+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-31807 | |||||||||
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Title | Cryo-EM structure of the Cas12c2-sgRNA binary complex | |||||||||
Map data | postprocess_masked.mrc from Relion | |||||||||
Sample |
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Keywords | cas12c / c2c3 / sgRNA / CRISPR / RNA binding protein-RNA complex | |||||||||
Biological species | uncultured archaeon (environmental samples) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.0 Å | |||||||||
Authors | Kurihara N / Hirano H / Tomita A / Kobayashi K | |||||||||
Funding support | Japan, 1 items
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Citation | Journal: Mol Cell / Year: 2022 Title: Structure of the type V-C CRISPR-Cas effector enzyme. Authors: Nina Kurihara / Ryoya Nakagawa / Hisato Hirano / Sae Okazaki / Atsuhiro Tomita / Kan Kobayashi / Tsukasa Kusakizako / Tomohiro Nishizawa / Keitaro Yamashita / David A Scott / Hiroshi ...Authors: Nina Kurihara / Ryoya Nakagawa / Hisato Hirano / Sae Okazaki / Atsuhiro Tomita / Kan Kobayashi / Tsukasa Kusakizako / Tomohiro Nishizawa / Keitaro Yamashita / David A Scott / Hiroshi Nishimasu / Osamu Nureki / Abstract: RNA-guided CRISPR-Cas nucleases are widely used as versatile genome-engineering tools. Recent studies identified functionally divergent type V Cas12 family enzymes. Among them, Cas12c2 binds a CRISPR ...RNA-guided CRISPR-Cas nucleases are widely used as versatile genome-engineering tools. Recent studies identified functionally divergent type V Cas12 family enzymes. Among them, Cas12c2 binds a CRISPR RNA (crRNA) and a trans-activating crRNA (tracrRNA) and recognizes double-stranded DNA targets with a short TN PAM. Here, we report the cryo-electron microscopy structures of the Cas12c2-guide RNA binary complex and the Cas12c2-guide RNA-target DNA ternary complex. The structures revealed that the crRNA and tracrRNA form an unexpected X-junction architecture, and that Cas12c2 recognizes a single T nucleotide in the PAM through specific hydrogen-bonding interactions with two arginine residues. Furthermore, our biochemical analyses indicated that Cas12c2 processes its precursor crRNA to a mature crRNA using the RuvC catalytic site through a unique mechanism. Collectively, our findings improve the mechanistic understanding of diverse type V CRISPR-Cas effectors. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_31807.map.gz | 4.4 MB | EMDB map data format | |
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Header (meta data) | emd-31807-v30.xml emd-31807.xml | 18.1 KB 18.1 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_31807_fsc.xml | 6.9 KB | Display | FSC data file |
Images | emd_31807.png | 104.8 KB | ||
Masks | emd_31807_msk_1.map | 27 MB | Mask map | |
Filedesc metadata | emd-31807.cif.gz | 6.5 KB | ||
Others | emd_31807_half_map_1.map.gz emd_31807_half_map_2.map.gz | 20.7 MB 20.7 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-31807 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-31807 | HTTPS FTP |
-Validation report
Summary document | emd_31807_validation.pdf.gz | 720.1 KB | Display | EMDB validaton report |
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Full document | emd_31807_full_validation.pdf.gz | 719.7 KB | Display | |
Data in XML | emd_31807_validation.xml.gz | 12.5 KB | Display | |
Data in CIF | emd_31807_validation.cif.gz | 17 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-31807 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-31807 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_31807.map.gz / Format: CCP4 / Size: 27 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | postprocess_masked.mrc from Relion | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.10667 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Mask #1
File | emd_31807_msk_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: run half2 class001 unfil.mrc from Relion
File | emd_31807_half_map_1.map | ||||||||||||
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Annotation | run_half2_class001_unfil.mrc from Relion | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: run half1 class001 unfil.mrc from Relion
File | emd_31807_half_map_2.map | ||||||||||||
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Annotation | run_half1_class001_unfil.mrc from Relion | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Cas12c2-sgRNA complex
Entire | Name: Cas12c2-sgRNA complex |
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Components |
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-Supramolecule #1: Cas12c2-sgRNA complex
Supramolecule | Name: Cas12c2-sgRNA complex / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: uncultured archaeon (environmental samples) |
-Supramolecule #2: Cas12c2
Supramolecule | Name: Cas12c2 / type: complex / ID: 2 / Parent: 1 / Macromolecule list: #1 |
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Source (natural) | Organism: uncultured archaeon (environmental samples) |
-Supramolecule #3: sgRNA
Supramolecule | Name: sgRNA / type: complex / ID: 3 / Parent: 1 / Macromolecule list: #2 |
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-Macromolecule #1: cas12c2
Macromolecule | Name: cas12c2 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: uncultured archaeon (environmental samples) |
Molecular weight | Theoretical: 138.348938 KDa |
Recombinant expression | Organism: Escherichia coli (E. coli) |
Sequence | String: MKIEEGKGHH HHHHMTKHSI PLHAFRNSGA DARKWKGRIA LLAKRGKETM RTLQFPLEMS EPEAAAINTT PFAVAYNAIE GTGKGTLFD YWAKLHLAGF RFFPSGGAAT IFRQQAVFED ASWNAAFCQQ SGKDWPWLVP SKLYERFTKA PREVAKKDGS K KSIEFTQE ...String: MKIEEGKGHH HHHHMTKHSI PLHAFRNSGA DARKWKGRIA LLAKRGKETM RTLQFPLEMS EPEAAAINTT PFAVAYNAIE GTGKGTLFD YWAKLHLAGF RFFPSGGAAT IFRQQAVFED ASWNAAFCQQ SGKDWPWLVP SKLYERFTKA PREVAKKDGS K KSIEFTQE NVANESHVSL VGASITDKTP EDQKEFFLKM AGALAEKFDS WKSANEDRIV AMKVIDEFLK SEGLHLPSLE NI AVKCSVE TKPDNATVAW HDAPMSGVQN LAIGVFATCA SRIDNIYDLN GGKLSKLIQE SATTPNVTAL SWLFGKGLEY FRT TDIDTI MQDFNIPASA KESIKPLVES AQAIPTMTVL GKKNYAPFRP NFGGKIDSWI ANYASRLMLL NDILEQIEPG FELP QALLD NETLMSGIDM TGDELKELIE AVYAWVDAAK QGLATLLGRG GNVDDAVQTF EQFSAMMDTL NGTLNTISAR YVRAV EMAG KDEARLEKLI ECKFDIPKWC KSVPKLVGIS GGLPKVEEEI KVMNAAFKDV RARMFVRFEE IAAYVASKGA GMDVYD ALE KRELEQIKKL KSAVPERAHI QAYRAVLHRI GRAVQNCSEK TKQLFSSKVI EMGVFKNPSH LNNFIFNQKG AIYRSPF DR SRHAPYQLHA DKLLKNDWLE LLAEISATLM ASESTEQMED ALRLERTRLQ LQLSGLPDWE YPASLAKPDI EVEIQTAL K MQLAKDTVTS DVLQRAFNLY SSVLSGLTFK LLRRSFSLKM RFSVADTTQL IYVPKVCDWA IPKQYLQAEG EIGIAARVV TESSPAKMVT EVEMKEPKAL GHFMQQAPHD WYFDASLGGT QVAGRIVEKG KEVGKERKLV GYRMRGNSAY KTVLDKSLVG NTELSQCSM IIEIPYTQTV DADFRAQVQA GLPKVSINLP VKETITASNK DEQMLFDRFV AIDLGERGLG YAVFDAKTLE L QESGHRPI KAITNLLNRT HHYEQRPNQR QKFQAKFNVN LSELRENTVG DVCHQINRIC AYYNAFPVLE YMVPDRLDKQ LK SVYESVT NRYIWSSTDA HKSARVQFWL GGETWEHPYL KSAKDKKPLV LSPGRGASGK GTSQTCSCCG RNPFDLIKDM KPR AKIAVV DGKAKLENSE LKLFERNLES KDDMLARRHR NERAGMEQPL TPGNYTVDEI KALLRANLRR APKNRRTKDT TVSE YHCVF SDCGKTMHAD ENAAVNIGGK FIADIEK |
-Macromolecule #2: sgRNA
Macromolecule | Name: sgRNA / type: rna / ID: 2 / Number of copies: 1 |
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Source (natural) | Organism: uncultured archaeon (environmental samples) |
Molecular weight | Theoretical: 36.147414 KDa |
Sequence | String: GGAUACCACC CGUGCAUUUC UGGAUCAAUG AUCCGUACCU CAAUGUCCGG GCGCGCAGCU AGAGCGACCU GAAGAAAUUC AGGUUGGGU UUGAGGGGAA AUUAGGUGCG CUU |
-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/RHODIUM / Mesh: 300 / Support film - Material: CARBON / Support film - topology: HOLEY ARRAY |
Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average exposure time: 5.0 sec. / Average electron dose: 54.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
+Image processing
-Atomic model buiding 1
Refinement | Space: RECIPROCAL / Protocol: FLEXIBLE FIT |
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Output model | PDB-7v93: |