Islam Md Serajul, Honma Masato, Nakabayashi Takakazu, Kinjo Masataka, Ohta Nobuhiro
Graduate School of Environmental Science, Hokkaido University, Sapporo 060-0810, Japan.
Int J Mol Sci. 2013 Jan 18;14(1):1952-63. doi: 10.3390/ijms14011952.
We have studied physiological parameters in a living cell using fluorescence lifetime imaging of endogenous chromophores. In this study, pH dependence of the fluorescence lifetime of flavin adenine dinucleotide (FAD), that is a significant cofactor exhibiting autofluorescence, has been investigated in buffer solution and in cells. The fluorescence lifetime of FAD remained unchanged with pH 5 to 9 in solution. However, the fluorescence lifetime in HeLa cells was found to decrease with increasing intracellular pH, suggesting that pH in a single cell can be estimated from the fluorescence lifetime imaging of FAD without adding exogenous fluorescent probes.
我们利用内源性发色团的荧光寿命成像技术研究了活细胞中的生理参数。在本研究中,我们在缓冲溶液和细胞中研究了黄素腺嘌呤二核苷酸(FAD)的荧光寿命对pH的依赖性,FAD是一种具有自发荧光的重要辅因子。在溶液中,FAD的荧光寿命在pH 5至9范围内保持不变。然而,我们发现HeLa细胞中的荧光寿命会随着细胞内pH值的升高而降低,这表明无需添加外源荧光探针,通过FAD的荧光寿命成像就可以估算单个细胞内的pH值。