Effects of incomplete decay in fluorescence lifetime estimation

Fluorescence lifetime imaging has emerged as an important microscopy technique, where high repetition rate lasers are the primary light sources. As fluorescence lifetime becomes comparable to intervals between consecutive excitation pulses, incomplete fluorescence decay from previous pulses can superimpose onto the subsequent decay measurements. Using a mathematical model, the incomplete decay effect has been shown to lead to overestimation of the amplitude average lifetime except in mono-exponential decays. An inverse model is then developed to correct the error from this effect and the theoretical simulations are tested by experimental results.

[1]  P. French,et al.  Time-resolved fluorescence microscopy , 2005 .

[2]  J. Taylor An Introduction to Error Analysis , 1982 .

[3]  J. Lakowicz Principles of fluorescence spectroscopy , 1983 .

[4]  Ammasi Periasamy,et al.  Characterization of two‐photon excitation fluorescence lifetime imaging microscopy for protein localization , 2004, Microscopy research and technique.

[5]  S. Ameer-Beg,et al.  Multiphoton time-domain fluorescence lifetime imaging microscopy: practical application to protein–protein interactions using global analysis , 2009, Journal of the Royal Society Interface.

[6]  Peter J. Parker,et al.  Imaging Protein Kinase Cα Activation in Cells , 1999 .

[7]  D. Elson,et al.  Fluorescence lifetime imaging microscopy for brain tumor image-guided surgery. , 2010, Journal of biomedical optics.

[8]  Hans C. Gerritsen,et al.  High-speed fluorescence lifetime imaging , 2004, SPIE BiOS.

[9]  H Szmacinski,et al.  Fluorescence lifetime imaging of intracellular calcium in COS cells using Quin-2. , 1994, Cell calcium.

[10]  Qiyin Fang,et al.  Single-shot acquisition of time-resolved fluorescence spectra using a multiple delay optical fiber bundle. , 2008, Optics letters.

[11]  R. Steiner,et al.  SLIM: A new method for molecular imaging , 2007, Microscopy research and technique.

[12]  H. Gerritsen,et al.  Fast fluorescence lifetime imaging of calcium in living cells. , 2004, Journal of biomedical optics.

[13]  Qiyin Fang,et al.  Characterization of Fluorescence Lifetime of Photofrin and Delta-Aminolevulinic Acid Induced Protoporphyrin IX in Living Cells Using Single- and Two-Photon Excitation , 2008, IEEE Journal of Selected Topics in Quantum Electronics.

[14]  Klaus Suhling,et al.  Time-resolved fluorescence microscopy , 2007, SPIE Optics East.

[15]  M A A Neil,et al.  Toward the clinical application of time-domain fluorescence lifetime imaging. , 2005, Journal of biomedical optics.

[16]  Elizabeth A Jares-Erijman,et al.  Imaging molecular interactions in living cells by FRET microscopy. , 2006, Current opinion in chemical biology.

[17]  A. Bergmann,et al.  Multispectral fluorescence lifetime imaging by TCSPC , 2007, Microscopy research and technique.

[18]  Borivoj Vojnovic,et al.  Global and pixel kinetic data analysis for FRET detection by multi-photon time-domain FLIM , 2005, SPIE BiOS.

[19]  H. van den Bergh,et al.  Frequency-domain fluorescence lifetime imaging for endoscopic clinical cancer photodetection: Apparatus design and preliminary results , 1997, Journal of Fluorescence.

[20]  T. Watson,et al.  Fluorescence lifetime endoscopy using TCSPC for the measurement of FRET in live cells , 2010, Optics express.

[21]  A. Coolen,et al.  The potential of optical proteomic technologies to individualize prognosis and guide rational treatment for cancer patients , 2009, Targeted Oncology.

[22]  D Barnes,et al.  Imaging protein kinase Calpha activation in cells. , 1999, Science.