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Open data
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Basic information
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Title | C. elegans L1 80S ribosome | |||||||||
![]() | Post-processed map | |||||||||
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![]() | Caenorhabditis / elegans / ribosome / 80S / L1 / larva / C. elegans | |||||||||
Biological species | ![]() ![]() | |||||||||
Method | subtomogram averaging / cryo EM / Resolution: 6.9 Å | |||||||||
![]() | Schioetz OH / Kaiser CJO / Klumpe S / Beck F / Plitzko JM | |||||||||
Funding support | ![]()
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![]() | ![]() Title: Serial Lift-Out: sampling the molecular anatomy of whole organisms. Authors: Oda Helene Schiøtz / Christoph J O Kaiser / Sven Klumpe / Dustin R Morado / Matthias Poege / Jonathan Schneider / Florian Beck / David P Klebl / Christopher Thompson / Jürgen M Plitzko / ![]() ![]() ![]() Abstract: Cryo-focused ion beam milling of frozen-hydrated cells and subsequent cryo-electron tomography (cryo-ET) has enabled the structural elucidation of macromolecular complexes directly inside cells. ...Cryo-focused ion beam milling of frozen-hydrated cells and subsequent cryo-electron tomography (cryo-ET) has enabled the structural elucidation of macromolecular complexes directly inside cells. Application of the technique to multicellular organisms and tissues, however, is still limited by sample preparation. While high-pressure freezing enables the vitrification of thicker samples, it prolongs subsequent preparation due to increased thinning times and the need for extraction procedures. Additionally, thinning removes large portions of the specimen, restricting the imageable volume to the thickness of the final lamella, typically <300 nm. Here we introduce Serial Lift-Out, an enhanced lift-out technique that increases throughput and obtainable contextual information by preparing multiple sections from single transfers. We apply Serial Lift-Out to Caenorhabditis elegans L1 larvae, yielding a cryo-ET dataset sampling the worm's anterior-posterior axis, and resolve its ribosome structure to 7 Å and a subregion of the 11-protofilament microtubule to 13 Å, illustrating how Serial Lift-Out enables the study of multicellular molecular anatomy. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 42.5 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 17.2 KB 17.2 KB | Display Display | ![]() |
FSC (resolution estimation) | ![]() | 8.1 KB | Display | ![]() |
Images | ![]() | 103.1 KB | ||
Masks | ![]() | 45.2 MB | ![]() | |
Filedesc metadata | ![]() | 4.5 KB | ||
Others | ![]() ![]() ![]() | 3.6 MB 23.2 MB 23.2 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 975.8 KB | Display | ![]() |
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Full document | ![]() | 975.4 KB | Display | |
Data in XML | ![]() | 14.7 KB | Display | |
Data in CIF | ![]() | 19.5 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | C: citing same article ( |
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Links
EMDB pages | ![]() ![]() |
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Map
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Annotation | Post-processed map | ||||||||||||||||||||
Voxel size | X=Y=Z: 2.98 Å | ||||||||||||||||||||
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Symmetry | Space group: 1 | ||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Mask #1
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-Additional map: Masked post-processed map
File | emd_17241_additional_1.map | ||||||||||||
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Annotation | Masked post-processed map | ||||||||||||
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-Half map: Half map 1
File | emd_17241_half_map_1.map | ||||||||||||
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Annotation | Half map 1 | ||||||||||||
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-Half map: Half map 2
File | emd_17241_half_map_2.map | ||||||||||||
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Annotation | Half map 2 | ||||||||||||
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Sample components
-Entire : C. elegans L1 larva, CGC strain NK2476
Entire | Name: C. elegans L1 larva, CGC strain NK2476 |
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Components |
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-Supramolecule #1: C. elegans L1 larva, CGC strain NK2476
Supramolecule | Name: C. elegans L1 larva, CGC strain NK2476 / type: complex / ID: 1 / Parent: 0 |
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Source (natural) | Organism: ![]() ![]() |
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | subtomogram averaging |
Aggregation state | tissue |
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Sample preparation
Buffer | pH: 7.5 / Details: M9 buffer + 20% Ficoll 400 |
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Grid | Model: Homemade / Material: COPPER / Mesh: 75 / Support film - Material: FORMVAR / Support film - topology: CONTINUOUS / Support film - Film thickness: 100 |
Vitrification | Cryogen name: NITROGEN / Details: High pressure freezing, Leica EM ICE. |
Details | Developmentally arrested L1 larvae |
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Electron microscopy
Microscope | FEI TITAN KRIOS |
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Specialist optics | Energy filter - Name: TFS Selectris X / Energy filter - Slit width: 10 eV |
Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Digitization - Dimensions - Width: 4096 pixel / Digitization - Dimensions - Height: 4096 pixel / Number real images: 1 / Average exposure time: 0.68 sec. / Average electron dose: 3.2 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | C2 aperture diameter: 50.0 µm / 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: 64000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |