Single-fluorophore orientation determination with multiview polarized illumination: modeling and microscope design

被引:9
作者
Chandler, Talon [1 ]
Mehta, Shalin [1 ,2 ,3 ]
Shroff, Hari [4 ,5 ]
Oldenbourg, Rudolf [2 ,6 ]
La Riviere, Patrick J. [1 ,5 ]
机构
[1] Univ Chicago, Dept Radiol, Chicago, IL 60637 USA
[2] Marine Biol Lab, Bell Ctr, Woods Hole, MA 02543 USA
[3] Chan Zuckerberg Biohub, San Francisco, CA 94158 USA
[4] Natl Inst Biomed Imaging & Bioengn, Sect High Resolut Opt Imaging, NIH, Bethesda, MD 20892 USA
[5] Marine Biol Lab, Whitman Ctr, Woods Hole, MA 02543 USA
[6] Brown Univ, Dept Phys, Providence, RI 02912 USA
关键词
FLUORESCENCE MICROSCOPY; DIPOLE ORIENTATION; DYNAMICS; POSITION; FIELD;
D O I
10.1364/OE.25.031309
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We investigate the use of polarized illumination in multiview microscopes for determining the orientation of single-molecule fluorescence transition dipoles. First, we relate the orientation of single dipoles to measurable intensities in multiview microscopes and develop an information-theoretic metric-the solid-angle uncertainty-to compare the ability of multiview microscopes to estimate the orientation of single dipoles. Next, we compare a broad class of microscopes using this metric-single-and dual-view microscopes with varying illumination polarization, illumination numerical aperture (NA), detection NA, obliquity, asymmetry, and exposure. We find that multi-view microscopes can measure all dipole orientations, while the orientations measurable with single-view microscopes is halved because of symmetries in the detection process. We also find that choosing a small illumination NA and a large detection NA are good design choices, that multiview microscopes can benefit from oblique illumination and detection, and that asymmetric NA microscopes can benefit from exposure asymmetry. (C) 2017 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:31309 / 31325
页数:17
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