Speckle-structured illumination for 3D phase and fluorescence computational microscopy

被引:26
|
作者
Yeh, Li-Hao [1 ]
Chowdhury, Shwetadwip [1 ]
Repina, Nicole A. [2 ]
Waller, Laura [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Elect Engn & Comp Sci, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Grad Program Bioengn, Berkeley, CA 94720 USA
来源
BIOMEDICAL OPTICS EXPRESS | 2019年 / 10卷 / 07期
基金
美国国家科学基金会;
关键词
OPTICAL DIFFRACTION TOMOGRAPHY; HIGH-RESOLUTION; WIDE-FIELD; HIGH-THROUGHPUT; FOURIER PTYCHOGRAPHY; LATERAL RESOLUTION; INTENSITY; SPEED; LIMIT; RECONSTRUCTION;
D O I
10.1364/BOE.10.003635
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
High-content biological microscopy targets high-resolution imaging across large fields-of-view, often achieved by computational imaging approaches. Previously, we demonstrated 2D multimodal high-content microscopy via structured illumination microscopy (SIM) with resolution > 2x the diffraction limit, using speckle illumination from Scotch tape. In this work, we extend the method to 3D by leveraging the fact that the speckle illumination is in fact a 3D structured pattern. We use both a coherent and an incoherent imaging model to develop algorithms for joint retrieval of the 3D super-resolved fluorescent and complex-held distributions of the sample. Our reconstructed images resolve features beyond the physical diffraction-limit set by the system's objective and demonstrate 3D multimodal imaging with similar to 0.6 x 0.6 x 6 mu m(3) resolution over a volume of similar to 314 x 500 x 24 mu m(3). (C) 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:3635 / 3653
页数:19
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