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A cell-based multiplex immunoassay platform using fluorescent protein-barcoded reporter cell lines.

dc.contributor.author Song, Shengli
dc.contributor.author Manook, Miriam
dc.contributor.author Kwun, Jean
dc.contributor.author Jackson, Annette M
dc.contributor.author Knechtle, Stuart J
dc.contributor.author Kelsoe, Garnett
dc.date.accessioned 2022-11-01T19:32:05Z
dc.date.available 2022-11-01T19:32:05Z
dc.date.issued 2021-11
dc.identifier 10.1038/s42003-021-02881-w
dc.identifier.issn 2399-3642
dc.identifier.issn 2399-3642
dc.identifier.uri https://hdl.handle.net/10161/26168
dc.description.abstract Multiplex immunoassays with acellular antigens are well-established based on solid-phase platforms such as the Luminex<sup>®</sup> 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.
dc.language eng
dc.publisher Springer Science and Business Media LLC
dc.relation.ispartof Communications biology
dc.relation.isversionof 10.1038/s42003-021-02881-w
dc.subject Antibodies
dc.subject Cell Line
dc.subject Epitopes
dc.subject Flow Cytometry
dc.subject Fluorescent Dyes
dc.subject Hemagglutinins
dc.subject Immunoassay
dc.subject Influenza A virus
dc.subject Membrane Proteins
dc.subject Mutation
dc.subject Protein Multimerization
dc.subject Receptors, CCR2
dc.subject Receptors, CCR5
dc.title A cell-based multiplex immunoassay platform using fluorescent protein-barcoded reporter cell lines.
dc.type Journal article
duke.contributor.id Kwun, Jean|0669479
duke.contributor.id Jackson, Annette M|0202070
duke.contributor.id Knechtle, Stuart J|0167915
duke.contributor.id Kelsoe, Garnett|0205291
dc.date.updated 2022-11-01T19:31:41Z
pubs.begin-page 1338
pubs.issue 1
pubs.organisational-group Duke
pubs.organisational-group School of Medicine
pubs.organisational-group Basic Science Departments
pubs.organisational-group Clinical Science Departments
pubs.organisational-group Institutes and Centers
pubs.organisational-group Immunology
pubs.organisational-group Medicine
pubs.organisational-group Surgery
pubs.organisational-group Medicine, Nephrology
pubs.organisational-group Surgery, Abdominal Transplant Surgery
pubs.organisational-group Surgery, Surgical Sciences
pubs.organisational-group Duke Cancer Institute
pubs.organisational-group Duke Clinical Research Institute
pubs.organisational-group Duke Human Vaccine Institute
pubs.publication-status Published
pubs.volume 4
duke.contributor.orcid Kwun, Jean|0000-0002-8563-5472
duke.contributor.orcid Jackson, Annette M|0000-0003-2648-2944
duke.contributor.orcid Knechtle, Stuart J|0000-0002-1625-385X


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