Background suppression by axially selective activation in single-molecule localization microscopy
Optics Letters, Vol. 35, Issue 6, pp. 886-888 (2010)
http://dx.doi.org/10.1364/OL.35.000886
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Abstract
Resolution of a few tens of nanometers has been achieved in fluorescence microscopy with photoswitchable molecules. However, for thick samples, the background brought by the crosstalk of unwanted on-state molecules is nonnegligible. Now we present a background suppression method by using two axial standing waves generated by the interference of two activation beams with the same phases and two deactivation beams with the opposite phases. With spatially incoherent illumination, most activated molecules are located in a thin layer. The performance of such method is simulated with the known photoswitching characteristic of Cy5. With suitable parameters, the thickness of the layer can reach
© 2010 Optical Society of America
OCIS Codes
(100.6640) Image processing : Superresolution
(180.6900) Microscopy : Three-dimensional microscopy
(170.2945) Medical optics and biotechnology : Illumination design
ToC Category:
Image Processing
History
Original Manuscript: November 10, 2009
Revised Manuscript: February 2, 2010
Manuscript Accepted: February 7, 2010
Published: March 15, 2010
Virtual Issues
Vol. 5, Iss. 7 Virtual Journal for Biomedical Optics
Citation
Danni Chen, Bin Yu, Junle Qu, and Hanben Niu, "Background suppression by axially selective activation in single-molecule localization microscopy," Opt. Lett. 35, 886-888 (2010)
http://www.opticsinfobase.org/vjbo/abstract.cfm?URI=ol-35-6-886
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