+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-42536 | |||||||||
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Title | CryoEM map of A/Shanghai/1/2013 H7 HA | |||||||||
Map data | Shanghai13H7_sharp | |||||||||
Sample |
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Keywords | cryoEMPEM / Flu Hemagglutinin / Central stem epitope / VIRAL PROTEIN | |||||||||
Biological species | Influenza A virus | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.1 Å | |||||||||
Authors | Huang J / Han J / Ward AB | |||||||||
Funding support | United States, 1 items
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Citation | Journal: Immunity / Year: 2024 Title: Eliciting a single amino acid change by vaccination generates antibody protection against group 1 and group 2 influenza A viruses. Authors: Rashmi Ray / Faez Amokrane Nait Mohamed / Daniel P Maurer / Jiachen Huang / Berk A Alpay / Larance Ronsard / Zhenfei Xie / Julianna Han / Monica Fernandez-Quintero / Quynh Anh Phan / Rebecca ...Authors: Rashmi Ray / Faez Amokrane Nait Mohamed / Daniel P Maurer / Jiachen Huang / Berk A Alpay / Larance Ronsard / Zhenfei Xie / Julianna Han / Monica Fernandez-Quintero / Quynh Anh Phan / Rebecca L Ursin / Mya Vu / Kathrin H Kirsch / Thavaleak Prum / Victoria C Rosado / Thalia Bracamonte-Moreno / Vintus Okonkwo / Julia Bals / Caitlin McCarthy / Usha Nair / Masaru Kanekiyo / Andrew B Ward / Aaron G Schmidt / Facundo D Batista / Daniel Lingwood / Abstract: Broadly neutralizing antibodies (bnAbs) targeting the hemagglutinin (HA) stem of influenza A viruses (IAVs) tend to be effective against either group 1 or group 2 viral diversity. In rarer cases, ...Broadly neutralizing antibodies (bnAbs) targeting the hemagglutinin (HA) stem of influenza A viruses (IAVs) tend to be effective against either group 1 or group 2 viral diversity. In rarer cases, intergroup protective bnAbs can be generated by human antibody paratopes that accommodate the conserved glycan differences between the group 1 and group 2 stems. We applied germline-engaging nanoparticle immunogens to elicit a class of cross-group bnAbs from physiological precursor frequency within a humanized mouse model. Cross-group protection depended on the presence of the human bnAb precursors within the B cell repertoire, and the vaccine-expanded antibodies enriched for an N55T substitution in the CDRH2 loop, a hallmark of the bnAb class. Structurally, this single mutation introduced a flexible fulcrum to accommodate glycosylation differences and could alone enable cross-group protection. Thus, broad IAV immunity can be expanded from the germline repertoire via minimal antigenic input and an exceptionally simple antibody development pathway. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_42536.map.gz | 203.8 MB | EMDB map data format | |
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Header (meta data) | emd-42536-v30.xml emd-42536.xml | 15.6 KB 15.6 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_42536_fsc.xml | 12.7 KB | Display | FSC data file |
Images | emd_42536.png | 62.1 KB | ||
Filedesc metadata | emd-42536.cif.gz | 5.2 KB | ||
Others | emd_42536_half_map_1.map.gz emd_42536_half_map_2.map.gz | 200.1 MB 200.1 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-42536 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-42536 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_42536.map.gz / Format: CCP4 / Size: 216 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | Shanghai13H7_sharp | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.725 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: Shanghai13H7 halfA
File | emd_42536_half_map_1.map | ||||||||||||
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Annotation | Shanghai13H7_halfA | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Shanghai13H7 halfB
File | emd_42536_half_map_2.map | ||||||||||||
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Annotation | Shanghai13H7_halfB | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : A/Shanghai/1/2013 H7 HA
Entire | Name: A/Shanghai/1/2013 H7 HA |
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Components |
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-Supramolecule #1: A/Shanghai/1/2013 H7 HA
Supramolecule | Name: A/Shanghai/1/2013 H7 HA / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: Influenza A virus |
-Macromolecule #1: A/Shanghai/1/2013 H7 HA
Macromolecule | Name: A/Shanghai/1/2013 H7 HA / type: protein_or_peptide / ID: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Influenza A virus |
Recombinant expression | Organism: Homo sapiens (human) |
Sequence | String: DKICLGHHAV SNGTKVNTLT ERGVEVVNAT ETVERTNIPR ICSKGKRTVD LGQCGLLGTI TGPPQCDQFL EFSADLIIER REGSDVCFPG KFVNEEALRQ ILRESGGIDK EAMGFTYSGI RTNGATSSCR RSGSSFYAEM KWLLSNTDNA AFPQMTKSYK NTRKNPALIV ...String: DKICLGHHAV SNGTKVNTLT ERGVEVVNAT ETVERTNIPR ICSKGKRTVD LGQCGLLGTI TGPPQCDQFL EFSADLIIER REGSDVCFPG KFVNEEALRQ ILRESGGIDK EAMGFTYSGI RTNGATSSCR RSGSSFYAEM KWLLSNTDNA AFPQMTKSYK NTRKNPALIV WGIHHSGSTA EQTKLYGSGN KLVTVGSSNY QQSFVPSPGA RTQVNGQSGR IDFHWLMLNP NDTVTFSFNG AFIAPDRASF LRGKSMGIQS GVQVDADCEG DCYYSGGTII SNLPFQNIDS RAVGKCPRYV KQRSLLLATG MKNVPEI PK GRGLFGAIAG FIENGWEGLI DGWYGFRHQN AQGEGTAADY KSTQSAIDQI TGKLNRLIEK TNQQFELIDN EFTEVEKQIG NVINWTRDSI TEVWSYNAEL LVAMENQHTI DLADSEMDKL YERVKRQLRE NAEEDGTGCF EIFHKCDDDC MASIRNNTYD HSKYREEAMQ NRIQID GSG YIPEAPRDGQ AYVRKDGEWV LLSTFLGSGL NDIFEAQKIE WHEGHHHHHH |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 0.7 mg/mL | ||||||||
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Buffer | pH: 7.4 Component:
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Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277.15 K / Instrument: FEI VITROBOT MARK IV |
-Electron microscopy
Microscope | TFS GLACIOS |
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Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELDBright-field microscopy / Nominal defocus max: 1.5 µm / Nominal defocus min: 0.7000000000000001 µm |
Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Average electron dose: 50.0 e/Å2 |