Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Tokyo, Japan.
Cell Signaling Group, WASEDA Bioscience Research Institute in Singapore (WABIOS), Singapore, Singapore.
Methods Mol Biol. 2021;2274:89-100. doi: 10.1007/978-1-0716-1258-3_9.
Advances in live-cell imaging have been accelerated by the development of various fluorescent indicators. However, indicators that are suitable for multicolor imaging remain a challenge to develop. Herein, we have developed a single fluorescent protein (FP)-based indicator using a semirational molecular design and a molecular evolution approach. We first inserted a ligand-binding domain into the vicinity of an FP chromophore to convert the conformational change induced by ligand binding into a change in fluorescence intensity. We then optimized the linker regions between the FP and the ligand-binding domain to greatly expand the dynamic range (F/F) of the indicator. Our design and optimization methods are highly versatile and can be used to develop any single FP-based indicators, which will further advance the utility of live-cell imaging.
活细胞成像的进展得益于各种荧光指示剂的发展。然而,开发适用于多色成像的指示剂仍然是一个挑战。在此,我们使用半理性的分子设计和分子进化方法,开发了一种基于单个荧光蛋白(FP)的指示剂。我们首先将配体结合域插入到 FP 发色团附近,将配体结合诱导的构象变化转化为荧光强度的变化。然后,我们优化了 FP 和配体结合域之间的连接区域,极大地扩展了指示剂的动态范围(F/F)。我们的设计和优化方法具有高度的通用性,可以用于开发任何基于单个 FP 的指示剂,这将进一步推进活细胞成像的应用。