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- EMDB-19254: HCV E1/E2 homodimer complex, ectodomain -

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Basic information

Entry
Database: EMDB / ID: EMD-19254
TitleHCV E1/E2 homodimer complex, ectodomain
Map data
Sample
  • Complex: HCV S52 E1E2
    • Protein or peptide: HCV E1
    • Protein or peptide: HCV E2
  • Ligand: 2-acetamido-2-deoxy-beta-D-glucopyranose
KeywordsHepatitis C virus S52 E1 E2 Homodimer Structure / VIRAL PROTEIN
Function / homology
Function and homology information


host cell mitochondrial membrane / host cell lipid droplet / symbiont-mediated suppression of host TRAF-mediated signal transduction / transformation of host cell by virus / symbiont-mediated perturbation of host cell cycle G1/S transition checkpoint / symbiont-mediated suppression of host JAK-STAT cascade via inhibition of STAT1 activity / symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of MAVS activity / lipid droplet / ribonucleoside triphosphate phosphatase activity / channel activity ...host cell mitochondrial membrane / host cell lipid droplet / symbiont-mediated suppression of host TRAF-mediated signal transduction / transformation of host cell by virus / symbiont-mediated perturbation of host cell cycle G1/S transition checkpoint / symbiont-mediated suppression of host JAK-STAT cascade via inhibition of STAT1 activity / symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of MAVS activity / lipid droplet / ribonucleoside triphosphate phosphatase activity / channel activity / monoatomic ion transmembrane transport / viral nucleocapsid / clathrin-dependent endocytosis of virus by host cell / RNA helicase activity / host cell perinuclear region of cytoplasm / host cell endoplasmic reticulum membrane / symbiont-mediated suppression of host type I interferon-mediated signaling pathway / induction by virus of host autophagy / ribonucleoprotein complex / viral RNA genome replication / cysteine-type endopeptidase activity / serine-type endopeptidase activity / RNA-dependent RNA polymerase activity / virus-mediated perturbation of host defense response / fusion of virus membrane with host endosome membrane / viral envelope / host cell nucleus / virion attachment to host cell / apoptotic process / host cell plasma membrane / structural molecule activity / virion membrane / proteolysis / RNA binding / zinc ion binding / ATP binding / membrane / plasma membrane / cytoplasm
Similarity search - Function
Hepatitus C virus, Non-structural 5a protein, C-terminal / Hepatitis C virus NS5A, 1B domain superfamily / Hepatitis C virus non-structural protein NS2, N-terminal domain / Hepatitis C virus non-structural protein NS2 / HCV NS5a protein C-terminal region / Hepatitis C virus, Non-structural protein NS4b / Hepatitis C virus, Core protein, N-terminal / Hepatitis C virus non-structural protein NS2, C-terminal domain / Hepatitis C virus core protein, chain A superfamily / : ...Hepatitus C virus, Non-structural 5a protein, C-terminal / Hepatitis C virus NS5A, 1B domain superfamily / Hepatitis C virus non-structural protein NS2, N-terminal domain / Hepatitis C virus non-structural protein NS2 / HCV NS5a protein C-terminal region / Hepatitis C virus, Non-structural protein NS4b / Hepatitis C virus, Core protein, N-terminal / Hepatitis C virus non-structural protein NS2, C-terminal domain / Hepatitis C virus core protein, chain A superfamily / : / Hepatitis C virus non-structural protein NS4b / Hepatitis C virus capsid protein / Hepatitis C virus, Non-structural 5a protein / Hepatitis C virus, Non-structural 5a protein, domain 1a / Hepatitis C virus non-structural 5a, 1B domain / NS5A domain 1a superfamily / Hepatitis C virus non-structural 5a zinc finger domain / Hepatitis C virus non-structural 5a domain 1b / Hepatitis C virus, Non-structural protein NS2 / : / NS3 RNA helicase, C-terminal helical domain / Hepacivirus nonstructural protein 2 (NS2) protease domain profile. / Hepatitis C virus non-structural 5a protein membrane anchor / Hepatitis C virus, Non-structural protein NS4a / Hepatitis C virus non-structural protein NS4a / Hepatitis C virus, Core protein, C-terminal / Hepatitis C virus core protein / Hepatitis C virus, Non-structural protein E2/NS1 / Hepatitis C virus non-structural protein E2/NS1 / Hepatitis C virus, Envelope glycoprotein E1 / Hepatitis C virus envelope glycoprotein E1 / RNA dependent RNA polymerase, hepatitis C virus / Viral RNA dependent RNA polymerase / Hepatitis C virus, NS3 protease, Peptidase S29 / Hepacivirus/Pegivirus NS3 protease domain profile. / Hepatitis C virus NS3 protease / DEAD box, Flavivirus / Flavivirus DEAD domain / Superfamilies 1 and 2 helicase C-terminal domain profile. / Superfamilies 1 and 2 helicase ATP-binding type-1 domain profile. / DEAD-like helicases superfamily / Helicase, C-terminal / Helicase superfamily 1/2, ATP-binding domain / Reverse transcriptase/Diguanylate cyclase domain / RNA-directed RNA polymerase, catalytic domain / RdRp of positive ssRNA viruses catalytic domain profile. / Peptidase S1, PA clan, chymotrypsin-like fold / Peptidase S1, PA clan / DNA/RNA polymerase superfamily / P-loop containing nucleoside triphosphate hydrolase
Similarity search - Domain/homology
Genome polyprotein / Genome polyprotein
Similarity search - Component
Biological speciesHepacivirus hominis
Methodsingle particle reconstruction / cryo EM / Resolution: 3.38 Å
AuthorsAugestad EH / Olesen CH / Groenberg C / Soerensen A / Velazquez-Moctezuma R / Fanalista M / Bukh J / Wang K / Gourdon P / Prentoe J
Funding support Denmark, 2 items
OrganizationGrant numberCountry
LundbeckfondenR324-2019-1375 Denmark
Novo Nordisk FoundationNNF20SA0064340 Denmark
CitationJournal: Nature / Year: 2024
Title: The hepatitis C virus envelope protein complex is a dimer of heterodimers.
Authors: Elias Honerød Augestad / Christina Holmboe Olesen / Christina Grønberg / Andreas Soerensen / Rodrigo Velázquez-Moctezuma / Margherita Fanalista / Jens Bukh / Kaituo Wang / Pontus Gourdon ...Authors: Elias Honerød Augestad / Christina Holmboe Olesen / Christina Grønberg / Andreas Soerensen / Rodrigo Velázquez-Moctezuma / Margherita Fanalista / Jens Bukh / Kaituo Wang / Pontus Gourdon / Jannick Prentoe /
Abstract: Fifty-eight million individuals worldwide are affected by chronic hepatitis C virus (HCV) infection, a primary driver of liver cancer for which no vaccine is available. The HCV envelope proteins E1 ...Fifty-eight million individuals worldwide are affected by chronic hepatitis C virus (HCV) infection, a primary driver of liver cancer for which no vaccine is available. The HCV envelope proteins E1 and E2 form a heterodimer (E1/E2), which is the target for neutralizing antibodies. However, the higher-order organization of these E1/E2 heterodimers, as well as that of any Hepacivirus envelope protein complex, remains unknown. Here we determined the cryo-electron microscopy structure of two E1/E2 heterodimers in a homodimeric arrangement. We reveal how the homodimer is established at the molecular level and provide insights into neutralizing antibody evasion and membrane fusion by HCV, as orchestrated by E2 motifs such as hypervariable region 1 and antigenic site 412, as well as the organization of the transmembrane helices, including two internal to E1. This study addresses long-standing questions on the higher-order oligomeric arrangement of Hepacivirus envelope proteins and provides a critical framework in the design of novel HCV vaccine antigens.
History
DepositionDec 22, 2023-
Header (metadata) releaseSep 4, 2024-
Map releaseSep 4, 2024-
UpdateOct 23, 2024-
Current statusOct 23, 2024Processing site: PDBe / Status: Released

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Structure visualization

Supplemental images

emd_19254.png

Downloads & links

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Map

FileDownload / File: emd_19254.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
Projections & slices

Image control

Size
Brightness
Contrast
Others
AxesZ (Sec.)Y (Row.)X (Col.)
0.82 Å/pix.
x 320 pix.
= 263.68 Å		0.82 Å/pix.
x 320 pix.
= 263.68 Å		0.82 Å/pix.
x 320 pix.
= 263.68 Å

Surface

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Slices (2/3)

Images are generated by Spider.

Voxel sizeX=Y=Z: 0.824 Å
Density

Histogram

Histogram (log scale)
Contour LevelBy AUTHOR: 0.5
Minimum - Maximum-0.4883369 - 1.3105427
Average (Standard dev.)0.003607222 (±0.030528467)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions320320320
Spacing320320320
CellA=B=C: 263.68 Å
α=β=γ: 90.0 °

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Supplemental data

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Mask #1

Fileemd_19254_msk_1.map
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Half map: #2

Fileemd_19254_half_map_1.map
Projections & Slices
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Histogram

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Half map: #1

Fileemd_19254_half_map_2.map
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Sample components

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Entire : HCV S52 E1E2

EntireName: HCV S52 E1E2
Components
  • Complex: HCV S52 E1E2
    • Protein or peptide: HCV E1
    • Protein or peptide: HCV E2
  • Ligand: 2-acetamido-2-deoxy-beta-D-glucopyranose

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Supramolecule #1: HCV S52 E1E2

SupramoleculeName: HCV S52 E1E2 / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2
Source (natural)Organism: Hepacivirus hominis
Molecular weightTheoretical: 200 KDa

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Macromolecule #1: HCV E1

MacromoleculeName: HCV E1 / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO
Source (natural)Organism: Hepacivirus hominis / Strain: S52
Molecular weightTheoretical: 13.212862 KDa
Recombinant expressionOrganism: Homo sapiens (human)
SequenceString:
EWRNTSGLYV LTNDCSNSSI VYEADDVILH TPGCVPCVQD DNTSTCWTPV TPTVAVRYVG ATTASIRSHV DLLVGAATLC SALYVGDMC GAVFLVGQAF TFRPRRHQTV QTCNCSLYPG HVSG

UniProtKB: Genome polyprotein

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Macromolecule #2: HCV E2

MacromoleculeName: HCV E2 / type: protein_or_peptide / ID: 2 / Number of copies: 2 / Enantiomer: LEVO
Source (natural)Organism: Hepacivirus hominis / Strain: S52
Molecular weightTheoretical: 36.466168 KDa
Recombinant expressionOrganism: Homo sapiens (human)
SequenceString: ETYVTGGSVA HSARGLTSLF SMGAKQKLQL VNTNGSWHIN STALNCNESI NTGFIAGLFY YHKFNSTGCP QRLSSCKPII SFRQGWGPL TDANITGPSD DRPYCWHYAP RPCSVVPASS VCGPVYCFTP SPVVVGTTDI KGKPTYNWGE NETDVFLLES L RPPSGRWF ...String:
ETYVTGGSVA HSARGLTSLF SMGAKQKLQL VNTNGSWHIN STALNCNESI NTGFIAGLFY YHKFNSTGCP QRLSSCKPII SFRQGWGPL TDANITGPSD DRPYCWHYAP RPCSVVPASS VCGPVYCFTP SPVVVGTTDI KGKPTYNWGE NETDVFLLES L RPPSGRWF GCAWMNSTGF LKTCGAPPCN IYGGEGDPEN ETDLFCPTDC FRKHPEATYS RCGAGPWLTP RCMVDYPYRL WH YPCTVNF TLFKVRMFVG GFEHRFTAAC NWTRGERCNI EDRDRSEQHP LLHSTTELAI LPCSFTPMPA LSTLGIHLHQ NIV DVQYLY G

UniProtKB: Genome polyprotein

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Macromolecule #5: 2-acetamido-2-deoxy-beta-D-glucopyranose

MacromoleculeName: 2-acetamido-2-deoxy-beta-D-glucopyranose / type: ligand / ID: 5 / Number of copies: 2 / Formula: NAG
Molecular weightTheoretical: 221.208 Da
Chemical component information

ChemComp-NAG:
2-acetamido-2-deoxy-beta-D-glucopyranose

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Experimental details

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Structure determination

Methodcryo EM
Processingsingle particle reconstruction
Aggregation stateparticle

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Sample preparation

BufferpH: 7.5
VitrificationCryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV

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Electron microscopy

MicroscopeFEI TITAN KRIOS
Image recordingFilm or detector model: GATAN K3 (6k x 4k) / Digitization - Dimensions - Width: 4092 pixel / Digitization - Dimensions - Height: 5760 pixel / Number grids imaged: 1 / Number real images: 13555 / Average electron dose: 50.0 e/Å2
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsC2 aperture diameter: 100.0 µm / Illumination mode: OTHER / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.5 µm / Nominal defocus min: 1.0 µm
Sample stageSpecimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

Startup modelType of model: INSILICO MODEL
Final reconstructionResolution.type: BY AUTHOR / Resolution: 3.38 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: cryoSPARC (ver. v 3.3.1) / Number images used: 105033
Initial angle assignmentType: MAXIMUM LIKELIHOOD / Software - Name: cryoSPARC (ver. v 3.3.1)
Final angle assignmentType: MAXIMUM LIKELIHOOD / Software - Name: cryoSPARC (ver. v 3.3.1)

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Atomic model buiding 1

Initial modelChain - Source name: AlphaFold / Chain - Initial model type: in silico model
RefinementSpace: REAL / Protocol: FLEXIBLE FIT / Overall B value: 100
Output model

PDB-8rk0:
HCV E1/E2 homodimer complex, ectodomain

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