Bridging fluorescence microscopy and electron microscopy

被引:76
作者
Giepmans, Ben N. G. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Cell Biol, Sect Mol Imaging & Elect Microscopy, NL-9713 AV Groningen, Netherlands
关键词
fluorescent proteins; tetracysteine biarsenical system; Quantum dots; correlative light and electron microscopy; Golgi apparatus;
D O I
10.1007/s00418-008-0460-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Development of new fluorescent probes and fluorescence microscopes has led to new ways to study cell biology. With the emergence of specialized microscopy units at most universities and research centers, the use of these techniques is well within reach for a broad research community. A major breakthrough in fluorescence microscopy in biology is the ability to follow specific targets on or in living cells, revealing dynamic localization and/or function of target molecules. One of the inherent limitations of fluorescence microscopy is the resolution. Several efforts are undertaken to overcome this limit. The traditional and most well-known way to achieve higher resolution imaging is by electron microscopy. Moreover, electron microscopy reveals organelles, membranes, macromolecules, and thus aids in the understanding of cellular complexity and localization of molecules of interest in relation to other structures. With the new probe development, a solid bridge between fluorescence microscopy and electron microscopy is being built, even leading to correlative imaging. This connection provides several benefits, both scientifically as well as practically. Here, I summarize recent developments in bridging microscopy.
引用
收藏
页码:211 / 217
页数:7
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