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A cell-based multiplex immunoassay platform using fluorescent protein-barcoded reporter cell lines
Multiplex immunoassays with acellular antigens are well-established based on solid-phase platforms such as the Luminex(®) technology. Cell barcoding by amine-reactive fluorescent dyes enables analogous cell-based multiplex assays, but requires multiple labeling reactions and quality checks prior to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8617053/ https://www.ncbi.nlm.nih.gov/pubmed/34824350 http://dx.doi.org/10.1038/s42003-021-02881-w |
Sumario: | Multiplex immunoassays with acellular antigens are well-established based on solid-phase platforms such as the Luminex(®) technology. Cell barcoding by amine-reactive fluorescent dyes enables analogous cell-based multiplex assays, but requires multiple labeling reactions and quality checks prior to every assay. Here we describe generation of stable, fluorescent protein-barcoded reporter cell lines suitable for multiplex screening of antibody to membrane proteins. The utility of this cell-based system, with the potential of a 256-plex cell panel, is demonstrated by flow cytometry deconvolution of barcoded cell panels expressing influenza A hemagglutinin trimers, or native human CCR2 or CCR5 multi-span proteins and their epitope-defining mutants. This platform will prove useful for characterizing immunity and discovering antibodies to membrane-associated proteins. |
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