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Novel lambda FRET spectral confocal microscopy imaging method

Novel lambda FRET spectral confocal microscopy imaging method We report a highly specific, sensitive, and robust method for analyzing fluorescence resonance energy transfer (FRET) based on spectral laser scanning confocal microscopy imaging. The lambda FRET (λFRET) algorithm comprises imaging of a FRET sample at multiple emission wavelengths rendering a FRET spectrum, which is separated into its donor and acceptor components to obtain a pixel‐based calculation of FRET efficiency. The method uses a novel off‐line precalibration procedure for spectral bleed‐through correction based on the acquisition of reference reflection images, which simplifies the method and reduces variability. λFRET method was validated using structurally characterized FRET standards with variable linker lengths and stoichiometries designed for this purpose. λFRET performed better than other well‐established methods, such as acceptor photobleaching and sensitized emission‐based methods, in terms of specificity, reproducibility, and sensitivity to distance variations. Moreover, λFRET analysis was unaffected by high fluorochrome spectral overlap and cellular autofluorescence. The λFRET method demonstrated outstanding performance in intra‐ and intermolecular FRET analysis in both fixed and live cell imaging studies. Microsc. Res. Tech., 2009. © 2008 Wiley‐Liss, Inc. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Microscopy Research and Technique Wiley

Novel lambda FRET spectral confocal microscopy imaging method

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References (23)

Publisher
Wiley
Copyright
Copyright © 2009 Wiley Subscription Services, Inc., A Wiley Company
ISSN
1059-910X
eISSN
1097-0029
DOI
10.1002/jemt.20633
pmid
18785251
Publisher site
See Article on Publisher Site

Abstract

We report a highly specific, sensitive, and robust method for analyzing fluorescence resonance energy transfer (FRET) based on spectral laser scanning confocal microscopy imaging. The lambda FRET (λFRET) algorithm comprises imaging of a FRET sample at multiple emission wavelengths rendering a FRET spectrum, which is separated into its donor and acceptor components to obtain a pixel‐based calculation of FRET efficiency. The method uses a novel off‐line precalibration procedure for spectral bleed‐through correction based on the acquisition of reference reflection images, which simplifies the method and reduces variability. λFRET method was validated using structurally characterized FRET standards with variable linker lengths and stoichiometries designed for this purpose. λFRET performed better than other well‐established methods, such as acceptor photobleaching and sensitized emission‐based methods, in terms of specificity, reproducibility, and sensitivity to distance variations. Moreover, λFRET analysis was unaffected by high fluorochrome spectral overlap and cellular autofluorescence. The λFRET method demonstrated outstanding performance in intra‐ and intermolecular FRET analysis in both fixed and live cell imaging studies. Microsc. Res. Tech., 2009. © 2008 Wiley‐Liss, Inc.

Journal

Microscopy Research and Technique – Wiley

Published: Jan 1, 2009

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