9OS5 image
Deposition Date 2025-05-23
Release Date 2025-09-03
Last Version Date 2026-03-18
Entry Detail
PDB ID:
9OS5
Title:
Human antibody Fab MPV498 bound to hMPV B2 post-fusion F
Biological Source:
Source Organism(s):
Expression System(s):
Method Details:
Experimental Method:
Resolution:
2.61 Å
Aggregation State:
PARTICLE
Reconstruction Method:
SINGLE PARTICLE
Macromolecular Entities
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Fusion glycoprotein F0
Gene (Uniprot):F
Chain IDs:A, B, C, D, E, F
Chain Length:465
Number of Molecules:6
Biological Source:human metapneumovirus
Protein Blast
Polymer Type:polypeptide(L)
Molecule:MPV498 Fab heavy chain
Chain IDs:G, I (auth: H), K (auth: I)
Chain Length:124
Number of Molecules:3
Biological Source:Homo sapiens
Protein Blast
Polymer Type:polypeptide(L)
Molecule:MPV498 Fab light chain
Chain IDs:H (auth: J), J (auth: K), L
Chain Length:100
Number of Molecules:3
Biological Source:Homo sapiens
Ligand Molecules
Primary Citation
Structural basis for childhood antibody recognition of the human metapneumovirus fusion protein.
Nat Commun 17 1267 1267 (2025)
PMID: 41455691 DOI: 10.1038/s41467-025-68021-8

Abstact

Human metapneumovirus (hMPV) is a significant cause of acute respiratory illness in children and older adults, with most children becoming seropositive by five years of age. The hMPV fusion (F) protein is the sole target of neutralizing antibodies, and while most common B-cell-targeted neutralizing epitopes on the hMPV F protein have been determined in hMPV-infected adults, the antibody response in hMPV-infected children remains undefined. We isolate five human monoclonal antibodies (mAbs) from hMPV-infected children, and evaluate their binding avidity, neutralization potency, epitope specificity, and in vivo efficacy. All mAbs are neutralizing, and epitope binning reveals four different epitopes targeted by the mAbs. Cryo-EM structures of four mAbs in complex with the hMPV F protein reveal epitopes on the hMPV F trimer surface as well as an intratrimer epitope located completely within the hMPV F trimer interface. Furthermore, we determine the prophylactic efficacy of the mAbs in protection against hMPV challenge in mice. These findings provide new insights into the immunodominant antigenic epitopes on the hMPV F protein in children and identify new mAbs for hMPV F disease prevention.

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Disease

Primary Citation of related structures
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