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Yorodumi- EMDB-58008: 2.3 angstrom cryoEM map of endogenous nucleosome core particle in... -
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Basic information
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| Title | 2.3 angstrom cryoEM map of endogenous nucleosome core particle in nuclear lysate | |||||||||
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Keywords | Nucleosome / Genome / Nucleoprotein / NUCLEAR PROTEIN | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.3 Å | |||||||||
Authors | Ker DS / Pellegrini L | |||||||||
| Funding support | United Kingdom, 1 items
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Citation | Journal: Biosci Rep / Year: 2026Title: High-resolution cryoEM of nucleosomes in nuclear extracts of mammalian cells. Authors: De-Sheng Ker / Hedaya Aboalnaga / Luca Pellegrini / ![]() Abstract: Frontier Structural Biology methods are transitioning from analysis of reconstituted macromolecular complexes in vitro to imaging of macromolecular assemblies within the physiological confines of the ...Frontier Structural Biology methods are transitioning from analysis of reconstituted macromolecular complexes in vitro to imaging of macromolecular assemblies within the physiological confines of the cell. Preparation of samples for in situ cryoEM analysis requires FIB milling or ultramicrotome sectioning, laborious and technically challenging procedures that are low-throughput and require a high degree of technical skills. We have devised a simple approach for cryoEM of nuclear macromolecular complexes that preserves to a high degree their physiological environment while removing the need for thin sectioning of the sample. The method requires only the preparation of nuclear extracts without additional purification or enrichment steps. We applied the method to obtain a 2.3 Å cryoEM structure of nucleosomes visualised directly in the nuclear lysate of human cells. #1: Journal: Biorxiv / Year: 2026Title: High-resolution cryoEM of nucleosomes in nuclear extracts of mammalian cells Authors: Ker DS / Aboalnaga H / Pellegrini L | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_58008.map.gz | 138.8 MB | EMDB map data format | |
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| Header (meta data) | emd-58008-v30.xml emd-58008.xml | 17.8 KB 17.8 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_58008_fsc.xml | 13.6 KB | Display | FSC data file |
| Images | emd_58008.png | 160.7 KB | ||
| Masks | emd_58008_msk_1.map | 274.6 MB | Mask map | |
| Filedesc metadata | emd-58008.cif.gz | 4.4 KB | ||
| Others | emd_58008_additional_1.map.gz emd_58008_half_map_1.map.gz emd_58008_half_map_2.map.gz | 232.2 MB 255.2 MB 255.2 MB | ||
| Archive directory | https://data.pdbj.org/pub/emdb/structures/EMD-58008 ftp://data.pdbj.org/pub/emdb/structures/EMD-58008 | HTTPS FTP |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_58008.map.gz / Format: CCP4 / Size: 274.6 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.929 Å | ||||||||||||||||||||||||||||||||||||
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_58008_msk_1.map | ||||||||||||
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-Additional map: Post-processed map by DeepEMhancer software
| File | emd_58008_additional_1.map | ||||||||||||
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| Annotation | Post-processed map by DeepEMhancer software | ||||||||||||
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-Half map: #2
| File | emd_58008_half_map_1.map | ||||||||||||
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-Half map: #1
| File | emd_58008_half_map_2.map | ||||||||||||
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Sample components
-Entire : Endogenous nucleosome core particle
| Entire | Name: Endogenous nucleosome core particle |
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| Components |
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-Supramolecule #1: Endogenous nucleosome core particle
| Supramolecule | Name: Endogenous nucleosome core particle / type: complex / 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 | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7.5 |
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| Grid | Model: Quantifoil R2/2 / Material: COPPER / Mesh: 300 / Support film - Material: CARBON / Support film - topology: CONTINUOUS / Support film - Film thickness: 20 / Pretreatment - Type: GLOW DISCHARGE |
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: TFS FALCON 4i (4k x 4k) / Average exposure time: 4.39 sec. / Average electron dose: 47.36 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: 2.0 µm / Nominal defocus min: 0.8 µm |
| Sample stage | Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Keywords
Homo sapiens (human)
Authors
United Kingdom, 1 items
Citation
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Processing
FIELD EMISSION GUN

