显微镜
荧光显微镜
纳米技术
光学切片
分辨率(逻辑)
活体细胞成像
光学显微镜
超分辨率
计算机科学
光激活定位显微镜
荧光
超分辨显微术
化学
光学
人工智能
图像(数学)
物理
材料科学
扫描电子显微镜
细胞
生物化学
作者
Rainer Heintzmann,Thomas Huser
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2017-11-10
卷期号:117 (23): 13890-13908
被引量:430
标识
DOI:10.1021/acs.chemrev.7b00218
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.
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