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- EMDB-5377: Direct electron detection yields cryo-EM reconstructions at resol... -
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Open data
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Basic information
Entry | Database: EMDB / ID: EMD-5377 | |||||||||
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Title | Direct electron detection yields cryo-EM reconstructions at resolutions beyond .75 Nyquist frequency | |||||||||
![]() | Icosahedral reconstruction of bacteriophage epsilon 15 | |||||||||
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![]() | Cryo-EM / Electron cryo-microscopy / Direct detection device / Active pixel sensor / CMOS detector / Nyquist frequency | |||||||||
Biological species | ![]() ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 7.9 Å | |||||||||
![]() | Bammes BE / Rochat RH / Jakana J / Chen D / Chiu W | |||||||||
![]() | ![]() Title: Direct electron detection yields cryo-EM reconstructions at resolutions beyond 3/4 Nyquist frequency. Authors: Benjamin E Bammes / Ryan H Rochat / Joanita Jakana / Dong-Hua Chen / Wah Chiu / ![]() Abstract: One limitation in electron cryo-microscopy (cryo-EM) is the inability to recover high-resolution signal from the image-recording media at the full-resolution limit of the transmission electron ...One limitation in electron cryo-microscopy (cryo-EM) is the inability to recover high-resolution signal from the image-recording media at the full-resolution limit of the transmission electron microscope. Direct electron detection using CMOS-based sensors for digitally recording images has the potential to alleviate this shortcoming. Here, we report a practical performance evaluation of a Direct Detection Device (DDD®) for biological cryo-EM at two different microscope voltages: 200 and 300 kV. Our DDD images of amorphous and graphitized carbon show strong per-pixel contrast with image resolution near the theoretical sampling limit of the data. Single-particle reconstructions of two frozen-hydrated bacteriophages, P22 and ε15, establish that the DDD is capable of recording usable signal for 3D reconstructions at about 4/5 of the Nyquist frequency, which is a vast improvement over the performance of conventional imaging media. We anticipate the unparalleled performance of this digital recording device will dramatically benefit cryo-EM for routine tomographic and single-particle structural determination of biological specimens. | |||||||||
History |
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Structure visualization
Movie |
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Structure viewer | EM map: ![]() ![]() ![]() |
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 112.8 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 10.4 KB 10.4 KB | Display Display | ![]() |
Images | ![]() | 110.2 KB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 78.3 KB | Display | ![]() |
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Full document | ![]() | 77.4 KB | Display | |
Data in XML | ![]() | 493 B | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
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Links
EMDB pages | ![]() ![]() |
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Map
File | ![]() | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Icosahedral reconstruction of bacteriophage epsilon 15 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 3.04 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
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Sample components
-Entire : Bacteriophage Epsilon-15
Entire | Name: Bacteriophage Epsilon-15 |
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Components |
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-Supramolecule #1000: Bacteriophage Epsilon-15
Supramolecule | Name: Bacteriophage Epsilon-15 / type: sample / ID: 1000 / Details: Sample was vitrified / Number unique components: 1 |
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-Supramolecule #1: Salmonella phage epsilon15
Supramolecule | Name: Salmonella phage epsilon15 / type: virus / ID: 1 / Name.synonym: Epsilon 15 / NCBI-ID: 215158 / Sci species name: Salmonella phage epsilon15 / Database: NCBI / Virus type: VIRION / Virus isolate: STRAIN / Virus enveloped: No / Virus empty: No / Syn species name: Epsilon 15 |
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Host (natural) | Organism: ![]() |
Virus shell | Shell ID: 1 / Name: capsid / Diameter: 700 Å / T number (triangulation number): 7 |
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | single particle reconstruction |
Aggregation state | particle |
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Sample preparation
Buffer | pH: 7.5 |
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Grid | Details: 400 mesh copper grid |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 95 % / Chamber temperature: 170 K / Instrument: OTHER / Details: Vitrification instrument: Vitrobot / Method: Blot for 1.5 seconds before plunging |
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Electron microscopy
Microscope | JEOL 3200FSC |
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Temperature | Min: 100 K / Max: 100 K / Average: 100 K |
Alignment procedure | Legacy - Astigmatism: objective lens astigmatism was corrected at 400,000 times magnification |
Specialist optics | Energy filter - Name: Omega / Energy filter - Lower energy threshold: 15.0 eV / Energy filter - Upper energy threshold: 20.0 eV |
Date | Mar 6, 2010 |
Image recording | Category: CCD / Film or detector model: DIRECT ELECTRON DE-12 (4k x 3k) / Digitization - Sampling interval: 6 µm / Number real images: 75 / Average electron dose: 20 e/Å2 Details: Digital images were collected on a CMOS type direct electron detection device DE-12 from Direct Electron |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Calibrated magnification: 20800 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 4.1 mm / Nominal defocus max: 3.0 µm / Nominal defocus min: 0.6 µm / Nominal magnification: 20000 |
Sample stage | Specimen holder: Eucentric / Specimen holder model: JEOL 3200FSC CRYOHOLDER |
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Image processing
Details | Grids were coated in thin carbon before applying sample |
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CTF correction | Details: Each Micrograph |
Final reconstruction | Algorithm: OTHER / Resolution.type: BY AUTHOR / Resolution: 7.9 Å / Resolution method: FSC 0.5 CUT-OFF / Software - Name: MPSA Details: Resolution was calculated at 7.9 Angstroms by the 0.5 FSC criterion and 6.8 Angstroms by the 0.143 FSC criterion both in comparison with the previously published 4.5 Angstrom resolution reconstruction. Number images used: 1380 |