Literature DB >> 14678512

Optimizing imaging parameters for the separation of multiple labels in a fluorescence image.

R Neher1, E Neher.   

Abstract

A theoretical analysis is presented on how to separate the contributions from individual, simultaneously present fluorophores in a spectrally resolved image. Equations are derived that allow the calculation of the signal-to-noise ratio of the estimates for such contributions, given the spectral information on the individual fluorophores, the excitation wavelengths and intensities, and the number and widths of the spectral detection channels. We then ask how such imaging parameters have to be chosen for optimal fluorophore separation. We optimize the signal-to-noise ratio or optimize a newly defined 'figure of merit', which is a measure of efficiency in the use of emitted photons. The influence of photobleaching on the resolution and on the choice of imaging parameters is discussed, as well as the additional resolution gained by including fluorescence lifetime information. A surprisingly small number of spectral channels are required for an almost optimal resolution, if the borders of these channels are optimally selected. The detailed consideration of photobleaching is found to be essential, whenever there is significant bleaching. Consideration of fluorescence lifetime information (in addition to spectral information) improves results, particularly when lifetimes differ by more than a factor of two.

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Year:  2004        PMID: 14678512     DOI: 10.1111/j.1365-2818.2004.01262.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  47 in total

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2.  Two-color STED microscopy of living synapses using a single laser-beam pair.

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3.  Fluorescence emission spectra of calcofluor stained yeast cell suspensions: heuristic assessment of basis spectra for their linear unmixing.

Authors:  Jaromír Plášek; Marek Dostál; Dana Gášková
Journal:  J Fluoresc       Date:  2012-04-27       Impact factor: 2.217

4.  Multicolor fluorescence nanoscopy in fixed and living cells by exciting conventional fluorophores with a single wavelength.

Authors:  Ilaria Testa; Christian A Wurm; Rebecca Medda; Ellen Rothermel; Claas von Middendorf; Jonas Fölling; Stefan Jakobs; Andreas Schönle; Stefan W Hell; Christian Eggeling
Journal:  Biophys J       Date:  2010-10-20       Impact factor: 4.033

5.  Signal/noise analysis of FRET-based sensors.

Authors:  Andrew Woehler; Jakub Wlodarczyk; Erwin Neher
Journal:  Biophys J       Date:  2010-10-06       Impact factor: 4.033

6.  Use of independent component analysis to improve signal-to-noise ratio in multi-probe fluorescence microscopy.

Authors:  L Dao; B Lucotte; B Glancy; L-C Chang; L-Y Hsu; R S Balaban
Journal:  J Microsc       Date:  2014-08-27       Impact factor: 1.758

7.  Quantitative multiphoton spectral imaging and its use for measuring resonance energy transfer.

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Journal:  Biophys J       Date:  2005-07-22       Impact factor: 4.033

Review 8.  Studying inner ear protein-protein interactions using FRET and FLIM.

Authors:  Richard Hallworth; Benjamin Currall; Michael G Nichols; Xudong Wu; Jian Zuo
Journal:  Brain Res       Date:  2006-04-13       Impact factor: 3.252

9.  Characterization of spectral FRET imaging microscopy for monitoring nuclear protein interactions.

Authors:  Ye Chen; Joshua P Mauldin; Richard N Day; Ammasi Periasamy
Journal:  J Microsc       Date:  2007-11       Impact factor: 1.758

10.  Three-dimensional FRET reconstruction microscopy for analysis of dynamic molecular interactions in live cells.

Authors:  Adam D Hoppe; Spencer L Shorte; Joel A Swanson; Rainer Heintzmann
Journal:  Biophys J       Date:  2008-03-13       Impact factor: 4.033

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