Light-sheet microscopy with digital Fourier analysis measures transport properties over large field-of-view

被引:28
|
作者
Wulstein, Devynn M. [1 ]
Regan, Kathryn E. [1 ]
Robertson-Anderson, Rae M. [1 ]
McGorty, Ryan [1 ]
机构
[1] Univ San Diego, Dept Phys & Biophys, San Diego, CA 92110 USA
来源
OPTICS EXPRESS | 2016年 / 24卷 / 18期
基金
美国国家科学基金会;
关键词
DIFFERENTIAL DYNAMIC MICROSCOPY; PLANE ILLUMINATION MICROSCOPY; CORRELATION SPECTROSCOPY; DIFFUSIVE DYNAMICS; DNA-MOLECULES; LIVING CELLS; NANOPARTICLES; EMBRYOS; POPULATIONS; EXCITATION;
D O I
10.1364/OE.24.020881
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Using light-sheet microscopy combined with digital Fourier methods we probe the dynamics of colloidal samples and DNA molecules. This combination, referred to as selective-plane illumination differential dynamic microscopy (SPIDDM), has the benefit of optical sectioning to study, with minimal photobleaching, thick samples allowing us to measure the diffusivity of colloidal particles at high volume fractions. Further, SPIDDM exploits the inherent spatially-varying thickness of Gaussian light-sheets. Where the excitation sheet is most focused, we capture high spatial frequency dynamics as the signal-to-background is high. In thicker regions, we capture the slower dynamics as diffusion out of the sheet takes longer. (C) 2016 Optical Society of America
引用
收藏
页码:20881 / 20894
页数:14
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