Department of Pharmacology, University of California, San Diego, San Diego, United States.
Department of Biomedical Engineering, Johns Hopkins University, Maryland, United States.
Elife. 2018 Jul 3;7:e35458. doi: 10.7554/eLife.35458.
Genetically encoded fluorescent biosensors have revolutionized the study of signal transduction by enabling the real-time tracking of signaling activities in live cells. Investigating the interaction between signaling networks has become increasingly important to understanding complex cellular phenomena, necessitating an update of the biosensor toolkit to allow monitoring and perturbing multiple activities simultaneously in the same cell. We therefore developed a new class of fluorescent biosensors based on homo-FRET, deemed FLuorescence Anisotropy REporters (FLAREs), which combine the multiplexing ability of single-color sensors with a quantitative, ratiometric readout. Using an array of color variants, we were able to demonstrate multiplexed imaging of three activity reporters simultaneously in the same cell. We further demonstrate the compatibility of FLAREs for use with optogenetic tools as well as intravital two-photon imaging.
基因编码荧光生物传感器通过实时跟踪活细胞中信号转导的活动,彻底改变了信号转导的研究。研究信号网络之间的相互作用对于理解复杂的细胞现象变得越来越重要,这需要更新生物传感器工具包,以允许在同一细胞中同时监测和干扰多种活性。因此,我们开发了一类基于同型 FRET 的新型荧光生物传感器,称为荧光各向异性报告子(FLAREs),它将单波长传感器的多路复用能力与定量、比率读数相结合。我们使用一系列颜色变体,成功地在同一细胞中同时实现了三种活性报告子的多路成像。我们还进一步证明了 FLAREs 与光遗传学工具以及活体双光子成像兼容。