High-content single-cell drug screening with phosphospecific flow cytometry

Peter O. Krutzik, Janelle M. Crane, Matthew R. Clutter, Garry P. Nolan*

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    155 Scopus citations

    Abstract

    Drug screening is often limited to cell-free assays involving purified enzymes, but it is arguably best applied against systems that represent disease states or complex physiological cellular networks. Here, we describe a high-content, cell-based drug discovery platform based on phosphospecific flow cytometry, or phosphoflow, that enabled screening for inhibitors against multiple endogenous kinase signaling pathways in heterogeneous primary cell populations at the single-cell level. From a library of small-molecule natural products, we identified pathway-selective inhibitors of Jak-Stat and MAP kinase signaling. Dose-response experiments in primary cells confirmed pathway selectivity, but importantly also revealed differential inhibition of cell types and new druggability trends across multiple compounds. Lead compound selectivity was confirmed in vivo in mice. Phosphoflow therefore provides a unique platform that can be applied throughout the drug discovery process, from early compound screening to in vivo testing and clinical monitoring of drug efficacy.

    Original languageEnglish (US)
    Pages (from-to)132-142
    Number of pages11
    JournalNature Chemical Biology
    Volume4
    Issue number2
    DOIs
    StatePublished - Feb 2008

    ASJC Scopus subject areas

    • Molecular Biology
    • Cell Biology

    Fingerprint Dive into the research topics of 'High-content single-cell drug screening with phosphospecific flow cytometry'. Together they form a unique fingerprint.

    Cite this