3-D reconstruction of cortical microtubules using multi-angle total internal reflection fluorescence microscopy

被引:0
|
作者
Jin, Luhong [1 ,2 ]
Xiu, Peng [3 ]
Zhou, Xiaoxu [1 ,2 ]
Fan, Jiannan [1 ,2 ]
Kuang, Cuifang [3 ]
Liu, Xu [3 ]
Xu, Yingke [1 ,2 ]
机构
[1] Zhejiang Univ, Dept Biomed Engn, Minist Educ, Key Lab Biomed Engn, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Zhejiang Prov Key Lab Cardiocerebral Vasc Detect, Hangzhou 310027, Zhejiang, Peoples R China
[3] Zhejiang Univ, Dept Opt Engn, State Key Lab Modern Opt Instrumentat, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
evanescent field; TIRFM; penetration depth; microtubules; reconstruction; RESOLUTION; LIGHT;
D O I
10.1117/12.2265976
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Total internal reflection fluorescence microscopy (TIRFM) has been widely used in biomedical research to visualize cellular processes near the cell surface. In this study, a novel multi-angle ring-illuminated TIRFM system, equipped with two galvo mirrors that are on conjugate plan of a 4f optical system was developed. Multi-angle TIRFM generates images with different penetration depths through the controlled variation of the incident angle of illuminating laser. We presented a method to perform three-dimensional (3-D) reconstruction of microtubules from multi-angle TIRFM images. The performance of our method was validated in simulated microtubules with variable signal-to-noise ratios (SNR) and the axial resolution and accuracy of reconstruction were evaluated in selecting different numbers of illumination angles or in different SNR conditions. In U373 cells, we reconstructed the 3-D localization of microtubules near the cell surface with high resolution using over a hundred different illumination angles. Theoretically, the presented TIRFM setup and 3D reconstruction method can achieve similar to 40 nm axial resolution in experimental conditions where SNR is as low as 2, with similar to 35 different illumination angles. Moreover, our system and reconstruction method have the potential to be used in live cells to track membrane dynamics in 3-D.
引用
收藏
页数:9
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