A neutralizing single-domain antibody that targets the trimer interface of the human metapneumovirus fusion protein.

ABSTRACT:

Importance

Human metapneumovirus (hMPV) is an important respiratory pathogen for which no licensed antivirals or vaccines exist. Single-domain antibodies represent promising antiviral biologics that can be easily produced and formatted. We describe the isolation and detailed characterization of two hMPV-neutralizing single-domain antibodies that are directed against the fusion protein F. One of these single-domain antibodies broadly neutralizes hMPV A and B strains, can prevent proteolytic maturation of F, and binds to an epitope in the F trimer interface. This suggests that hMPV pre-F undergoes trimer opening or "breathing" on infectious virions, exposing a vulnerable site for neutralizing antibodies. Finally, we show that this single-domain antibody, fused to a human IgG1 Fc, can

SUBMITTER: Ballegeer M 

PROVIDER: S-EPMC10790764 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature