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STED nanoscopy with fluorescent quantum dots

Janina Hanne, Henning J. Falk, Frederik Görlitz, Patrick Hoyer, Johann Engelhardt, Steffen J. Sahl and Stefan W. Hell ()
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Janina Hanne: German Cancer Research Center (DKFZ)
Henning J. Falk: German Cancer Research Center (DKFZ)
Frederik Görlitz: German Cancer Research Center (DKFZ)
Patrick Hoyer: German Cancer Research Center (DKFZ)
Johann Engelhardt: German Cancer Research Center (DKFZ)
Steffen J. Sahl: Max Planck Institute for Biophysical Chemistry
Stefan W. Hell: German Cancer Research Center (DKFZ)

Nature Communications, 2015, vol. 6, issue 1, 1-6

Abstract: Abstract 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 775 nm STED laser light. A resolution of presently ∼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 >1,000 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.

Date: 2015
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DOI: 10.1038/ncomms8127

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