Abstract

.We demonstrate the possibility of measuring FRET efficiency with a low-cost frequency-domain fluorescence lifetime imaging microscope (FD-FLIM). The system utilizes single-frequency-modulated excitation, which enables the use of cost-effective laser sources and electronics, simplification of data acquisition and analysis, and a dual-channel detection capability. Following calibration with coumarin 6, we measured the apparent donor lifetime in mTFP1-mVenus FRET standards expressed in living cells. We evaluated the system’s sensitivity by differentiating the short and long lifetimes of mTFP1 corresponding to the known standards’ high and low FRET efficiency, respectively. Furthermore, we show that the lifetime of the vinculin tension sensor, VinTS, at focal adhesions () is significantly () longer than the lifetime of the unloaded TSMod probe (). The pixel dwell time was for samples expressing the FRET standards, with signal typically an order of magnitude higher than VinTS. The apparent FRET efficiency () of the standards, calculated from the measured apparent lifetime, was linearly related to their known FRET efficiency by a factor of 0.92 to 0.99 (). This relationship serves as a calibration curve to convert apparent FRET to true FRET and circumvent the need to measure multiexponential lifetime decays. This approach yielded a FRET efficiency of 18% to 19.5%, for VinTS, in agreement with published values. Taken together, our results demonstrate a cost-effective, fast, and sensitive FD-FLIM approach with the potential to facilitate applications of FLIM in mechanobiology and FRET-based biosensing.

Highlights

  • Fluorescence resonance energy transfer (FRET) probes consisting of molecular springs inserted between a fluorescent donor and acceptor pair have been the focus of much recent interest

  • We show that the fluorescence resonance energy transfer (FRET) efficiency (EaFpRpET) estimated based on the apparent lifetime can be related by a linear fit to the known true EFRET of the constructs

  • We further demonstrate measurements of FRET efficiency in the vinculin tension probe, VinTS10 at focal adhesions

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Summary

Introduction

While the subcellular localization of adhesion molecules and the architecture of focal adhesions can be imaged by conventional and by super-resolution fluorescence microscopy,[5,6] actual tension measurements require techniques that are sensitive to piconewton level forces at the cellular and subcellular scales. To this end, fluorescence resonance energy transfer (FRET) probes consisting of molecular springs inserted between a fluorescent donor and acceptor pair have been the focus of much recent interest. The ability to quantify accurately their FRET efficiency presents a challenge for microscopic imaging

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