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Open data
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Basic information
Entry | ![]() | |||||||||
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Title | Cryo-EM structure of partial VP4 from simian rotavirus SA11 | |||||||||
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![]() | VIRUS / ROTAVIRUS / VP4 | |||||||||
Function / homology | ![]() host cytoskeleton / viral outer capsid / symbiont entry into host cell via permeabilization of host membrane / host cell endoplasmic reticulum / virion attachment to host cell / host cell plasma membrane / membrane Similarity search - Function | |||||||||
Biological species | ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.84 Å | |||||||||
![]() | Huang Y / Sun H / Zheng Q / Li S / Ge S / Xia N | |||||||||
Funding support | 1 items
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![]() | ![]() Title: A single residue switch mediates the broad neutralization of Rotaviruses. Authors: Yang Huang / Feibo Song / Yuanjun Zeng / Hui Sun / Roufang Sheng / Xuechun Wang / Liqin Liu / Guoxing Luo / Yanan Jiang / Yaling Chen / Mengxuan Zhang / Shiyin Zhang / Ying Gu / Hai Yu / ...Authors: Yang Huang / Feibo Song / Yuanjun Zeng / Hui Sun / Roufang Sheng / Xuechun Wang / Liqin Liu / Guoxing Luo / Yanan Jiang / Yaling Chen / Mengxuan Zhang / Shiyin Zhang / Ying Gu / Hai Yu / Shaowei Li / Tingdong Li / Qingbing Zheng / Shengxiang Ge / Jun Zhang / Ningshao Xia / ![]() Abstract: Broadly neutralizing antibodies (bNAbs) could offer escape-tolerant and lasting protection against viral infections and therefore guide development of broad-spectrum vaccines. The increasing ...Broadly neutralizing antibodies (bNAbs) could offer escape-tolerant and lasting protection against viral infections and therefore guide development of broad-spectrum vaccines. The increasing challenge posed by viral evolution and immune evasion intensifies the importance of the discovery of bNAbs and their underlying neutralization mechanism. Here, focusing on the pivotal viral protein VP4 of rotavirus (RV), we identify a potent bNAb, 7H13, exhibiting broad-spectrum neutralization across diverse RV genotypes and demonstrating strong prevention of virus infection in female mice. A combination of time-resolved cryo-electron microscopy (cryo-EM) and in situ cryo-electron tomography (cryo-ET) analysis reveals a counterintuitive dynamic process of virus inactivation, in which 7H13 asymmetrically binds to a conserved epitope in the capsid-proximal aspect of VP4, triggers a conformational switch in a critical residue-F418-thereby disrupts the meta-stable conformation of VP4 essential for normal viral infection. Structure-guided mutagenesis corroborates the essential role of the 7H13 heavy chain I54 in activating F418 switch and destabilizing VP4. These findings define an atypical NAbs' neutralization mechanism and reveal a potential type of virus vulnerable site for universal vaccine and therapeutics design. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 157 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 18 KB 18 KB | Display Display | ![]() |
Images | ![]() | 48 KB | ||
Filedesc metadata | ![]() | 5.4 KB | ||
Others | ![]() ![]() | 165.1 MB 165.1 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 8ygrMC ![]() 8ygsC ![]() 8ygtC ![]() 8yguC M: atomic model generated by this map C: citing same article ( |
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Similar structure data | Similarity search - Function & homology ![]() |
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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 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_39260_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_39260_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
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Sample components
-Entire : Rotavirus A
Entire | Name: ![]() |
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Components |
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-Supramolecule #1: Rotavirus A
Supramolecule | Name: Rotavirus A / type: virus / ID: 1 / Parent: 0 / Macromolecule list: all / NCBI-ID: 28875 / Sci species name: Rotavirus A / Sci species strain: SA11 / Virus type: VIRION / Virus isolate: STRAIN / Virus enveloped: No / Virus empty: No |
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-Supramolecule #2: Partial VP4 of rotavirus
Supramolecule | Name: Partial VP4 of rotavirus / type: complex / ID: 2 / Parent: 1 / Macromolecule list: all |
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Source (natural) | Organism: ![]() |
-Macromolecule #1: Outer capsid protein VP4
Macromolecule | Name: Outer capsid protein VP4 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 64.861418 KDa |
Sequence | String: GYKMASLIYR QLLTNSYTVD LSDEIQEIGS TKSQNVTINP GPFAQTGYAP VNWGPGEIND STTVEPLLDG PYQPTTFNPP VDYWMLLAP TTPGVIVEGT NNTDRWLATI LIEPNVQSEN RTYTIFGIQE QLTVSNTSQD QWKFIDVVKT TANGSIGQYG P LLSSPKLY ...String: GYKMASLIYR QLLTNSYTVD LSDEIQEIGS TKSQNVTINP GPFAQTGYAP VNWGPGEIND STTVEPLLDG PYQPTTFNPP VDYWMLLAP TTPGVIVEGT NNTDRWLATI LIEPNVQSEN RTYTIFGIQE QLTVSNTSQD QWKFIDVVKT TANGSIGQYG P LLSSPKLY AVMKHNEKLY TYEGQTPNAR TAHYSTTNYD SVNMTAFCDF YIIPRSEESK CTEYINNGLP PIQNTRNVVP LS LTARDVI HYRAQANEDI VISKTSLWKE MQYNRDITIR FKFANTIIKS GGLGYKWSEI SFKPANYQYT YTRDGEEVTA HTT CSVNGV NDFSFNGGSL PTDFVVSKFE VIKENSYVYI DYWDDSQAFR NVVYVRSLAA NLNSVMCTGG SYNFSLPVGQ WPVL TGGAV SLHSAGVTLS TQFTDFVSLN SLRFRFRLAV EEPHFKLTRT RLSRLYGLPA ANPNNGKEYY EIAGRFSLIS LVPSN HDYQ TPIANSVTVR QDLERQLGEL REEFNALSQE IAMSQLIDLA LLPLDMFSMF SGIKSTIDAA KSMATNVMKK FKKSGL ANS VSTLTDSLSD AASSISRG UniProtKB: Outer capsid protein VP4 |
-Macromolecule #2: Outer capsid protein VP4
Macromolecule | Name: Outer capsid protein VP4 / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 64.889465 KDa |
Sequence | String: GYKMASLIYR QLLTNSYTVD LSDEIQEIGS TKSQNVTINP GPFAQTGYAP VNWGPGEIND STTVEPLLDG PYQPTTFNPP VDYWMLLAP TTPGVIVEGT NNTDRWLATI LIEPNVQSEN RTYTIFGIQE QLTVSNTSQD QWKFIDVVKT TANGSIGQYG P LLSSPKLY ...String: GYKMASLIYR QLLTNSYTVD LSDEIQEIGS TKSQNVTINP GPFAQTGYAP VNWGPGEIND STTVEPLLDG PYQPTTFNPP VDYWMLLAP TTPGVIVEGT NNTDRWLATI LIEPNVQSEN RTYTIFGIQE QLTVSNTSQD QWKFIDVVKT TANGSIGQYG P LLSSPKLY AVMKHNEKLY TYEGQTPNAR TAHYSTTNYD SVNMTAFCDF YIIPRSEESK CTEYINNGLP PIQNTRNVVP LS LTARDVI HYRAQVNEDI VISKTSLWKE MQYNRDITIR FKFANTIIKS GGLGYKWSEI SFKPANYQYT YTRDGEEVTA HTT CSVNGV NDFSFNGGSL PTDFVVSKFE VIKENSYVYI DYWDDSQAFR NVVYVRSLAA NLNSVMCTGG SYNFSLPVGQ WPVL TGGAV SLHSAGVTLS TQFTDFVSLN SLRFRFRLAV EEPHFKLTRT RLSRLYGLPA ANPNNGKEYY EIAGRFSLIS LVPSN HDYQ TPIANSVTVR QDLERQLGEL REEFNALSQE IAMSQLIDLA LLPLDMFSMF SGIKSTIDAA KSMATNVMKK FKKSGL ANS VSTLTDSLSD AASSISRG UniProtKB: Outer capsid protein VP4 |
-Macromolecule #3: Outer capsid protein VP4
Macromolecule | Name: Outer capsid protein VP4 / type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 64.891465 KDa |
Sequence | String: GYKMASLIYR QLLTNSYTVD LSDEIQEIGS TKSQNVTINP GPFAQTGYAP VNWGPGEIND STTVEPLLDG PYQPTTFNPP VDYWMLLAP TTPGVIVEGT NNTDRWLATI LIEPNVQSEN RTYTIFGIQE QLTVSNTSQD QWKFIDVAKT TANGSIEQYG P LLSSPKLY ...String: GYKMASLIYR QLLTNSYTVD LSDEIQEIGS TKSQNVTINP GPFAQTGYAP VNWGPGEIND STTVEPLLDG PYQPTTFNPP VDYWMLLAP TTPGVIVEGT NNTDRWLATI LIEPNVQSEN RTYTIFGIQE QLTVSNTSQD QWKFIDVAKT TANGSIEQYG P LLSSPKLY AVMKHNKKLY TYEGQTPNAR TGHYSTTNYD SVNMTAFCDF YIIPRSEESK CTEYINNGLP PIQNTRNVVP LS LTARDVI HYRAQANEDI VISKTSLWKE MQYNRDITIR FKFANTIIKS GGLGYKWSEI SFKPANYQYT YTRDGEEVTA HTT CSVNGV NDFSFNGGSL PTDFVVSKFE VIKENSYVYI DYWDDSQAFR NVVYVRSLAA NLNSVMCTGG SYNFSLPVGQ WPVL TGGAV SLHSAGVTLS TQFTDFVSLN SLRFRFRLAV EEPHFKLTRT RLSRLYGLPA ANPNNGKEYY EIAGRFSLIS LVPSN HDYQ TPIANSVTVR QDLERQLGEL REEFNALSQE IAMSQLIDLA LLPLDMFSMF SGIKSTIDAA KSMATNVMKK FKKSGL ANS VSTLTDSLSD AASSISRG UniProtKB: Outer capsid protein VP4 |
-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: 7.4 |
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Vitrification | Cryogen name: ETHANE |
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Electron microscopy
Microscope | FEI TECNAI F30 |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 40.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 3.0 µm / Nominal defocus min: 0.7000000000000001 µm |
Experimental equipment | ![]() Model: Tecnai F30 / Image courtesy: FEI Company |
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Image processing
Startup model | Type of model: OTHER |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 3.84 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 367118 |
Initial angle assignment | Type: MAXIMUM LIKELIHOOD / Details: cryosparc local refine |
Final angle assignment | Type: MAXIMUM LIKELIHOOD / Details: cryosparc local refine |