Optical photon reassignment with increased axial resolution by structured illumination

被引:21
作者
Roth, Stephan [1 ]
Heintzmann, Rainer [1 ,2 ,3 ]
机构
[1] Leibniz Inst Photon Technol, Albert Einstein Str 9, D-07745 Jena, Germany
[2] Friedrich Schiller Univ Jena, Inst Phys Chem, Helmholtzweg 4, D-07743 Jena, Germany
[3] Friedrich Schiller Univ Jena, Abbe Ctr Photon, Helmholtzweg 4, D-07743 Jena, Germany
来源
Methods and Applications in Fluorescence | 2016年 / 4卷 / 04期
关键词
microscopy; superresolution microscopy; confocal microscopy; reassignment microscopy; scanning microscopy; AiryScan; MICROSCOPY; LIVE;
D O I
10.1088/2050-6120/4/4/045005
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Fluorescent microscopy methods linked to the reassignment principle as image scanning microscopy (ISM), re-scan confocal (RSC), optical photon reassignment (OPRA) and instant structured illumination microscopy (iSIM) have the potential to replace confocal microscopy as the standard microscopy technique. Photon reassignment methods are known to link the most important properties in biological imaging as resolution, sensitivity, imaging speed and combinability with fluorophores in an elegant way. On the example of OPRA, we show how this method could be easily extended to the third dimension. If OPRA is used in combination with a structured illumination pattern the sectioning ability can be improved while maintaining the very high signal intensity. We present a detailed analysis about the imaging properties of OPRA in three dimensions and show experimental results on biological samples.
引用
收藏
页码:1 / 6
页数:6
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