Super-Resolution Structured Illumination Microscopy

被引:416
作者
Heintzmann, Rainer [1 ,2 ,3 ]
Huser, Thomas [4 ,5 ,6 ]
机构
[1] Leibniz Inst Photon Technol, Albert Einstein Str 9, D-07745 Jena, Germany
[2] Friedrich Schiller Univ Jena, Inst Phys Chem, D-07745 Jena, Germany
[3] Friedrich Schiller Univ Jena, Abbe Ctr Photon, D-07745 Jena, Germany
[4] Univ Bielefeld, Dept Phys, Biomol Photon, Univ Str 25, D-33615 Bielefeld, Germany
[5] Univ Calif Davis, Dept Internal Med, Sacramento, CA 95817 USA
[6] Univ Calif Davis, NSF Ctr Biophoton, Sacramento, CA 95817 USA
基金
欧盟地平线“2020”;
关键词
PATTERNED EXCITATION MICROSCOPY; FLUORESCENCE MICROSCOPY; LATERAL RESOLUTION; LIVE CELLS; STIMULATED-EMISSION; EXTENDED RESOLUTION; OPTICAL RESOLUTION; LIGHT-MICROSCOPY; LIVING CELLS; IMAGE;
D O I
10.1021/acs.chemrev.7b00218
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Super-resolved structured illumination microscopy (SR-SIM) is among the most rapidly growing fluorescence microscopy techniques that can surpass the optical diffraction limit. The strength of SR-SIM is that it can be readily applied to samples prepared for conventional fluorescence microscopy, requiring no sophisticated sample preparation protocols. As an extension of wide-field fluorescence microscopy, it is inherently capable of multicolor imaging and optical sectioning and, with sufficiently fast implementations, permits live cell imaging. Image reconstruction, however, currently relies on sophisticated computational procedures, susceptible to reconstruction artifacts, requiring trained users to recognize and avoid them. Here, we review the latest developments in SR-SIM research. Starting from a historical overview of the development of SR-SIM, we review how this method can be implemented in various experimental schemes, we provide an overview of the important parameters involved in successful image reconstruction, we summarize recent biological applications, and we provide a brief outlook of the directions in which we believe SR-SIM is headed in the future.
引用
收藏
页码:13890 / 13908
页数:19
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