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

Ilya V Smirnov, Danica F Besavilla, Karin Schön, Hannes Axelsson, Davide Angeletti
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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.

动态MUNANA分析揭示了甲型流感病毒神经氨酸酶的功能相关抗体表位。
甲型流感病毒神经氨酸酶(NA)作为疫苗开发的靶点正受到关注。在这项研究中,我们提出了动态MUNANA测定作为鉴定特异性靶向NA上功能表位的单克隆抗体(mab)的工具。通过分析Michaelis-Menten曲线参数(Km和Vmax)的变化,我们揭示了不同的抗体介导的抑制机制。此外,我们开发了一个基于网络的应用程序,促进了分析结果的有效处理和统计推断。我们采用动态MUNANA法检测新开发的针对广泛使用的PR8 H1N1毒株NA的单抗。其中,对NA酶参数有强烈影响的单克隆抗体更有可能选择对病毒整体酶活性有重大影响的逃逸突变体。综上所述,当与ELLA结合时,动态MUNANA是一种快速分析推测结合位点和na特异性单克隆抗体效果的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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