Kinetic MUNANA assay reveals functionally relevant antibody epitopes on Influenza A virus neuraminidase

Influenza A virus neuraminidase (NA) is drawing attention as a target for vaccine development. In this study, we propose kinetic MUNANA assay as a tool to identify monoclonal antibodies (mAbs) that specifically target functional epitopes on NA. By analyzing changes in the parameters of the Michaelis-Menten curve (Km and Vmax), we revealed distinct mechanisms of Ab-mediated inhibition. Additionally, we developed a web-based application facilitating efficient processing of the assay results and enabling statistical inference. We employed the kinetic MUNANA assay to test newly developed mAbs targeting NA of the widely used PR8 H1N1 strain. Among these, mAbs with strong effect on NA enzymatic parameters were more likely to select for escape mutants that had a substantial impact on the overall enzymatic activity of the virus. In summary, when combined with ELLA, kinetic MUNANA is a rapid method to profile the putative binding site and the effect of NA-specific mAbs.

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Publication Details

Journal
npj Viruses
Published
2025-05-10
DOI
https://doi.org/10.1038/s44298-025-00123-y
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Kinetic MUNANA assay reveals functionally relevant antibody epitopes on Influenza A virus neuraminidase

Hannes Axelsson, И. В. Смирнов, Davide Angeletti, Danica F. Besavilla et al.
npj Viruses
Influenza Virus Research Studies
article

Kinetic MUNANA assay reveals functionally relevant antibody epitopes on Influenza A virus neuraminidase

Hannes Axelsson, И. В. Смирнов, Davide Angeletti, Danica F. Besavilla, Karin Schön
article en

Abstract

Influenza A virus neuraminidase (NA) is drawing attention as a target for vaccine development. In this study, we propose kinetic MUNANA assay as a tool to identify monoclonal antibodies (mAbs) that specifically target functional epitopes on NA. By analyzing changes in the parameters of the Michaelis-Menten curve (Km and Vmax), we revealed distinct mechanisms of Ab-mediated inhibition. Additionally, we developed a web-based application facilitating efficient processing of the assay results and enabling statistical inference. We employed the kinetic MUNANA assay to test newly developed mAbs targeting NA of the widely used PR8 H1N1 strain. Among these, mAbs with strong effect on NA enzymatic parameters were more likely to select for escape mutants that had a substantial impact on the overall enzymatic activity of the virus. In summary, when combined with ELLA, kinetic MUNANA is a rapid method to profile the putative binding site and the effect of NA-specific mAbs.

npj VirusesVol. 3(1)
University of Gothenburg (SE)
Knut och Alice Wallenbergs Stiftelse, Vetenskapsrådet, Svenska Läkaresällskapet, HORIZON EUROPE European Research Council
Good health and well-being
Openalex Percentile: Top 85%
Influenza Virus Research Studies
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