Hancock Michael K, Xia Menghang, Frey Elizabeth S, Sakamuru Srilatha, Bi Kun
Invitrogen Corporation, Discovery Assays and Services, 501 Charmany Drive, Madison, WI 53719, USA.
Curr Chem Genomics. 2009 Feb 5;3:1-6. doi: 10.2174/1875397300903010001.
Moderate environmental and physiological stressors are known to initiate protective heat shock response (HSR) leading to cell survival. HSR is largely mediated by the activation of heat shock factor (HSF), resulting in increased heat shock protein expression. Dysregulation of the HSR signaling has been associated with various diseases including cancer, inflammation and neurodegenerative disorders. Compounds that can modulate HSR have been pursued for the treatment of these diseases. To facilitate the discovery of HSR modulators, we developed a high-throughput amenable betalactamase transcriptional reporter gene assay for monitoring the function of HSF. HeLa cells were engineered to express the beta-lactamase reporter under the control of HSF response elements (HSE) present in the HSP70 gene promoter. The HSE-beta lactamase (HSE-bla) reporter gene assay was validated by using HSF-specific siRNAs and known small molecule modulators. Taking the advantage of fluorescence resonance energy transfer (FRET)-based cell permeable betalactamase substrate, this assay can be miniaturized into 1536-well format. Our results demonstrate that the assay is robust and can be applied to high-throughput screening (HTS) for modulators of HSR.
已知适度的环境和生理应激源会引发保护性热休克反应(HSR),从而导致细胞存活。HSR主要由热休克因子(HSF)的激活介导,导致热休克蛋白表达增加。HSR信号传导的失调与包括癌症、炎症和神经退行性疾病在内的各种疾病有关。能够调节HSR的化合物已被用于治疗这些疾病。为了促进HSR调节剂的发现,我们开发了一种适用于高通量的β-内酰胺酶转录报告基因检测方法,用于监测HSF的功能。将HeLa细胞进行基因改造,使其在HSP70基因启动子中存在的HSF反应元件(HSE)的控制下表达β-内酰胺酶报告基因。通过使用HSF特异性siRNA和已知的小分子调节剂对HSE-β-内酰胺酶(HSE-bla)报告基因检测方法进行了验证。利用基于荧光共振能量转移(FRET)的细胞可渗透β-内酰胺酶底物,该检测方法可小型化为1536孔板形式。我们的结果表明,该检测方法具有稳健性,可应用于HSR调节剂的高通量筛选(HTS)。