Optical Sectioning and High Resolution in Single-Slice Structured Illumination Microscopy by Thick Slice Blind-SIM Reconstruction

被引:46
作者
Jost, Aurelie [1 ,2 ]
Tolstik, Elen [1 ,2 ]
Feldmann, Polina [1 ,2 ]
Wicker, Kai [1 ,2 ,3 ]
Sentenac, Anne [4 ]
Heintzmann, Rainer [1 ,2 ,5 ]
机构
[1] Univ Jena, Inst Phys Chem, Abbe Ctr Photon, D-07743 Jena, Germany
[2] Leibniz Inst Photon Technol, Jena, Germany
[3] Carl Zeiss, Corp Res & Technol, Jena, Germany
[4] Aix Marseille Univ, CNRS, Inst Fresnel, Marseille, France
[5] Kings Coll London, Randall Div, London, England
关键词
FLUORESCENCE MICROSCOPY; LIGHT;
D O I
10.1371/journal.pone.0132174
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The microscope image of a thick fluorescent sample taken at a given focal plane is plagued by out-of-focus fluorescence and diffraction limited resolution. In this work, we show that a single slice of Structured Illumination Microscopy (two or three beam SIM) data can be processed to provide an image exhibiting tight sectioning and high transverse resolution. Our reconstruction algorithm is adapted from the blind-SIM technique which requires very little knowledge of the illumination patterns. It is thus able to deal with illumination distortions induced by the sample or illumination optics. We named this new algorithm thick slice blind-SIM because it models a three-dimensional sample even though only a single two-dimensional plane of focus was measured.
引用
收藏
页数:10
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