Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, NY, USA.
Methods Mol Biol. 2021;2350:43-68. doi: 10.1007/978-1-0716-1593-5_4.
Förster resonance energy transfer (FRET) biosensors are popular and useful for directly observing cellular signaling pathways in living cells. Until recently, multiplex imaging of genetically encoded FRET biosensors to simultaneously monitor several protein activities in one cell was limited due to a lack of spectrally compatible FRET pair of fluorescent proteins. With the recent development of miRFP series of near-infrared (NIR) fluorescent proteins, we are now able to extend the spectrum of FRET biosensors beyond blue-green-yellow into NIR. These new NIR FRET biosensors enable direct multiplex imaging together with commonly used cyan-yellow FRET biosensors. We describe herein a method to produce cell lines harboring two compatible FRET biosensors. We will then discuss how to directly multiplex-image these FRET biosensors in living cells. The approaches described herein are generally applicable to any combinations of genetically encoded, ratiometric FRET biosensors utilizing the cyan-yellow and NIR fluorescence.
Förster 共振能量转移(FRET)生物传感器在直接观察活细胞中的细胞信号通路方面非常受欢迎且非常有用。直到最近,由于缺乏光谱兼容的荧光蛋白 FRET 对,多色成像的遗传编码 FRET 生物传感器同时监测一个细胞中的几种蛋白质活性仍然受到限制。随着近红外(NIR)荧光蛋白 miRFP 系列的最新发展,我们现在能够将 FRET 生物传感器的光谱扩展到蓝-绿-黄之外的 NIR。这些新的 NIR FRET 生物传感器能够与常用的青-黄 FRET 生物传感器一起直接进行多色成像。本文描述了一种产生携带两个兼容 FRET 生物传感器的细胞系的方法。然后,我们将讨论如何直接在活细胞中对这些 FRET 生物传感器进行多色成像。本文中描述的方法通常适用于利用青-黄和 NIR 荧光的任何组合的遗传编码、比率 FRET 生物传感器。