+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-13779 | |||||||||
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Title | cryo iDPC-STEM structure recorded with CSA 3.0 | |||||||||
Map data | cryo iDPC-STEM structure recorded with CSA 3.0 | |||||||||
Sample |
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Keywords | tobacco mosaic virus / RNA virus / VIRUS | |||||||||
Function / homology | Tobacco mosaic virus-like, coat protein / Tobacco mosaic virus-like, coat protein superfamily / Virus coat protein (TMV like) / helical viral capsid / structural molecule activity / identical protein binding / Capsid protein Function and homology information | |||||||||
Biological species | Tobacco mosaic virus (strain vulgare) | |||||||||
Method | helical reconstruction / cryo EM / Resolution: 4.3 Å | |||||||||
Authors | Sachse C / Leidl ML | |||||||||
Funding support | Germany, 1 items
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Citation | Journal: Nat Methods / Year: 2022 Title: Single-particle cryo-EM structures from iDPC-STEM at near-atomic resolution. Authors: Ivan Lazić / Maarten Wirix / Max Leo Leidl / Felix de Haas / Daniel Mann / Maximilian Beckers / Evgeniya V Pechnikova / Knut Müller-Caspary / Ricardo Egoavil / Eric G T Bosch / Carsten Sachse / Abstract: In electron cryomicroscopy (cryo-EM), molecular images of vitrified biological samples are obtained by conventional transmission microscopy (CTEM) using large underfocuses and subsequently ...In electron cryomicroscopy (cryo-EM), molecular images of vitrified biological samples are obtained by conventional transmission microscopy (CTEM) using large underfocuses and subsequently computationally combined into a high-resolution three-dimensional structure. Here, we apply scanning transmission electron microscopy (STEM) using the integrated differential phase contrast mode also known as iDPC-STEM to two cryo-EM test specimens, keyhole limpet hemocyanin (KLH) and tobacco mosaic virus (TMV). The micrographs show complete contrast transfer to high resolution and enable the cryo-EM structure determination for KLH at 6.5 Å resolution, as well as for TMV at 3.5 Å resolution using single-particle reconstruction methods, which share identical features with maps obtained by CTEM of a previously acquired same-sized TMV data set. These data show that STEM imaging in general, and in particular the iDPC-STEM approach, can be applied to vitrified single-particle specimens to determine near-atomic resolution cryo-EM structures of biological macromolecules. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_13779.map.gz | 7.1 MB | EMDB map data format | |
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Header (meta data) | emd-13779-v30.xml emd-13779.xml | 15.4 KB 15.4 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_13779_fsc.xml | 10.7 KB | Display | FSC data file |
Images | emd_13779.png | 120.5 KB | ||
Masks | emd_13779_msk_1.map | 103 MB | Mask map | |
Filedesc metadata | emd-13779.cif.gz | 5.3 KB | ||
Others | emd_13779_half_map_1.map.gz emd_13779_half_map_2.map.gz | 80.5 MB 80.6 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-13779 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-13779 | HTTPS FTP |
-Validation report
Summary document | emd_13779_validation.pdf.gz | 809.5 KB | Display | EMDB validaton report |
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Full document | emd_13779_full_validation.pdf.gz | 809 KB | Display | |
Data in XML | emd_13779_validation.xml.gz | 16.4 KB | Display | |
Data in CIF | emd_13779_validation.cif.gz | 21 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-13779 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-13779 | HTTPS FTP |
-Related structure data
Related structure data | 7q23MC 7q22C 7q2qC 7q2rC 7q2sC M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_13779.map.gz / Format: CCP4 / Size: 30.9 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | cryo iDPC-STEM structure recorded with CSA 3.0 | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. generated in cubic-lattice coordinate | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.23 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Mask #1
File | emd_13779_msk_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: half-map2
File | emd_13779_half_map_1.map | ||||||||||||
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Annotation | half-map2 | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: half-map1
File | emd_13779_half_map_2.map | ||||||||||||
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Annotation | half-map1 | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Tobacco mosaic virus
Entire | Name: Tobacco mosaic virus |
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Components |
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-Supramolecule #1: Tobacco mosaic virus
Supramolecule | Name: Tobacco mosaic virus / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: Tobacco mosaic virus (strain vulgare) |
Molecular weight | Theoretical: 131 kDa/nm |
-Macromolecule #1: Capsid protein
Macromolecule | Name: Capsid protein / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Tobacco mosaic virus (strain vulgare) / Strain: vulgare |
Molecular weight | Theoretical: 17.091998 KDa |
Sequence | String: SYSITTPSQF VFLSSAWADP IELINLCTNA LGNQFQTQQA RTVVQRQFSE VWKPSPQVTV RFPDSDFKVY RYNAVLDPLV TALLGAFDT RNRIIEVENQ ANPTTAETLD ATRRVDDATV AIRSAINNLI VELIRGTGSY NRSSFESSSG LVWT UniProtKB: Capsid protein |
-Macromolecule #2: RNA (5'-R(P*GP*AP*A)-3')
Macromolecule | Name: RNA (5'-R(P*GP*AP*A)-3') / type: rna / ID: 2 / Number of copies: 1 |
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Source (natural) | Organism: Tobacco mosaic virus (strain vulgare) / Strain: vulgare |
Molecular weight | Theoretical: 958.66 Da |
Sequence | String: GAA |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | helical reconstruction |
Aggregation state | helical array |
-Sample preparation
Concentration | 90 mg/mL |
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Buffer | pH: 7.4 |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV Details: blot force of +10 and a duration for blotting of 10 seconds. |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Details | iDPC-STEM |
Image recording | Film or detector model: OTHER / Average electron dose: 35.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: OTHER / Imaging mode: OTHER |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |