Geisinger Clinic, Danville, PA, USA.
Department of Urology, Dokkyo Medical University, Tochigi, Japan.
Methods Mol Biol. 2023;2693:1-11. doi: 10.1007/978-1-0716-3342-7_1.
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.
热休克反应(HSR)是一种细胞机制,用于对抗急性蛋白毒性应激。在真核生物中,HSR 的转录激活受热休克因子 1(HSF1)调控。HSF1 的激活诱导热休克蛋白(HSPs)的表达,这些 HSPs 作为分子伴侣发挥作用,以折叠和维持错误折叠蛋白的三维结构。HSR 的程度和持续时间的调节受多种生化机制控制,包括 HSF1 的翻译后修饰和许多蛋白质-蛋白质相互作用。在本章中,我们描述了一种使用半衰期短的荧光素酶报告基因检测法在转录水平上评估 HSR 激活和失活的方法。该测定法可用于进一步表征 HSR,也可用于筛选小分子诱导剂、放大器或抑制剂。