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 |
|