Terai Kenta, Imanishi Ayako, Li Chunjie, Matsuda Michiyuki
Laboratory of Bioimaging and Cell Signaling, Graduate School of Biostudies, Kyoto University.
Research Center for Dynamic Living Systems, Graduate School of Biostudies, Kyoto University.
Cell Struct Funct. 2019 Nov 2;44(2):153-169. doi: 10.1247/csf.18035. Epub 2019 Mar 21.
Two decades have passed since the development of the first calcium indicator based on the green fluorescent protein (GFP) and the principle of Förster resonance energy transfer (FRET). During this period, researchers have advanced many novel ideas for the improvement of such genetically encoded FRET biosensors, which have allowed them to expand their targets from small molecules to signaling proteins and physicochemical properties. Although the merits of "genetically encoded" FRET biosensors became clear once various cell lines were established and several transgenic organisms were generated, the road to these developments was not necessarily a smooth one. Moreover, even today the development of new FRET biosensors remains a very labor-intensive, trial-and-error process. Therefore, at this junction, it may be worthwhile to summarize the progress of the FRET biosensor and discuss the future direction of its development and application.Key words: FRET, biosensor, fluorescent protein.
自基于绿色荧光蛋白(GFP)和福斯特共振能量转移(FRET)原理的首个钙指示剂问世以来,二十年已经过去了。在此期间,研究人员提出了许多新颖的想法来改进此类基因编码的FRET生物传感器,这使他们能够将目标从小分子扩展到信号蛋白和物理化学性质。尽管一旦建立了各种细胞系并培育出几种转基因生物,“基因编码”FRET生物传感器的优点就变得显而易见,但这些发展之路并非一帆风顺。此外,即使在今天,新型FRET生物传感器的开发仍然是一个劳动密集型的试错过程。因此,在这个节点上,总结FRET生物传感器的进展并讨论其未来的发展和应用方向可能是值得的。关键词:FRET、生物传感器、荧光蛋白。