Resolution enhancement by subtraction of confocal signals taken at different pinhole sizes

被引:78
作者
Heintzmann, R
Sarafis, V
Munroe, P
Nailon, J
Hanley, QS
Jovin, TM
机构
[1] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
[2] Univ Queensland, Sch Elect & Comp Engn, St Lucia, Qld 4072, Australia
[3] Univ New S Wales, Electron Microscopy Unit, Sydney, NSW 2052, Australia
[4] Univ Queensland, Ctr Microscopy & Microanal, St Lucia, Qld 4072, Australia
关键词
subtractive imaging; superresolution; composite image; Fourier-space weighting; weighted averaging;
D O I
10.1016/S0968-4328(03)00054-4
中图分类号
TH742 [显微镜];
学科分类号
摘要
Subtractive imaging in confocal fluorescence light microscopy is based on the subtraction of a suitably weighted widefield image from a confocal image. An approximation to a widefield image can be obtained by detection with an opened confocal pinhole. The subtraction of images enhances the resolution in-plane as well as along the optic axis. Due to the linearity of the approach, the effect of subtractive imaging in Fourier-space corresponds to a reduction of low spatial frequency contributions leading to a relative enhancement of the high frequencies. Along the direction of the optic axis this also results in an improved sectioning. Image processing can achieve a similar effect. However, a 3D volume dataset must be acquired and processed, yielding a result essentially identical to subtractive imaging but superior in signal-to-noise ratio. The latter can be increased further with the technique of weighted averaging in Fourier-space. A comparison of 2D and 3D experimental data analysed with subtractive imaging, the equivalent Fourier-space processing of the confocal data only, and Fourier-space weighted averaging is presented. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:293 / 300
页数:8
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