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Yorodumi- EMDB-32600: Structure of Coxsackievirus A10 for critical dose measurement at ... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-32600 | |||||||||
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Title | Structure of Coxsackievirus A10 for critical dose measurement at 120 kV | |||||||||
Map data | Coxsackievirus A10 at 120 kV for critical dose measurement. | |||||||||
Sample |
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Keywords | Coxsackievirus A10 / VIRUS | |||||||||
Biological species | Coxsackievirus A10 | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.49 Å | |||||||||
Authors | Zhu DJ / Zhang XZ | |||||||||
Funding support | China, 1 items
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Citation | Journal: Commun Biol / Year: 2022 Title: An electron counting algorithm improves imaging of proteins with low-acceleration-voltage cryo-electron microscope. Authors: Dongjie Zhu / Huigang Shi / Chunling Wu / Xinzheng Zhang / Abstract: Relative to the 300-kV accelerating field, electrons accelerated under lower voltages are potentially scattered more strongly. Lowering the accelerate voltage has been suggested to enhance the signal- ...Relative to the 300-kV accelerating field, electrons accelerated under lower voltages are potentially scattered more strongly. Lowering the accelerate voltage has been suggested to enhance the signal-to-noise ratio (SNR) of cryo-electron microscopy (cryo-EM) images of small-molecular-weight proteins (<100 kD). However, the detection efficient of current Direct Detection Devices (DDDs) and temporal coherence of cryo-EM decrease at lower voltage, leading to loss of SNR. Here, we present an electron counting algorithm to improve the detection of low-energy electrons. The counting algorithm increased the SNR of 120-kV and 200-kV cryo-EM image from a Falcon III camera by 8%, 20% at half the Nyquist frequency and 21%, 80% at Nyquist frequency, respectively, resulting in a considerable improvement in resolution of 3D reconstructions. Our results indicate that with further improved temporal coherence and a dedicated designed camera, a 120-kV cryo-electron microscope has potential to match the 300-kV microscope at imaging small proteins. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_32600.map.gz | 162 MB | EMDB map data format | |
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Header (meta data) | emd-32600-v30.xml emd-32600.xml | 8.1 KB 8.1 KB | Display Display | EMDB header |
Images | emd_32600.png | 152.4 KB | ||
Filedesc metadata | emd-32600.cif.gz | 3.7 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-32600 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-32600 | HTTPS FTP |
-Validation report
Summary document | emd_32600_validation.pdf.gz | 671.9 KB | Display | EMDB validaton report |
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Full document | emd_32600_full_validation.pdf.gz | 671.5 KB | Display | |
Data in XML | emd_32600_validation.xml.gz | 7.6 KB | Display | |
Data in CIF | emd_32600_validation.cif.gz | 8.7 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-32600 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-32600 | HTTPS FTP |
-Related structure data
Related structure data | C: citing same article (ref.) |
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-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_32600.map.gz / Format: CCP4 / Size: 343 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | Coxsackievirus A10 at 120 kV for critical dose measurement. | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.03 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Sample components
-Entire : Coxsackievirus A10
Entire | Name: Coxsackievirus A10 |
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Components |
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-Supramolecule #1: Coxsackievirus A10
Supramolecule | Name: Coxsackievirus A10 / type: virus / ID: 1 / Parent: 0 / NCBI-ID: 42769 / Sci species name: Coxsackievirus A10 / Virus type: VIRION / Virus isolate: OTHER / Virus enveloped: No / Virus empty: No |
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-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 7.4 |
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Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Detector mode: OTHER / Digitization - Dimensions - Width: 5760 pixel / Digitization - Dimensions - Height: 4092 pixel / Average electron dose: 36.82 e/Å2 |
Electron beam | Acceleration voltage: 120 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 1.8 µm / Nominal defocus min: 0.6 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Startup model | Type of model: EMDB MAP EMDB ID: |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 3.49 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: RELION (ver. 3.1) / Number images used: 25237 |
Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
Final angle assignment | Type: MAXIMUM LIKELIHOOD |