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Open data
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Basic information
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| Title | Cryo-EM of CarbIF tube | |||||||||
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Keywords | dipeptides / micelle / PROTEIN FIBRIL | |||||||||
| Biological species | synthetic construct (others) | |||||||||
| Method | helical reconstruction / cryo EM / Resolution: 3.2 Å | |||||||||
Authors | Sonani RR / Bianco S / Adams DJ / Egelman EH | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Faraday Discuss / Year: 2025Title: Cryo-EM for atomic characterization of supramolecular gels. Authors: Ravi R Sonani / Simona Bianco / Mark A B Kreutzberger / Dave J Adams / Edward H Egelman / ![]() Abstract: While there have been great advances in the design and synthesis of supramolecular gels, their characterization methods have largely stayed the same, with electron microscopy of dried samples, or ...While there have been great advances in the design and synthesis of supramolecular gels, their characterization methods have largely stayed the same, with electron microscopy of dried samples, or small-angle scattering and spectroscopy dominating the approaches used. Although these methods provide valuable insights into structural properties, they are unable to unambiguously generate reliable atomic models that can further guide the site-specific modification of supramolecular gelators. Cryogenic electron microscopy (cryo-EM), allowing the high-resolution imaging of the sample in a hydrated state, has emerged as the dominant technique in structural biology, but has yet to become a routine method in materials science. Here, we describe the use of cryo-EM to determine the atomic structure of the tubular micelle formed by the dipeptide CarbIF, revealing the mechanism of assembly and gelation. Using the CarbIF micelle as an example, we highlight some of the challenges in using cryo-EM to study such materials, and how determination of the helical symmetry can be the most difficult aspect of such a project. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_45610.map.gz | 53.8 MB | EMDB map data format | |
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| Header (meta data) | emd-45610-v30.xml emd-45610.xml | 12.2 KB 12.2 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_45610_fsc.xml | 8.4 KB | Display | FSC data file |
| Images | emd_45610.png | 49.2 KB | ||
| Filedesc metadata | emd-45610.cif.gz | 3.8 KB | ||
| Others | emd_45610_half_map_1.map.gz emd_45610_half_map_2.map.gz | 59.3 MB 59.3 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-45610 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-45610 | HTTPS FTP |
-Validation report
| Summary document | emd_45610_validation.pdf.gz | 808.7 KB | Display | EMDB validaton report |
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| Full document | emd_45610_full_validation.pdf.gz | 808.2 KB | Display | |
| Data in XML | emd_45610_validation.xml.gz | 16.4 KB | Display | |
| Data in CIF | emd_45610_validation.cif.gz | 21.4 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-45610 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-45610 | HTTPS FTP |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_45610.map.gz / Format: CCP4 / Size: 64 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: 1.08 Å | ||||||||||||||||||||||||||||||||||||
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: #1
| File | emd_45610_half_map_1.map | ||||||||||||
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-Half map: #2
| File | emd_45610_half_map_2.map | ||||||||||||
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Sample components
-Entire : CarbIF tubular micelle
| Entire | Name: CarbIF tubular micelle |
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| Components |
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-Supramolecule #1: CarbIF tubular micelle
| Supramolecule | Name: CarbIF tubular micelle / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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| Source (natural) | Organism: synthetic construct (others) |
-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: 11 |
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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: 2.2 µm / Nominal defocus min: 1.2 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Keywords
Authors
United States, 1 items
Citation
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Processing
FIELD EMISSION GUN

