Combination of structured illumination and single molecule localization microscopy in one setup

被引:42
作者
Rossberger, Sabrina [1 ,2 ]
Best, Gerrit [1 ,2 ]
Baddeley, David [3 ,4 ]
Heintzmann, Rainer [5 ,6 ,7 ]
Birk, Udo [1 ,8 ]
Dithmar, Stefan [2 ]
Cremer, Christoph [1 ,8 ,9 ]
机构
[1] Heidelberg Univ, Kirchhoff Inst Phys, D-69120 Heidelberg, Germany
[2] Heidelberg Univ, Dept Ophthalmol, D-69120 Heidelberg, Germany
[3] Univ Auckland, Dept Physiol, Auckland, New Zealand
[4] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
[5] Univ Jena, Inst Phys Chem, D-07743 Jena, Germany
[6] Inst Photon Technol, Jena, Germany
[7] Kings Coll London, Randall Div, London, England
[8] Inst Mol Biol, Mainz, Germany
[9] Heidelberg Univ, Inst Pharm & Mol Biotechnol, D-69120 Heidelberg, Germany
关键词
super-resolution microscopy; single molecule localization microscopy (SMLM); structured illumination microscopy (SIM); imaging; SPDM; OPTICAL RECONSTRUCTION MICROSCOPY; PATTERNED EXCITATION MICROSCOPY; FIELD FLUORESCENCE NANOSCOPY; RESOLUTION LIMIT; DIFFRACTION-LIMIT; LIGHT-MICROSCOPY; LIVE CELLS; SUPERRESOLUTION; IMPROVEMENT; PROBES;
D O I
10.1088/2040-8978/15/9/094003
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Understanding the positional and structural aspects of biological nanostructures simultaneously is as much a challenge as a desideratum. In recent years, highly accurate (20 nm) positional information of optically isolated targets down to the nanometer range has been obtained using single molecule localization microscopy (SMLM), while highly resolved (100 nm) spatial information has been achieved using structured illumination microscopy (SIM). In this paper, we present a high-resolution fluorescence microscope setup which combines the advantages of SMLM with SIM in order to provide high-precision localization and structural information in a single setup. Furthermore, the combination of the wide-field SIM image with the SMLM data allows us to identify artifacts produced during the visualization process of SMLM data, and potentially also during the reconstruction process of SIM images. We describe the SMLM-SIM combo and software, and apply the instrument in a first proof-of-principle to the same region of H3K293 cells to achieve SIM images with high structural resolution (in the 100 nm range) in overlay with the highly accurate position information of localized single fluorophores. Thus, with its robust control software, efficient switching between the SMLM and SIM mode, fully automated and user-friendly acquisition and evaluation software, the SMLM-SIM combo is superior over existing solutions.
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页数:13
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