使用多重六元荧光素酶测定同时检测细胞通路。

Q2 Biochemistry, Genetics and Molecular Biology Current Protocols in Molecular Biology Pub Date : 2020-06-01 DOI:10.1002/cpmb.122
Alejandro Sarrion-Perdigones, Lyra Chang, Yezabel Gonzalez, Tatiana Gallego-Flores, Damian W Young, Koen J T Venken
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引用次数: 3

摘要

多重实验可以分析同一细胞中的多种细胞信号通路,需要在大动态范围内报告正交遗传编码报告。荧光素酶是一种成本效益高,用途广泛的候选物,其输出信号可以以多路方式敏感地检测到。常用的双荧光素酶报告分析检测一种与单个细胞途径偶联的荧光素酶,另一种与控制途径偶联的荧光素酶用于正常化目的。我们已经将这种方法扩展到多重六元荧光素酶检测,可以报告五种细胞信号通路和一种控制,每一种都由一种独特的荧光素酶编码。六种荧光素酶发出的光可以通过使用两种不同的底物来区分,每种底物对三种荧光素酶都有特异性,然后用带通滤波器对三种荧光素酶发出的光进行光谱分解。在这里,我们详细介绍了如何使用组成型CMV启动子作为归一化控制,通过五种特定信号通路(即c-Myc、NF-κβ、TGF-β、p53和MAPK/JNK)的转录反应元件进行多重六元荧光素酶检测来监测通路通量的方案。提供了用于制备用于多重报告基因测定的报告载体质粒、进行细胞培养和多重荧光素酶报告载体质粒转染、执行多重荧光素酶测定以及分析和解释由适当配备以检测不同发光的平板阅读器获得的数据的方案。©2020 Wiley期刊有限责任公司基本方案1:多重六元荧光素酶测定载体的制备基本方案2:多重六元荧光素酶测定的细胞培养工作基本方案3:荧光素酶报告质粒转染,然后进行药物和重组蛋白处理基本方案4:执行多重六元荧光素酶测定。
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Simultaneous Examination of Cellular Pathways using Multiplex Hextuple Luciferase Assaying.

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.

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Current Protocols in Molecular Biology
Current Protocols in Molecular Biology Biochemistry, Genetics and Molecular Biology-Molecular Biology
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