Development of a fast TCSPC FLIM-FRET imaging system

Simon P. Poland, Simao Coelho, Nikola Krstajić, David Tyndall, Richard Walker, James Monypenny, David Day Uei Li, Robert Henderson, Simon Ameer-Beg

Research output: Chapter in Book/Report/Conference proceedingConference contribution book

15 Citations (Scopus)

Abstract

Forster/Fluorescence resonant energy transfer (FRET) has become an extremely important technique to explore biological interactions in cells and tissues. As the non-radiative transfer of energy from the donor to acceptor occurs typically only within 1-10nm, FRET measurement allows the user to detect localisation events between proteinconjugated fluorophores. Compared to other techniques, the use of time correlated single photon counting (TCSPC) to measure fluorescence lifetime (FLIM) has become the gold standard for measuring FRET interactions in cells. The technique is fundamentally superior to all existing techniques due to its near ideal counting efficiency, inherent low excitation light flux (reduced photobleaching and toxicity) and time resolution. Unfortunately due to its slow acquisition time when compared with other techniques, such as Frequency-domain lifetime determination or anisotropy, this makes it impractical for measuring dynamic protein interactions in cells. The relatively slow acquisition time of TCSPC FLIMFRET is simply due to the system usually employing a single-beam scanning approach where each lifetime (and thus FRET interaction) is determined individually on a voxel by voxel basis. In this paper we will discuss the development a microscope system which will parallelize TCSPC for FLIM-FRET in a multi-beam multi-detector format. This will greatly improve the speed at which the system can operate, whilst maintaining both the high temporal resolution and the high signal-to-noise for which typical TCPSC systems are known for. We demonstrate this idea using spatial light modulator (SLM) generated beamlets and single photon avalanche detector (SPAD) array. The performance is evaluated on a plant specimen. 

LanguageEnglish
Title of host publicationProceedings of SPIE 8588
Subtitle of host publicationMultiphoton Microscopy in the Biomedical Sciences XIII
Place of PublicationBellingham, Washington
Volume8588
DOIs
Publication statusPublished - 12 Jun 2013
EventMultiphoton Microscopy in the Biomedical Sciences XIII - San Francisco, CA, United Kingdom
Duration: 3 Feb 20135 Feb 2013

Conference

ConferenceMultiphoton Microscopy in the Biomedical Sciences XIII
CountryUnited Kingdom
CitySan Francisco, CA
Period3/02/135/02/13

Fingerprint

Energy Transfer
Photons
Imaging systems
Energy transfer
counting
Fluorescence
energy transfer
life (durability)
fluorescence
photons
Cell Communication
acquisition
cells
Avalanches
interactions
Detectors
Photobleaching
Light
Fluorophores
detectors

Keywords

  • FLIM-FRET
  • fluorescence lifetime
  • in-vivo imaging
  • multifocal scanning
  • multiphoton microscopy
  • TCSPC

Cite this

Poland, S. P., Coelho, S., Krstajić, N., Tyndall, D., Walker, R., Monypenny, J., ... Ameer-Beg, S. (2013). Development of a fast TCSPC FLIM-FRET imaging system. In Proceedings of SPIE 8588: Multiphoton Microscopy in the Biomedical Sciences XIII (Vol. 8588). [85880X] Bellingham, Washington. https://doi.org/10.1117/12.2004199
Poland, Simon P. ; Coelho, Simao ; Krstajić, Nikola ; Tyndall, David ; Walker, Richard ; Monypenny, James ; Li, David Day Uei ; Henderson, Robert ; Ameer-Beg, Simon. / Development of a fast TCSPC FLIM-FRET imaging system. Proceedings of SPIE 8588: Multiphoton Microscopy in the Biomedical Sciences XIII. Vol. 8588 Bellingham, Washington, 2013.
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Poland, SP, Coelho, S, Krstajić, N, Tyndall, D, Walker, R, Monypenny, J, Li, DDU, Henderson, R & Ameer-Beg, S 2013, Development of a fast TCSPC FLIM-FRET imaging system. in Proceedings of SPIE 8588: Multiphoton Microscopy in the Biomedical Sciences XIII. vol. 8588, 85880X, Bellingham, Washington, Multiphoton Microscopy in the Biomedical Sciences XIII, San Francisco, CA, United Kingdom, 3/02/13. https://doi.org/10.1117/12.2004199

Development of a fast TCSPC FLIM-FRET imaging system. / Poland, Simon P.; Coelho, Simao; Krstajić, Nikola; Tyndall, David; Walker, Richard; Monypenny, James; Li, David Day Uei; Henderson, Robert; Ameer-Beg, Simon.

Proceedings of SPIE 8588: Multiphoton Microscopy in the Biomedical Sciences XIII. Vol. 8588 Bellingham, Washington, 2013. 85880X.

Research output: Chapter in Book/Report/Conference proceedingConference contribution book

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AU - Poland, Simon P.

AU - Coelho, Simao

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AU - Walker, Richard

AU - Monypenny, James

AU - Li, David Day Uei

AU - Henderson, Robert

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N2 - Forster/Fluorescence resonant energy transfer (FRET) has become an extremely important technique to explore biological interactions in cells and tissues. As the non-radiative transfer of energy from the donor to acceptor occurs typically only within 1-10nm, FRET measurement allows the user to detect localisation events between proteinconjugated fluorophores. Compared to other techniques, the use of time correlated single photon counting (TCSPC) to measure fluorescence lifetime (FLIM) has become the gold standard for measuring FRET interactions in cells. The technique is fundamentally superior to all existing techniques due to its near ideal counting efficiency, inherent low excitation light flux (reduced photobleaching and toxicity) and time resolution. Unfortunately due to its slow acquisition time when compared with other techniques, such as Frequency-domain lifetime determination or anisotropy, this makes it impractical for measuring dynamic protein interactions in cells. The relatively slow acquisition time of TCSPC FLIMFRET is simply due to the system usually employing a single-beam scanning approach where each lifetime (and thus FRET interaction) is determined individually on a voxel by voxel basis. In this paper we will discuss the development a microscope system which will parallelize TCSPC for FLIM-FRET in a multi-beam multi-detector format. This will greatly improve the speed at which the system can operate, whilst maintaining both the high temporal resolution and the high signal-to-noise for which typical TCPSC systems are known for. We demonstrate this idea using spatial light modulator (SLM) generated beamlets and single photon avalanche detector (SPAD) array. The performance is evaluated on a plant specimen. 

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KW - fluorescence lifetime

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ER -

Poland SP, Coelho S, Krstajić N, Tyndall D, Walker R, Monypenny J et al. Development of a fast TCSPC FLIM-FRET imaging system. In Proceedings of SPIE 8588: Multiphoton Microscopy in the Biomedical Sciences XIII. Vol. 8588. Bellingham, Washington. 2013. 85880X https://doi.org/10.1117/12.2004199