Laboratory of Chemical Biology, Department of Biomedical Engineering, Eindhoven University of Technology , P.O. Box 513, 5600MB Eindhoven, The Netherlands.
ACS Chem Biol. 2013 Oct 18;8(10):2133-9. doi: 10.1021/cb400427b. Epub 2013 Aug 30.
Elucidation of subcellular signaling networks by multiparameter imaging is hindered by a lack of sensitive FRET pairs spectrally compatible with the classic CFP/YFP pair. Here, we present a generic strategy to enhance the traditionally poor sensitivity of red FRET sensors by developing self-associating variants of mOrange and mCherry that allow sensors to switch between well-defined on- and off states. Requiring just a single mutation of the mFruit domain, this new FRET pair improved the dynamic range of protease sensors up to 10-fold and was essential to generate functional red variants of CFP-YFP-based Zn(2+) sensors. The large dynamic range afforded by the new red FRET pair allowed simultaneous use of differently colored Zn(2+) FRET sensors to image Zn(2+) over a broad concentration range in the same cellular compartment.
通过多参数成像阐明细胞内信号转导网络受到限制,因为缺乏与经典 CFP/YFP 对光谱兼容的灵敏 FRET 对。在这里,我们提出了一种通用策略,通过开发 mOrange 和 mCherry 的自缔合变体来增强红色 FRET 传感器的传统低灵敏度,使传感器能够在明确定义的开和关状态之间切换。该新的 FRET 对仅需要 mFruit 结构域的单个突变,就将蛋白酶传感器的动态范围提高了 10 倍,对于生成基于 CFP-YFP 的 Zn(2+)传感器的功能性红色变体至关重要。新的红色 FRET 对提供的大动态范围允许同时使用不同颜色的 Zn(2+)FRET 传感器,在同一细胞区室中对广泛浓度范围内的 Zn(2+)进行成像。