Abstract

We introduce two new alternative experimental realizations of dual focus fluorescence correlation spectroscopy (2fFCS), a method which allows for obtaining absolute diffusion coefficient of fast moving fluorescing molecules at nanomolar concentrations, based on fast polarization modulation of the excitation beam by a resonant electro-optical modulator. The first approach rotates every second linearly polarized laser pulse by 90 degrees to obtain independent intensity readout for both foci, similar to original design. The second approach combines polarization modulation of cw laser and fluorescence lifetime correlation spectroscopy (FLCS) like analysis to obtain clean correlation curves for both overlapping foci. We tested our new approaches with different lasers and samples, revealed a need for intensity cross-talk corrections by comparing the methods with each other and discussed experimental artifacts stemming from improper polarization alignment and detector afterpulsing. The advantages of our solutions are that the polarization rotation approach requires just one pulsed laser for each wavelength, that the polarization modulation approach even mitigates the need of pulsed lasers by using standard cw lasers and that it allows the DIC prism to be placed at an arbitrary angle. As a consequence the presented experimental solutions for 2fFCS can be more easily implemented into commercial laser scanning microscopes.

Highlights

  • Determination of diffusion coefficients in live cells or in model systems is usually achieved by fluorescence based methods like Fluorescence Recovery After Photobleaching (FRAP) [1], Fluorescence Correlation Spectroscopy (FCS) [2] [3] or fluorescence Single Particle Tracking (SPT) [4]

  • We have shown that 2fFCS setups based on fast electro-optical modulator (EOM) polarization rotation and modulation are complementary tools to classical 2fFCS setup which uses two perpendicularly oriented linearly polarized pulsed lasers

  • We have experimentally confirmed that our 2fFCS EOM polarization rotation and modulation setups are not limited to only one excitation wavelength, but can be used independently of the excitation wavelength

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Summary

Introduction

Determination of diffusion coefficients in live cells or in model systems is usually achieved by fluorescence based methods like Fluorescence Recovery After Photobleaching (FRAP) [1], Fluorescence Correlation Spectroscopy (FCS) [2] [3] or fluorescence Single Particle Tracking (SPT) [4]. These methods are highly complementary, each exploring different concentration, spatial and time ranges. A strong feature of FCS is its concentration range mostly suiting molecules abundance under cellular conditions (micromolar to nanomolar concentrations) and its coverage of long time span from nanoseconds to seconds.

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