Germond Arno, Fujita Hideaki, Ichimura Taro, Watanabe Tomonobu M
Laboratory for Comprehensive Bioimaging, RIKEN Quantitative Biology Center (QBiC), 6-2-3 Furuedai, Suita, Osaka, 565-0874, Japan.
WPI Immunology Frontier Research Center, Osaka University, 1-3 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Biophys Rev. 2016 Jun;8(2):121-138. doi: 10.1007/s12551-016-0195-9. Epub 2016 Apr 29.
Over the past decades many researchers have made major contributions towards the development of genetically encoded (GE) fluorescent sensors derived from fluorescent proteins. GE sensors are now used to study biological phenomena by facilitating the measurement of biochemical behaviors at various scales, ranging from single molecules to single cells or even whole animals. Here, we review the historical development of GE fluorescent sensors and report on their current status. We specifically focus on the development strategies of the GE sensors used for measuring pH, ion concentrations (e.g., chloride and calcium), redox indicators, membrane potential, temperature, pressure, and molecular crowding. We demonstrate that these fluroescent protein-based sensors have a shared history of concepts and development strategies, and we highlight the most original concepts used to date. We believe that the understanding and application of these various concepts will pave the road for the development of future GE sensors and lead to new breakthroughs in bioimaging.
在过去几十年里,许多研究人员对源自荧光蛋白的基因编码(GE)荧光传感器的发展做出了重大贡献。GE传感器现在被用于研究生物现象,通过促进在各种尺度上测量生化行为,范围从单分子到单细胞甚至整个动物。在这里,我们回顾GE荧光传感器的历史发展并报告其当前状态。我们特别关注用于测量pH值、离子浓度(如氯离子和钙离子)、氧化还原指示剂、膜电位、温度、压力和分子拥挤程度的GE传感器的开发策略。我们证明这些基于荧光蛋白的传感器在概念和开发策略上有共同的历史,并且我们突出了迄今为止使用的最原始的概念。我们相信对这些各种概念的理解和应用将为未来GE传感器的发展铺平道路,并在生物成像方面带来新的突破。