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Yorodumi- EMDB-35850: Cellular components at INS-1E cell periphery under second phase o... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-35850 | |||||||||
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Title | Cellular components at INS-1E cell periphery under second phase of glucose-stimulated insulin secretion | |||||||||
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Sample |
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Keywords | insulin secretion / cytoskeleton / CYTOSOLIC PROTEIN | |||||||||
Biological species | Rattus (rat) | |||||||||
Method | electron tomography / cryo EM | |||||||||
Authors | Li W / Li A / Yu B / Zhang X / Liu X / White K / Stevens R / Baumeister W / Sali A / Jasnin M / Sun L | |||||||||
Funding support | 1 items
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Citation | Journal: Nat Commun / Year: 2024 Title: In situ structure of actin remodeling during glucose-stimulated insulin secretion using cryo-electron tomography. Authors: Weimin Li / Angdi Li / Bing Yu / Xiaoxiao Zhang / Xiaoyan Liu / Kate L White / Raymond C Stevens / Wolfgang Baumeister / Andrej Sali / Marion Jasnin / Liping Sun / Abstract: Actin mediates insulin secretion in pancreatic β-cells through remodeling. Hampered by limited resolution, previous studies have offered an ambiguous depiction as depolymerization and ...Actin mediates insulin secretion in pancreatic β-cells through remodeling. Hampered by limited resolution, previous studies have offered an ambiguous depiction as depolymerization and repolymerization. We report the in situ structure of actin remodeling in INS-1E β-cells during glucose-stimulated insulin secretion at nanoscale resolution. After remodeling, the actin filament network at the cell periphery exhibits three marked differences: 12% of actin filaments reorient quasi-orthogonally to the ventral membrane; the filament network mainly remains as cell-stabilizing bundles but partially reconfigures into a less compact arrangement; actin filaments anchored to the ventral membrane reorganize from a "netlike" to a "blooming" architecture. Furthermore, the density of actin filaments and microtubules around insulin secretory granules decreases, while actin filaments and microtubules become more densely packed. The actin filament network after remodeling potentially precedes the transport and release of insulin secretory granules. These findings advance our understanding of actin remodeling and its role in glucose-stimulated insulin secretion. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_35850.map.gz | 1 GB | EMDB map data format | |
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Header (meta data) | emd-35850-v30.xml emd-35850.xml | 7.7 KB 7.7 KB | Display Display | EMDB header |
Images | emd_35850.png | 108.6 KB | ||
Filedesc metadata | emd-35850.cif.gz | 3.4 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-35850 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-35850 | HTTPS FTP |
-Validation report
Summary document | emd_35850_validation.pdf.gz | 404 KB | Display | EMDB validaton report |
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Full document | emd_35850_full_validation.pdf.gz | 403.5 KB | Display | |
Data in XML | emd_35850_validation.xml.gz | 4.3 KB | Display | |
Data in CIF | emd_35850_validation.cif.gz | 4.8 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-35850 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-35850 | 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_35850.map.gz / Format: CCP4 / Size: 1.1 GB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||
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Projections & slices | Image control
Images are generated by Spider. generated in cubic-lattice coordinate | ||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 13.412 Å | ||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Sample components
-Entire : INS-1E cell
Entire | Name: INS-1E cell |
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Components |
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-Supramolecule #1: INS-1E cell
Supramolecule | Name: INS-1E cell / type: cell / ID: 1 / Parent: 0 |
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Source (natural) | Organism: Rattus (rat) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | electron tomography |
Aggregation state | cell |
-Sample preparation
Buffer | pH: 7.45 |
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Vitrification | Cryogen name: ETHANE |
Sectioning | Other: NO SECTIONING |
Fiducial marker | Manufacturer: aurion / Diameter: 10 nm |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 2.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 8.0 µm / Nominal defocus min: 5.0 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Final reconstruction | Number images used: 61 |
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