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- EMDB-42859: Prehairpin intermediate of SARS-CoV-2 Spike in membrane -

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Basic information

Entry
Database: EMDB / ID: EMD-42859
TitlePrehairpin intermediate of SARS-CoV-2 Spike in membrane
Map data
Sample
  • Complex: Prehairpin intermediate of SARS-CoV-2 Spike in membrane
KeywordsComplex / VIRAL PROTEIN
Biological speciesSevere acute respiratory syndrome coronavirus 2
Methodsubtomogram averaging / cryo EM / Resolution: 24.0 Å
AuthorsLi W / Mothes W / Grunst MW / Qin Z
Funding support United States, 1 items
OrganizationGrant numberCountry
National Institutes of Health/National Institute Of Allergy and Infectious Diseases (NIH/NIAID)AI163395 United States
CitationJournal: Science / Year: 2024
Title: Structure and inhibition of SARS-CoV-2 spike refolding in membranes.
Authors: Michael W Grunst / Zhuan Qin / Esteban Dodero-Rojas / Shilei Ding / Jérémie Prévost / Yaozong Chen / Yanping Hu / Marzena Pazgier / Shenping Wu / Xuping Xie / Andrés Finzi / José N ...Authors: Michael W Grunst / Zhuan Qin / Esteban Dodero-Rojas / Shilei Ding / Jérémie Prévost / Yaozong Chen / Yanping Hu / Marzena Pazgier / Shenping Wu / Xuping Xie / Andrés Finzi / José N Onuchic / Paul C Whitford / Walther Mothes / Wenwei Li /
Abstract: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein binds the receptor angiotensin converting enzyme 2 (ACE2) and drives virus-host membrane fusion through refolding of its ...The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein binds the receptor angiotensin converting enzyme 2 (ACE2) and drives virus-host membrane fusion through refolding of its S2 domain. Whereas the S1 domain contains high sequence variability, the S2 domain is conserved and is a promising pan-betacoronavirus vaccine target. We applied cryo-electron tomography to capture intermediates of S2 refolding and understand inhibition by antibodies to the S2 stem-helix. Subtomogram averaging revealed ACE2 dimers cross-linking spikes before transitioning into S2 intermediates, which were captured at various stages of refolding. Pan-betacoronavirus neutralizing antibodies targeting the S2 stem-helix bound to and inhibited refolding of spike prehairpin intermediates. Combined with molecular dynamics simulations, these structures elucidate the process of SARS-CoV-2 entry and reveal how pan-betacoronavirus S2-targeting antibodies neutralize infectivity by arresting prehairpin intermediates.
History
DepositionNov 17, 2023-
Header (metadata) releaseAug 28, 2024-
Map releaseAug 28, 2024-
UpdateAug 28, 2024-
Current statusAug 28, 2024Processing site: RCSB / Status: Released

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Structure visualization

Supplemental images

Downloads & links

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Map

FileDownload / File: emd_42859.map.gz / Format: CCP4 / Size: 30.5 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
Projections & slices

Image control

Size
Brightness
Contrast
Others
AxesZ (Sec.)Y (Row.)X (Col.)
2.69 Å/pix.
x 200 pix.
= 538.4 Å
2.69 Å/pix.
x 200 pix.
= 538.4 Å
2.69 Å/pix.
x 200 pix.
= 538.4 Å

Surface

Projections

Slices (1/3)

Slices (1/2)

Slices (2/3)

Images are generated by Spider.

Voxel sizeX=Y=Z: 2.692 Å
Density
Contour LevelBy AUTHOR: 0.07
Minimum - Maximum-0.14698935 - 0.2854132
Average (Standard dev.)-0.000000000006124 (±0.020710835)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions200200200
Spacing200200200
CellA=B=C: 538.39996 Å
α=β=γ: 90.0 °

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Supplemental data

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Mask #1

Fileemd_42859_msk_1.map
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Sample components

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Entire : Prehairpin intermediate of SARS-CoV-2 Spike in membrane

EntireName: Prehairpin intermediate of SARS-CoV-2 Spike in membrane
Components
  • Complex: Prehairpin intermediate of SARS-CoV-2 Spike in membrane

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Supramolecule #1: Prehairpin intermediate of SARS-CoV-2 Spike in membrane

SupramoleculeName: Prehairpin intermediate of SARS-CoV-2 Spike in membrane
type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2
Source (natural)Organism: Severe acute respiratory syndrome coronavirus 2

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Experimental details

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Structure determination

Methodcryo EM
Processingsubtomogram averaging
Aggregation stateparticle

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Sample preparation

BufferpH: 7.4
VitrificationCryogen name: ETHANE

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Electron microscopy

MicroscopeFEI TITAN KRIOS
Specialist opticsPhase plate: VOLTA PHASE PLATE / Energy filter - Name: GIF Quantum LS / Energy filter - Slit width: 20 eV
Image recordingFilm or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 3.0 e/Å2
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsC2 aperture diameter: 50.0 µm / Calibrated defocus max: 0.8 µm / Calibrated defocus min: 0.2 µm / Illumination mode: OTHER / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 0.5 µm / Nominal defocus min: 0.5 µm / Nominal magnification: 64000
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

Final reconstructionApplied symmetry - Point group: C1 (asymmetric) / Resolution.type: BY AUTHOR / Resolution: 24.0 Å / Resolution method: FSC 0.143 CUT-OFF / Number subtomograms used: 2106
ExtractionNumber tomograms: 275 / Number images used: 2163
Final angle assignmentType: OTHER
FSC plot (resolution estimation)

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