DMD-based LED-illumination Super-resolution and optical sectioning microscopy

被引:262
作者
Dan, Dan [1 ]
Lei, Ming [1 ]
Yao, Baoli [1 ]
Wang, Wen [2 ,3 ]
Winterhalder, Martin [4 ]
Zumbusch, Andreas [4 ]
Qi, Yujiao [1 ]
Xia, Liang [2 ,3 ]
Yan, Shaohui [1 ]
Yang, Yanlong [1 ]
Gao, Peng [1 ]
Ye, Tong [1 ]
Zhao, Wei [1 ]
机构
[1] Chinese Acad Sci, Xian Inst Opt & Precis Mech, State Key Lab Transient Opt & Photon, Xian 710119, Peoples R China
[2] Fourth Mil Med Univ, Dept Anat, Xian 710032, Peoples R China
[3] Fourth Mil Med Univ, KK Leung Brain Res Ctr, Xian 710032, Peoples R China
[4] Univ Konstanz, Dept Chem, D-78457 Constance, Germany
来源
SCIENTIFIC REPORTS | 2013年 / 3卷
关键词
STRUCTURED-ILLUMINATION; FLUORESCENCE MICROSCOPY; RESOLUTION LIMIT; LIGHT; CELLS;
D O I
10.1038/srep01116
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Super-resolution three-dimensional (3D) optical microscopy has incomparable advantages over other high-resolution microscopic technologies, such as electron microscopy and atomic force microscopy, in the study of biological molecules, pathways and events in live cells and tissues. We present a novel approach of structured illumination microscopy (SIM) by using a digital micromirror device (DMD) for fringe projection and a low-coherence LED light for illumination. The lateral resolution of 90 nm and the optical sectioning depth of 120 mm were achieved. The maximum acquisition speed for 3D imaging in the optical sectioning mode was 1.63107 pixels/second, which was mainly limited by the sensitivity and speed of the CCD camera. In contrast to other SIM techniques, the DMD-based LED-illumination SIM is cost-effective, ease of multi-wavelength switchable and speckle-noise-free. The 2D super-resolution and 3D optical sectioning modalities can be easily switched and applied to either fluorescent or non-fluorescent specimens.
引用
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页数:7
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