Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas.
Department of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, Texas.
Curr Protoc Mol Biol. 2020 Jun;131(1):e122. doi: 10.1002/cpmb.122.
Multiplex experimentation that can assay multiple cellular signaling pathways in the same cells requires orthogonal genetically encoded reporters that report over large dynamic ranges. Luciferases are cost-effective, versatile candidates whose output signals can be sensitively detected in a multiplex fashion. Commonly used dual luciferase reporter assays detect one luciferase that is coupled to a single cellular pathway and a second that is coupled to a control pathway for normalization purposes. We have expanded this approach to multiplex hextuple luciferase assays that can report on five cellular signaling pathways and one control, each of which is encoded by a unique luciferase. Light emission by the six luciferases can be distinguished by the use of two distinct substrates, each specific for three luciferases, followed by spectral decomposition of the light emitted by each of the three luciferase enzymes with bandpass filters. Here, we present detailed protocols on how to perform multiplex hextuple luciferase assaying to monitor pathway fluxes through transcriptional response elements for five specific signaling pathways (i.e., c-Myc, NF-κβ, TGF-β, p53, and MAPK/JNK) using the constitutive CMV promoter as normalization control. Protocols are provided for preparing reporter vector plasmids for multiplex reporter assaying, performing cell culture and multiplex luciferase reporter vector plasmid transfection, executing multiplex luciferase assays, and analyzing and interpreting data obtained by a plate reader appropriately equipped to detect the different luminescences. © 2020 Wiley Periodicals LLC. Basic Protocol 1: Preparation of vectors for multiplex hextuple luciferase assaying Basic Protocol 2: Cell culture work for multiplex hextuple luciferase assays Basic Protocol 3: Transfection of luciferase reporter plasmids followed by drug and recombinant protein treatments Basic Protocol 4: Performing the multiplex hextuple luciferase assay.
多重实验可以在同一细胞中测定多个细胞信号通路,这需要正交的遗传编码报告器,其报告范围大。荧光素酶是具有成本效益的多功能候选物,其输出信号可以以高灵敏度的方式以多重方式检测。常用的双荧光素酶报告基因检测方法检测一种与单个细胞途径偶联的荧光素酶和一种与对照途径偶联的第二种荧光素酶,用于归一化目的。我们已经扩展了这种方法,以进行六重荧光素酶多重检测,该方法可以报告五个细胞信号通路和一个对照,每个通路都由独特的荧光素酶编码。通过使用两种独特的底物来区分六种荧光素酶的发光,每种底物都特异性地与三种荧光素酶结合,然后用带通滤波器对每种三种荧光素酶发出的光进行光谱分解。在这里,我们提供了详细的协议,介绍如何进行六重荧光素酶多重检测,以监测通过五个特定信号通路(即 c-Myc、NF-κβ、TGF-β、p53 和 MAPK/JNK)的转录反应元件的途径通量,使用组成型 CMV 启动子作为归一化对照。提供了用于制备多重报告基因检测载体质粒的方案,进行细胞培养和六重荧光素酶报告基因载体质粒转染,执行六重荧光素酶检测,以及分析和解释适当配备以检测不同发光的平板读数器获得的数据。 © 2020 威立出版社。基本方案 1:六重荧光素酶检测载体质粒的制备基本方案 2:六重荧光素酶检测的细胞培养工作基本方案 3:荧光素酶报告质粒转染后进行药物和重组蛋白处理基本方案 4:进行六重荧光素酶检测。