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bioRxivBiophysics

Analyzing engineered point spread functions using phasor-based single-molecule localization microscopy

K. J. A. Martens, A. Jabermoradi, S. Yang, J. Hohlbein

PDFDOIPreprint

Abstract

The point spread function (PSF) of single molecule emitters can be engineered in the Fourier plane to encode three-dimensional localization information, creating double-helix, saddle-point or tetra-pod PSFs. Here, we describe and assess adaptations of the phasor-based single-molecule localization microscopy (pSMLM) algorithm to localize single molecules using these PSFs with sub-pixel accuracy. For double-helix, pSMLM identifies the two individual lobes and uses their relative rotation for obtaining z-resolved localizations, while for saddle-point or tetra-pod, a novel phasor-based deconvolution approach is used. The pSMLM software package delivers similar precision and recall rates to the best-in-class software package (SMAP) at signal-to-noise ratios typical for organic fluorophores. pSMLM substantially improves the localization rate by a factor of 2 - 4x on a standard CPU, with 1-1.5{middle dot}104 (double-helix) or 2.5{middle dot}105 (saddle-point/tetra-pod) localizations/second.

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