Literature DB >> 19335458

Imaging lifetime and anisotropy spectra in the frequency domain.

Y Zhou1, J M Dickenson, Q S Hanley.   

Abstract

We report the development of a system combining the capabilities of fluorescence imaging spectroscopy (x, lambda, I), fluorescence lifetime (tau) and static and dynamic fluorescence anisotropy (r), enabling the wide-field measurement of the spectroscopic parameters of fluorophores: (x, lambda, I, tau, r). The system employs a frequency domain data collection strategy with a modulated light emitting diode as the light source. A polarization rotator placed in the excitation path after a polarizer allows alternating parallel and perpendicular images to be collected without moving parts. A second polarizer on the emission side serves as the analyzer, leading to estimations of the wavelength-dependent dynamic anisotropies. The spectrograph has a nominal range of 365-920 nm; however, the light-emitting diodes and filter sets used in this study restricted the usable range from about 510 to 700 nm. The system was tested on rhodamine 6G (R6G) solutions containing 0, 15, 37, 45, 59, 74 and 91 glycerol. These experiments gave rotational diffusion results comparing favourably with literature values while also demonstrating a trend towards shorter measured lifetimes at high refractive index. The ability of the system to resolve mixtures was tested on mixtures of anti-human IgG-FITC (gamma-chain-specific) and R6G. These fluorophores have similar lifetimes but could be separated using anisotropy parameters. The imaging capabilities of the system were tested on mixtures of fluorescent beads with glycerol solutions of R6G.

Entities:  

Year:  2009        PMID: 19335458     DOI: 10.1111/j.1365-2818.2009.03145.x

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


  7 in total

Review 1.  Fluorescence polarization/anisotropy in diagnostics and imaging.

Authors:  David M Jameson; Justin A Ross
Journal:  Chem Rev       Date:  2010-05-12       Impact factor: 60.622

2.  Global analysis of dynamic fluorescence anisotropy by a polarized phasor approach.

Authors:  Yanzhou Zhou; Long Wu; Qinruo Wang; Yonghua Wang
Journal:  J Fluoresc       Date:  2010-06-08       Impact factor: 2.217

3.  Multi-target spectrally resolved fluorescence lifetime imaging microscopy.

Authors:  Thomas Niehörster; Anna Löschberger; Ingo Gregor; Benedikt Krämer; Hans-Jürgen Rahn; Matthias Patting; Felix Koberling; Jörg Enderlein; Markus Sauer
Journal:  Nat Methods       Date:  2016-01-25       Impact factor: 28.547

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

Authors:  Yanzhou Zhou; Yulei Bai; Ci Chen; John M Dickenson
Journal:  J Fluoresc       Date:  2013-03-15       Impact factor: 2.217

5.  When one plus one does not equal two: fluorescence anisotropy in aggregates and multiply labeled proteins.

Authors:  Zahra Zolmajd-Haghighi; Quentin S Hanley
Journal:  Biophys J       Date:  2014-04-01       Impact factor: 4.033

Review 6.  Caught in the act: quantifying protein behaviour in living cells.

Authors:  Diane S Lidke; Bridget S Wilson
Journal:  Trends Cell Biol       Date:  2009-10-02       Impact factor: 20.808

7.  Simultaneous FRAP, FLIM and FAIM for measurements of protein mobility and interaction in living cells.

Authors:  James A Levitt; Penny E Morton; Gilbert O Fruhwirth; George Santis; Pei-Hua Chung; Maddy Parsons; Klaus Suhling
Journal:  Biomed Opt Express       Date:  2015-09-08       Impact factor: 3.732

  7 in total

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