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Yorodumi- EMDB-22073: Cryo-EM structure of piggyBac transposase synaptic complex with h... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-22073 | |||||||||
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Title | Cryo-EM structure of piggyBac transposase synaptic complex with hairpin DNA (SNHP) | |||||||||
Map data | ||||||||||
Sample |
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Keywords | piggyBac / synaptic complex / hairpin DNA / transposase / DNA BINDING PROTEIN-DNA complex | |||||||||
Function / homology | PiggyBac transposable element-derived protein / Transposase IS4 / Transposase Function and homology information | |||||||||
Biological species | Trichoplusia ni (cabbage looper) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.66 Å | |||||||||
Authors | Chen Q / Hickman AB | |||||||||
Funding support | United States, 1 items
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Citation | Journal: Nat Commun / Year: 2020 Title: Structural basis of seamless excision and specific targeting by piggyBac transposase. Authors: Qiujia Chen / Wentian Luo / Ruth Ann Veach / Alison B Hickman / Matthew H Wilson / Fred Dyda / Abstract: The piggyBac DNA transposon is used widely in genome engineering applications. Unlike other transposons, its excision site can be precisely repaired without leaving footprints and it integrates ...The piggyBac DNA transposon is used widely in genome engineering applications. Unlike other transposons, its excision site can be precisely repaired without leaving footprints and it integrates specifically at TTAA tetranucleotides. We present cryo-EM structures of piggyBac transpososomes: a synaptic complex with hairpin DNA intermediates and a strand transfer complex capturing the integration step. The results show that the excised TTAA hairpin intermediate and the TTAA target adopt essentially identical conformations, providing a mechanistic link connecting the two unique properties of piggyBac. The transposase forms an asymmetric dimer in which the two central domains synapse the ends while two C-terminal domains form a separate dimer that contacts only one transposon end. In the strand transfer structure, target DNA is severely bent and the TTAA target is unpaired. In-cell data suggest that asymmetry promotes synaptic complex formation, and modifying ends with additional transposase binding sites stimulates activity. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_22073.map.gz | 20.1 MB | EMDB map data format | |
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Header (meta data) | emd-22073-v30.xml emd-22073.xml | 14.7 KB 14.7 KB | Display Display | EMDB header |
Images | emd_22073.png | 44 KB | ||
Filedesc metadata | emd-22073.cif.gz | 6.3 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-22073 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-22073 | HTTPS FTP |
-Validation report
Summary document | emd_22073_validation.pdf.gz | 516.8 KB | Display | EMDB validaton report |
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Full document | emd_22073_full_validation.pdf.gz | 516.4 KB | Display | |
Data in XML | emd_22073_validation.xml.gz | 5.6 KB | Display | |
Data in CIF | emd_22073_validation.cif.gz | 6.3 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-22073 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-22073 | HTTPS FTP |
-Related structure data
Related structure data | 6x68MC 6x67C C: citing same article (ref.) M: atomic model generated by this map |
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Similar structure data |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_22073.map.gz / Format: CCP4 / Size: 26.2 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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Sample components
-Entire : piggyBac transposase complex with hairpin DNA
Entire | Name: piggyBac transposase complex with hairpin DNA |
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Components |
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-Supramolecule #1: piggyBac transposase complex with hairpin DNA
Supramolecule | Name: piggyBac transposase complex with hairpin DNA / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 |
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Source (natural) | Organism: Trichoplusia ni (cabbage looper) |
-Macromolecule #1: Transposase
Macromolecule | Name: Transposase / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: Trichoplusia ni (cabbage looper) |
Molecular weight | Theoretical: 68.012969 KDa |
Recombinant expression | Organism: Homo sapiens (human) |
Sequence | String: MGSSLDDEHI LSALLQSDDE LVGEDSDSEI SDHVSEDDVQ SDTEEAFIDE VHEVQPTSSG SEILDEQNVI EQPGSSLASN KILTLPQRT IRGKNKHCWS TSKSTRRSRV SALNIVRSQR GPTRMCRNIY DPLLCFKLFF TDEIISEIVK WTNAEISLKR R ESMTGATF ...String: MGSSLDDEHI LSALLQSDDE LVGEDSDSEI SDHVSEDDVQ SDTEEAFIDE VHEVQPTSSG SEILDEQNVI EQPGSSLASN KILTLPQRT IRGKNKHCWS TSKSTRRSRV SALNIVRSQR GPTRMCRNIY DPLLCFKLFF TDEIISEIVK WTNAEISLKR R ESMTGATF RDTNEDEIYA FFGILVMTAV RKDNHMSTDD LFDRSLSMVY VSVMSRDRFD FLIRCLRMDD KSIRPTLREN DV FTPVRKI WDLFIHQCIQ NYTPGAHLTI DEQLLGFRGR CPFRMYIPNK PSKYGIKILM MCDSGTKYMI NGMPYLGRGT QTN GVPLGE YYVKELSKPV RGSCRNITCD NWFTSIPLAK NLLQEPYKLT IVGTVRSNKR EIPEVLKNSR SRPVGTSMFC FDGP LTLVS YKPKPAKMVY LLSSCDEDAS INESTGKPQM VMYYNQTKGG VDTLDQMCSV MTCSRKTNRW PMALLYGMIN IACIN SFII YSHNVSSKGE KVQSRKKFMR NLYMSLTSSF MRKRLEAPTL KRYLRDNISN ILPNEVPGTS DDSTEEPVTK KRTYCT YCP SKIRRKANAS CKKCKKVICR EHNIDMCQSC F UniProtKB: Transposase |
-Macromolecule #2: hairpin DNA
Macromolecule | Name: hairpin DNA / type: dna / ID: 2 / Number of copies: 2 / Classification: DNA |
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Source (natural) | Organism: Trichoplusia ni (cabbage looper) |
Molecular weight | Theoretical: 22.813643 KDa |
Sequence | String: (DC)(DA)(DT)(DG)(DC)(DG)(DT)(DC)(DA)(DA) (DT)(DT)(DT)(DT)(DA)(DC)(DG)(DC)(DA)(DG) (DA)(DC)(DT)(DA)(DT)(DC)(DT)(DT)(DT) (DC)(DT)(DA)(DG)(DG)(DG)(DT)(DT)(DA)(DA) (DC) (DC)(DC)(DT)(DA)(DG)(DA) ...String: (DC)(DA)(DT)(DG)(DC)(DG)(DT)(DC)(DA)(DA) (DT)(DT)(DT)(DT)(DA)(DC)(DG)(DC)(DA)(DG) (DA)(DC)(DT)(DA)(DT)(DC)(DT)(DT)(DT) (DC)(DT)(DA)(DG)(DG)(DG)(DT)(DT)(DA)(DA) (DC) (DC)(DC)(DT)(DA)(DG)(DA)(DA)(DA) (DG)(DA)(DT)(DA)(DG)(DT)(DC)(DT)(DG)(DC) (DG)(DT) (DA)(DA)(DA)(DA)(DT)(DT)(DG) (DA)(DC)(DG)(DC)(DA)(DT)(DG) |
-Macromolecule #3: CALCIUM ION
Macromolecule | Name: CALCIUM ION / type: ligand / ID: 3 / Number of copies: 4 / Formula: CA |
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Molecular weight | Theoretical: 40.078 Da |
-Macromolecule #4: ZINC ION
Macromolecule | Name: ZINC ION / type: ligand / ID: 4 / Number of copies: 4 / Formula: ZN |
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Molecular weight | Theoretical: 65.409 Da |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 0.8 mg/mL | |||||||||||||||
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Buffer | pH: 8 Component:
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Grid | Model: C-flat-1.2/1.3 / Material: GOLD / Mesh: 300 / Support film - Material: CARBON / Support film - topology: HOLEY / Support film - Film thickness: 400 / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 60 sec. / Pretreatment - Atmosphere: AIR | |||||||||||||||
Vitrification | Cryogen name: METHANE / Chamber humidity: 100 % / Chamber temperature: 298 K / Instrument: FEI VITROBOT MARK IV |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: SUPER-RESOLUTION / Average exposure time: 10.0 sec. / Average electron dose: 73.7 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: TUNGSTEN HAIRPIN |
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: REAL / Protocol: AB INITIO MODEL / Overall B value: 109 / Target criteria: Correlation coefficient |
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Output model | PDB-6x68: |