STED nanoscopy with fluorescent quantum dots

被引:169
作者
Hanne, Janina [1 ]
Falk, Henning J. [1 ]
Goerlitz, Frederik [1 ]
Hoyer, Patrick [1 ]
Engelhardt, Johann [1 ]
Sahl, Steffen J. [2 ]
Hell, Stefan W. [1 ,2 ]
机构
[1] German Canc Res Ctr, Opt Nanoscopy Div, D-69120 Heidelberg, Germany
[2] Max Planck Inst Biophys Chem, Dept NanoBiophoton, D-37077 Gottingen, Germany
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
关键词
LIVE CELLS; MICROSCOPY; RESOLUTION; DEPLETION; SUBDIFFRACTION; LUMINESCENCE; BLINKING; EMISSION;
D O I
10.1038/ncomms8127
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The widely popular class of quantum-dot molecular labels could so far not be utilized as standard fluorescent probes in STED (stimulated emission depletion) nanoscopy. This is because broad quantum-dot excitation spectra extend deeply into the spectral bands used for STED, thus compromising the transient fluorescence silencing required for attaining super-resolution. Here we report the discovery that STED nanoscopy of several red-emitting commercially available quantum dots is in fact successfully realized by the increasingly popular 775nm STED laser light. A resolution of presently similar to 50 nm is demonstrated for single quantum dots, and sub-diffraction resolution is further shown for imaging of quantum-dot-labelled vimentin filaments in fibroblasts. The high quantum-dot photostability enables repeated STED recordings with 41,000 frames. In addition, we have evidence that the tendency of quantum-dot labels to blink is largely suppressed by combined action of excitation and STED beams. Quantum-dot STED significantly expands the realm of application of STED nanoscopy, and, given the high stability of these probes, holds promise for extended time-lapse imaging.
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页数:6
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