[English] 日本語
Yorodumi- EMDB-2910: Cryo electron microscopy of actively translating human polysomes ... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-2910 | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Title | Cryo electron microscopy of actively translating human polysomes (pre-recycling state). | |||||||||
Map data | pre-recycling state of human polysomes | |||||||||
Sample |
| |||||||||
Keywords | mammalian ribosome / translation / polysome / cryo electron microscopy / elongation cycle | |||||||||
Biological species | Homo sapiens (human) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 8.0 Å | |||||||||
Authors | Behrmann E / Loerke J / Budkevich TV / Yamamoto K / Schmidt A / Penczek PA / Vos MR / Burger J / Mielke T / Scheerer P / Spahn CMT | |||||||||
Citation | Journal: Cell / Year: 2015 Title: Structural snapshots of actively translating human ribosomes. Authors: Elmar Behrmann / Justus Loerke / Tatyana V Budkevich / Kaori Yamamoto / Andrea Schmidt / Pawel A Penczek / Matthijn R Vos / Jörg Bürger / Thorsten Mielke / Patrick Scheerer / Christian M T Spahn / Abstract: Macromolecular machines, such as the ribosome, undergo large-scale conformational changes during their functional cycles. Although their mode of action is often compared to that of mechanical ...Macromolecular machines, such as the ribosome, undergo large-scale conformational changes during their functional cycles. Although their mode of action is often compared to that of mechanical machines, a crucial difference is that, at the molecular dimension, thermodynamic effects dominate functional cycles, with proteins fluctuating stochastically between functional states defined by energetic minima on an energy landscape. Here, we have used cryo-electron microscopy to image ex-vivo-derived human polysomes as a source of actively translating ribosomes. Multiparticle refinement and 3D variability analysis allowed us to visualize a variety of native translation intermediates. Significantly populated states include not only elongation cycle intermediates in pre- and post-translocational states, but also eEF1A-containing decoding and termination/recycling complexes. Focusing on the post-translocational state, we extended this assessment to the single-residue level, uncovering striking details of ribosome-ligand interactions and identifying both static and functionally important dynamic elements. | |||||||||
History |
|
-Structure visualization
Movie |
Movie viewer |
---|---|
Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_2910.map.gz | 8.8 MB | EMDB map data format | |
---|---|---|---|---|
Header (meta data) | emd-2910-v30.xml emd-2910.xml | 10.7 KB 10.7 KB | Display Display | EMDB header |
Images | pre-rec.tif | 2.2 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-2910 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-2910 | HTTPS FTP |
-Validation report
Summary document | emd_2910_validation.pdf.gz | 255.6 KB | Display | EMDB validaton report |
---|---|---|---|---|
Full document | emd_2910_full_validation.pdf.gz | 254.7 KB | Display | |
Data in XML | emd_2910_validation.xml.gz | 6.1 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-2910 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-2910 | HTTPS FTP |
-Related structure data
Related structure data | 2875C 2902C 2903C 2904C 2905C 2906C 2907C 2908C 2909C 2911C 5aj0C C: citing same article (ref.) |
---|---|
Similar structure data |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
---|---|
Related items in Molecule of the Month |
-Map
File | Download / File: emd_2910.map.gz / Format: CCP4 / Size: 29.8 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Annotation | pre-recycling state of human polysomes | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.89 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
|
-Supplemental data
-Sample components
-Entire : Native ribosomal complex from polysomes - pre-recycling state
Entire | Name: Native ribosomal complex from polysomes - pre-recycling state |
---|---|
Components |
|
-Supramolecule #1000: Native ribosomal complex from polysomes - pre-recycling state
Supramolecule | Name: Native ribosomal complex from polysomes - pre-recycling state type: sample / ID: 1000 / Details: The sample was monodisperse / Number unique components: 1 |
---|---|
Molecular weight | Experimental: 4.5 MDa / Theoretical: 4.5 MDa |
-Supramolecule #1: 80S ribosomal complex
Supramolecule | Name: 80S ribosomal complex / type: complex / ID: 1 / Name.synonym: 80S ribosome Details: The sample was isolated as polysomes from the cell. Structural analysis shows that the complex contains 2 tRNAs and mRNA. Recombinant expression: No / Ribosome-details: ribosome-eukaryote: ALL |
---|---|
Source (natural) | Organism: Homo sapiens (human) / synonym: Human / Tissue: Kidney / Cell: HEK 293T / Location in cell: Cytoplasm |
Molecular weight | Experimental: 4.5 MDa / Theoretical: 4.5 MDa |
-Experimental details
-Structure determination
Method | cryo EM |
---|---|
Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 3.5 mg/mL |
---|---|
Buffer | pH: 7.5 Details: 20 mM Hepes-KOH, pH 7.5, 100 mM KCl, 1.5 mM MgCl2, 0.5 mM spermidine, 0.04 mM spermine, 1 mM DTT |
Grid | Details: Quantifoil grids with additional continuous carbon support |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 93 K / Instrument: FEI VITROBOT MARK II / Method: blot for 2-4 seconds before plunging |
-Electron microscopy #1
Microscopy ID | 1 |
---|---|
Microscope | FEI POLARA 300 |
Details | Data was collected automatically with Leginon |
Date | Aug 20, 2012 |
Image recording | Category: CCD / Film or detector model: TVIPS TEMCAM-F416 (4k x 4k) / Number real images: 51282 / Average electron dose: 20 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Calibrated magnification: 205000 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.0 mm / Nominal defocus max: 4.5 µm / Nominal defocus min: 2.0 µm / Nominal magnification: 115000 |
Sample stage | Specimen holder model: GATAN LIQUID NITROGEN |
Experimental equipment | Model: Tecnai Polara / Image courtesy: FEI Company |
-Electron microscopy #2
Microscopy ID | 2 |
---|---|
Microscope | FEI TITAN KRIOS |
Date | Nov 29, 2012 |
Image recording | Category: CCD / Film or detector model: FEI FALCON II (4k x 4k) / Number real images: 51282 / Average electron dose: 20 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Calibrated magnification: 172000 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 4.5 µm / Nominal defocus min: 1.5 µm / Nominal magnification: 96000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
CTF correction | Details: Each micrograph |
---|---|
Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Algorithm: OTHER / Resolution.type: BY AUTHOR / Resolution: 8.0 Å / Resolution method: OTHER / Software - Name: Signature, CTFFind3, Spider, SPARX Details: Maps were calculated from 2 datasets using SSNR-weighted combination. Number images used: 60986 |