Background suppression in fluorescence nanoscopy with stimulated emission double depletion

被引:0
|
作者
Gao, Peng [1 ,2 ]
Prunsche, Benedikt [2 ]
Zhou, Lu [1 ,2 ]
Nienhaus, Karin [2 ]
Nienhaus, G. Ulrich [1 ,2 ,3 ,4 ]
机构
[1] Karlsruhe Inst Technol, Inst Nanotechnol, D-76344 Eggenstein Leopoldshafen, Germany
[2] Karlsruhe Inst Technol, Inst Appl Phys, D-76128 Karlsruhe, Germany
[3] Karlsruhe Inst Technol, Inst Toxicol & Genet, D-76344 Eggenstein Leopoldshafen, Germany
[4] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
关键词
OPTICAL RECONSTRUCTION MICROSCOPY; DIFFRACTION RESOLUTION LIMIT; CORRELATION SPECTROSCOPY; STED MICROSCOPY; FCS; DIFFUSION; MEMBRANE; DYNAMICS; BREAKING; PROTEIN;
D O I
10.1038/NPHOTON.2016.279
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Stimulated emission depletion (STED) fluorescence nanoscopy is a powerful super-resolution imaging technique based on the confinement of fluorescence emission to the central subregion of an observation volume through de-excitation of fluorophores in the periphery via stimulated emission. Here, we introduce stimulated emission double depletion ( STEDD) as a method to selectively remove artificial background intensity. In this approach, a first, conventional STED pulse is followed by a second, delayed Gaussian STED pulse that specifically depletes the central region, thus leaving only background. Thanks to time-resolved detection we can remove this background intensity voxel by voxel by taking the weighted difference of photons collected before and after the second STED pulse. STEDD thus yields background-suppressed super-resolved images as well as STED-based fluorescence correlation spectroscopy data. Furthermore, the proposed method is also beneficial when considering lower-power, less redshifted depletion pulses.
引用
收藏
页码:163 / +
页数:8
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