Fluorescence microscopy with super-resolved optical sections

被引:80
作者
Egner, A
Hell, SW [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept NanoBiophoton, D-37077 Gottingen, Germany
[2] German Canc Res Ctr, Div High Resolut Opt Microscopy, D-69120 Heidelberg, Germany
关键词
D O I
10.1016/j.tcb.2005.02.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The fluorescence microscope, especially its confocal variant, has become a standard tool in cell biology research for delivering 3D-images of intact cells. However, the resolution of any standard optical microscope is at least 3 times poorer along the axis of the lens that in its focal plane. Here, we review principles and applications of an emerging family of fluorescence microscopes, such as Vi microscopes,which improve axial resolution by a factor of seven by employing two opposing lenses. Noninvasive axial sections of 80-160 nm thickness deliver more faithful 3D-images of subcellular features, providing a new opportunity to significantly enhance our understanding of cellular structure and function.
引用
收藏
页码:207 / 215
页数:9
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