| Literature DB >> 19550524 |
S Kumar, C Dunsby, P A A De Beule, D M Owen, U Anand, P M P Lanigan, R K P Benninger, D M Davis, M A A Neil, P Anand, C Benham, A Naylor, P M W French.
Abstract
We report a multifocal multiphoton time-correlated single photon counting (TCSPC) fluorescence lifetime imaging (FLIM) microscope system that uses a 16 channel multi-anode PMT detector. Multiphoton excitation minimizes out-of-focus photobleaching, multifocal excitation reduces non-linear in-plane photobleaching effects and TCSPC electronics provide photon-efficient detection of the fluorescence decay profile. TCSPC detection is less prone to bleaching- and movement-induced artefacts compared to wide-field time-gated or frequency-domain FLIM. This microscope is therefore capable of acquiring 3-D FLIM images at significantly increased speeds compared to single beam multiphoton microscopy and we demonstrate this with live cells expressing a GFP tagged protein. We also apply this system to time-lapse FLIM of NAD(P)H autofluorescence in single live cells and report measurements on the change in the fluorescence decay profile following the application of a known metabolic inhibitor.Entities:
Year: 2007 PMID: 19550524 DOI: 10.1364/oe.15.012548
Source DB: PubMed Journal: Opt Express ISSN: 1094-4087 Impact factor: 3.894