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Updated: May 2, 2026

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
Published on: December 10, 2013
Quantifying classical and quantum bounds for resolving closely spaced, non-interacting, simultaneously emitting
Armine I Dingilian1,2,3, Aarnah Kurella4, Div Chamria3,5
1Center for Biophysics and Quantitative Biology, University of Illinois Urbana-Champaign, Urbana, Illinois 61801, USA.
Abstract:
Recent theoretical and experimental work has shown that the quantum Fisher information associated with estimating the separation between two optical point sources remains finite at small separations, effectively opening up new routes to super-resolution imaging of simultaneously emitting sources. Most studies to date, however, implicitly invoke the scalar approximation, which is not appropriate in the context of high-numerical-aperture microscopy. Utilizing parameter estimation theory, here we consider the estimation of separation between two closely spaced dipole emitters, a commonly employed model for single-molecule optical beacons. We consider two limiting cases: one in which the orientations of the emitters are fixed and equal, and another in which both dipoles freely sample all of orientation space over the course of the measurement. We quantify precision limits using quantum and classical variants of the Fisher information and Cramér-Rao bound. In all cases, the vectorial nature of the emission complicates the analyses, but with appropriate filtering of the collected light in the azimuthal-radial polarization basis, a previously proposed scheme to saturate the quantum Fisher information via image inversion interferometry can be salvaged.
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