• DocumentCode
    2300502
  • Title

    Far-field optical nanoscopy

  • Author

    Hell, Stefan W.

  • Author_Institution
    Dept. of NanoBiophotonics, Max Planck Inst. for Biophys. Chem., Göttingen, Germany
  • fYear
    2010
  • fDate
    7-11 Nov. 2010
  • Firstpage
    3
  • Lastpage
    4
  • Abstract
    In this paper physical concepts that radically break the diffraction barrier in focusing fluorescence microscopy has been discussed. They share a common strategy: exploiting selected molecular transitions of the fluorescent marker to neutralize the limiting role of diffraction. The first viable concept of this kind was Stimulated Emission Depletion (STED) microscopy. In its simplest variant, STED microscopy uses a focused beam for fluorescence excitation, along with a red-shifted doughnut-shaped beam for subsequent quenching of fluorescent molecules by stimulated emission.
  • Keywords
    fluorescence; molecular biophysics; nanobiotechnology; optical microscopy; proteins; radiation quenching; red shift; stimulated emission; STED microscopy; diffraction barrier; far-field optical nanoscopy; fluorescence excitation; fluorescence microscopy; quenching; red-shifted doughnut-shaped beam; selected molecular transitions; stimulated emission depletion microscopy;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    IEEE Photonics Society, 2010 23rd Annual Meeting of the
  • Conference_Location
    Denver, CO
  • ISSN
    -
  • Print_ISBN
    978-1-4244-5368-9
  • Electronic_ISBN
    -
  • Type

    conf

  • DOI
    10.1109/PHOTONICS.2010.5698725
  • Filename
    5698725