Structured illumination fluorescence microscopy with distorted excitations using a filtered blind-SIM algorithm

被引:65
作者
Ayuk, R. [1 ]
Giovannini, H. [1 ]
Jost, A. [3 ,4 ]
Mudry, E. [1 ]
Girard, J. [1 ]
Mangeat, T. [2 ]
Sandeau, N. [1 ]
Heintzmann, R. [3 ,4 ]
Wicker, K. [3 ,4 ]
Belkebir, K. [1 ]
Sentenac, A. [1 ]
机构
[1] Aix Marseille Univ, Inst Fresnel, F-13013 Marseille, France
[2] Univ Toulouse 3, CNRS, LBCMCP, F-31062 Toulouse, France
[3] Inst Photon Technol, Jena, Germany
[4] Univ Jena, Inst Phys Chem, Abbe Ctr Photon, D-07743 Jena, Germany
关键词
RESOLUTION; SUPERRESOLUTION; LIMIT;
D O I
10.1364/OL.38.004723
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Structured illumination microscopy (SIM) is a powerful technique for obtaining super-resolved fluorescence maps of samples, but it is very sensitive to aberrations or misalignments affecting the excitation patterns. Here, we present a reconstruction algorithm that is able to process SIM data even if the illuminations are strongly distorted. The approach is an extension of the recent blind-SIM technique, which reconstructs simultaneously the sample and the excitation patterns without a priori information on the latter. Our algorithm was checked on synthetic and experimental data using distorted and nondistorted illuminations. The reconstructions were similar to that obtained by up-to-date SIM methods when the illuminations were periodic and remained artifact-free when the illuminations were strongly distorted. (C) 2013 Optical Society of America
引用
收藏
页码:4723 / 4726
页数:4
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