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- EMDB-18137: HK68 cryo-EM structure achieved via rapid-spray and vitrification... -

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Entry
Database: EMDB / ID: EMD-18137
TitleHK68 cryo-EM structure achieved via rapid-spray and vitrification for grid preparation
Map data
Sample
  • Complex: CryoEM reconstruction of Influenza A virus (HK68) hemagglutinin bound to an Affimer reagent
  • Protein or peptide: HK68
KeywordsInhibitor / Antiviral / Influenza A Virus / Complex / ANTIVIRAL PROTEIN
Biological speciesInfluenza A virus / H3N2 subtype (virus)
Methodsingle particle reconstruction / cryo EM / Resolution: 4.3 Å
AuthorsDebski-Antoniak O / Flynn A / Klebl PD / Tiede C / Muench S / Tomlinson D / Fontana J
Funding support1 items
OrganizationGrant numberCountry
Other private
CitationJournal: mBio / Year: 2024
Title: Exploiting the Affimer platform against influenza A virus.
Authors: Oliver Debski-Antoniak / Alex Flynn / David P Klebl / Moisés H Rojas Rechy / Christian Tiede / Ian A Wilson / Stephen P Muench / Darren Tomlinson / Juan Fontana /
Abstract: Influenza A virus (IAV) is well known for its pandemic potential. While current surveillance and vaccination strategies are highly effective, therapeutic approaches are often short-lived due to the ...Influenza A virus (IAV) is well known for its pandemic potential. While current surveillance and vaccination strategies are highly effective, therapeutic approaches are often short-lived due to the high mutation rates of IAV. Recently, monoclonal antibodies (mAbs) have emerged as a promising therapeutic approach, both against current strains and future IAV pandemics. In addition to mAbs, several antibody-like alternatives exist, which aim to improve upon mAbs. Among these, Affimers stand out for their short development time, high expression levels in , and animal-free production. In this study, we utilized the Affimer platform to isolate and produce specific and potent inhibitors of IAV. Using a monomeric version of the IAV trimeric hemagglutinin (HA) fusion protein, we isolated 12 Affimers that inhibit IAV infection . Two of these Affimers were characterized in detail and exhibited nanomolar-binding affinities to the target H3 HA protein, specifically binding to the HA1 head domain. Cryo-electron microscopy (cryo-EM), employing a novel spray approach to prepare cryo-grids, allowed us to image HA-Affimer complexes. Combined with functional assays, we determined that these Affimers inhibit IAV by blocking the interaction of HA with the host-cell receptor, sialic acid. Furthermore, these Affimers inhibited IAV strains closely related to the one used for their isolation. Overall, our results support the use of Affimers as a viable alternative to existing targeted therapies for IAV and highlight their potential as diagnostic reagents.
IMPORTANCE: Influenza A virus is one of the few viruses that can cause devastating pandemics. Due to the high mutation rates of this virus, annual vaccination is required, and antivirals are short- ...IMPORTANCE: Influenza A virus is one of the few viruses that can cause devastating pandemics. Due to the high mutation rates of this virus, annual vaccination is required, and antivirals are short-lived. Monoclonal antibodies present a promising approach to tackle influenza virus infections but are associated with some limitations. To improve on this strategy, we explored the Affimer platform, which are antibody-like proteins made in bacteria. By performing phage-display against a monomeric version of influenza virus fusion protein, an established viral target, we were able to isolate Affimers that inhibit influenza virus infection . We characterized the mechanism of inhibition of the Affimers by using assays targeting different stages of the viral replication cycle. We additionally characterized HA-Affimer complex structure, using a novel approach to prepare samples for cryo-electron microscopy. Overall, these results show that Affimers are a promising tool against influenza virus infection.
History
DepositionAug 5, 2023-
Header (metadata) releaseAug 14, 2024-
Map releaseAug 14, 2024-
UpdateAug 28, 2024-
Current statusAug 28, 2024Processing site: PDBe / Status: Released

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Structure visualization

Supplemental images

Downloads & links

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Map

FileDownload / File: emd_18137.map.gz / Format: CCP4 / Size: 103 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
Projections & slices

Image control

Size
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AxesZ (Sec.)Y (Row.)X (Col.)
1.07 Å/pix.
x 300 pix.
= 321. Å
1.07 Å/pix.
x 300 pix.
= 321. Å
1.07 Å/pix.
x 300 pix.
= 321. Å

Surface

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Images are generated by Spider.

Voxel sizeX=Y=Z: 1.07 Å
Density
Contour LevelBy AUTHOR: 0.0142
Minimum - Maximum-0.040159293 - 0.06751043
Average (Standard dev.)-0.0000089299165 (±0.0017481442)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions300300300
Spacing300300300
CellA=B=C: 321.00003 Å
α=β=γ: 90.0 °

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Supplemental data

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Mask #1

Fileemd_18137_msk_1.map
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Additional map: #1

Fileemd_18137_additional_1.map
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Half map: #1

Fileemd_18137_half_map_1.map
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Sample components

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Entire : CryoEM reconstruction of Influenza A virus (HK68) hemagglutinin b...

EntireName: CryoEM reconstruction of Influenza A virus (HK68) hemagglutinin bound to an Affimer reagent
Components
  • Complex: CryoEM reconstruction of Influenza A virus (HK68) hemagglutinin bound to an Affimer reagent
  • Protein or peptide: HK68

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Supramolecule #1: CryoEM reconstruction of Influenza A virus (HK68) hemagglutinin b...

SupramoleculeName: CryoEM reconstruction of Influenza A virus (HK68) hemagglutinin bound to an Affimer reagent
type: complex / ID: 1 / Parent: 0
Source (natural)Organism: Influenza A virus

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Macromolecule #1: HK68

MacromoleculeName: HK68 / type: protein_or_peptide / ID: 1 / Enantiomer: DEXTRO
Source (natural)Organism: H3N2 subtype (virus)
Recombinant expressionOrganism: Escherichia coli-Pichia pastoris shuttle vector pPpGUT1 (others)
SequenceString: ADPGATLCLG HHAVPNGTLV KTITDDQIEV TNATELVQSS STGKICNNPH RILDGIDCTL IDALLGDPHC DVFQNETWDL FVERSKAFSN CYPYDVPDYA SLRSLVASSG TLEFITEGFT WTGVTQNGGS NACKRGPGSG FFSRLNWLTK SGSTYPVLNV TMPNNDNFDK ...String:
ADPGATLCLG HHAVPNGTLV KTITDDQIEV TNATELVQSS STGKICNNPH RILDGIDCTL IDALLGDPHC DVFQNETWDL FVERSKAFSN CYPYDVPDYA SLRSLVASSG TLEFITEGFT WTGVTQNGGS NACKRGPGSG FFSRLNWLTK SGSTYPVLNV TMPNNDNFDK LYIWGVHHPS TNQEQTSLYV QASGRVTVST RRSQQTIIPN IGSRPWVRGL SSRISIYWTI VKPGDVLVIN SNGNLIAPRG YFKMRTGKSS IMRSDAPIDT CISECITPNG SIPNDKPFQN VNKITYGACP KYVKQNTLKL ATGMRNVPEK QTRGLFGAIA GFIENGWEGM IDGWYGFRHQ NSEGTGQAAD LKSTQAAIDQ INGKLNRVIE KTNEKFHQIE KEFSEVEGRI QDLEKYVEDT KIDLWSYNAE LLVALENQHT IDLTDSEMNK LFEKTGRQLR ENAEDMGNGC FKIYHKCDNA CIESIRNGTY DHDVYRDEAL NNRFQIK

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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: 7.4
VitrificationCryogen name: ETHANE

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Electron microscopy

MicroscopeFEI TITAN KRIOS
Image recordingFilm or detector model: FEI FALCON IV (4k x 4k) / Average electron dose: 56.2 e/Å2
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsIllumination mode: FLOOD BEAM / Imaging mode: OTHER / Nominal defocus max: 4.0 µm / Nominal defocus min: 2.0 µm
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

Startup modelType of model: NONE
Final reconstructionResolution.type: BY AUTHOR / Resolution: 4.3 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 129501
Initial angle assignmentType: ANGULAR RECONSTITUTION
Final angle assignmentType: ANGULAR RECONSTITUTION
FSC plot (resolution estimation)

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