1 Department of Chemistry, University of Kentucky, Lexington, KY, USA.
SLAS Discov. 2017 Apr;22(4):399-407. doi: 10.1177/2472555216684333. Epub 2017 Jan 6.
Dysregulated transcription, translation, and protein degradation are common features of cancer cells, regardless of specific genetic profiles. Several clinical anticancer agents take advantage of this characteristic vulnerability and interfere with the processes of transcription and translation or inhibit protein degradation. However, traditional assays that follow the process of protein production and removal require multistep processing and are not easily amenable to high-throughput screening. The use of recombinant fluorescent proteins provides a convenient solution to this problem, and moreover, photoconvertable fluorescent proteins allow for ratiometric detection of both new protein production and removal of existing proteins. Here, the photoconvertable protein Dendra2 is used in the development of in-cell assays of protein production and degradation that are optimized and validated for high-throughput screening. Conversion from the green to red emissive form can be achieved using a high-intensity light-emitting diode array, producing a stable pool of the red fluorescent form of Dendra2. This allows for rates of protein production or removal to be quantified in a plate reader or by fluorescence microscopy, providing a means to measure the potencies of inhibitors that affect these key processes.
转录、翻译和蛋白质降解失调是癌细胞的共同特征,而与特定的遗传特征无关。几种临床抗癌药物利用了这种特征性的脆弱性,干扰转录和翻译过程或抑制蛋白质降解。然而,跟踪蛋白质产生和去除过程的传统检测方法需要多步处理,并且不容易适用于高通量筛选。重组荧光蛋白的使用为这个问题提供了一个方便的解决方案,而且,光可转换的荧光蛋白允许对新蛋白质的产生和现有蛋白质的去除进行比率检测。在这里,光可转换蛋白 Dendra2 用于开发细胞内蛋白质产生和降解的检测方法,这些方法经过优化和验证可用于高通量筛选。使用高强度发光二极管阵列可以从绿色发射形式转换为红色发射形式,从而产生稳定的 Dendra2 红色荧光形式的储备库。这使得可以在板读数器或荧光显微镜中定量蛋白质的产生或去除率,提供了一种测量影响这些关键过程的抑制剂效力的方法。