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Yorodumi- EMDB-19546: Human mitochondrial ribosome in complex with antibiotic tigecycli... -
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Open data
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Basic information
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| Title | Human mitochondrial ribosome in complex with antibiotic tigecycline, Class empty mtLSU body (local-filter) | |||||||||
Map data | Class empty, mtLSU body local-filter | |||||||||
Sample |
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Keywords | antibiotics / immunometabolism / mitochondrial ribosomes / tetracyclines / T cells. / RIBOSOME | |||||||||
| Biological species | Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.2 Å | |||||||||
Authors | Khawaja A / Nguyen MD / Singh V / Rorbach J | |||||||||
| Funding support | Sweden, 1 items
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Citation | Journal: Nat Commun / Year: 2025Title: T cell toxicity induced by tigecycline binding to the mitochondrial ribosome. Authors: Qiuya Shao / Anas Khawaja / Minh Duc Nguyen / Vivek Singh / Jingdian Zhang / Yong Liu / Joel Nordin / Monika Adori / C Axel Innis / Xaquin Castro Dopico / Joanna Rorbach / ![]() Abstract: Tetracyclines are essential bacterial protein synthesis inhibitors under continual development to combat antibiotic resistance yet suffer from unwanted side effects. Mitoribosomes - responsible for ...Tetracyclines are essential bacterial protein synthesis inhibitors under continual development to combat antibiotic resistance yet suffer from unwanted side effects. Mitoribosomes - responsible for generating oxidative phosphorylation (OXPHOS) subunits - share structural similarities with bacterial machinery and may suffer from cross-reactivity. Since lymphocytes rely upon OXPHOS upregulation to establish immunity, we set out to assess the impact of ribosome-targeting antibiotics on human T cells. We find tigecycline, a third-generation tetracycline, to be the most cytotoxic compound tested. In vitro, 5-10 μM tigecycline inhibits mitochondrial but not cytosolic translation, mitochondrial complex I, III and IV expression, and curtails the activation and expansion of unique T cell subsets. By cryo-EM, we find tigecycline to occupy three sites on T cell mitoribosomes. In addition to the conserved A-site found in bacteria, tigecycline also attaches to the peptidyl transferase center of the large subunit. Furthermore, a third, distinct binding site on the large subunit, aligns with helices analogous to those in bacteria, albeit lacking methylation in humans. The data provide a mechanism to explain part of the anti-inflammatory effects of these drugs and inform antibiotic design. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_19546.map.gz | 8.7 MB | EMDB map data format | |
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| Header (meta data) | emd-19546-v30.xml emd-19546.xml | 13 KB 13 KB | Display Display | EMDB header |
| Images | emd_19546.png | 65 KB | ||
| Filedesc metadata | emd-19546.cif.gz | 3.9 KB | ||
| Others | emd_19546_half_map_1.map.gz emd_19546_half_map_2.map.gz | 475.8 MB 475.8 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-19546 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-19546 | HTTPS FTP |
-Validation report
| Summary document | emd_19546_validation.pdf.gz | 823.2 KB | Display | EMDB validaton report |
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| Full document | emd_19546_full_validation.pdf.gz | 822.8 KB | Display | |
| Data in XML | emd_19546_validation.xml.gz | 18.8 KB | Display | |
| Data in CIF | emd_19546_validation.cif.gz | 22.7 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-19546 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-19546 | 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_19546.map.gz / Format: CCP4 / Size: 512 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Class empty, mtLSU body local-filter | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.01 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: Class empty, mtLSU body local-filter, half map A
| File | emd_19546_half_map_1.map | ||||||||||||
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| Annotation | Class empty, mtLSU body local-filter, half map A | ||||||||||||
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| Density Histograms |
-Half map: Class empty, mtLSU body local-filter, half map B
| File | emd_19546_half_map_2.map | ||||||||||||
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| Annotation | Class empty, mtLSU body local-filter, half map B | ||||||||||||
| Projections & Slices |
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| Density Histograms |
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Sample components
-Entire : Human mitochondrial ribosome in complex with mRNA, A-site and P-s...
| Entire | Name: Human mitochondrial ribosome in complex with mRNA, A-site and P-site tRNA and antibiotic tigecycline. |
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| Components |
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-Supramolecule #1: Human mitochondrial ribosome in complex with mRNA, A-site and P-s...
| Supramolecule | Name: Human mitochondrial ribosome in complex with mRNA, A-site and P-site tRNA and antibiotic tigecycline. 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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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 45.0 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: 1.6 µm / Nominal defocus min: 0.4 µm / Nominal magnification: 165000 |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



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











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Processing
FIELD EMISSION GUN

