IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v6y2015i1d10.1038_ncomms8127.html
   My bibliography  Save this article

STED nanoscopy with fluorescent quantum dots

Author

Listed:
  • 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)
    Max Planck Institute for Biophysical Chemistry)

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.

Suggested Citation

  • Janina Hanne & Henning J. Falk & Frederik Görlitz & Patrick Hoyer & Johann Engelhardt & Steffen J. Sahl & Stefan W. Hell, 2015. "STED nanoscopy with fluorescent quantum dots," Nature Communications, Nature, vol. 6(1), pages 1-6, November.
  • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms8127
    DOI: 10.1038/ncomms8127
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms8127
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms8127?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms8127. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.