Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

8EAY

HMPV F complex with 4I3 Fab

Summary for 8EAY
Entry DOI10.2210/pdb8eay/pdb
EMDB information27808 27990
DescriptorFusion glycoprotein F0, 4I3 heavy chain protein, 4I3 light chain protein (3 entities in total)
Functional Keywordshuman antibodies, rsv and mpv fusion protein, complex cryo-em structure, viral protein and antiviral protein, biosynthetic protein
Biological sourceHuman metapneumovirus A (human)
More
Total number of polymer chains3
Total formula weight69859.11
Authors
Wen, X.,Jardetzky, T.S. (deposition date: 2022-08-30, release date: 2023-08-16, Last modification date: 2024-11-13)
Primary citationWen, X.,Suryadevara, N.,Kose, N.,Liu, J.,Zhan, X.,Handal, L.S.,Williamson, L.E.,Trivette, A.,Carnahan, R.H.,Jardetzky, T.S.,Crowe Jr., J.E.
Potent cross-neutralization of respiratory syncytial virus and human metapneumovirus through a structurally conserved antibody recognition mode.
Cell Host Microbe, 31:1288-1300.e6, 2023
Cited by
PubMed Abstract: Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) infections pose a significant health burden. Using pre-fusion conformation fusion (F) proteins, we isolated a panel of anti-F antibodies from a human donor. One antibody (RSV-199) potently cross-neutralized 8 RSV and hMPV strains by recognizing antigenic site III, which is partially conserved in RSV and hMPV F. Next, we determined the cryoelectron microscopy (cryo-EM) structures of RSV-199 bound to RSV F trimers, hMPV F monomers, and an unexpected dimeric form of hMPV F. These structures revealed how RSV-199 engages both RSV and hMPV F proteins through conserved interactions of the antibody heavy-chain variable region and how variability within heavy-chain complementarity-determining region 3 (HCDR3) can be accommodated at the F protein interface in site-III-directed antibodies. Furthermore, RSV-199 offered enhanced protection against RSV A and B strains and hMPV in cotton rats. These findings highlight the mechanisms of broad neutralization and therapeutic potential of RSV-199.
PubMed: 37516111
DOI: 10.1016/j.chom.2023.07.002
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.33 Å)
Structure validation

237735

数据于2025-06-18公开中

PDB statisticsPDBj update infoContact PDBjnumon