Ohta Yusaku, Kamagata Takanori, Mukai Asuka, Takada Shinji, Nagai Takeharu, Horikawa Kazuki
Division of Bioimaging, Institute of Biomedical Sciences, Tokushima University Graduate School , 3-18-15 Kuramoto-cho, Tokushima City, Tokushima 770-8503, Japan.
Okazaki Institute for Integrative Bioscience and National Institute for Basic Biology, National Institutes of Natural Sciences , Okazaki, Aichi 444-8787, Japan.
ACS Chem Biol. 2016 Jul 15;11(7):1816-22. doi: 10.1021/acschembio.6b00221. Epub 2016 Jun 1.
Genetically encoded indicators driven by the Förster resonance energy transfer (FRET) mechanism are reliable tools for live imaging. While the properties of FRET-based indicators have been improved over the years, they often suffer from a poor dynamic range due to the lack of comprehensive understanding about how to apply an appropriate strategy to optimize the FRET parameters. One of the most successful optimizations is the incorporation of circularly permuted fluorescent proteins (cpFPs). To better understand the effects of this strategy, we systematically investigated the properties of the indicators by utilizing a set of FRET backbones consisting of native or one of the most effective cp variants (cp173FPs) with considerations of their order. As a result, the ordering of donor and acceptor FPs, which has been ignored in previous studies, was found to significantly affect the dynamic range of indicators. By utilizing these backbones, we succeeded in improving a cGMP indicator with 3.6-fold increased dynamic range and in generating an ultrasensitive cAMP indicator capable of environmental imaging, demonstrating the practical importance of the ordering of donors and acceptors in the engineering of FRET-based indicators.
由Förster共振能量转移(FRET)机制驱动的基因编码指示剂是用于活细胞成像的可靠工具。尽管多年来基于FRET的指示剂的性能有所改善,但由于缺乏对如何应用适当策略来优化FRET参数的全面理解,它们常常存在动态范围较差的问题。最成功的优化之一是引入了环状排列的荧光蛋白(cpFPs)。为了更好地理解这种策略的效果,我们通过使用一组由天然或最有效的cp变体之一(cp173FPs)组成的FRET骨架,并考虑它们的顺序,系统地研究了指示剂的性能。结果发现,供体和受体荧光蛋白的顺序在以前的研究中被忽略了,它会显著影响指示剂的动态范围。通过使用这些骨架,我们成功地改进了一种cGMP指示剂,其动态范围增加了3.6倍,并生成了一种能够进行环境成像的超灵敏cAMP指示剂,证明了供体和受体顺序在基于FRET的指示剂工程中的实际重要性。