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Open data
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Basic information
Entry | ![]() | |||||||||
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Title | Tetrahymena Ribozyme scaffolded TABV xrRNA | |||||||||
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![]() | Ribozyme / xrRNA / Scaffold / RNA | |||||||||
Biological species | ![]() ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.46 Å | |||||||||
![]() | Langeberg CJ / Kieft JS | |||||||||
Funding support | ![]()
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![]() | ![]() Title: A generalizable scaffold-based approach for structure determination of RNAs by cryo-EM. Authors: Conner J Langeberg / Jeffrey S Kieft / ![]() Abstract: Single-particle cryo-electron microscopy (cryo-EM) can reveal the structures of large and often dynamic molecules, but smaller biomolecules (≤50 kDa) remain challenging targets due to their ...Single-particle cryo-electron microscopy (cryo-EM) can reveal the structures of large and often dynamic molecules, but smaller biomolecules (≤50 kDa) remain challenging targets due to their intrinsic low signal to noise ratio. Methods to help resolve small proteins have been applied but development of similar approaches to aid in structural determination of small, structured RNA elements have lagged. Here, we present a scaffold-based approach that we used to recover maps of sub-25 kDa RNA domains to 4.5-5.0 Å. While lacking the detail of true high-resolution maps, these maps are suitable for model building and preliminary structure determination. We demonstrate this method helped faithfully recover the structure of several RNA elements of known structure, and that it promises to be generalized to other RNAs without disturbing their native fold. This approach may streamline the sample preparation process and reduce the optimization required for data collection. This first-generation scaffold approach provides a robust system to aid in RNA structure determination by cryo-EM and lays the groundwork for further scaffold optimization to achieve higher resolution. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 254.3 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 14.5 KB 14.5 KB | Display Display | ![]() |
FSC (resolution estimation) | ![]() | 16.9 KB | Display | ![]() |
Images | ![]() | 50.5 KB | ||
Filedesc metadata | ![]() | 5.2 KB | ||
Others | ![]() ![]() | 474.7 MB 474.7 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 723.2 KB | Display | ![]() |
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Full document | ![]() | 722.8 KB | Display | |
Data in XML | ![]() | 26.7 KB | Display | |
Data in CIF | ![]() | 35.2 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 8tjuMC ![]() 8tjqC ![]() 8tjvC ![]() 8tjxC M: atomic model generated by this map C: citing same article ( |
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Links
EMDB pages | ![]() ![]() |
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Map
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Voxel size | X=Y=Z: 0.8255 Å | ||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_41311_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_41311_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
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Sample components
-Entire : Tetrahymena Ribozyme scaffolded TABV xrRNA
Entire | Name: Tetrahymena Ribozyme scaffolded TABV xrRNA |
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Components |
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-Supramolecule #1: Tetrahymena Ribozyme scaffolded TABV xrRNA
Supramolecule | Name: Tetrahymena Ribozyme scaffolded TABV xrRNA / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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Source (natural) | Organism: ![]() |
-Macromolecule #1: DNA/RNA (416-MER)
Macromolecule | Name: DNA/RNA (416-MER) / type: other / ID: 1 / Number of copies: 1 Classification: polydeoxyribonucleotide/polyribonucleotide hybrid |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 134.331484 KDa |
Sequence | String: GGCAAGGUAC GGCAUAUGGA UGCAGUUCAC AGACUAAAUG UCGGUCGGGG AAGAUGUAUU CUUCUCAUAA GAUAUAGUCG GACCUCUCC UUAAUGGGAG CUAGCGGAUG AAGUGAUGCA ACACUGGAGC CGCUGGGAAC UAAUUUGUAU GCGAAAGUAU A UUGAUUAG ...String: GGCAAGGUAC GGCAUAUGGA UGCAGUUCAC AGACUAAAUG UCGGUCGGGG AAGAUGUAUU CUUCUCAUAA GAUAUAGUCG GACCUCUCC UUAAUGGGAG CUAGCGGAUG AAGUGAUGCA ACACUGGAGC CGCUGGGAAC UAAUUUGUAU GCGAAAGUAU A UUGAUUAG UUUUGGAG(DG)(DA) (DG)(DG)(DG)(DA)(DA)AAGUU AUCAGGCAUG CACCUGGUAG CUAGUCUUUA A ACCAAUAG AUUGCAUCGG UUUAAAAGGC AAGACCGUCA AAUUGCGGGA AAGGGGUCAA CAGCCGUUCA GUACCAAGUC UC AGGGGAA ACUUUGAGAU GGCCUUGCAA AGGGUAUGGU AAUAAGCUGA CGGACAUGGU CCUAACCACG CAGCCAAGUC CUA AGUGCC GUAGGGGCUU GAGAACCCCC CCUCCCCACU C |
Recombinant expression | Organism: in vitro transcription vector pT7-Fluc(deltai) (others) |
-Macromolecule #2: MAGNESIUM ION
Macromolecule | Name: MAGNESIUM ION / type: ligand / ID: 2 / Number of copies: 27 / Formula: MG |
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Molecular weight | Theoretical: 24.305 Da |
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | single particle reconstruction |
Aggregation state | particle |
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Sample preparation
Buffer | pH: 7.5 Component:
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Grid | Model: C-flat-1.2/1.3 / Material: COPPER / Mesh: 50 / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 6 sec. / Pretreatment - Atmosphere: OTHER | |||||||||
Vitrification | Cryogen name: ETHANE |
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Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 50.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.0 µm / Nominal defocus min: 0.8 µm |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |