van der Krogt Gerard N M, Ogink Janneke, Ponsioen Bas, Jalink Kees
Division of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
PLoS One. 2008 Apr 2;3(4):e1916. doi: 10.1371/journal.pone.0001916.
We recently reported on CFP-Epac-YFP, an Epac-based single polypeptide FRET reporter to resolve cAMP levels in living cells. In this study, we compared and optimized the fluorescent protein donor/acceptor pairs for use in biosensors such as CFP-Epac-YFP. Our strategy was to prepare a wide range of constructs consisting of different donor and acceptor fluorescent proteins separated by a short linker. Constructs were expressed in HEK293 cells and tested for FRET and other relevant properties. The most promising pairs were subsequently used in an attempt to improve the FRET span of the Epac-based cAMP sensor. The results show significant albeit not perfect correlation between performance in the spacer construct and in the Epac sensor. Finally, this strategy enabled us to identify improved sensors both for detection by sensitized emission and by fluorescent lifetime imaging. The present overview should be helpful in guiding development of future FRET sensors.
我们最近报道了CFP-Epac-YFP,一种基于Epac的单多肽FRET报告基因,用于解析活细胞中的cAMP水平。在本研究中,我们比较并优化了用于CFP-Epac-YFP等生物传感器的荧光蛋白供体/受体对。我们的策略是制备一系列由短接头分隔的不同供体和受体荧光蛋白组成的构建体。构建体在HEK293细胞中表达,并测试其FRET及其他相关特性。随后使用最有前景的配对来尝试提高基于Epac的cAMP传感器的FRET跨度。结果表明,间隔构建体和Epac传感器的性能之间存在显著但并不完美的相关性。最后,该策略使我们能够识别出通过敏化发射和荧光寿命成像进行检测的改进型传感器。本综述应有助于指导未来FRET传感器的开发。