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Yorodumi- EMDB-26653: Native Lassa glycoprotein in complex with neutralizing antibodies... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-26653 | |||||||||
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Title | Native Lassa glycoprotein in complex with neutralizing antibodies 8.9F and 37.2D | |||||||||
Map data | ||||||||||
Sample |
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Keywords | Lassa virus / Neutralizing antibody / N-linked glycans complex / VIRAL PROTEIN / VIRAL PROTEIN-IMMUNE SYSTEM complex | |||||||||
Function / homology | Function and homology information host cell Golgi membrane / receptor-mediated endocytosis of virus by host cell / host cell endoplasmic reticulum membrane / fusion of virus membrane with host endosome membrane / viral envelope / virion attachment to host cell / host cell plasma membrane / virion membrane / membrane / metal ion binding Similarity search - Function | |||||||||
Biological species | Lassa virus / Homo sapiens (human) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 2.77 Å | |||||||||
Authors | Li H / Saphire EO | |||||||||
Funding support | United States, 1 items
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Citation | Journal: Sci Transl Med / Year: 2022 Title: A cocktail of protective antibodies subverts the dense glycan shield of Lassa virus. Authors: Haoyang Li / Tierra Buck / Michelle Zandonatti / Jieyun Yin / Alex Moon-Walker / Jingru Fang / Anatoliy Koval / Megan L Heinrich / Megan M Rowland / Ruben Diaz Avalos / Sharon L Schendel / ...Authors: Haoyang Li / Tierra Buck / Michelle Zandonatti / Jieyun Yin / Alex Moon-Walker / Jingru Fang / Anatoliy Koval / Megan L Heinrich / Megan M Rowland / Ruben Diaz Avalos / Sharon L Schendel / Diptiben Parekh / Dawid Zyla / Adrian Enriquez / Stephanie Harkins / Brian Sullivan / Victoria Smith / Onyeka Chukwudozie / Reika Watanabe / James E Robinson / Robert F Garry / Luis M Branco / Kathryn M Hastie / Erica Ollmann Saphire / Abstract: Developing potent therapeutics and effective vaccines are the ultimate goals in controlling infectious diseases. Lassa virus (LASV), the causative pathogen of Lassa fever (LF), infects hundreds of ...Developing potent therapeutics and effective vaccines are the ultimate goals in controlling infectious diseases. Lassa virus (LASV), the causative pathogen of Lassa fever (LF), infects hundreds of thousands annually, but effective antivirals or vaccines against LASV infection are still lacking. Furthermore, neutralizing antibodies against LASV are rare. Here, we describe biochemical analyses and high-resolution cryo-electron microscopy structures of a therapeutic cocktail of three broadly protective antibodies that target the LASV glycoprotein complex (GPC), previously identified from survivors of multiple LASV infections. Structural and mechanistic analyses reveal compatible neutralizing epitopes and complementary neutralization mechanisms that offer high potency, broad range, and resistance to escape. These antibodies either circumvent or exploit specific glycans comprising the extensive glycan shield of GPC. Further, they require mammalian glycosylation, native GPC cleavage, and proper GPC trimerization. These findings guided engineering of a next-generation GPC antigen suitable for future neutralizing antibody and vaccine discovery. Together, these results explain protective mechanisms of rare, broad, and potent antibodies and identify a strategy for the rational design of therapeutic modalities against LF and related infectious diseases. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_26653.map.gz | 254.4 MB | EMDB map data format | |
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Header (meta data) | emd-26653-v30.xml emd-26653.xml | 20.1 KB 20.1 KB | Display Display | EMDB header |
Images | emd_26653.png | 120.7 KB | ||
Filedesc metadata | emd-26653.cif.gz | 6.5 KB | ||
Others | emd_26653_half_map_1.map.gz emd_26653_half_map_2.map.gz | 475.6 MB 475.6 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-26653 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-26653 | HTTPS FTP |
-Validation report
Summary document | emd_26653_validation.pdf.gz | 1.2 MB | Display | EMDB validaton report |
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Full document | emd_26653_full_validation.pdf.gz | 1.2 MB | Display | |
Data in XML | emd_26653_validation.xml.gz | 18.9 KB | Display | |
Data in CIF | emd_26653_validation.cif.gz | 22.2 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-26653 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-26653 | HTTPS FTP |
-Related structure data
Related structure data | 7uotMC 7uovC M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_26653.map.gz / Format: CCP4 / Size: 512 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 0.66 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_26653_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_26653_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Native Lassa glycoprotein in complex with 8.9F-scFv and 37.2D-scFv
Entire | Name: Native Lassa glycoprotein in complex with 8.9F-scFv and 37.2D-scFv |
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Components |
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-Supramolecule #1: Native Lassa glycoprotein in complex with 8.9F-scFv and 37.2D-scFv
Supramolecule | Name: Native Lassa glycoprotein in complex with 8.9F-scFv and 37.2D-scFv type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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-Macromolecule #1: Glycoprotein G1
Macromolecule | Name: Glycoprotein G1 / type: protein_or_peptide / ID: 1 / Number of copies: 3 / Enantiomer: LEVO |
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Source (natural) | Organism: Lassa virus / Strain: Mouse/Sierra Leone/Josiah/1976 |
Molecular weight | Theoretical: 29.064402 KDa |
Recombinant expression | Organism: Homo sapiens (human) |
Sequence | String: MGQIVTFFQE VPHVIEEVMN IVLIALSVLA VLKGLYNFAT CGLVGLVTFL LLCGRSCTTS LYKGVYELQT LELNMETLNM TMPLSCTKN NSHHYIMVGN ETGLELTLTN TSIINHKFCN LSDAHKKNLY DHALMSIIST FHLSIPNFNQ YEAMSCDFNG G KISVQYNL ...String: MGQIVTFFQE VPHVIEEVMN IVLIALSVLA VLKGLYNFAT CGLVGLVTFL LLCGRSCTTS LYKGVYELQT LELNMETLNM TMPLSCTKN NSHHYIMVGN ETGLELTLTN TSIINHKFCN LSDAHKKNLY DHALMSIIST FHLSIPNFNQ YEAMSCDFNG G KISVQYNL SHSYAGDAAN HCGTVANGVL QTFMRMAWGG SYIALDSGRG NWDCIMTSYQ YLIIQNTTWE DHCQFSRPSP IG YLGLLSQ RTRDIYISRR LL UniProtKB: Pre-glycoprotein polyprotein GP complex |
-Macromolecule #2: Glycoprotein G2
Macromolecule | Name: Glycoprotein G2 / type: protein_or_peptide / ID: 2 / Number of copies: 3 / Enantiomer: LEVO |
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Source (natural) | Organism: Lassa virus / Strain: Mouse/Sierra Leone/Josiah/1976 |
Molecular weight | Theoretical: 26.797973 KDa |
Recombinant expression | Organism: Homo sapiens (human) |
Sequence | String: GTFTWTLSDS EGKDTPGGYC LTRWMLIEAE LKCFGNTAVA KCNEKHDEEF CDMLRLFDFN KQAIQRLKAE AQTSIQLINK AVNALINDQ LIMKNHLRDI MGIPYCNYSK YWYLNHTTTG RTSLPKCWLV SNGSYLNETH FSDDIEQQAD NMITEMLQKE Y MERQGKTP ...String: GTFTWTLSDS EGKDTPGGYC LTRWMLIEAE LKCFGNTAVA KCNEKHDEEF CDMLRLFDFN KQAIQRLKAE AQTSIQLINK AVNALINDQ LIMKNHLRDI MGIPYCNYSK YWYLNHTTTG RTSLPKCWLV SNGSYLNETH FSDDIEQQAD NMITEMLQKE Y MERQGKTP LGLVDLFVFS TSFYLISIFL HLVKIPTHRH IVGKSCPKPH RLNHMGICSC GLYKQPGVPV KWKR UniProtKB: Pre-glycoprotein polyprotein GP complex |
-Macromolecule #3: 37.2D light chain (variable domain)
Macromolecule | Name: 37.2D light chain (variable domain) / type: protein_or_peptide / ID: 3 / Number of copies: 3 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 11.412506 KDa |
Recombinant expression | Organism: Drosophila melanogaster (fruit fly) |
Sequence | String: ETTLTQSPAT LSVSPGETAT LSCRASQNVI NNLAWYQQKP GQAPRLLIYG ASTRATGIPA RFSGSGSGTE FTLTISSMQS EDFAVYYCQ QYNDWPRSFG QGTRLD |
-Macromolecule #4: 37.2D heavy chain (variable domain)
Macromolecule | Name: 37.2D heavy chain (variable domain) / type: protein_or_peptide / ID: 4 / Number of copies: 3 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 13.946536 KDa |
Recombinant expression | Organism: Drosophila melanogaster (fruit fly) |
Sequence | String: EVQLVQSGAE VKKPGASVKV SCKASGYTFT KYGISWVRQA PGQGLEWMGW ISAFNGYTRY GQRFQGKVTM TTDTSTNTAS LEVRTLTSN DTAVYYCARQ YPDQYSSSGW PRLFAMDVWG QGTTVTV |
-Macromolecule #5: 8.9F heavy chain (variable domain)
Macromolecule | Name: 8.9F heavy chain (variable domain) / type: protein_or_peptide / ID: 5 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 15.002536 KDa |
Recombinant expression | Organism: Drosophila melanogaster (fruit fly) |
Sequence | String: QGTLRESGPG LVRPSETLSL TCGVSGYSIS SGYYWGWIRQ PPGKGLEWIG NIYRSGSTYY NPSLKSRVTV SIDTSKNQFS LKLNSVTAA DTAVYYCARS GIKVADDYYY EMDVWGQGTD DYSYAMDVWG QGTTVTV |
-Macromolecule #6: 8.9F light chain (variable domain)
Macromolecule | Name: 8.9F light chain (variable domain) / type: protein_or_peptide / ID: 6 / Number of copies: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 11.445485 KDa |
Recombinant expression | Organism: Drosophila melanogaster (fruit fly) |
Sequence | String: QAVLTQPASV SGSPGQSITI SCTAANSDIG DFAFVSWYQQ RPDKAPKLMV YEVSSRPSGV SNRFSGSKSG NTASLTISGL QAEDEADYY CTSYTSSSTF VFGTGTKVTV |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 7.5 |
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Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / 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: 2.0 µm / Nominal defocus min: 1.0 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Startup model | Type of model: NONE |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 2.77 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 148826 |
Initial angle assignment | Type: NOT APPLICABLE |
Final angle assignment | Type: NOT APPLICABLE |