| Literature DB >> 29177649 |
Toshiki Kijima1, Takanori Eguchi2, Len Neckers3, Thomas L Prince4.
Abstract
The heat shock response (HSR) is a cellular mechanism for counteracting acute proteotoxic stress. In eukaryotes, transcriptional activation of the HSR is regulated by heat shock factor 1 (HSF1). Activation of HSF1 induces the expression of heat shock proteins (HSPs) that function as molecular chaperones to fold and maintain the three-dimensional structure of misfolded proteins. The regulation of the degree and duration of the HSR is controlled by multiple biochemical mechanisms that include posttranslational modification of HSF1 and numerous protein-protein interactions. In this chapter, we describe a method to evaluate the activation and deactivation of the HSR at the transcriptional level using a short half-life luciferase reporter assay. This assay can be used to further characterize the HSR or as a screen for small-molecule inducers, amplifiers, or repressors.Entities:
Keywords: Drug screen; Heat shock factor 1 (HSF1); Heat shock protein 90 (HSP90); Heat shock response; Luciferase assay; Real-time
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Year: 2018 PMID: 29177649 PMCID: PMC8054299 DOI: 10.1007/978-1-4939-7477-1_3
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745