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Yorodumi- EMDB-29567: Mouse apoferritin from data collected on Glacios microscope equip... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-29567 | |||||||||
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Title | Mouse apoferritin from data collected on Glacios microscope equipped with a Falcon 3 camera operating in integrating mode, in 50-100 nm ice thickness | |||||||||
Map data | Mouse apoferritin from data collected on Glacios microscope equipped with a Falcon 3 camera operating in integrating mode, in 50-100 nm ice thickness | |||||||||
Sample |
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Keywords | Mouse apoferritin / Glacios / Falcon 3 / integrating mode / 50-100nm ice thickness / METAL BINDING PROTEIN | |||||||||
Biological species | mouse (mice) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 4.64 Å | |||||||||
Authors | Neselu K / Wang B / Rice WJ / Potter CS / Carragher B / Chua EYD | |||||||||
Funding support | United States, 2 items
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Citation | Journal: J Struct Biol X / Year: 2023 Title: Measuring the effects of ice thickness on resolution in single particle cryo-EM. Authors: Kasahun Neselu / Bing Wang / William J Rice / Clinton S Potter / Bridget Carragher / Eugene Y D Chua / Abstract: Ice thickness is a critical parameter in single particle cryo-EM - too thin ice can break during imaging or exclude the sample of interest, while ice that is too thick contributes to more inelastic ...Ice thickness is a critical parameter in single particle cryo-EM - too thin ice can break during imaging or exclude the sample of interest, while ice that is too thick contributes to more inelastic scattering that precludes obtaining high resolution reconstructions. Here we present the practical effects of ice thickness on resolution, and the influence of energy filters, accelerating voltage, or detector mode. We collected apoferritin data with a wide range of ice thicknesses on three microscopes with different instrumentation and settings. We show that on a 300 kV microscope, using a 20 eV energy filter slit has a greater effect on improving resolution in thicker ice; that operating at 300 kV instead of 200 kV accelerating voltage provides significant resolution improvements at an ice thickness above 150 nm; and that on a 200 kV microscope using a detector operating in super resolution mode enables good reconstructions for up to 200 nm ice thickness, while collecting in counting instead of linear mode leads to improvements in resolution for ice of 50-150 nm thickness. Our findings can serve as a guide for users seeking to optimize data collection or sample preparation routines for both single particle and in situ cryo-EM. We note that most in situ data collection is done on samples in a range of ice thickness above 150 nm so these results may be especially relevant to that community. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_29567.map.gz | 59.7 MB | EMDB map data format | |
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Header (meta data) | emd-29567-v30.xml emd-29567.xml | 14.6 KB 14.6 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_29567_fsc.xml | 8.4 KB | Display | FSC data file |
Images | emd_29567.png | 42 KB | ||
Filedesc metadata | emd-29567.cif.gz | 4.4 KB | ||
Others | emd_29567_half_map_1.map.gz emd_29567_half_map_2.map.gz | 59 MB 59 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-29567 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-29567 | HTTPS FTP |
-Validation report
Summary document | emd_29567_validation.pdf.gz | 842.2 KB | Display | EMDB validaton report |
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Full document | emd_29567_full_validation.pdf.gz | 841.8 KB | Display | |
Data in XML | emd_29567_validation.xml.gz | 16.7 KB | Display | |
Data in CIF | emd_29567_validation.cif.gz | 21.2 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-29567 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-29567 | 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_29567.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | Mouse apoferritin from data collected on Glacios microscope equipped with a Falcon 3 camera operating in integrating mode, in 50-100 nm ice thickness | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.204 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #1
File | emd_29567_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #2
File | emd_29567_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Mouse apoferritin
Entire | Name: Mouse apoferritin |
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Components |
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-Supramolecule #1: Mouse apoferritin
Supramolecule | Name: Mouse apoferritin / type: complex / ID: 1 / Parent: 0 |
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Source (natural) | Organism: mouse (mice) |
Molecular weight | Theoretical: 450 KDa |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 8 mg/mL | ||||||||||||
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Buffer | pH: 7.5 Component:
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Grid | Model: UltrAuFoil R1.2/1.3 / Support film - Material: GOLD / Support film - topology: HOLEY | ||||||||||||
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 295.15 K / Instrument: FEI VITROBOT MARK IV |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Specialist optics | Energy filter - Name: GIF Bioquantum / Energy filter - Slit width: 20 eV |
Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Number grids imaged: 1 / Average exposure time: 2.0 sec. / Average electron dose: 51.22 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 100.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.0 µm / Nominal defocus min: 0.8 µm / Nominal magnification: 81000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |