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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | In situ human 80S ribosome (Focused on 40S head) | |||||||||
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Sample |
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Keywords | In situ / RIBOSOME | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.64 Å | |||||||||
Authors | Wei Z / Yong Z | |||||||||
| Funding support | 1 items
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Citation | Journal: Nat Commun / Year: 2025Title: Visualizing the translation landscape in human cells at high resolution. Authors: Wei Zheng / Yuekang Zhang / Jimin Wang / Shuhui Wang / Pengxin Chai / Elizabeth J Bailey / Chenghao Zhu / Wangbiao Guo / Swapnil C Devarkar / Shenping Wu / Jianfeng Lin / Kai Zhang / Jun Liu ...Authors: Wei Zheng / Yuekang Zhang / Jimin Wang / Shuhui Wang / Pengxin Chai / Elizabeth J Bailey / Chenghao Zhu / Wangbiao Guo / Swapnil C Devarkar / Shenping Wu / Jianfeng Lin / Kai Zhang / Jun Liu / Ivan B Lomakin / Yong Xiong / ![]() Abstract: Comprehensive in situ structures of macromolecules can transform our understanding of biology and advance human health. Here, we map protein synthesis inside human cells in detail by combining ...Comprehensive in situ structures of macromolecules can transform our understanding of biology and advance human health. Here, we map protein synthesis inside human cells in detail by combining automated cryo-focused ion beam (FIB) milling and in situ single-particle cryo electron microscopy (cryo-EM). With this in situ cryo-EM approach, we resolved a 2.2 Å consensus structure of the human 80S ribosome and unveiled 23 functional states, nearly all better than 3 Å resolution. Compared to in vitro studies, we observed variations in ribosome structures, distinct environments of ion and polyamine binding, and associated proteins such as EDF1 and NACβ that are typically not enriched with purified ribosomes. We also detected additional peptide-related density features on the ribosome and visualized ribosome-ribosome interactions in helical polysomes. Finally, high-resolution structures from cells treated with homoharringtonine and cycloheximide revealed a distinct translational landscape and a spermidine that interacts with cycloheximide at the E site, one of the numerous polyamines that also bind native ribosomes. These results underscore the value of high-resolution in situ studies in the native environment. | |||||||||
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_71443.map.gz | 363.8 MB | EMDB map data format | |
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| Header (meta data) | emd-71443-v30.xml emd-71443.xml | 14.1 KB 14.1 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_71443_fsc.xml | 19 KB | Display | FSC data file |
| Images | emd_71443.png | 12.4 KB | ||
| Masks | emd_71443_msk_1.map | 729 MB | Mask map | |
| Filedesc metadata | emd-71443.cif.gz | 4 KB | ||
| Others | emd_71443_half_map_1.map.gz emd_71443_half_map_2.map.gz | 676.2 MB 676.1 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-71443 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-71443 | HTTPS FTP |
-Validation report
| Summary document | emd_71443_validation.pdf.gz | 1.1 MB | Display | EMDB validaton report |
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| Full document | emd_71443_full_validation.pdf.gz | 1.1 MB | Display | |
| Data in XML | emd_71443_validation.xml.gz | 28.3 KB | Display | |
| Data in CIF | emd_71443_validation.cif.gz | 37.3 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-71443 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-71443 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9p6zC ![]() 9p72C ![]() 9p73C ![]() 9p76C ![]() 9p7fC ![]() 9p7gC ![]() 9p7hC ![]() 9p7iC ![]() 9p7jC ![]() 9p7kC ![]() 9p7lC ![]() 9p7nC ![]() 9p7oC ![]() 9p7wC ![]() 9p7xC ![]() 9p7yC ![]() 9p8bC ![]() 9p8hC ![]() 9p8iC ![]() 9p9hC ![]() 9p9iC ![]() 9p9jC ![]() 9p9kC ![]() 9pa7C ![]() 9pbeC ![]() 9pkgC C: citing same article ( |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_71443.map.gz / Format: CCP4 / Size: 729 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: 0.89 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_71443_msk_1.map | ||||||||||||
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| Density Histograms |
-Half map: #1
| File | emd_71443_half_map_1.map | ||||||||||||
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| Density Histograms |
-Half map: #2
| File | emd_71443_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : In situ human ribosome (Focused on 40S with SERBP1 CTD)
| Entire | Name: In situ human ribosome (Focused on 40S with SERBP1 CTD) |
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| Components |
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-Supramolecule #1: In situ human ribosome (Focused on 40S with SERBP1 CTD)
| Supramolecule | Name: In situ human ribosome (Focused on 40S with SERBP1 CTD) 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 | cell |
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Sample preparation
| Buffer | pH: 7.4 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | FEI TECNAI F30 |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 50.0 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: 2.0 µm / Nominal defocus min: 1.2 µm |
| Experimental equipment | ![]() Model: Tecnai F30 / Image courtesy: FEI Company |
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About Yorodumi




Keywords
Homo sapiens (human)
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Processing
FIELD EMISSION GUN

