebola virus to illuminate assembly intermediates, as well as a 9 Å map of the complete intracellular assembly. This structure reveals a previously unresolved third and outer layer of NP complexed with VP35. The intrinsically disordered region, together with the C-terminal domain of this outer layer of NP, provides the constant width between intracellular nucleocapsid bundles and likely functions as a flexible tether to the viral matrix protein in the virion. A comparison of intracellular nucleocapsids with prior in-virion nucleocapsid structures reveals that the nucleocapsid further condenses vertically in the virion. The interfaces responsible for nucleocapsid assembly are highly conserved and offer targets for broadly effective antivirals. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_42515.map.gz | 580.6 KB | EMDB map data format | |
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Header (meta data) | emd-42515-v30.xml emd-42515.xml | 14.5 KB 14.5 KB | Display Display | EMDB header |
Images | emd_42515.png | 94.7 KB | ||
Masks | emd_42515_msk_1.map | 1.4 MB | Mask map | |
Filedesc metadata | emd-42515.cif.gz | 4.4 KB | ||
Others | emd_42515_half_map_1.map.gz emd_42515_half_map_2.map.gz | 1 MB 1 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-42515 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-42515 | HTTPS FTP |
-Validation report
Summary document | emd_42515_validation.pdf.gz | 704.5 KB | Display | EMDB validaton report |
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Full document | emd_42515_full_validation.pdf.gz | 704 KB | Display | |
Data in XML | emd_42515_validation.xml.gz | 7.3 KB | Display | |
Data in CIF | emd_42515_validation.cif.gz | 8.5 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42515 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-42515 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_42515.map.gz / Format: CCP4 / Size: 1.4 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | intracellular Ebola virus nucelocapsid from cells expressing NP, VP24 and VP35 | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 5.37 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Mask #1
File | emd_42515_msk_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: half map1
File | emd_42515_half_map_1.map | ||||||||||||
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Annotation | half map1 | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: half map2
File | emd_42515_half_map_2.map | ||||||||||||
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Annotation | half map2 | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Ebola virus - Mayinga, Zaire, 1976
Entire | Name: Ebola virus - Mayinga, Zaire, 1976 |
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Components |
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-Supramolecule #1: Ebola virus - Mayinga, Zaire, 1976
Supramolecule | Name: Ebola virus - Mayinga, Zaire, 1976 / type: virus / ID: 1 / Parent: 0 / NCBI-ID: 128952 / Sci species name: Ebola virus - Mayinga, Zaire, 1976 / Virus type: VIRUS-LIKE PARTICLE / Virus isolate: OTHER / Virus enveloped: No / Virus empty: No |
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Host (natural) | Organism: Homo sapiens (human) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | subtomogram averaging |
Aggregation state | cell |
-Sample preparation
Buffer | pH: 7.2 |
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Grid | Model: Quantifoil / Material: COPPER / Mesh: 200 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE |
Vitrification | Cryogen name: ETHANE-PROPANE |
Details | FIB-milled-plunge-frozen cell expressing EBOV NP, VP24 and VP35 |
-Electron microscopy
Microscope | TFS KRIOS |
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Specialist optics | Energy filter - Name: GIF Bioquantum / Energy filter - Slit width: 20 eV |
Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 3.5 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 70.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 5.5 µm / Nominal defocus min: 4.5 µm |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Resolution.type: BY AUTHOR / Resolution: 17.57 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: RELION (ver. 3.1) / Number subtomograms used: 8371 |
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Extraction | Number tomograms: 10 / Number images used: 39000 |
Final 3D classification | Number classes: 3 / Avg.num./class: 13000 / Software - Name: RELION (ver. 3.1) |
Final angle assignment | Type: MAXIMUM LIKELIHOOD / Software - Name: RELION (ver. 3.1) |