Department of Aerospace and Mechanical Engineering, University of Notre Dame, Notre Dame, IN 46556, USA.
Department of Bioengineering, University of California, San Diego, CA 92092, USA.
Sensors (Basel). 2020 Sep 3;20(17):4998. doi: 10.3390/s20174998.
Fluorescence resonance energy transfer (FRET)-based biosensors have advanced live cell imaging by dynamically visualizing molecular events with high temporal resolution. FRET-based biosensors with spectrally distinct fluorophore pairs provide clear contrast between cells during dual FRET live cell imaging. Here, we have developed a new FRET-based Ca biosensor using EGFP and FusionRed fluorophores (FRET-GFPRed). Using different filter settings, the developed biosensor can be differentiated from a typical FRET-based Ca biosensor with ECFP and YPet (YC3.6 FRET Ca biosensor, FRET-CFPYPet). A high-frequency ultrasound (HFU) with a carrier frequency of 150 MHz can target a subcellular region due to its tight focus smaller than 10 µm. Therefore, HFU offers a new single cell stimulations approach for FRET live cell imaging with precise spatial resolution and repeated stimulation for longitudinal studies. Furthermore, the single cell level intracellular delivery of a desired FRET-based biosensor into target cells using HFU enables us to perform dual FRET imaging of a cell pair. We show that a cell pair is defined by sequential intracellular delivery of the developed FRET-GFPRed and FRET-CFPYPet into two target cells using HFU. We demonstrate that a FRET-GFPRed exhibits consistent 10-15% FRET response under typical ionomycin stimulation as well as under a new stimulation strategy with HFU.
荧光共振能量转移(FRET)生物传感器通过以高时间分辨率动态可视化分子事件,推动了活细胞成像的发展。具有明显光谱特征的荧光团对的 FRET 生物传感器在双 FRET 活细胞成像期间为细胞之间提供了清晰的对比度。在这里,我们使用 EGFP 和 FusionRed 荧光团(FRET-GFPRed)开发了一种新的基于 FRET 的 Ca 生物传感器。使用不同的滤光片设置,可以将开发的生物传感器与具有 ECFP 和 YPet 的典型 FRET 基于 Ca 的生物传感器(YC3.6 FRET Ca 生物传感器,FRET-CFPYPet)区分开来。由于其小于 10 µm 的紧密焦点,具有 150 MHz 载波频率的高频超声(HFU)可以靶向亚细胞区域。因此,HFU 为 FRET 活细胞成像提供了一种新的单细胞刺激方法,具有精确的空间分辨率和重复刺激以进行纵向研究。此外,使用 HFU 将所需的基于 FRET 的生物传感器以单细胞水平递送到靶细胞内,使我们能够对细胞对进行双 FRET 成像。我们表明,通过 HFU 顺序将开发的 FRET-GFPRed 和 FRET-CFPYPet 递送到两个靶细胞内,可以定义一对细胞。我们证明,在典型的离子霉素刺激以及 HFU 的新刺激策略下,FRET-GFPRed 表现出一致的 10-15%FRET 响应。