Polarized illumination coded structured illumination microscopy (picoSIM): experimental results

被引:4
作者
Appelt, Daniel [1 ,5 ]
Ehler, Elisabeth [1 ]
Mukherjee, Sapna Shukla [2 ,3 ,4 ]
Heintzmann, Rainer [1 ,2 ,3 ,4 ]
Wicker, Kai [2 ,3 ,4 ,6 ]
机构
[1] Kings Coll London, Randall Div Cell & Mol Biophys, Guys Campus, London SE1 1UL, England
[2] Leibniz Inst Photon Technol, Albert Einstein Str 9, D-07745 Jena, Germany
[3] Friedrich Schiller Univ Jena, Inst Phys Chem, Helmholtzweg 4, D-07743 Jena, Germany
[4] Friedrich Schiller Univ Jena, Abbe Ctr Photon, Helmholtzweg 4, D-07743 Jena, Germany
[5] Arthrex GmbH, Erwin Hielscher Str 9, D-81249 Munich, Germany
[6] Carl Zeiss, ZEISS Innovat Hub Dresden, Else Kroner Fresenius Ctr Digital Hlth, Fetscherstr 74, D-01307 Dresden, Germany
来源
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 2022年 / 380卷 / 2220期
关键词
resolution; super-resolution; structured illumination; fluorescence; sectioning; RESOLUTION; EXCITATION; PHASE;
D O I
10.1098/rsta.2021.0193
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
07 ; 0710 ; 09 ;
摘要
The need for acquiring at least three images to reconstruct an optical section of a sample limits the acquisition rate in structured illumination microscopy (SIM) for optical sectioning. In polarized illumination coded structured illumination microscopy (picoSIM) the three individual light patterns are encoded in a single polarized illumination light distribution, enabling the acquisition of the complete SIM data in a single exposure. Here, we describe our experimental set-up and show experimental results acquired with sequential and single-shot picoSIM. This article is part of the Theo Murphy meeting issue 'Super-resolution structured illumination microscopy (part 2)'.
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页数:12
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