Literature DB >> 23494166

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

Yanzhou Zhou1, Yulei Bai, Ci Chen, John M Dickenson.   

Abstract

As the hardware of FLIM technique becomes mature, the most important criterion for FLIM application is the correct interpretation of its data. In this research, first of all, a more orthogonal phasor approach, called as Modified Phasor Approach (MPA), is put forward. It is a way to calculate the lifetime of the complex fluorescent process, and a rule to measure how much the fluorescence process deviates from single exponential decay. Secondly, MPA is used to analysis the time-resolved fluorescence processes of the transfected CHO-K1 Cell lines expressing adenosine receptor A1R tagged by CYP and YFP, measured in the channel of the acceptor. The image of the fluorescence lifetime and the multiplication of the fluorescence lifetime and deviation from single exponential decay reveal the details of the Homo-FRET. In one word, MPA provides the physical meaning in its whole modified phasor space, and broadens the way for the application of the fluorescence lifetime imaging.

Mesh:

Year:  2013        PMID: 23494166     DOI: 10.1007/s10895-013-1193-y

Source DB:  PubMed          Journal:  J Fluoresc        ISSN: 1053-0509            Impact factor:   2.217


  10 in total

1.  Graphical representation and multicomponent analysis of single-frequency fluorescence lifetime imaging microscopy data.

Authors:  A H A Clayton; Q S Hanley; P J Verveer
Journal:  J Microsc       Date:  2004-01       Impact factor: 1.758

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

Authors:  P J Verveer; P I H Bastiaens
Journal:  J Microsc       Date:  2003-01       Impact factor: 1.758

Review 3.  FRET imaging.

Authors:  Elizabeth A Jares-Erijman; Thomas M Jovin
Journal:  Nat Biotechnol       Date:  2003-11       Impact factor: 54.908

4.  AB-plot assisted determination of fluorophore mixtures in a fluorescence lifetime microscope using spectra or quenchers.

Authors:  Q S Hanley; A H A Clayton
Journal:  J Microsc       Date:  2005-04       Impact factor: 1.758

5.  Polar plot representation for frequency-domain analysis of fluorescence lifetimes.

Authors:  Glen I Redford; Robert M Clegg
Journal:  J Fluoresc       Date:  2005-09       Impact factor: 2.217

6.  The phasor approach to fluorescence lifetime imaging analysis.

Authors:  Michelle A Digman; Valeria R Caiolfa; Moreno Zamai; Enrico Gratton
Journal:  Biophys J       Date:  2007-11-02       Impact factor: 4.033

7.  Global analysis of time correlated single photon counting FRET-FLIM data.

Authors:  Hernan E Grecco; Pedro Roda-Navarro; Peter J Verveer
Journal:  Opt Express       Date:  2009-04-13       Impact factor: 3.894

8.  Quantitative analysis of fluorescence lifetime imaging made easy.

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

9.  Imaging lifetime and anisotropy spectra in the frequency domain.

Authors:  Y Zhou; J M Dickenson; Q S Hanley
Journal:  J Microsc       Date:  2009-04       Impact factor: 1.758

10.  Quantitative comparison of polar approach versus fitting method in time domain FLIM image analysis.

Authors:  A Leray; C Spriet; D Trinel; R Blossey; Y Usson; L Héliot
Journal:  Cytometry A       Date:  2010-12-02       Impact factor: 4.355

  10 in total

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