Literature DB >> 2752091

Padé-Laplace method for analysis of fluorescence intensity decay.

Z Bajzer1, A C Myers, S S Sedarous, F G Prendergast.   

Abstract

This novel approach to the analysis of multiexponential functions is based on the combined use of the Laplace transform and Padé approximants (Yeramian, E., and P. Claverie. 1987. Nature (Lond.). 326:169-174). It is similar in principle to the well-known Isenberg method of moments (Isenberg, I. 1983. Biophys. J. 43:141-148) traditionally applied to the analysis of fluorescence decay. The advantage of the Padé-Laplace method lies in its ability to detect the number of components in a multiexponential function as well as their parameters. In this paper we modified the original method so that it can be applied to the analysis of multifrequency phase/modulation measurements of fluorescence decay. The method was tested first on simulated data. It afforded recovery up to four distinct lifetime components (and their fractional contributions). In the case of simulated data corresponding to continuous lifetime distributions (nonexponential decay), the results of the analysis by the Padé-Laplace method indicated the absence of discrete exponential components. The method was also applied to real phase/modulation data gathered on known fluorophores and their mixtures and on tryptophan fluorescence in phospholipase A2. The lifetime and fraction recoveries were consistent with those obtained from standard methods involving nonlinear least-square fitting.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2752091      PMCID: PMC1280453          DOI: 10.1016/S0006-3495(89)82653-0

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  8 in total

1.  Analyzing the distribution of decay constants in pulse-fluorimetry using the maximum entropy method.

Authors:  A K Livesey; J C Brochon
Journal:  Biophys J       Date:  1987-11       Impact factor: 4.033

2.  A systems-theory approach to the analysis of multiexponential fluorescence decay.

Authors:  J Eisenfeld; C C Ford
Journal:  Biophys J       Date:  1979-04       Impact factor: 4.033

3.  Interpretation of fluorescence decays in proteins using continuous lifetime distributions.

Authors:  J R Alcala; E Gratton; F G Prendergast
Journal:  Biophys J       Date:  1987-06       Impact factor: 4.033

4.  Nanosecond fluorescence spectroscopy of macromolecules.

Authors:  J Yguerabide
Journal:  Methods Enzymol       Date:  1972       Impact factor: 1.600

Review 5.  Time-resolved fluorescence of proteins.

Authors:  J M Beechem; L Brand
Journal:  Annu Rev Biochem       Date:  1985       Impact factor: 23.643

6.  Robust estimation in pulse fluorometry. A study of the method of moments and least squares.

Authors:  I Isenberg
Journal:  Biophys J       Date:  1983-08       Impact factor: 4.033

7.  A continuously variable frequency cross-correlation phase fluorometer with picosecond resolution.

Authors:  E Gratton; M Limkeman
Journal:  Biophys J       Date:  1983-12       Impact factor: 4.033

8.  Complex photophysics of the single tryptophan of porcine pancreatic phospholipase A2, its zymogen, and an enzyme/micelle complex.

Authors:  R D Ludescher; J J Volwerk; G H de Haas; B S Hudson
Journal:  Biochemistry       Date:  1985-12-03       Impact factor: 3.162

  8 in total
  3 in total

1.  Robust reconstruction of the rate constant distribution using the phase function method.

Authors:  Yajun Zhou; Xiaowei Zhuang
Journal:  Biophys J       Date:  2006-09-15       Impact factor: 4.033

2.  Padé-Laplace method for the analysis of time-resolved fluorescence decay curves.

Authors:  Z Bajzer; J C Sharp; S S Sedarous; F G Prendergast
Journal:  Eur Biophys J       Date:  1990       Impact factor: 1.733

3.  Bimodal control of a Ca(2+)-activated Cl(-) channel by different Ca(2+) signals.

Authors:  A Kuruma; H C Hartzell
Journal:  J Gen Physiol       Date:  2000-01       Impact factor: 4.086

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.