Literature DB >> 7299035

Correction of timing errors in photomultiplier tubes used in phase-modulation fluorometry.

J R Lakowicz, H Cherek, A Balter.   

Abstract

The measurement of fluorescence lifetimes is known to be hindered by the wavelength-dependent and photocathode area-dependent time response of photomultiplier tubes. A simple and direct method is described to minimize these effects in photomultiplier tubes used for phase-modulation fluorometry. Reference fluorophores of known lifetime were used in place of the usual scattering reference. The emission wavelengths of the reference and sample were matched by either filters or a monochromator, and the use of a fluorophore rather than a scatterer decreases the differences in spatial distribution of light emanating from the reference and sample. Thus photomultiplier tube artifacts are minimized. Five reference fluorophores were selected on the basis of availability, ease of solution preparation, and constancy of lifetime with temperature and emission wavelength. These compounds are p-terphenyl, PPO, PPD, POPOP and dimethyl POPOP. These compounds are dissolved in ethanol to give standard solutions that can be used over the temperature range from -55 to +55 degrees C. Purging with inert gas is not necessary. The measured phase and modulation of the reference solution is used, in conjunction with the known reference lifetime, to calculate the actual phase and modulation of the excitation beam. The use of standard fluorophores does not require separate experiments to quantify photomultiplier effects, and does not increase the time required for the measurement of fluorescence lifetimes. Examples are presented which demonstrate the elimination of artifactual photomultiplier effects in measurements of the lifetimes of NADH (0.4 ns) and indole solutions quenched by iodide. In addition, the use of these reference solutions increases the accuracy of fluorescence lifetime measurements ranging to 30 ns. We judge this method to provide more reliable lifetime measurements by the phase and modulation method. The test solutions and procedures we describe may be used by other laboratories to evaluate the performance of their phase fluorometers.

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Year:  1981        PMID: 7299035     DOI: 10.1016/0165-022x(81)90012-9

Source DB:  PubMed          Journal:  J Biochem Biophys Methods        ISSN: 0165-022X


  33 in total

1.  Background suppression in frequency-domain fluorometry.

Authors:  J R Lakowicz; I Gryczynski; Z Gryczynski; M L Johnson
Journal:  Anal Biochem       Date:  2000-01-01       Impact factor: 3.365

2.  Real-time background suppression during frequency domain lifetime measurements.

Authors:  Petr Herman; Badri P Maliwal; Joseph R Lakowicz; Baldri P Maliwal
Journal:  Anal Biochem       Date:  2002-10-01       Impact factor: 3.365

3.  Quantification of allosteric influence of Escherichia coli phosphofructokinase by frequency domain fluorescence.

Authors:  Audrey S Pham; Gregory D Reinhart
Journal:  Biophys J       Date:  2003-07       Impact factor: 4.033

4.  Nonmonotonic alterations in the fluorescence anisotropy of polar head group labeled fluorophores during the lamellar to hexagonal phase transition of phospholipids.

Authors:  X Han; R W Gross
Journal:  Biophys J       Date:  1992-08       Impact factor: 4.033

5.  Fluorescence lifetime imaging.

Authors:  J R Lakowicz; H Szmacinski; K Nowaczyk; K W Berndt; M Johnson
Journal:  Anal Biochem       Date:  1992-05-01       Impact factor: 3.365

6.  Resolution of multicomponent fluorescence emission using frequency-dependent phase angle and modulation spectra.

Authors:  J R Lakowicz; R Jayaweera; H Szmacinski; W Wiczk
Journal:  Anal Chem       Date:  1990-09-15       Impact factor: 6.986

7.  Nanosecond fluorescence microscopy. Emission kinetics of fura-2 in single cells.

Authors:  S M Keating; T G Wensel
Journal:  Biophys J       Date:  1991-01       Impact factor: 4.033

8.  Kinetics of formation of fluorescent products from hexanal and L-lysine in a two-phase system.

Authors:  H Stapelfeldt; L H Skibsted
Journal:  Lipids       Date:  1996-11       Impact factor: 1.880

9.  Biotin binding changes the conformation and decreases tryptophan accessibility of streptavidin.

Authors:  G P Kurzban; G Gitlin; E A Bayer; M Wilchek; P M Horowitz
Journal:  J Protein Chem       Date:  1990-12

10.  Membrane structural domains. Resolution limits using diphenylhexatriene fluorescence decay.

Authors:  D A Barrow; B R Lentz
Journal:  Biophys J       Date:  1985-08       Impact factor: 4.033

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