Extended field of view of light-sheet fluorescence microscopy by scanning multiple focus-shifted Gaussian beam arrays

被引:16
|
作者
Liu, Chao [1 ,2 ]
Bai, Chen [1 ]
Yu, Xianghua [1 ]
Yan, Shaohui [1 ]
Zhou, Yuan [1 ,2 ]
Li, Xing [1 ,2 ]
Min, Junwei [1 ]
Yang, Yanlong [1 ]
Dan, Dan [1 ]
Yao, Baoli [1 ,2 ]
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
基金
中国国家自然科学基金;
关键词
ILLUMINATION MICROSCOPY;
D O I
10.1364/OE.418707
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Light-sheet fluorescence microscopy (LSFM) facilitates high temporal-spatial resolution, low photobleaching and phototoxicity for long-term volumetric imaging. However, when a high axial resolution or optical sectioning capability is required, the field of view (FOV) is limited. Here, we propose to generate a large FOV of light-sheet by scanning multiple focus-shifted Gaussian beam arrays (MGBA) while keeping the high axial resolution. The positions of the beam waists of the multiple Gaussian beam arrays are shifted in both axial and lateral directions in an optimized arranged pattern, and then scanned along the direction perpendicular to the propagation axis to form an extended FOV of light-sheet. Complementary beam subtraction method is also adopted to further improve axial resolution. Compared with the single Gaussian light-sheet method, the proposed method extends the FOV from 12 mu m to 200 mu m while sustaining the axial resolution of 0.73 mu m. Both numerical simulation and experiment on samples are performed to verify the effectiveness of the method. (C) 2021 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:6158 / 6168
页数:11
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