+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-19767 | ||||||||||||
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Title | Structure of a 2873 Scaffold Base DNA Origami V1 | ||||||||||||
Map data | |||||||||||||
Sample |
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Keywords | DNA Origami / Multilayer / Square lattice / 2873 scaffold / DNA | ||||||||||||
Biological species | synthetic construct (others) | ||||||||||||
Method | single particle reconstruction / cryo EM / Resolution: 8.6 Å | ||||||||||||
Authors | Ali K / Georg K / Volodymyr M / Johanna G / Maximilian NH / Lukas K / Simone C / Hendrik D | ||||||||||||
Funding support | European Union, Germany, 3 items
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Citation | Journal: Nano Lett / Year: 2024 Title: Designing Rigid DNA Origami Templates for Molecular Visualization Using Cryo-EM. Authors: Ali Khoshouei / Georg Kempf / Volodymyr Mykhailiuk / Johanna Mariko Griessing / Maximilian Nicolas Honemann / Lukas Kater / Simone Cavadini / Hendrik Dietz / Abstract: DNA origami, a method for constructing nanostructures from DNA, offers potential for diverse scientific and technological applications due to its ability to integrate various molecular ...DNA origami, a method for constructing nanostructures from DNA, offers potential for diverse scientific and technological applications due to its ability to integrate various molecular functionalities in a programmable manner. In this study, we examined the impact of internal crossover distribution and the compositional uniformity of staple strands on the structure of multilayer DNA origami using cryogenic electron microscopy (cryo-EM) single-particle analysis. A refined DNA object was utilized as an alignment framework in a host-guest model, where we successfully resolved an 8 kDa thrombin binding aptamer (TBA) linked to the host object. Our results broaden the spectrum of DNA in structural applications. | ||||||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_19767.map.gz | 44.9 MB | EMDB map data format | |
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Header (meta data) | emd-19767-v30.xml emd-19767.xml | 13.3 KB 13.3 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_19767_fsc.xml | 9.7 KB | Display | FSC data file |
Images | emd_19767.png | 57.5 KB | ||
Filedesc metadata | emd-19767.cif.gz | 4.1 KB | ||
Others | emd_19767_half_map_1.map.gz emd_19767_half_map_2.map.gz | 58 MB 58 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-19767 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-19767 | HTTPS FTP |
-Validation report
Summary document | emd_19767_validation.pdf.gz | 700.9 KB | Display | EMDB validaton report |
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Full document | emd_19767_full_validation.pdf.gz | 700.4 KB | Display | |
Data in XML | emd_19767_validation.xml.gz | 16.7 KB | Display | |
Data in CIF | emd_19767_validation.cif.gz | 21.7 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-19767 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-19767 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_19767.map.gz / Format: CCP4 / Size: 75.1 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_19767_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #2
File | emd_19767_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Structure of a 2873 Scaffold Base DNA Origami V1
Entire | Name: Structure of a 2873 Scaffold Base DNA Origami V1 |
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Components |
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-Supramolecule #1: Structure of a 2873 Scaffold Base DNA Origami V1
Supramolecule | Name: Structure of a 2873 Scaffold Base DNA Origami V1 / type: complex / ID: 1 / Parent: 0 |
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Source (natural) | Organism: synthetic construct (others) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 8 |
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Grid | Model: Quantifoil R1.2/1.3 / Material: COPPER / Pretreatment - Type: GLOW DISCHARGE |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: FEI FALCON III (4k 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: 2.5 µm / Nominal defocus min: 0.5 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |