Recent advancements in structured-illumination microscopy toward live-cell imaging

被引:64
作者
Hirano, Yasuhiro [1 ]
Matsuda, Atsushi [1 ,2 ]
Hiraoka, Yasushi [1 ,2 ]
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, 1-3 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Natl Inst Informat & Commun Technol, Adv ICT Res Inst Kobe, Nishi Ku, Kobe, Hyogo 6512492, Japan
关键词
structured-illumination microscopy; super-resolution; temporal resolution; live-cell imaging; low illumination intensity; FLUORESCENCE MICROSCOPY; PUPIL-SEGMENTATION; DIFFRACTION-LIMIT; RESOLUTION LIMIT; ADAPTIVE OPTICS; RECONSTRUCTION; DYNAMICS; IMPROVES; EMBRYOS;
D O I
10.1093/jmicro/dfv034
中图分类号
TH742 [显微镜];
学科分类号
摘要
Fluorescence microscopy allows us to observe fluorescently labeled molecules in diverse biological processes and organelle structures within living cells. However, the diffraction limit restricts its spatial resolution to about half of its wavelength, limiting the capability of biological observation at the molecular level. Structured-illumination microscopy (SIM), a type of super-resolution microscopy, doubles the spatial resolution in all three dimensions by illuminating the sample with a patterned excitation light, followed by computer reconstruction. SIM uses a relatively low illumination power compared with other methods of super-resolution microscopy and is easily available for multicolor imaging. SIM has great potential for meeting the requirements of live-cell imaging. Recent developments in diverse types of SIM have achieved higher spatial (similar to 50 nm lateral) and temporal (similar to 100 Hz) resolutions. Here, we review recent advancements in SIM and discuss its application in noninvasive live-cell imaging.
引用
收藏
页码:237 / 249
页数:13
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