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Protocol for high-throughput compound screening using flow cytometry in THP-1 cells

Flow cytometry is a valuable method for analyzing protein expressions at the single cell level but can be difficult to apply to large numbers of samples. This protocol provides instructions to perform a high-throughput small molecule screen using flow cytometry analysis of THP-1 cells, a human monoc...

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Detalles Bibliográficos
Autores principales: Spangenberg, Stephan H., Zavareh, Reza Beheshti, Lairson, Luke L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985391/
https://www.ncbi.nlm.nih.gov/pubmed/33778785
http://dx.doi.org/10.1016/j.xpro.2021.100400
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author Spangenberg, Stephan H.
Zavareh, Reza Beheshti
Lairson, Luke L.
author_facet Spangenberg, Stephan H.
Zavareh, Reza Beheshti
Lairson, Luke L.
author_sort Spangenberg, Stephan H.
collection PubMed
description Flow cytometry is a valuable method for analyzing protein expressions at the single cell level but can be difficult to apply to large numbers of samples. This protocol provides instructions to perform a high-throughput small molecule screen using flow cytometry analysis of THP-1 cells, a human monocytic leukemia cell line. We describe a methodology for identifying compounds that regulate PD-L1 surface expression in IFN-γ-stimulated cells, which has been successfully used to screen a collection of ∼200,000 compounds. For complete details on the use and execution of this protocol, please refer to Zavareh et al. (2020).
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spelling pubmed-79853912021-03-25 Protocol for high-throughput compound screening using flow cytometry in THP-1 cells Spangenberg, Stephan H. Zavareh, Reza Beheshti Lairson, Luke L. STAR Protoc Protocol Flow cytometry is a valuable method for analyzing protein expressions at the single cell level but can be difficult to apply to large numbers of samples. This protocol provides instructions to perform a high-throughput small molecule screen using flow cytometry analysis of THP-1 cells, a human monocytic leukemia cell line. We describe a methodology for identifying compounds that regulate PD-L1 surface expression in IFN-γ-stimulated cells, which has been successfully used to screen a collection of ∼200,000 compounds. For complete details on the use and execution of this protocol, please refer to Zavareh et al. (2020). Elsevier 2021-03-19 /pmc/articles/PMC7985391/ /pubmed/33778785 http://dx.doi.org/10.1016/j.xpro.2021.100400 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Spangenberg, Stephan H.
Zavareh, Reza Beheshti
Lairson, Luke L.
Protocol for high-throughput compound screening using flow cytometry in THP-1 cells
title Protocol for high-throughput compound screening using flow cytometry in THP-1 cells
title_full Protocol for high-throughput compound screening using flow cytometry in THP-1 cells
title_fullStr Protocol for high-throughput compound screening using flow cytometry in THP-1 cells
title_full_unstemmed Protocol for high-throughput compound screening using flow cytometry in THP-1 cells
title_short Protocol for high-throughput compound screening using flow cytometry in THP-1 cells
title_sort protocol for high-throughput compound screening using flow cytometry in thp-1 cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985391/
https://www.ncbi.nlm.nih.gov/pubmed/33778785
http://dx.doi.org/10.1016/j.xpro.2021.100400
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