扫描电镜
显微镜
受激发射
化学
纳米技术
活体细胞成像
超分辨显微术
荧光显微镜
光学
荧光
物理
扫描共焦电子显微镜
激光器
材料科学
生物化学
细胞
作者
Hans Blom,Jerker Widengren
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2017-03-06
卷期号:117 (11): 7377-7427
被引量:339
标识
DOI:10.1021/acs.chemrev.6b00653
摘要
Despite its short history, diffraction-unlimited fluorescence microscopy techniques have already made a substantial imprint in the biological sciences. In this review, we describe how stimulated emission depletion (STED) imaging originally evolved, how it compares to other optical super-resolution imaging techniques, and what advantages it provides compared to previous golden-standards for biological microscopy, such as diffraction-limited optical microscopy and electron microscopy. We outline the prerequisites for successful STED imaging experiments, emphasizing the equally critical roles of instrumentation, sample preparation, and photophysics, and describe major evolving strategies for how to push the borders of STED imaging even further in life science. Finally, we provide examples of how STED nanoscopy can be applied, within three different fields with particular potential for STED imaging experiments: neuroscience, plasma membrane biophysics, and subcellular clinical diagnostics. In these areas, and in many more, STED imaging can be expected to play an increasingly important role in the future.
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