Zaccolo M, Pozzan T
Dipartimento di Scienze Biomediche Sperimentali and Centro CNR per le Biomembrane, University of Padova, Italy.
IUBMB Life. 2000 May;49(5):375-9. doi: 10.1080/152165400410218.
Since the cloning and the eterologous expression of the Green Fluorescence Protein (GFP), a number of applications have been reported where protein location within the cell or gene expression is revealed by fluorescent imaging of living cells. Modified GFPs, however, can now be exploited not only as a fluorescent reporter but also as a dynamic marker of intracellular signalling events, such as fluctuations in the levels of the second messengers Ca2+ and cAMP, or as a probe for detecting changes in pH in various cell compartments. These genetically manipulated GFPs allow monitoring of the biochemistry of the cell in real time and thus offer the possibility to gain a more precise view of the functioning of live cells.
自从绿色荧光蛋白(GFP)被克隆并实现异源表达以来,已经有许多应用报道,通过活细胞的荧光成像来揭示细胞内蛋白质的定位或基因表达情况。然而,经过修饰的GFP现在不仅可以用作荧光报告分子,还可以作为细胞内信号事件的动态标记物,比如第二信使Ca2+和cAMP水平的波动,或者作为检测各种细胞区室pH变化的探针。这些经过基因操作的GFP能够实时监测细胞的生物化学过程,从而提供了更精确地了解活细胞功能的可能性。