Laboratory of Bioimaging and Cell Signaling, Graduate School of Biostudies, Kyoto University, Kyoto, Japan.
Cancer Sci. 2012 Apr;103(4):614-9. doi: 10.1111/j.1349-7006.2011.02196.x. Epub 2012 Feb 3.
The constituents of the oncogene signal transduction pathway are promising targets for anticancer drugs. Despite the wealth of available knowledge regarding their molecular properties, the spatiotemporal regulation of the signaling molecules remains elusive. Biosensors based on the principle of FRET have been developed to visualize the activities of the signaling molecules in living cells. However, difficulties in the development of sensitive FRET biosensors have prevented their widespread use in cancer research. The lack of cell lines constitutively expressing a FRET biosensor has also limited their use. In this review, we will introduce the principle of FRET-based biosensors, describe an optimized backbone of the FRET biosensors, techniques to express FRET biosensors stably in the cells, and discuss the future perspectives of FRET biosensors in cancer research.
癌基因信号转导途径的组成部分是有前途的抗癌药物靶点。尽管关于它们的分子特性有丰富的知识,但信号分子的时空调节仍然难以捉摸。基于 FRET 原理的生物传感器已被开发出来,用于可视化活细胞中信号分子的活性。然而,敏感 FRET 生物传感器的开发困难阻碍了它们在癌症研究中的广泛应用。缺乏稳定表达 FRET 生物传感器的细胞系也限制了它们的使用。在这篇综述中,我们将介绍基于 FRET 的生物传感器的原理,描述 FRET 生物传感器的优化骨架,稳定表达 FRET 生物传感器的技术,并讨论 FRET 生物传感器在癌症研究中的未来前景。