Paper
25 February 2010 dSTORM: real-time subdiffraction-resolution fluorescence imaging with organic fluorophores
Mark Schüttpelz, Steve Wolter, Sebastian van de Linde, Mike Heilemann, Markus Sauer
Author Affiliations +
Abstract
In the recent past, a variety of methods have been developed to circumvent the diffraction barrier of light which restricts optical resolution to about 200 nm in the image plane. Single-molecule based photoswitching microscopy such as direct stochastic optical reconstruction microscopy (dSTORM) has been successfully implemented for subdiffraction-resolution fluorescence imaging. The major drawback of this technique has been that the reconstruction of subdiffraction-resolution images requires substantially more time than the actual experiment and prevented real-time imaging. Here we present a new computational algorithm enabling subdiffraction-resolution fast imaging of cellular structures with ~20 nm optical resolution in less than 10 seconds.
© (2010) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Mark Schüttpelz, Steve Wolter, Sebastian van de Linde, Mike Heilemann, and Markus Sauer "dSTORM: real-time subdiffraction-resolution fluorescence imaging with organic fluorophores", Proc. SPIE 7571, Single Molecule Spectroscopy and Imaging III, 75710V (25 February 2010); https://doi.org/10.1117/12.848105
Lens.org Logo
CITATIONS
Cited by 6 scholarly publications.
Advertisement
Advertisement
RIGHTS & PERMISSIONS
Get copyright permission  Get copyright permission on Copyright Marketplace
KEYWORDS
Luminescence

Microscopy

Image processing

Data processing

Real time imaging

Image resolution

Super resolution

Back to Top