Abstract
Background: Phospholipase C (PLC) isozymes are increasingly attractive therapeutic targets; however, pharmacological modulators are lacking. Results: A facile fluorescent high-throughput screen was developed and used to identify small molecule inhibitors of PLC activity. Conclusion: The new assay is robust and suitable for the rapid discovery of novel PLC modulators. Significance: This new methodology eliminates the major roadblock hampering the discovery of small molecule PLC inhibitors. © 2013 by The American Society for Biochemistry and Molecular Biology, Inc.
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CITATION STYLE
Huang, W., Barrett, M., Hajicek, N., Hicks, S., Harden, T. K., Sondek, J., & Zhang, Q. (2013). Small molecule inhibitors of phospholipase C from a novel high-throughput screen. Journal of Biological Chemistry, 288(8), 5840–5848. https://doi.org/10.1074/jbc.M112.422501
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