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- EMDB-19046: DNA bound type IV-A1 CRISPR effector complex from P. oleovorans -
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Open data
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Basic information
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Title | DNA bound type IV-A1 CRISPR effector complex from P. oleovorans | ||||||||||||
![]() | composite map used for final refinement | ||||||||||||
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![]() | CRISPR / crRNA / DNA binding / type IV CRISPR-Cas / CRISPRi / nuclease deficient / GENE REGULATION | ||||||||||||
Function / homology | CRISPR-associated protein, Csf1 family / CRISPR type IV/AFERR-associated protein Csf2 / CRISPR type AFERR-associated protein Csf1 / CRISPR type AFERR-associated protein Csf2 / CRISPR type AFERR-associated protein Csf3 / Uncharacterized protein![]() | ||||||||||||
Biological species | ![]() | ||||||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.0 Å | ||||||||||||
![]() | Miksys A / Cepaite R / Malinauskaite L / Pausch P | ||||||||||||
Funding support | European Union, 3 items
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![]() | ![]() Title: Structural variation of types IV-A1- and IV-A3-mediated CRISPR interference. Authors: R Čepaitė / N Klein / A Mikšys / S Camara-Wilpert / V Ragožius / F Benz / A Skorupskaitė / H Becker / G Žvejytė / N Steube / G K A Hochberg / L Randau / R Pinilla-Redondo / L ...Authors: R Čepaitė / N Klein / A Mikšys / S Camara-Wilpert / V Ragožius / F Benz / A Skorupskaitė / H Becker / G Žvejytė / N Steube / G K A Hochberg / L Randau / R Pinilla-Redondo / L Malinauskaitė / P Pausch / ![]() ![]() ![]() ![]() Abstract: CRISPR-Cas mediated DNA-interference typically relies on sequence-specific binding and nucleolytic degradation of foreign genetic material. Type IV-A CRISPR-Cas systems diverge from this general ...CRISPR-Cas mediated DNA-interference typically relies on sequence-specific binding and nucleolytic degradation of foreign genetic material. Type IV-A CRISPR-Cas systems diverge from this general mechanism, using a nuclease-independent interference pathway to suppress gene expression for gene regulation and plasmid competition. To understand how the type IV-A system associated effector complex achieves this interference, we determine cryo-EM structures of two evolutionarily distinct type IV-A complexes (types IV-A1 and IV-A3) bound to cognate DNA-targets in the presence and absence of the type IV-A signature DinG effector helicase. The structures reveal how the effector complexes recognize the protospacer adjacent motif and target-strand DNA to form an R-loop structure. Additionally, we reveal differences between types IV-A1 and IV-A3 in DNA interactions and structural motifs that allow for in trans recruitment of DinG. Our study provides a detailed view of type IV-A mediated DNA-interference and presents a structural foundation for engineering type IV-A-based genome editing tools. | ||||||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 166.6 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 34.7 KB 34.7 KB | Display Display | ![]() |
FSC (resolution estimation) | ![]() ![]() | 11.8 KB 11.9 KB | Display Display | ![]() |
Images | ![]() | 80.5 KB | ||
Filedesc metadata | ![]() | 8.1 KB | ||
Others | ![]() ![]() ![]() ![]() ![]() | 148.2 MB 167.9 MB 89.3 MB 165.3 MB 165.3 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 8rc3MC ![]() 8rc2C ![]() 8rfjC ![]() 8s35C ![]() 8s36C ![]() 8s37C C: citing same article ( M: atomic model generated by this map |
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Similar structure data | Similarity search - Function & homology ![]() |
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Links
EMDB pages | ![]() ![]() |
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Map
File | ![]() | ||||||||||||||||||||||||||||||||||||
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Annotation | composite map used for final refinement | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.1 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Additional map: Unsharpened map of the whole complex
File | emd_19046_additional_1.map | ||||||||||||
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Annotation | Unsharpened map of the whole complex | ||||||||||||
Projections & Slices |
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Density Histograms |
-Additional map: Sharpened map of the whole complex
File | emd_19046_additional_2.map | ||||||||||||
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Annotation | Sharpened map of the whole complex | ||||||||||||
Projections & Slices |
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Density Histograms |
-Additional map: Composite sharpened map processed with EMReady, used for...
File | emd_19046_additional_3.map | ||||||||||||
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Annotation | Composite sharpened map processed with EMReady, used for initial model building | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Unsharpened half map A of the whole complex
File | emd_19046_half_map_1.map | ||||||||||||
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Annotation | Unsharpened half map A of the whole complex | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Unsharpened half map B of the whole complex
File | emd_19046_half_map_2.map | ||||||||||||
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Annotation | Unsharpened half map B of the whole complex | ||||||||||||
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Density Histograms |
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Sample components
+Entire : Type IV-A1 CRISPR-Cas effector complex from Pseudomonas oleovoran...
+Supramolecule #1: Type IV-A1 CRISPR-Cas effector complex from Pseudomonas oleovoran...
+Supramolecule #2: Type IV-A1 CRISPR-Cas effector complex from Pseudomonas oleovoran...
+Supramolecule #3: Target DNA
+Macromolecule #1: CRISPR type AFERR-associated protein Csf2
+Macromolecule #2: CRISPR type AFERR-associated protein Csf3
+Macromolecule #3: CRISPR type AFERR-associated protein Csf1
+Macromolecule #7: CRISPR type AFERR-associated protein Csf5
+Macromolecule #4: crRNA
+Macromolecule #5: Target strand (TS) DNA
+Macromolecule #6: Non-target strand (NTS) DNA
+Macromolecule #8: ZINC ION
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | single particle reconstruction |
Aggregation state | particle |
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Sample preparation
Concentration | 0.5 mg/mL | ||||||
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Buffer | pH: 7.5 / Component:
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Grid | Model: Quantifoil R1.2/1.3 / Material: COPPER / Mesh: 300 / Support film - Material: CARBON / Support film - topology: CONTINUOUS / Support film - Film thickness: 2 / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 7 sec. / Pretreatment - Atmosphere: AIR / Details: 20 mA | ||||||
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
Microscope | TFS GLACIOS |
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Image recording | Film or detector model: FEI FALCON III (4k x 4k) / Detector mode: COUNTING / Digitization - Dimensions - Width: 4096 pixel / Digitization - Dimensions - Height: 4096 pixel / Number grids imaged: 1 / Number real images: 2332 / Average exposure time: 48.0 sec. / Average electron dose: 30.0 e/Å2 |
Electron beam | Acceleration voltage: 200 kV / Electron source: ![]() |
Electron optics | Calibrated defocus max: 2.0 µm / Calibrated defocus min: 1.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.0 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 92000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
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Image processing
-Atomic model buiding 1
Initial model | Chain - Source name: AlphaFold / Chain - Initial model type: in silico model |
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Refinement | Space: REAL / Protocol: AB INITIO MODEL |
Output model | ![]() PDB-8rc3: |