Stimulated Emission Depletion Microscopy

被引:274
作者
Blom, Hans [1 ]
Widengren, Jerker [2 ]
机构
[1] Royal Inst Technol KTH, Dept Appl Phys, SciLifeLab, S-17165 Solna, Sweden
[2] Royal Inst Technol KTH, Dept Appl Phys, Albanova Univ Ctr, S-10691 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
FLUORESCENCE CORRELATION SPECTROSCOPY; SUBCORTICAL CYTOSKELETON PERIODICITY; DIFFRACTION RESOLUTION BARRIER; ENHANCED RAMAN-SPECTROSCOPY; NANOSCALE CHEMICAL-ANALYSIS; NEEDLE-ASPIRATION-CYTOLOGY; LASER-SCANNING-MICROSCOPE; SINGLE-MOLECULE DETECTION; FIELD OPTICAL NANOSCOPY; 3D WIDEFIELD MICROSCOPY;
D O I
10.1021/acs.chemrev.6b00653
中图分类号
O6 [化学];
学科分类号
0703 ;
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.
引用
收藏
页码:7377 / 7427
页数:51
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