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Open data
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Basic information
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Title | Pseudosymmetric protein nanocage GI9-F7 (local refinement) | |||||||||
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![]() | Fusion protein / Structural Genomics / Seattle Structural Genomics Center for Infectious Disease / SSGCID / pseudosymmetric protein nanocages / VIRAL PROTEIN | |||||||||
Biological species | synthetic construct (others) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 4.0 Å | |||||||||
![]() | Park YJ / Dowling QM / King NP / Seattle Structural Genomics Center for Infectious Disease (SSGCID) / Veesler D | |||||||||
Funding support | ![]()
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![]() | ![]() Title: Hierarchical design of pseudosymmetric protein nanocages. Authors: Quinton M Dowling / Young-Jun Park / Chelsea N Fries / Neil C Gerstenmaier / Sebastian Ols / Erin C Yang / Adam J Wargacki / Annie Dosey / Yang Hsia / Rashmi Ravichandran / Carl D Walkey / ...Authors: Quinton M Dowling / Young-Jun Park / Chelsea N Fries / Neil C Gerstenmaier / Sebastian Ols / Erin C Yang / Adam J Wargacki / Annie Dosey / Yang Hsia / Rashmi Ravichandran / Carl D Walkey / Anika L Burrell / David Veesler / David Baker / Neil P King / ![]() Abstract: Discrete protein assemblies ranging from hundreds of kilodaltons to hundreds of megadaltons in size are a ubiquitous feature of biological systems and perform highly specialized functions. Despite ...Discrete protein assemblies ranging from hundreds of kilodaltons to hundreds of megadaltons in size are a ubiquitous feature of biological systems and perform highly specialized functions. Despite remarkable recent progress in accurately designing new self-assembling proteins, the size and complexity of these assemblies has been limited by a reliance on strict symmetry. Here, inspired by the pseudosymmetry observed in bacterial microcompartments and viral capsids, we developed a hierarchical computational method for designing large pseudosymmetric self-assembling protein nanomaterials. We computationally designed pseudosymmetric heterooligomeric components and used them to create discrete, cage-like protein assemblies with icosahedral symmetry containing 240, 540 and 960 subunits. At 49, 71 and 96 nm diameter, these nanocages are the largest bounded computationally designed protein assemblies generated to date. More broadly, by moving beyond strict symmetry, our work substantially broadens the variety of self-assembling protein architectures that are accessible through design. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 1.3 GB | ![]() | |
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Header (meta data) | ![]() ![]() | 21.3 KB 21.3 KB | Display Display | ![]() |
Images | ![]() | 57 KB | ||
Filedesc metadata | ![]() | 6 KB | ||
Others | ![]() ![]() ![]() | 717.8 MB 1.3 GB 1.3 GB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 880.7 KB | Display | ![]() |
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Full document | ![]() | 880.4 KB | Display | |
Data in XML | ![]() | 23.6 KB | Display | |
Data in CIF | ![]() | 28.6 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
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Links
EMDB pages | ![]() ![]() |
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Map
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Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.686 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Additional map: #1
File | emd_47038_additional_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_47038_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #2
File | emd_47038_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
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Sample components
-Entire : Pseudosymmetric protein nanocages: GI9-F7 nanocage
Entire | Name: Pseudosymmetric protein nanocages: GI9-F7 nanocage |
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Components |
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-Supramolecule #1: Pseudosymmetric protein nanocages: GI9-F7 nanocage
Supramolecule | Name: Pseudosymmetric protein nanocages: GI9-F7 nanocage / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: synthetic construct (others) |
-Macromolecule #1: Pseudosymmetric protein nanocage GI9-F7 A chain
Macromolecule | Name: Pseudosymmetric protein nanocage GI9-F7 A chain / type: protein_or_peptide / ID: 1 / Number of copies: 3 / Enantiomer: LEVO |
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Source (natural) | Organism: synthetic construct (others) |
Molecular weight | Theoretical: 24.330975 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: GSHHHHHHGS EKAAKAEEAA RKMEELFKEH KIVAVLRANS VEEAKKKALA VFLGGVHLIE ITFTVPDADT VIKELSFLKE MGAIIGAGT VTSVEQCREA VESGAEFIVS PHLDEEISQF CKEEGVFYMP GVMTPTELYK AMKLGHTILK LFPGEVVGPQ F VEAMKGPF ...String: GSHHHHHHGS EKAAKAEEAA RKMEELFKEH KIVAVLRANS VEEAKKKALA VFLGGVHLIE ITFTVPDADT VIKELSFLKE MGAIIGAGT VTSVEQCREA VESGAEFIVS PHLDEEISQF CKEEGVFYMP GVMTPTELYK AMKLGHTILK LFPGEVVGPQ F VEAMKGPF PNVKFVPTGG VNLDNVCEWF EAGVLAVGVG SALVEGTPVE VAEKAKAFVE KIEGCTE |
-Macromolecule #2: Pseudosymmetric protein nanocage GI9-F7 C chain
Macromolecule | Name: Pseudosymmetric protein nanocage GI9-F7 C chain / type: protein_or_peptide / ID: 2 / Number of copies: 3 / Enantiomer: LEVO |
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Source (natural) | Organism: synthetic construct (others) |
Molecular weight | Theoretical: 23.530266 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MKMEELFKEH KIVAVLRANS REEAIEIALA VFAGGVHLIE ITFTVPDADE VIKRLEMLKR AGAIIGAGTV TSVEQCREAV ESGAEFIVS PHLDEEISQF CKEEGVFYMP GVMTPTELVK AMKLGHTILK LFPGEVVGPQ FVEAMKGPFP NVKFVPTGGV N LDNVCEWF ...String: MKMEELFKEH KIVAVLRANS REEAIEIALA VFAGGVHLIE ITFTVPDADE VIKRLEMLKR AGAIIGAGTV TSVEQCREAV ESGAEFIVS PHLDEEISQF CKEEGVFYMP GVMTPTELVK AMKLGHTILK LFPGEVVGPQ FVEAMKGPFP NVKFVPTGGV N LDNVCEWF EAGVLAVGVG SALVEGKPSE VAEKARRFVK KIRGCTEGSL EHHHHHH |
-Macromolecule #3: Pseudosymmetric protein nanocage GI9-F7 B chain
Macromolecule | Name: Pseudosymmetric protein nanocage GI9-F7 B chain / type: protein_or_peptide / ID: 3 / Number of copies: 3 / Enantiomer: LEVO |
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Source (natural) | Organism: synthetic construct (others) |
Molecular weight | Theoretical: 22.115564 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MKMEELFKEH KIVAVLRANS VEEAISKALA VFAGGVHLIE ITFTVPDADQ VIKELEFLKE AGAIIGAGTV TSVEQCREAV ESGAEFIVS FHLDEEISQF CKEEGVFYMP GVMTPTELVK AMKLGHTILK LVPGEVVGPQ FVEAMKGPFP NVKFVPTGGV N LDNVCEWF ...String: MKMEELFKEH KIVAVLRANS VEEAISKALA VFAGGVHLIE ITFTVPDADQ VIKELEFLKE AGAIIGAGTV TSVEQCREAV ESGAEFIVS FHLDEEISQF CKEEGVFYMP GVMTPTELVK AMKLGHTILK LVPGEVVGPQ FVEAMKGPFP NVKFVPTGGV N LDNVCEWF EAGVLAVGVG SALVEGEPAE VAELAIRFVE KIRGCTE |
-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: 8 |
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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 (6k x 4k) / Average electron dose: 60.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.5 µm / Nominal defocus min: 0.5 µm |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
Startup model | Type of model: NONE |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 4.0 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: cryoSPARC / Number images used: 795360 |
Initial angle assignment | Type: PROJECTION MATCHING |
Final angle assignment | Type: PROJECTION MATCHING |