Superresolution fluorescence microscopy for 3D reconstruction of thick samples

被引:14
作者
Park, Sangjun [1 ,2 ,3 ]
Kang, Wooyoung [1 ,2 ,3 ]
Kwon, Yeong-Dae [3 ,4 ]
Shim, Jaehoon [5 ]
Kim, Siyong [5 ]
Kaang, Bong-Kiun [5 ]
Hohng, Sungchul [1 ,2 ,3 ]
机构
[1] Seoul Natl Univ, Dept Phys & Astron, Seoul, South Korea
[2] Seoul Natl Univ, Inst Appl Phys, Seoul, South Korea
[3] Seoul Natl Univ, Natl Ctr Creat Res Initiat, Seoul, South Korea
[4] Seoul Natl Univ, Res Inst Basic Sci, Seoul, South Korea
[5] Seoul Natl Univ, Sch Biol Sci, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Line-scan confocal microscopy; DNA-PAINT; Superresolution microscopy; Single-molecule localization microscopy; Three-dimensional reconstruction; DIFFRACTION RESOLUTION LIMIT; DNA-PAINT; ILLUMINATION MICROSCOPY; PLANE ILLUMINATION; EXCHANGE-PAINT; CELLS; LOCALIZATION; PROBES; BREAKING; SPECTRIN;
D O I
10.1186/s13041-018-0361-z
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Three-dimensional (3D) reconstruction of thick samples using superresolution fluorescence microscopy remains challenging due to high level of background noise and fast photobleaching of fluorescence probes. We develop superresolution fluorescence microscopy that can reconstruct 3D structures of thick samples with both high localization accuracy and no photobleaching problem. The background noise is reduced by optically sectioning the sample using line-scan confocal microscopy, and the photobleaching problem is overcome by using the DNA-PAINT (Point Accumulation for Imaging in Nanoscale Topography). As demonstrations, we take 3D superresolution images of microtubules of a whole cell, and two-color 3D images of microtubules and mitochondria. We also present superresolution images of chemical synapse of a mouse brain section at different z-positions ranging from 0 mu m to 100 mu m.
引用
收藏
页数:9
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