Literature DB >> 27782585

A wide-field TCSPC FLIM system based on an MCP PMT with a delay-line anode.

Wolfgang Becker1, Liisa M Hirvonen2, James Milnes3, Thomas Conneely3, Ottmar Jagutzki4, Holger Netz1, Stefan Smietana1, Klaus Suhling2.   

Abstract

We report on the implementation of a wide-field time-correlated single photon counting (TCSPC) method for fluorescence lifetime imaging (FLIM). It is based on a 40 mm diameter crossed delay line anode detector, where the readout is performed by three standard TCSPC boards. Excitation is performed by a picosecond diode laser with 50 MHz repetition rate. The photon arrival timing is obtained directly from the microchannel plates, with an instrumental response of ∼190 to 230 ps full width at half maximum depending on the position on the photocathode. The position of the photon event is obtained from the pulse propagation time along the two delay lines, one in x and one in y. One end of a delay line is fed into the "start" input of the corresponding TCSPC board, and the other end is delayed by 40 ns and fed into the "stop" input. The time between start and stop is directly converted into position, with a resolution of 200-250 μm. The data acquisition software builds up the distribution of the photons over their spatial coordinates, x and y, and their times after the excitation pulses, typically into 512 × 512 pixels and 1024 time channels per pixel. We apply the system to fluorescence lifetime imaging of cells labelled with Alexa 488 phalloidin in an epi-fluorescence microscope and discuss the application of our approach to other fluorescence microscopy methods.

Entities:  

Year:  2016        PMID: 27782585     DOI: 10.1063/1.4962864

Source DB:  PubMed          Journal:  Rev Sci Instrum        ISSN: 0034-6748            Impact factor:   1.523


  6 in total

1.  Advanced Fluorescence Microscopy Methods to Study Dynamics of Fluorescent Proteins In Vivo.

Authors:  Marcela Díaz; Leonel Malacrida
Journal:  Methods Mol Biol       Date:  2023

2.  Differences between FLIM phasor analyses for data collected with the Becker and Hickl SPC830 card and with the FLIMbox card.

Authors:  Suman Ranjit; Leonel Malacrida; Enrico Gratton
Journal:  Microsc Res Tech       Date:  2018-10-08       Impact factor: 2.769

Review 3.  Wide-field time-correlated single photon counting-based fluorescence lifetime imaging microscopy.

Authors:  Klaus Suhling; Liisa M Hirvonen; Wolfgang Becker; Stefan Smietana; Holger Netz; James Milnes; Thomas Conneely; Alix Le Marois; Ottmar Jagutzki; Fred Festy; Zdeněk Petrášek; Andrew Beeby
Journal:  Nucl Instrum Methods Phys Res A       Date:  2019-10-21       Impact factor: 1.455

4.  Quantitative real-time imaging of intracellular FRET biosensor dynamics using rapid multi-beam confocal FLIM.

Authors:  James A Levitt; Simon P Poland; Nikola Krstajic; Karin Pfisterer; Ahmet Erdogan; Paul R Barber; Maddy Parsons; Robert K Henderson; Simon M Ameer-Beg
Journal:  Sci Rep       Date:  2020-03-20       Impact factor: 4.379

5.  Lightsheet fluorescence lifetime imaging microscopy with wide-field time-correlated single photon counting.

Authors:  Liisa M Hirvonen; Jakub Nedbal; Norah Almutairi; Thomas A Phillips; Wolfgang Becker; Thomas Conneely; James Milnes; Susan Cox; Stephen Stürzenbaum; Klaus Suhling
Journal:  J Biophotonics       Date:  2019-11-25       Impact factor: 3.207

Review 6.  High-throughput, multi-parametric, and correlative fluorescence lifetime imaging.

Authors:  Chetan Poudel; Ioanna Mela; Clemens F Kaminski
Journal:  Methods Appl Fluoresc       Date:  2020-02-20       Impact factor: 3.009

  6 in total

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