Literature DB >> 11489073

Frequency-domain fluorescence microscopy with the LED as a light source.

P Herman1, B P Maliwal, H J Lin, J R Lakowicz.   

Abstract

We describe a frequency-domain lifetime fluorometer based on a microscope and a modulated light-emitting diode (LED) excitation source (370/460 nm), which operates in the frequency range 120 Hz--250 MHz. We collected multifrequency phase and modulation fluorescence responses from cellular areas as small as 10--15 microm in diameter. We also collected fluorescence lifetime data from cells stained by a lipophilic coumarin sensitized europium fluorophore, Coum-Eu, with a millisecond lifetime, and Ru(bpy)(2)phe-C(12),with microsecond lifetime. Nanosecond lifetimes from native nuclei stained with SYTO 14 and SYTO 16 probes were measured as well. We demonstrate that a simple LED excitation source can, for many applications, successfully replace complex and expensive laser systems, which have been used for cellular frequency-domain lifetime measurements. As the LEDs are very stable with low noise, it will be possible to image even smaller sample areas using brighter LEDs. With availability of modulated LEDs emitting at several wavelengths covering almost the entire visible spectrum it is easy to assemble a system for the fluorophore of choice. The ability to select an excitation source for a given fluorophore and low price make such an excitation source even more practical.

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Year:  2001        PMID: 11489073     DOI: 10.1046/j.1365-2818.2001.00943.x

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


  11 in total

1.  Long-wavelength long-lifetime luminophores.

Authors:  B P Maliwal; Z Gryczynski; J R Lakowicz
Journal:  Anal Chem       Date:  2001-09-01       Impact factor: 6.986

2.  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

3.  Parallel excitation-emission multiplexed fluorescence lifetime confocal microscopy for live cell imaging.

Authors:  Ming Zhao; Yu Li; Leilei Peng
Journal:  Opt Express       Date:  2014-05-05       Impact factor: 3.894

4.  Mercury free microscopy: an opportunity for core facility directors.

Authors:  T Regan Baird; Daniel Kaufman; Claire M Brown
Journal:  J Biomol Tech       Date:  2014-07

5.  Long-term monitoring of live cell proliferation in presence of PVP-Hypericin: a new strategy using ms pulses of LED and the fluorescent dye CFSE.

Authors:  Rozhin Penjweini; Hans G Loew; Michael R Hamblin; Karl W Kratky
Journal:  J Microsc       Date:  2011-10-04       Impact factor: 1.758

6.  Determination of photoluminescence quantum yields in dilute solution using non-monochromatic excitation light.

Authors:  Tarik Aaboub; Aicha Boukhriss; Said Gmouh; Martinus H V Werts
Journal:  Photochem Photobiol Sci       Date:  2022-10-21       Impact factor: 4.328

7.  Development of Low-Cost Instrumentation for Single Point Autofluorescence Lifetime Measurements.

Authors:  João Lagarto; Jonathan D Hares; Christopher Dunsby; Paul M W French
Journal:  J Fluoresc       Date:  2017-05-25       Impact factor: 2.217

8.  Selective detection of NADPH oxidase in polymorphonuclear cells by means of NAD(P)H-based fluorescence lifetime imaging.

Authors:  R Niesner; P Narang; H Spiecker; V Andresen; K-H Gericke; M Gunzer
Journal:  J Biophys       Date:  2008-11-16

9.  LED arrays as cost effective and efficient light sources for widefield microscopy.

Authors:  Dinu F Albeanu; Edward Soucy; Tomokazu F Sato; Markus Meister; Venkatesh N Murthy
Journal:  PLoS One       Date:  2008-05-14       Impact factor: 3.240

10.  Frequency domain photoacoustic and fluorescence microscopy.

Authors:  Gregor Langer; Bianca Buchegger; Jaroslaw Jacak; Thomas A Klar; Thomas Berer
Journal:  Biomed Opt Express       Date:  2016-06-20       Impact factor: 3.732

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