University of Massachusetts, Amherst, MA, 01003, USA.
Angew Chem Int Ed Engl. 2019 Dec 9;58(50):18271-18275. doi: 10.1002/anie.201911799. Epub 2019 Oct 24.
Precisely determining the intracellular concentrations of metabolites and signaling molecules is critical in studying cell biology. Fluorogenic RNA-based sensors have emerged to detect various targets in living cells. However, it is still challenging to apply these genetically encoded sensors to quantify the cellular concentrations and distributions of targets. Herein, using a pair of orthogonal fluorogenic RNA aptamers, DNB and Broccoli, we engineered a modular sensor system to apply the DNB-to-Broccoli fluorescence ratio to quantify the cell-to-cell variations of target concentrations. These ratiometric sensors can be broadly applied for live-cell imaging and quantification of metabolites, signaling molecules, and other synthetic compounds.
精确测定细胞内代谢物和信号分子的浓度对于研究细胞生物学至关重要。基于荧光的 RNA 传感器已经出现,可以用于检测活细胞中的各种靶标。然而,将这些基因编码的传感器应用于定量靶标在细胞内的浓度和分布仍然具有挑战性。在此,我们使用一对正交的荧光 RNA 适体(DNB 和 Broccoli),设计了一种模块化的传感器系统,将 DNB 到 Broccoli 的荧光比值用于定量靶标浓度的细胞间变化。这些比率型传感器可以广泛应用于代谢物、信号分子和其他合成化合物的活细胞成像和定量。