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Open data
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Basic information
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| Title | Cryo-EM of VEVAG Peptide 1 | |||||||||
Map data | FULL MAP | |||||||||
Sample |
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Keywords | peptide fiber / helical polymer / protein fibril | |||||||||
| Biological species | synthetic construct (others) | |||||||||
| Method | helical reconstruction / cryo EM / Resolution: 3.2 Å | |||||||||
Authors | Rich-New ST / Wang R / Zia A / Tovar JD / Wang F | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: ACS Macro Lett / Year: 2025Title: Cryo-EM Visualization of Intermolecular π-Electron Interactions within π-Conjugated Peptidic Supramolecular Polymers. Authors: Shane T Rich-New / Runlai Wang / Ayisha Zia / Fengbin Wang / John D Tovar / ![]() Abstract: The self-assembly of "π-peptides" - molecules with π-electron cores substituted with two or more oligopeptide chains - brings organic electronic function into biologically relevant nanomaterials. ...The self-assembly of "π-peptides" - molecules with π-electron cores substituted with two or more oligopeptide chains - brings organic electronic function into biologically relevant nanomaterials. π-Peptides assemble into fibrillar nanomaterials as driven by enthalpic peptide-based hydrogen bonding networks and pi-core-based quadrupolar interactions. A large body of spectroscopic, morphological and computational studies informs on the nature of the self-assembly process and the resulting nanostructures, but detailed structural information has remained elusive. Inspired by the recent use of cryogenic electron microscopy (cryo-EM) to provide high-resolution structures for synthetic peptide nanomaterials, we present here the use of cryo-EM to offer ca. 3 Å resolution of π-peptide nanomaterial assemblies, visualizing for the first time the nature of the intermolecular π-core electronic interactions responsible for energy transport through these supramolecular materials. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_70201.map.gz | 107.1 MB | EMDB map data format | |
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| Header (meta data) | emd-70201-v30.xml emd-70201.xml | 14.8 KB 14.8 KB | Display Display | EMDB header |
| Images | emd_70201.png | 67 KB | ||
| Filedesc metadata | emd-70201.cif.gz | 4.7 KB | ||
| Others | emd_70201_half_map_1.map.gz emd_70201_half_map_2.map.gz | 109.9 MB 110.7 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-70201 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-70201 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9o7jMC ![]() 9o7kC ![]() 9o7lC M: atomic model generated by this map C: citing same article ( |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_70201.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | FULL MAP | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.12 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: HALF MAP B
| File | emd_70201_half_map_1.map | ||||||||||||
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| Annotation | HALF MAP B | ||||||||||||
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| Density Histograms |
-Half map: HALF MAP A
| File | emd_70201_half_map_2.map | ||||||||||||
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| Annotation | HALF MAP A | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : VEVAG peptide fibril
| Entire | Name: VEVAG peptide fibril |
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| Components |
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-Supramolecule #1: VEVAG peptide fibril
| Supramolecule | Name: VEVAG peptide fibril / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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| Source (natural) | Organism: synthetic construct (others) |
-Macromolecule #1: pi-conjugated peptide
| Macromolecule | Name: pi-conjugated peptide / type: protein_or_peptide / ID: 1 / Number of copies: 6 / Enantiomer: LEVO |
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| Source (natural) | Organism: synthetic construct (others) |
| Molecular weight | Theoretical: 473.52 Da |
| Sequence | String: GAVEV |
-Macromolecule #2: 4,4'-(thiophene-2,5-diyl)dibenzoic acid
| Macromolecule | Name: 4,4'-(thiophene-2,5-diyl)dibenzoic acid / type: ligand / ID: 2 / Number of copies: 3 / Formula: A1B9Y |
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| Molecular weight | Theoretical: 324.35 Da |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | helical reconstruction |
| Aggregation state | filament |
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Sample preparation
| Buffer | pH: 7 |
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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: 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: 1.0 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
| Final reconstruction | Applied symmetry - Helical parameters - Δz: 4.75 Å Applied symmetry - Helical parameters - Δ&Phi: -4.29 ° Applied symmetry - Helical parameters - Axial symmetry: C2 (2 fold cyclic) Resolution.type: BY AUTHOR / Resolution: 3.2 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 304634 |
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
| Startup model | Type of model: NONE |
| Final angle assignment | Type: NOT APPLICABLE |
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Keywords
Authors
United States, 1 items
Citation




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FIELD EMISSION GUN
