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Lightsheet fluorescence lifetime imaging microscopy with wide‐field time‐correlated single photon counting

We report on wide‐field time‐correlated single photon counting (TCSPC)‐based fluorescence lifetime imaging microscopy (FLIM) with lightsheet illumination. A pulsed diode laser is used for excitation, and a crossed delay line anode image intensifier, effectively a single‐photon sensitive camera, is u...

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Detalles Bibliográficos
Autores principales: Hirvonen, Liisa M., Nedbal, Jakub, Almutairi, Norah, Phillips, Thomas A., Becker, Wolfgang, Conneely, Thomas, Milnes, James, Cox, Susan, Stürzenbaum, Stephen, Suhling, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY‐VCH Verlag GmbH & Co. KGaA 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065631/
https://www.ncbi.nlm.nih.gov/pubmed/31661595
http://dx.doi.org/10.1002/jbio.201960099
Descripción
Sumario:We report on wide‐field time‐correlated single photon counting (TCSPC)‐based fluorescence lifetime imaging microscopy (FLIM) with lightsheet illumination. A pulsed diode laser is used for excitation, and a crossed delay line anode image intensifier, effectively a single‐photon sensitive camera, is used to record the position and arrival time of the photons with picosecond time resolution, combining low illumination intensity of microwatts with wide‐field data collection. We pair this detector with the lightsheet illumination technique, and apply it to 3D FLIM imaging of dye gradients in human cancer cell spheroids, and C. elegans. [Image: see text]