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Open data
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Basic information
| Entry | ![]() | |||||||||||||||
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| Title | METIS asymmetric triangular wireframe DNA origami | |||||||||||||||
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Sample |
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| Biological species | Escherichia virus M13 | |||||||||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 13.0 Å | |||||||||||||||
Authors | Li S / Wang X / Zhang K / Chiu W / Bathe M | |||||||||||||||
| Funding support | United States, 4 items
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Citation | Journal: Sci Adv / Year: 2022Title: Planar 2D wireframe DNA origami. Authors: Xiao Wang / Shanshan Li / Hyungmin Jun / Torsten John / Kaiming Zhang / Hannah Fowler / Jonathan P K Doye / Wah Chiu / Mark Bathe / ![]() Abstract: Two-dimensional (2D) DNA origami is widely used for applications ranging from excitonics to single-molecule biophysics. Conventional, single-layer 2D DNA origami exhibits flexibility and curvature in ...Two-dimensional (2D) DNA origami is widely used for applications ranging from excitonics to single-molecule biophysics. Conventional, single-layer 2D DNA origami exhibits flexibility and curvature in solution; however, that may limit its suitability as a 2D structural template. In contrast, 2D wireframe DNA origami rendered with six-helix bundle edges offers local control over duplex orientations with enhanced in-plane rigidity. Here, we investigate the 3D structure of these assemblies using cryo-electron microscopy (cryo-EM). 3D reconstructions reveal a high degree of planarity and homogeneity in solution for polygonal objects with and without internal mesh, enabling 10-Å resolution for a triangle. Coarse-grained simulations were in agreement with cryo-EM data, offering molecular structural insight into this class of 2D DNA origami. Our results suggest that these assemblies may be valuable for 2D material applications and geometries that require high structural fidelity together with local control over duplex orientations, rather than parallel duplex assembly. | |||||||||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_26328.map.gz | 26.8 MB | EMDB map data format | |
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| Header (meta data) | emd-26328-v30.xml emd-26328.xml | 12.4 KB 12.4 KB | Display Display | EMDB header |
| Images | emd_26328.png | 50.2 KB | ||
| Others | emd_26328_half_map_1.map.gz emd_26328_half_map_2.map.gz | 49 MB 49 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-26328 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-26328 | HTTPS FTP |
-Validation report
| Summary document | emd_26328_validation.pdf.gz | 621.4 KB | Display | EMDB validaton report |
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| Full document | emd_26328_full_validation.pdf.gz | 621 KB | Display | |
| Data in XML | emd_26328_validation.xml.gz | 12 KB | Display | |
| Data in CIF | emd_26328_validation.cif.gz | 13.8 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-26328 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-26328 | 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_26328.map.gz / Format: CCP4 / Size: 52.7 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: 1.4 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: #1
| File | emd_26328_half_map_1.map | ||||||||||||
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-Half map: #2
| File | emd_26328_half_map_2.map | ||||||||||||
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Sample components
-Entire : METIS asymmetric triangular wireframe DNA origami
| Entire | Name: METIS asymmetric triangular wireframe DNA origami |
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| Components |
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-Supramolecule #1: METIS asymmetric triangular wireframe DNA origami
| Supramolecule | Name: METIS asymmetric triangular wireframe DNA origami / type: complex / Chimera: Yes / ID: 1 / Parent: 0 |
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| Source (natural) | Organism: Escherichia virus M13 |
-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: 7.8 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | FEI TALOS ARCTICA |
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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: 200 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 3.5 µm / Nominal defocus min: 1.5 µm |
| Experimental equipment | ![]() Model: Talos Arctica / Image courtesy: FEI Company |
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Image processing
| Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 13.0 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 95277 |
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| Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
| Final angle assignment | Type: MAXIMUM LIKELIHOOD |
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About Yorodumi




Escherichia virus M13
Authors
United States, 4 items
Citation







Z (Sec.)
Y (Row.)
X (Col.)




































FIELD EMISSION GUN
