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Yorodumi- EMDB-49477: Computationally optimized broadly reactive influenza B hemaggluti... -
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Open data
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Basic information
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| Title | Computationally optimized broadly reactive influenza B hemagglutinin BC2 bound by antibody #46 | |||||||||
Map data | sharpened map after spIsoNet correction | |||||||||
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Keywords | influenza / antibody / cell entry / hemagglutination / VIRAL PROTEIN / VIRAL PROTEIN-Immune System complex | |||||||||
| Function / homology | Function and homology informationviral budding from plasma membrane / host cell surface receptor binding / endocytosis involved in viral entry into host cell / fusion of virus membrane with host plasma membrane / fusion of virus membrane with host endosome membrane / viral envelope / virion attachment to host cell / host cell plasma membrane / virion membrane / membrane Similarity search - Function | |||||||||
| Biological species | Homo sapiens (human) / Influenza B virus | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.5 Å | |||||||||
Authors | Dzimianski JV / Kunkel I / Balasco Serrao VH / DuBois RM | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Front Immunol / Year: 2026Title: Human broadly neutralizing influenza B virus antibodies recognizing hemagglutinin computationally optimized broadly reactive antigens. Authors: Yailin Campos Mota / John V Dzimianski / Mariana Lopez / Robert A Richardson / Ted M Ross / Ian J A Kunkel / Sara M O'Rourke / Vitor Hugo Balasco Serrão / Rebecca M DuBois / Giuseppe A Sautto / ![]() Abstract: INTRODUCTION: Influenza B viruses (IBVs) are responsible for severe disease and death, similarly to influenza A viruses (IAVs), with a higher number of infections happening in children and the ...INTRODUCTION: Influenza B viruses (IBVs) are responsible for severe disease and death, similarly to influenza A viruses (IAVs), with a higher number of infections happening in children and the elderly. Despite the inclusion of an IBV component in the seasonal influenza vaccine, rates of vaccine effectiveness (VE) are still variable and low in many previous seasons. METHODS: In this work, longitudinal profiling of IBV hemagglutinin (HA)-specific B-cell responses was described following influenza vaccination in 15 vaccinated participants over four consecutive ...METHODS: In this work, longitudinal profiling of IBV hemagglutinin (HA)-specific B-cell responses was described following influenza vaccination in 15 vaccinated participants over four consecutive influenza seasons. These individuals belonged to different age groups and monoclonal antibodies (mAbs) showing broad binding and functional antibody profiles were isolated from the plasmablasts of one individual. RESULTS: These individuals possessed different breadths and magnitudes of antibody responses to a panel of IBV historical and more recent vaccine strains. In particular, young adults (age 23-33) ...RESULTS: These individuals possessed different breadths and magnitudes of antibody responses to a panel of IBV historical and more recent vaccine strains. In particular, young adults (age 23-33) showed a higher magnitude and breadth of antibody response compared to middle-aged (age 55-58) and elderly (age 65-77) participants who instead showed a lower albeit detectable antibody response. Interestingly, one of the isolated mAbs, mAb #46, had the broadest response with a broad binding and potent functional activity against historical and recent IBV strains spanning both Victoria and Yamagata lineages and including binding to IBV computationally optimized broadly reactive antigen (COBRA) HAs. Importantly, mAb #46 administration, either therapeutically or prophylactically, fully protected IBV-challenged mice. Structural characterization of the mAb #46-HA complex by cryo-electron microscopy single-particle analysis revealed that mAb #46 targets a conserved epitope within the HA receptor binding site. DISCUSSION: This study highlights the presence of broadly neutralizing antibodies in the human repertoire that may be recalled by vaccination with COBRA HA, although this hypothesis will be confirmed ...DISCUSSION: This study highlights the presence of broadly neutralizing antibodies in the human repertoire that may be recalled by vaccination with COBRA HA, although this hypothesis will be confirmed in upcoming clinical trials. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_49477.map.gz | 370.7 MB | EMDB map data format | |
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| Header (meta data) | emd-49477-v30.xml emd-49477.xml | 35.3 KB 35.3 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_49477_fsc.xml | 19 KB | Display | FSC data file |
| Images | emd_49477.png | 42.1 KB | ||
| Masks | emd_49477_msk_1.map | 729 MB | Mask map | |
| Filedesc metadata | emd-49477.cif.gz | 7.7 KB | ||
| Others | emd_49477_additional_1.map.gz emd_49477_additional_2.map.gz emd_49477_additional_3.map.gz emd_49477_half_map_1.map.gz emd_49477_half_map_2.map.gz | 676.5 MB 359.9 MB 676.5 MB 676.5 MB 676.5 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-49477 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-49477 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9njaMC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_49477.map.gz / Format: CCP4 / Size: 729 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | sharpened map after spIsoNet correction | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.5727 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_49477_msk_1.map | ||||||||||||
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-Additional map: spIsoNet corrected half map A
| File | emd_49477_additional_1.map | ||||||||||||
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| Annotation | spIsoNet corrected half map A | ||||||||||||
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-Additional map: unsharpened map
| File | emd_49477_additional_2.map | ||||||||||||
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| Annotation | unsharpened map | ||||||||||||
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-Additional map: spIsoNet corrected half map B
| File | emd_49477_additional_3.map | ||||||||||||
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| Annotation | spIsoNet corrected half map B | ||||||||||||
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-Half map: half map B
| File | emd_49477_half_map_1.map | ||||||||||||
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| Annotation | half map B | ||||||||||||
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| Density Histograms |
-Half map: half map A
| File | emd_49477_half_map_2.map | ||||||||||||
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| Annotation | half map A | ||||||||||||
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Sample components
-Entire : Complex of a viral protein with two antibodies
| Entire | Name: Complex of a viral protein with two antibodies |
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| Components |
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-Supramolecule #1: Complex of a viral protein with two antibodies
| Supramolecule | Name: Complex of a viral protein with two antibodies / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#3 |
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| Source (natural) | Organism: Homo sapiens (human) |
-Macromolecule #1: Fab A Light Chain
| Macromolecule | Name: Fab A Light Chain / type: protein_or_peptide / ID: 1 / Number of copies: 3 / Enantiomer: LEVO |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 23.206629 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: QLANFGSEEL TQAPSVSVSP GQTATITCRG DALGDRSASW YRQKSGQSPL LVIYENFRRP SGIPERFSGS KSGNTATLTV SGTQTMDEA HYYCQTGDST TVLFGGGTQL IVLGQPKAAP SVTLFPPSSE ELQANKATLV CLISDFYPGA VTVAWKADSS P VKAGVETT ...String: QLANFGSEEL TQAPSVSVSP GQTATITCRG DALGDRSASW YRQKSGQSPL LVIYENFRRP SGIPERFSGS KSGNTATLTV SGTQTMDEA HYYCQTGDST TVLFGGGTQL IVLGQPKAAP SVTLFPPSSE ELQANKATLV CLISDFYPGA VTVAWKADSS P VKAGVETT TPSKQSNNKY AASSYLSLTP EQWKSHRSYS CQVTHEGSTV EKTVAPTECS |
-Macromolecule #2: Fab A Heavy Chain
| Macromolecule | Name: Fab A Heavy Chain / type: protein_or_peptide / ID: 2 / Number of copies: 3 / Enantiomer: LEVO |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 24.845973 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: QVQLVQSGAE VKKPGSSVKV SCKASGDAFI SFAINWVRQA PGQGPEWMGE FIPFLTRATY AQKFQDRVRM TADHSTTTAY LEIIGLKPE DTAVYFCARE LGSWPNDVGA GKYFDPWGQG TLVTVSSAST KGPSVFPLAP SSKSTSGGTA ALGCLVKDYF P EPVTVSWN ...String: QVQLVQSGAE VKKPGSSVKV SCKASGDAFI SFAINWVRQA PGQGPEWMGE FIPFLTRATY AQKFQDRVRM TADHSTTTAY LEIIGLKPE DTAVYFCARE LGSWPNDVGA GKYFDPWGQG TLVTVSSAST KGPSVFPLAP SSKSTSGGTA ALGCLVKDYF P EPVTVSWN SGALTSGVHT FPAVLQSSGL YSLSSVVTVP SSSLGTQTYI CNVNHKPSNT KVDKKVEPKS CDKTH |
-Macromolecule #3: Hemagglutinin
| Macromolecule | Name: Hemagglutinin / type: protein_or_peptide / ID: 3 / Number of copies: 3 / Enantiomer: LEVO |
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| Source (natural) | Organism: Influenza B virus |
| Molecular weight | Theoretical: 57.375242 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: DRICTGITSS NSPHVVKTAT QGEVNVTGVI PLTTTPTKSH FANLKGTKTR GKLCPKCLNC TDLDVALGRP KCMGTIPSAK ASILHEVRP VTSGCFPIMH DRTKIRQLPN LLRGYENIRL STHNVINAEK APGGPYRIGT SGSCPNVTNG NGFFATMAWA V PKNDNNKT ...String: DRICTGITSS NSPHVVKTAT QGEVNVTGVI PLTTTPTKSH FANLKGTKTR GKLCPKCLNC TDLDVALGRP KCMGTIPSAK ASILHEVRP VTSGCFPIMH DRTKIRQLPN LLRGYENIRL STHNVINAEK APGGPYRIGT SGSCPNVTNG NGFFATMAWA V PKNDNNKT ATNPLTVEVP YICTEGEDQI TVWGFHSDNE TQMKKLYGDS KPQKFTSSAN GVTTHYVSQI GGFPNQTEDG GL PQSGRIV VDYMVQKSGK TGTIVYQRGI LLPQKVWCAS GRSKVIKGSL PLIGEADCLH EKYGGLNKSK PYYTGEHAKA IGN CPIWVK TPLKLANGTK YRPPAKLLKE RGFFGAIAGF LEGGWEGMIA GWHGYTSHGA HGVAVAADLK STQEAINKIT KNLN SLSEL EVKNLQRLSG AMDELHNEIL ELDEKVDDLR ADTISSQIEL AVLLSNEGII NSEDEHLLAL ERKLKKMLGP SAVDI GNGC FETKHKCNQT CLDRIAAGTF NAGEFSLPTF DSLNITAASS GRLVPR UniProtKB: Hemagglutinin |
-Macromolecule #5: 2-acetamido-2-deoxy-beta-D-glucopyranose
| Macromolecule | Name: 2-acetamido-2-deoxy-beta-D-glucopyranose / type: ligand / ID: 5 / Number of copies: 6 / Formula: NAG |
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| Molecular weight | Theoretical: 221.208 Da |
| Chemical component information | ![]() ChemComp-NAG: |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7.4 |
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| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 298 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 BIOCONTINUUM (6k x 4k) / Number grids imaged: 2 / Number real images: 35025 / Average electron dose: 50.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.8000000000000003 µm / Nominal defocus min: 0.5 µm |
| Sample stage | Specimen 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
-Atomic model buiding 1
| Initial model |
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| Refinement | Protocol: RIGID BODY FIT | ||||||||
| Output model | ![]() PDB-9nja: |
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About Yorodumi



Keywords
Homo sapiens (human)
Influenza B virus
Authors
United States, 1 items
Citation









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FIELD EMISSION GUN


