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 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.
Duke Scholars
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- Receptors, CCR5
- Receptors, CCR2
- Protein Multimerization
- Mutation
- Membrane Proteins
- Influenza A virus
- Immunoassay
- Hemagglutinins
- Fluorescent Dyes
- Flow Cytometry
Citation
Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Receptors, CCR5
- Receptors, CCR2
- Protein Multimerization
- Mutation
- Membrane Proteins
- Influenza A virus
- Immunoassay
- Hemagglutinins
- Fluorescent Dyes
- Flow Cytometry