[English] 日本語
Yorodumi- EMDB-5774: A Two-Pronged Structural Analysis of Retroviral Maturation Indica... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-5774 | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Title | A Two-Pronged Structural Analysis of Retroviral Maturation Indicates that Core Formation Proceeds by a Disassembly-Reassembly Pathway Rather than a Displacive Transition | |||||||||
Map data | Reconstruction of the inner particles (T=1) of the 30 nm RSV-CASP | |||||||||
Sample |
| |||||||||
Keywords | Cryo-EM / Rous Sarcoma Virus Structure / in vitro assembled capsids / spacer peptide | |||||||||
Biological species | Rous sarcoma virus | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 20.0 Å | |||||||||
Authors | Keller PW / Huang RK / England M / Waki K / Cheng N / Heymann JB / Craven RC / Freed EO / Steven AC | |||||||||
Citation | Journal: J Virol / Year: 2013 Title: A two-pronged structural analysis of retroviral maturation indicates that core formation proceeds by a disassembly-reassembly pathway rather than a displacive transition. Authors: Paul W Keller / Rick K Huang / Matthew R England / Kayoko Waki / Naiqian Cheng / J Bernard Heymann / Rebecca C Craven / Eric O Freed / Alasdair C Steven / Abstract: Retrovirus maturation involves sequential cleavages of the Gag polyprotein, initially arrayed in a spherical shell, leading to formation of capsids with polyhedral or conical morphology. Evidence ...Retrovirus maturation involves sequential cleavages of the Gag polyprotein, initially arrayed in a spherical shell, leading to formation of capsids with polyhedral or conical morphology. Evidence suggests that capsids assemble de novo inside maturing virions from dissociated capsid (CA) protein, but the possibility persists of a displacive pathway in which the CA shell remains assembled but is remodeled. Inhibition of the final cleavage between CA and spacer peptide SP1/SP blocks the production of mature capsids. We investigated whether retention of SP might render CA assembly incompetent by testing the ability of Rous sarcoma virus (RSV) CA-SP to assemble in vitro into icosahedral capsids. Capsids were indeed assembled and were indistinguishable from those formed by CA alone, indicating that SP was disordered. We also used cryo-electron tomography to characterize HIV-1 particles produced in the presence of maturation inhibitor PF-46396 or with the cleavage-blocking CA5 mutation. Inhibitor-treated virions have a shell that resembles the CA layer of the immature Gag shell but is less complete. Some CA protein is generated but usually not enough for a mature core to assemble. We propose that inhibitors like PF-46396 bind to the Gag lattice where they deny the protease access to the CA-SP1 cleavage site and prevent the release of CA. CA5 particles, which exhibit no cleavage at the CA-SP1 site, have spheroidal shells with relatively thin walls. It appears that this lattice progresses displacively toward a mature-like state but produces neither conical cores nor infectious virions. These observations support the disassembly-reassembly pathway for core formation. | |||||||||
History |
|
-Structure visualization
Movie |
Movie viewer |
---|---|
Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_5774.map.gz | 151 MB | EMDB map data format | |
---|---|---|---|---|
Header (meta data) | emd-5774-v30.xml emd-5774.xml | 13.4 KB 13.4 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_5774_fsc.xml | 3.3 KB | Display | FSC data file |
Images | emd_5774.png emd_5774_1.png | 183.4 KB 886.3 KB | ||
Masks | emd_5774_msk_1.map | 40.9 MB | Mask map | |
Others | emd_5774_additional_1.map.gz | 151 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-5774 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-5774 | HTTPS FTP |
-Validation report
Summary document | emd_5774_validation.pdf.gz | 78.1 KB | Display | EMDB validaton report |
---|---|---|---|---|
Full document | emd_5774_full_validation.pdf.gz | 77.2 KB | Display | |
Data in XML | emd_5774_validation.xml.gz | 494 B | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-5774 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-5774 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
---|
-Map
File | Download / File: emd_5774.map.gz / Format: CCP4 / Size: 159.7 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Annotation | Reconstruction of the inner particles (T=1) of the 30 nm RSV-CASP | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.27 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
|
-Supplemental data
-Segmentation: Use to mask only the inner capsid.
Annotation | Use to mask only the inner capsid. | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
File | emd_5774_msk_1.map | ||||||||||||
Projections & Slices |
| ||||||||||||
Density Histograms |
-Supplemental map: emd 5774 additional 1.map
File | emd_5774_additional_1.map | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Projections & Slices |
| ||||||||||||
Density Histograms |
-Sample components
-Entire : Icosahedral assembly of Rous sarcoma virus capsid proteins with s...
Entire | Name: Icosahedral assembly of Rous sarcoma virus capsid proteins with spacer peptide (inner particle) |
---|---|
Components |
|
-Supramolecule #1000: Icosahedral assembly of Rous sarcoma virus capsid proteins with s...
Supramolecule | Name: Icosahedral assembly of Rous sarcoma virus capsid proteins with spacer peptide (inner particle) type: sample / ID: 1000 / Details: Inner shell of the 30nm particle Oligomeric state: Icosahedral shell composed of 12 pentamers Number unique components: 1 |
---|---|
Molecular weight | Theoretical: 1.5 MDa |
-Supramolecule #1: Rous sarcoma virus
Supramolecule | Name: Rous sarcoma virus / type: virus / ID: 1 / NCBI-ID: 11886 / Sci species name: Rous sarcoma virus / Virus type: VIRUS-LIKE PARTICLE / Virus isolate: SPECIES / Virus enveloped: No / Virus empty: Yes |
---|---|
Host (natural) | Organism: Gallus gallus (chicken) / synonym: VERTEBRATES |
Host system | Organism: Escherichia coli (E. coli) / Recombinant strain: BL21 |
Virus shell | Shell ID: 1 / Name: inner particles / T number (triangulation number): 1 |
-Experimental details
-Structure determination
Method | cryo EM |
---|---|
Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 2 mg/mL |
---|---|
Buffer | pH: 7.5 Details: 10 mM Tris-HCl, 75 mM sodium chloride, 0.05 mM EDTA, 0.5 M sodium phosphate |
Grid | Details: Holey carbon film on R2/2 400 mesh copper grid |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 90 % / Chamber temperature: 93.15 K / Instrument: LEICA KF80 / Details: Vitrification carried out in nitrogen atmosphere. Method: 4.0 microliter sample dropped onto grid, blotted on one side for 2 second, then plunged. |
-Electron microscopy
Microscope | FEI/PHILIPS CM200FEG |
---|---|
Temperature | Average: 93.15 K |
Date | Sep 24, 2011 |
Image recording | Category: FILM / Film or detector model: KODAK SO-163 FILM / Digitization - Scanner: NIKON SUPER COOLSCAN 9000 / Digitization - Sampling interval: 6.35 µm / Number real images: 17 / Average electron dose: 15 e/Å2 / Details: scanning at 4000 dpi / Bits/pixel: 16 |
Electron beam | Acceleration voltage: 120 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2 mm / Nominal defocus max: 2.1 µm / Nominal defocus min: 0.7 µm / Nominal magnification: 50000 |
Sample stage | Specimen holder model: GATAN LIQUID NITROGEN |