Literature DB >> 12535178

Evaluation of global analysis algorithms for single frequency fluorescence lifetime imaging microscopy data.

P J Verveer1, P I H Bastiaens.   

Abstract

Global analysis of fluorescence lifetime image microscopy (FLIM) data can be used to obtain an accurate fit of multi-exponential fluorescence decays. In particular, it can be used to fit a bi-exponential decay to single frequency FLIM data, which is not possible with conventional fitting techniques. Bi-exponential fluorescence decay models can be used to analyse quantitatively single frequency FLIM data from samples that exhibit fluorescence resonance energy transfer (FRET). Global analysis algorithms simultaneously fit multiple measurements acquired under different experimental conditions to achieve higher accuracy. To demonstrate that bi-exponential models can indeed be fitted to single frequency data, we derive an analytical solution for the special case of two measurements and use this solution to illustrate the properties of global analysis algorithms. We also derive a novel global analysis algorithm that is optimized for single frequency FLIM data, and demonstrate that it is superior to earlier algorithms in terms of computational requirements.

Year:  2003        PMID: 12535178     DOI: 10.1046/j.1365-2818.2003.01093.x

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


  21 in total

1.  Multi-dimensional time-correlated single photon counting (TCSPC) fluorescence lifetime imaging microscopy (FLIM) to detect FRET in cells.

Authors:  R R Duncan; A Bergmann; M A Cousin; D K Apps; M J Shipston
Journal:  J Microsc       Date:  2004-07       Impact factor: 1.758

2.  Methodological considerations for global analysis of cellular FLIM/FRET measurements.

Authors:  Nur Aida Adbul Rahim; Serge Pelet; Roger D Kamm; Peter T C So
Journal:  J Biomed Opt       Date:  2012-02       Impact factor: 3.170

3.  Global analysis of dynamic fluorescence anisotropy by a polarized phasor approach.

Authors:  Yanzhou Zhou; Long Wu; Qinruo Wang; Yonghua Wang
Journal:  J Fluoresc       Date:  2010-06-08       Impact factor: 2.217

4.  Fluorescence lifetime heterogeneity resolution in the frequency domain by lifetime moments analysis.

Authors:  Alessandro Esposito; Hans C Gerritsen; Fred S Wouters
Journal:  Biophys J       Date:  2005-09-16       Impact factor: 4.033

5.  Pitfalls and their remedies in time-resolved fluorescence spectroscopy and microscopy.

Authors:  Martin vandeVen; Marcel Ameloot; Bernard Valeur; Noël Boens
Journal:  J Fluoresc       Date:  2005-05       Impact factor: 2.217

6.  Quantitative lifetime unmixing of multiexponentially decaying fluorophores using single-frequency fluorescence lifetime imaging microscopy.

Authors:  Gert-Jan Kremers; Erik B van Munster; Joachim Goedhart; Theodorus W J Gadella
Journal:  Biophys J       Date:  2008-03-21       Impact factor: 4.033

7.  Ultrafast Method for the Analysis of Fluorescence Lifetime Imaging Microscopy Data Based on the Laguerre Expansion Technique.

Authors:  Javier A Jo; Qiyin Fang; Laura Marcu
Journal:  IEEE J Quantum Electron       Date:  2005       Impact factor: 2.318

8.  Quantitative analysis of fluorescence lifetime imaging made easy.

Authors:  Fred S Wouters; Alessandro Esposito
Journal:  HFSP J       Date:  2008-01-18

9.  Processing of fluorescence lifetime image using modified phasor approach: homo-FRET from the acceptor.

Authors:  Yanzhou Zhou; Yulei Bai; Ci Chen; John M Dickenson
Journal:  J Fluoresc       Date:  2013-03-15       Impact factor: 2.217

10.  Electrostatic interactions positively regulate K-Ras nanocluster formation and function.

Authors:  Sarah J Plowman; Nicholas Ariotti; Andrew Goodall; Robert G Parton; John F Hancock
Journal:  Mol Cell Biol       Date:  2008-05-05       Impact factor: 4.272

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