DeCuzzi Nicholaus L, Hu Jason Y, Xu Florene, Rodriguez Brayant, Pargett Michael, Albeck John G
Department of Molecular and Cellular Biology, University of California, Davis.
bioRxiv. 2024 Dec 2:2024.11.30.626109. doi: 10.1101/2024.11.30.626109.
Cell fate decisions are regulated by intricate signaling networks, with Extracellular signal-Regulated Kinase (ERK) being a central regulator. However, ERK is rarely the only signaling pathway involved, creating a need to study multiple signaling pathways simultaneously at the single-cell level. Many existing fluorescent biosensors for ERK and other pathways have significant spectral overlap, limiting their ability to be multiplexed. To address this limitation, we developed two novel red-FRET ERK biosensors, REKAR67 and REKAR76, which operate in the 670-720 nm range using miRFP670nano3 and miRFP720. REKAR67 and REKAR76 differ in fluorophore position, which impacts biosensor characteristics; REKAR67 displayed a higher dynamic range but greater signal variance than REKAR76. Mixed populations of REKAR67 or REKAR76 displayed similar Signal-to-Noise ratio (SNR), but in clonal cell populations, REKAR76 had a significantly higher SNR. Overall, our red-FRET ERK biosensors were highly consistent with existing ERK FRET biosensors and in reporting ERK activity and are spectrally compatible with CFP/YFP FRET and cpGFP -based biosensors. Both REKAR biosensors expand the available methods for measuring single-cell ERK activity.
细胞命运决定由复杂的信号网络调控,细胞外信号调节激酶(ERK)是核心调节因子。然而,ERK很少是唯一涉及的信号通路,这就需要在单细胞水平同时研究多种信号通路。许多现有的用于ERK和其他通路的荧光生物传感器存在显著的光谱重叠,限制了它们进行多路复用的能力。为解决这一限制,我们开发了两种新型的红色荧光共振能量转移(FRET)ERK生物传感器,REKAR67和REKAR76,它们使用miRFP670nano3和miRFP720在670 - 720 nm范围内发挥作用。REKAR67和REKAR76在荧光团位置上有所不同,这影响生物传感器的特性;REKAR67显示出更高的动态范围,但比REKAR76具有更大的信号方差。REKAR67或REKAR76的混合群体显示出相似的信噪比(SNR),但在克隆细胞群体中,REKAR76具有显著更高的SNR。总体而言,我们的红色FRET ERK生物传感器在报告ERK活性方面与现有的ERK FRET生物传感器高度一致,并且在光谱上与基于CFP/YFP FRET和cpGFP的生物传感器兼容。两种REKAR生物传感器都扩展了测量单细胞ERK活性的可用方法。