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Open data
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Basic information
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| Title | MEDUSA-Complex | |||||||||
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Sample |
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Keywords | Multivalency / supramolecular assemblies / FNAP / directed evolution / antivirals / SELEX / aptamers / DNA | |||||||||
| Biological species | synthetic construct (others) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 20.0 Å | |||||||||
Authors | Duhoo Y / Kononenko A | |||||||||
| Funding support | Switzerland, 1 items
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Citation | Journal: Nat Nanotechnol / Year: 2025Title: Evolution of multivalent supramolecular assemblies of aptamers with target-defined spatial organization. Authors: Artem Kononenko / Vincenzo Caroprese / Yoan Duhoo / Cem Tekin / Maartje M C Bastings / ![]() Abstract: Rapid identification of neutralizing molecules against new and mutating viruses is key to efficiently combating biorisk. Current binder identification techniques use a monovalent library of potential ...Rapid identification of neutralizing molecules against new and mutating viruses is key to efficiently combating biorisk. Current binder identification techniques use a monovalent library of potential binders. Interestingly, proteins on pathogens are often homo-oligomeric-for example, the SARS-CoV-2 spike protein is a homotrimer. Here we describe a simple strategy, MEDUSA (multivalent evolved DNA-based supramolecular assembly), to evolve multivalent assemblies of aptamers with precise interligand spacing and three-fold symmetry, mirroring the geometric structure of many viral capsid proteins. MEDUSA allowed the selection of potent SARS-CoV-2 spike binders structurally distinct from any known aptamers. Decoupling the geometric and structural rigidity contributions toward selectivity made it possible to connect form to function, as demonstrated by the design of tunable fluorescent sensors. This approach offers a blueprint for targeting geometrically defined pathogen structures and developing rapid-response tools for emerging pathogens. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_52510.map.gz | 7.6 MB | EMDB map data format | |
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| Header (meta data) | emd-52510-v30.xml emd-52510.xml | 15.3 KB 15.3 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_52510_fsc.xml | 4.8 KB | Display | FSC data file |
| Images | emd_52510.png | 22.3 KB | ||
| Filedesc metadata | emd-52510.cif.gz | 4.3 KB | ||
| Others | emd_52510_half_map_1.map.gz emd_52510_half_map_2.map.gz | 7.4 MB 7.4 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-52510 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-52510 | HTTPS FTP |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_52510.map.gz / Format: CCP4 / Size: 8 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: 3.72 Å | ||||||||||||||||||||||||||||||||||||
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: #1
| File | emd_52510_half_map_1.map | ||||||||||||
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| Density Histograms |
-Half map: #2
| File | emd_52510_half_map_2.map | ||||||||||||
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Sample components
-Entire : MEDUSA complex
| Entire | Name: MEDUSA complex |
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| Components |
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-Supramolecule #1: MEDUSA complex
| Supramolecule | Name: MEDUSA complex / type: complex / ID: 1 / Parent: 0 Details: Nano assembly of functionalized nucleic acid polymer on the DNA scaffold. |
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| Source (natural) | Organism: synthetic construct (others) |
| Molecular weight | Theoretical: 69 KDa |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 0.35 mg/mL | |||||||||
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| Buffer | pH: 7 Component:
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| Grid | Model: Quantifoil R1.2/1.3 / Material: COPPER / Mesh: 400 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 90 sec. / Pretreatment - Atmosphere: AIR / Details: 15mA on GloQube Plus | |||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 95 % / Chamber temperature: 288 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS GLACIOS |
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| Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Number grids imaged: 1 / Number real images: 1196 / Average electron dose: 50.0 e/Å2 |
| Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 20.0 µm / Calibrated magnification: 150000 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 5.0 µm / Nominal defocus min: 0.5 µm |
| Sample stage | Cooling holder cryogen: NITROGEN |
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Keywords
Authors
Switzerland, 1 items
Citation
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Processing
FIELD EMISSION GUN
