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Yorodumi- EMDB-1460: Near-atomic resolution using electron cryomicroscopy and single-p... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-1460 | |||||||||
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Title | Near-atomic resolution using electron cryomicroscopy and single-particle reconstruction. | |||||||||
Map data | Map of rotavirus DLP, filtered at 3.8 Angstrom resolution (cosine edge mask), and sharpened with a B-factor of -450 Angstrom squared. The deposited file contains 1/8th of the entire volume. | |||||||||
Sample |
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Biological species | Bovine rotavirus | |||||||||
Method | single particle reconstruction / cryo EM / negative staining / Resolution: 5.1 Å | |||||||||
Authors | Zhang X / Settembre E / Xu C / Dormitzer PR | |||||||||
Citation | Journal: Proc Natl Acad Sci U S A / Year: 2008 Title: Near-atomic resolution using electron cryomicroscopy and single-particle reconstruction. Authors: Xing Zhang / Ethan Settembre / Chen Xu / Philip R Dormitzer / Richard Bellamy / Stephen C Harrison / Nikolaus Grigorieff / Abstract: Electron cryomicroscopy (cryo-EM) yields images of macromolecular assemblies and their components, from which 3D structures can be determined, by using an image processing method commonly known as ...Electron cryomicroscopy (cryo-EM) yields images of macromolecular assemblies and their components, from which 3D structures can be determined, by using an image processing method commonly known as "single-particle reconstruction." During the past two decades, this technique has become an important tool for 3D structure determination, but it generally has not been possible to determine atomic models. In principle, individual molecular images contain high-resolution information contaminated by a much higher level of noise. In practice, it has been unclear whether current averaging methods are adequate to extract this information from the background. We present here a reconstruction, obtained by using recently developed image processing methods, of the rotavirus inner capsid particle ("double-layer particle" or DLP) at a resolution suitable for interpretation by an atomic model. The result establishes single-particle reconstruction as a high-resolution technique. We show by direct comparison that the cryo-EM reconstruction of viral protein 6 (VP6) of the rotavirus DLP is similar in clarity to a 3.8-A resolution map obtained from x-ray crystallography. At this resolution, most of the amino acid side chains produce recognizable density. The icosahedral symmetry of the particle was an important factor in achieving this resolution in the cryo-EM analysis, but as the size of recordable datasets increases, single-particle reconstruction also is likely to yield structures at comparable resolution from samples of much lower symmetry. This potential has broad implications for structural cell biology. | |||||||||
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_1460.map.gz | 104.5 MB | EMDB map data format | |
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Header (meta data) | emd-1460-v30.xml emd-1460.xml | 16.6 KB 16.6 KB | Display Display | EMDB header |
Images | 1460.gif | 101.6 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-1460 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-1460 | HTTPS FTP |
-Validation report
Summary document | emd_1460_validation.pdf.gz | 341.6 KB | Display | EMDB validaton report |
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Full document | emd_1460_full_validation.pdf.gz | 340.7 KB | Display | |
Data in XML | emd_1460_validation.xml.gz | 6.7 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-1460 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-1460 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_1460.map.gz / Format: CCP4 / Size: 116.4 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Map of rotavirus DLP, filtered at 3.8 Angstrom resolution (cosine edge mask), and sharpened with a B-factor of -450 Angstrom squared. The deposited file contains 1/8th of the entire volume. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.238 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 : Bovine rotavirus DLP
+Supramolecule #1000: Bovine rotavirus DLP
+Macromolecule #1: VP1
+Macromolecule #2: VP2
+Macromolecule #3: VP3
+Macromolecule #4: VP6
+Macromolecule #5: dsRNA 1
+Macromolecule #6: dsRNA 2
+Macromolecule #7: dsRNA 3
+Macromolecule #8: dsRNA 4
+Macromolecule #9: dsRNA 5
+Macromolecule #10: dsRNA 6
+Macromolecule #11: dsRNA 7
+Macromolecule #12: dsRNA 8
+Macromolecule #13: dsRNA 9
+Macromolecule #14: dsRNA 10
+Macromolecule #15: dsRNA 11
-Experimental details
-Structure determination
Method | negative staining, cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 5 mg/mL |
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Buffer | pH: 7.4 |
Staining | Type: NEGATIVE / Details: Ice |
Grid | Details: Lacy carbon and C-falt |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 30 % / Instrument: HOMEMADE PLUNGER Details: Vitrification instrument: Home-made. Vitrification carried out in air at room temperature Method: Blot for 3 seconds before plunging |
-Electron microscopy
Microscope | FEI TECNAI F30 |
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Temperature | Average: 90 K |
Alignment procedure | Legacy - Astigmatism: objective lens astigmatism was corrected Legacy - Electron beam tilt params: 0 |
Date | Jun 1, 2007 |
Image recording | Category: FILM / Film or detector model: KODAK SO-163 FILM / Digitization - Scanner: ZEISS SCAI / Digitization - Sampling interval: 7 µm / Number real images: 386 / Average electron dose: 15 e/Å2 / Od range: 1 / Bits/pixel: 8 |
Tilt angle min | 0 |
Tilt angle max | 0 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Calibrated magnification: 56540 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2 mm / Nominal defocus max: 3.5 µm / Nominal defocus min: 1.1 µm / Nominal magnification: 59000 |
Sample stage | Specimen holder: Eucentric, side-entry / Specimen holder model: GATAN LIQUID NITROGEN |
Experimental equipment | Model: Tecnai F30 / Image courtesy: FEI Company |
-Image processing
Details | Particles were selected using the computer program SIGNATURE |
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CTF correction | Details: Each particle |
Final reconstruction | Applied symmetry - Point group: I (icosahedral) / Algorithm: OTHER / Resolution.type: BY AUTHOR / Resolution: 5.1 Å / Resolution method: OTHER / Software - Name: FREALIGN / Details: Ewald sphere curvature was not corrected / Number images used: 8400 |