High-resolution imaging in two-photon excitation microscopy using in situ estimations of the point spread function

被引:27
|
作者
Doi, Atsushi [1 ]
Oketani, Ryosuke [2 ]
Nawa, Yasunori [2 ]
Fujita, Katsumasa [2 ]
机构
[1] Olympus Corp, 2-3 Kuboyama Cho, Hachioji, Tokyo 1928512, Japan
[2] Osaka Univ, Dept Appl Phys, 2-1 Yamadaoka, Suita, Osaka 5650871, Japan
来源
BIOMEDICAL OPTICS EXPRESS | 2018年 / 9卷 / 01期
关键词
STIMULATED-EMISSION-DEPLETION; STRUCTURED ILLUMINATION MICROSCOPY; FLUORESCENCE CONFOCAL MICROSCOPY; LATERAL RESOLUTION; MULTIPHOTON MICROSCOPY; OPTICAL MICROSCOPY; SINGLE-WAVELENGTH; STED MICROSCOPY; SUPERRESOLUTION; DEPTH;
D O I
10.1364/BOE.9.000202
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We present a technique for improving the spatial resolution of two-photon excitation microscopy; our technique combines annular illumination with an in situ estimation of the point spread function (PSF) used for deconvolution. For the in situ estimation of the PSF, we developed a technique called autocorrelation scanning, in which a sample is imaged by the scanning of two excitation foci that arc overlapped over various distances. The image series obtained with the variation of the distance between the two foci provides the autocorrelation function of the PSF, which can be used to estimate the PSF at specific positions within a sample. We proved the principle and the effectiveness of this technique through observations of a fluorescent biological sample, and we confirmed that the improvement in the spatial resolution was similar to 1.7 times that of typical two-photon excitation microscopy by observing a mouse brain phantom at a depth of 200 mu m. (C) 2017 Optical Society of America
引用
收藏
页码:202 / 213
页数:12
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