Single shot, three dimensional fluorescence microscopy with a spatially rotating point spread function

被引:39
|
作者
Wang, Zhaojun [1 ,2 ]
Cai, Yanan [1 ,2 ]
Liang, Yansheng [1 ,2 ]
Zhou, Xing [1 ,2 ]
Yan, Shaohui [1 ]
Dan, Dan [1 ]
Bianco, Piero R. [3 ]
Lei, Ming [1 ]
Yao, Baoli [1 ]
机构
[1] Chinese Acad Sci, Xian Inst Opt & Precis Mech, State Key Lab Transient Opt & Photon, Xian 710119, shaanxi, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Univ Buffalo, Dept Microbiol & Immunol, 12 Capen Hall, Buffalo, NY 14214 USA
来源
BIOMEDICAL OPTICS EXPRESS | 2017年 / 8卷 / 12期
基金
美国国家卫生研究院;
关键词
EXTENDED DEPTH; FIELD; LIGHT;
D O I
10.1364/BOE.8.005493
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A wide-field fluorescence microscope with a double-helix point spread function (PSF) is constructed to obtain the specimen's three-dimensional distribution with a single snapshot. Spiral-phase-based computer-generated holograms (CGHs) are adopted to make the depth-of-field of the microscope adjustable. The impact of system aberrations on the double-helix PSF at high numerical aperture is analyzed to reveal the necessity of the aberration correction. A modified cepstrum-based reconstruction scheme is promoted in accordance with properties of the new double-helix PSF. The extended depth-of-field images and the corresponding depth maps for both a simulated sample and a tilted section slice of bovine pulmonary artery endothelial (BPAE) cells are recovered, respectively, verifying that the depth-of-field is properly extended and the depth of the specimen can be estimated at a precision of 23.4mn. This three-dimensional fluorescence microscope with a framerate-rank time resolution is suitable for studying the fast developing process of thin and sparsely distributed micron-scale cells in extended depth-of-field. (C) 2017 Optical Society of America under the terms of the USA Open Access Publishing Agreement
引用
收藏
页码:5493 / 5506
页数:14
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