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Yorodumi- EMDB-54280: Cryo-electron tomogram of apoptosis-induced HeLa cell expressing ... -
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Open data
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Basic information
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| Title | Cryo-electron tomogram of apoptosis-induced HeLa cell expressing Apaf1-SNAP | |||||||||
Map data | Cryo-electron tomogram of apoptosis-induced HeLa cell expressing Apaf1-SNAP | |||||||||
Sample |
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Keywords | Apoptosome / Caspase-activation / HeLa cell / APOPTOSIS | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | electron tomography / cryo EM | |||||||||
Authors | Borgeaud AC / Ganeva I / Klein C / Stooss A / Ross-Kaschitza D / Wu L / Riley JS / Tait SWG / Lemmin T / Kaufmann T / Kukulski W | |||||||||
| Funding support | Switzerland, 1 items
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Citation | Journal: Nat Commun / Year: 2025Title: Large transient assemblies of Apaf1 constitute the apoptosome in cells. Authors: Alicia C Borgeaud / Iva Ganeva / Calvin Klein / Amandine Stooss / Daniela Ross-Kaschitza / Liyang Wu / Joel S Riley / Stephen W G Tait / Thomas Lemmin / Thomas Kaufmann / Wanda Kukulski / ![]() Abstract: Upon cell death signals, the apoptotic protease-activating factor Apaf1 and cytochrome c interact to form the apoptosome complex. The apoptosome is crucial for mitochondrial apoptosis, as it ...Upon cell death signals, the apoptotic protease-activating factor Apaf1 and cytochrome c interact to form the apoptosome complex. The apoptosome is crucial for mitochondrial apoptosis, as it activates caspases that dismantle the cell. However, the in vivo assembly mechanism and appearance of the apoptosome remain unclear. We show that upon onset of apoptosis, Apaf1 molecules accumulate into multiple foci per cell. Disassembly of the foci correlates with cell survival. Structurally, Apaf1 foci resemble organelle-sized, cloud-like assemblies. They form through specific interactions with cytochrome c, contain caspase-9, and depend on procaspase-9 expression for their formation. We propose that Apaf1 foci correspond to the apoptosome in cells. Transientness and ultrastructure of Apaf1 foci suggest that the dynamic spatiotemporal organisation of apoptosome components regulates progression of apoptosis. | |||||||||
| History |
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_54280.map.gz | 42.5 MB | EMDB map data format | |
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| Header (meta data) | emd-54280-v30.xml emd-54280.xml | 11.1 KB 11.1 KB | Display Display | EMDB header |
| Images | emd_54280.png | 243.4 KB | ||
| Filedesc metadata | emd-54280.cif.gz | 3.9 KB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-54280 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-54280 | HTTPS FTP |
-Validation report
| Summary document | emd_54280_validation.pdf.gz | 554.1 KB | Display | EMDB validaton report |
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| Full document | emd_54280_full_validation.pdf.gz | 553.6 KB | Display | |
| Data in XML | emd_54280_validation.xml.gz | 2.2 KB | Display | |
| Data in CIF | emd_54280_validation.cif.gz | 2.7 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-54280 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-54280 | HTTPS FTP |
-Related structure data
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_54280.map.gz / Format: CCP4 / Size: 103.4 MB / Type: IMAGE STORED AS SIGNED BYTE | ||||||||||||||||||||
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| Annotation | Cryo-electron tomogram of apoptosis-induced HeLa cell expressing Apaf1-SNAP | ||||||||||||||||||||
| Voxel size | X=Y=Z: 17.82 Å | ||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
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Sample components
-Entire : HeLa cell expressing Apaf1-SNAP, treated with ABT-737 and QVD
| Entire | Name: HeLa cell expressing Apaf1-SNAP, treated with ABT-737 and QVD |
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| Components |
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-Supramolecule #1: HeLa cell expressing Apaf1-SNAP, treated with ABT-737 and QVD
| Supramolecule | Name: HeLa cell expressing Apaf1-SNAP, treated with ABT-737 and QVD type: cell / ID: 1 / Parent: 0 |
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| Source (natural) | Organism: Homo sapiens (human) |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | electron tomography |
| Aggregation state | cell |
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Sample preparation
| Buffer | pH: 7.4 |
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| Vitrification | Cryogen name: ETHANE |
| Sectioning | Focused ion beam - Instrument: OTHER / Focused ion beam - Ion: OTHER / Focused ion beam - Voltage: 30 / Focused ion beam - Current: 1 / Focused ion beam - Duration: 2000 / Focused ion beam - Temperature: 80 K / Focused ion beam - Initial thickness: 1000 / Focused ion beam - Final thickness: 200 Focused ion beam - Details: Rough milling started at 30 kV and 1 nA current, progressively lowered to final 23 pA at 16 kV for fine milling.. The value given for _em_focused_ion_beam.instrument is ...Focused ion beam - Details: Rough milling started at 30 kV and 1 nA current, progressively lowered to final 23 pA at 16 kV for fine milling.. The value given for _em_focused_ion_beam.instrument is TFS Aquilos 2. This is not in a list of allowed values {'OTHER', 'DB235'} so OTHER is written into the XML file. |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Average electron dose: 1.0 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: 5.0 µm / Nominal defocus min: 5.0 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
| Final reconstruction | Software - Name: IMOD / Number images used: 117 |
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| CTF correction | Type: PHASE FLIPPING ONLY |
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About Yorodumi



Keywords
Homo sapiens (human)
Authors
Switzerland, 1 items
Citation




FIELD EMISSION GUN
