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Yorodumi- EMDB-11870: Tomogram of the actin network in an extracted and fixed mouse fib... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-11870 | |||||||||
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Title | Tomogram of the actin network in an extracted and fixed mouse fibroblast lamellipodium. | |||||||||
Map data | Sample tomogram of an extracted and fixed mouse fibroblast lamellipodium. | |||||||||
Sample |
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Biological species | Mus musculus (house mouse) | |||||||||
Method | electron tomography / cryo EM | |||||||||
Authors | Faessler F / Dimchev G / Hodirnau VV / Wan W / Schur FKM | |||||||||
Funding support | Austria, 1 items
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Citation | Journal: Nat Commun / Year: 2020 Title: Cryo-electron tomography structure of Arp2/3 complex in cells reveals new insights into the branch junction. Authors: Florian Fäßler / Georgi Dimchev / Victor-Valentin Hodirnau / William Wan / Florian K M Schur / Abstract: The actin-related protein (Arp)2/3 complex nucleates branched actin filament networks pivotal for cell migration, endocytosis and pathogen infection. Its activation is tightly regulated and involves ...The actin-related protein (Arp)2/3 complex nucleates branched actin filament networks pivotal for cell migration, endocytosis and pathogen infection. Its activation is tightly regulated and involves complex structural rearrangements and actin filament binding, which are yet to be understood. Here, we report a 9.0 Å resolution structure of the actin filament Arp2/3 complex branch junction in cells using cryo-electron tomography and subtomogram averaging. This allows us to generate an accurate model of the active Arp2/3 complex in the branch junction and its interaction with actin filaments. Notably, our model reveals a previously undescribed set of interactions of the Arp2/3 complex with the mother filament, significantly different to the previous branch junction model. Our structure also indicates a central role for the ArpC3 subunit in stabilizing the active conformation. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_11870.map.gz | 33.3 MB | EMDB map data format | |
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Header (meta data) | emd-11870-v30.xml emd-11870.xml | 12.5 KB 12.5 KB | Display Display | EMDB header |
Images | emd_11870.png | 143.8 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-11870 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-11870 | HTTPS FTP |
-Validation report
Summary document | emd_11870_validation.pdf.gz | 155.4 KB | Display | EMDB validaton report |
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Full document | emd_11870_full_validation.pdf.gz | 154.5 KB | Display | |
Data in XML | emd_11870_validation.xml.gz | 4 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-11870 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-11870 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_11870.map.gz / Format: CCP4 / Size: 52.7 MB / Type: IMAGE STORED AS SIGNED BYTE | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Sample tomogram of an extracted and fixed mouse fibroblast lamellipodium. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 17.096 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 : Actin network in a mouse fibroblast lamellipodium
Entire | Name: Actin network in a mouse fibroblast lamellipodium |
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Components |
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-Supramolecule #1: Actin network in a mouse fibroblast lamellipodium
Supramolecule | Name: Actin network in a mouse fibroblast lamellipodium / type: cell / ID: 1 / Parent: 0 / Macromolecule list: #1-#8 Details: Branched actin network of extracted and fixed mouse fibroblast lamellipodium |
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Source (natural) | Organism: Mus musculus (house mouse) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | electron tomography |
Aggregation state | cell |
-Sample preparation
Buffer | pH: 6.1 Component:
Details: Adjust to pH 6.1 using NaOH | ||||||||||||
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Grid | Model: Quantifoil R2/2 / Material: GOLD / Mesh: 200 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Atmosphere: AIR Details: After glow discharging of the grid and prior to the seeding of cells, the grid was coated using 25ug/ml Fibronectin | ||||||||||||
Vitrification | Cryogen name: ETHANE / Chamber humidity: 80 % / Chamber temperature: 277 K Details: Leica GP2, 3,5sec back-blotting, sensor on, 0,1mm movement after contact, manually pre-blotted within the chamber prior to the application of fiducials. | ||||||||||||
Sectioning | Other: NO SECTIONING | ||||||||||||
Fiducial marker | Manufacturer: AURION / Diameter: 10 nm |
-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 real images: 61 / Average exposure time: 1.21 sec. / Average electron dose: 2.79 e/Å2 Details: Images were collected in movie-mode with 7 frames per tilt |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: -0.0055 µm / Nominal defocus min: -0.00175 µm / Nominal magnification: 42000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Final reconstruction | Algorithm: BACK PROJECTION / Software - Name: IMOD (ver. 4.9.12) / Number images used: 61 |
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