Dixit Ram, Cyr Richard, Gilroy Simon
Biology Department, The Pennsylvania State University, 208 Mueller Laboratory, University Park, PA 16802, USA.
Plant J. 2006 Feb;45(4):599-615. doi: 10.1111/j.1365-313X.2006.02658.x.
The intrinsically fluorescent proteins (IFPs), such as the green, cyan and yellow fluorescent proteins, have revolutionized how we can image the dynamics of cellular events. Intrinsically fluorescent proteins have been used as reporter genes to monitor transcriptional regulation, as targeted markers for organelles and subcellular structures, in fusion proteins to directly observe protein motility and dynamics, and in sensors designed to show changes in cellular environments ranging from pH to protein kinase activity. The IFPs hold tremendous potential to reveal the dynamic processes that underlie plant cell function; however, as with all technology there are artifacts and pitfalls inherent in their use. In this review, we highlight some of the practical issues in using IFPs for live cell imaging. These include choice of the appropriate IFP, dealing with autofluorescence, photobleaching and phototoxicity, and application of approaches such as fluorescence resonance energy transfer (FRET), fluorescence lifetime imaging (FLIM) and fluorescence recovery after photobleaching (FRAP) to gain high-resolution data about protein dynamics within the cell. We also discuss some of the more common artifacts associated with these fluorescence imaging approaches and suggest controls that should help both spot these problems and suggest their solutions.
诸如绿色、青色和黄色荧光蛋白等内在荧光蛋白,彻底改变了我们对细胞事件动态进行成像的方式。内在荧光蛋白已被用作报告基因来监测转录调控,作为细胞器和亚细胞结构的靶向标记,用于融合蛋白中以直接观察蛋白质的运动性和动态变化,以及用于设计的传感器中以显示从pH值到蛋白激酶活性等细胞环境的变化。内在荧光蛋白在揭示植物细胞功能背后的动态过程方面具有巨大潜力;然而,与所有技术一样,其使用过程中存在一些假象和陷阱。在本综述中,我们重点介绍了使用内在荧光蛋白进行活细胞成像的一些实际问题。这些问题包括选择合适的内在荧光蛋白、处理自发荧光、光漂白和光毒性,以及应用诸如荧光共振能量转移(FRET)、荧光寿命成像(FLIM)和光漂白后荧光恢复(FRAP)等方法来获取有关细胞内蛋白质动态的高分辨率数据。我们还讨论了与这些荧光成像方法相关的一些更常见的假象,并提出了有助于发现这些问题并提出解决方案的对照方法。