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Updated: Apr 27, 2026

Three-dimensional Super Resolution Microscopy of F-actin Filaments by Interferometric PhotoActivated Localization Microscopy iPALM
Published on: December 1, 2016
Three-dimensional super-resolution and localization of dense clusters of single molecules
Anthony Barsic1, Ginni Grover1, Rafael Piestun1
1Department of Electrical, Computer, and Energy Engineering, University of Colorado at Boulder UCB 425, Boulder, Colorado 80309, USA.
Abstract:
When a single molecule is detected in a wide-field microscope, the image approximates the point spread function of the system. However, as the distribution of molecules becomes denser and their images begin to overlap, existing solutions to determine the number of molecules present and their precise three-dimensional locations can tolerate little to no overlap. We propose a localization scheme that can identify several overlapping molecule images while maintaining high localization precision. A solution to this problem involving matched optical and digital techniques, as here proposed, can substantially increase the allowable labeling density and accelerate the data collection time of single-molecule localization microscopy by more than one order of magnitude.
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