Multifocal Multiphoton Microscopy with Adaptive Optical Correction

    Student thesis: Doctoral ThesisDoctor of Philosophy

    Abstract

    Multiphoton microscopy (MPM) is a remarkably versatile technique in biological
    imaging. MPM provides increased depth over confocal imaging and can be
    combined with other imaging techniques such as fluorescence lifetime
    imaging microscopy (FLIM), adding functional information. FLIM read-­‐out
    is relatively straightforward using time-­‐correlated single photon counting
    (TCSPC). Fluorescence lifetime detection enhances the power of multiphoton
    imaging to allow three dimensional, concentration independent, measurements
    of environmental parameters such as pH, Oxygen tension and Ca2+ in addtion
    to the interaction or conformational modification of proteins by Förster
    resonant energy transfer (FRET); the latter is a particular focus of the Dimbleby
    research groups at King’s College London. However, there are significant
    limitations in both FLIM and MM. Limitations of TCSPC-­‐FLIM include prolonged
    acquisition times along with signal and resolution degradation as a function
    of depth. This thesis demonstrates advancements multiphoton fluorescence
    lifetime imaging through improvements in two principal areas: speed
    and resolution at depth.
    In order to improve acquistion rates a multifocal multiphoton microscope
    (MMM) capable of rapid, parallelized TCSPC-­‐FLIM was developed-­‐MegaFLI.
    Acquisitions demonstrate rapid 3-­‐dimensional, high temporal resolution
    FLIM in vivo Zebrafish. Performed by massively parallel excitation/detection
    the speed is signficantly improved by a factor of 64. In parallel to the
    MegaFLI project, a second microscope employing adaptive optical
    correction has been developed.
    The introduction of Adaptive Optics (AO) serves to improve imaging quality
    by counteracting the refractive index heterogeneities introduced by the
    sample, limiting the imaging depth. Incorporated with a single beam scanning
    FLIM system, a pupil-­‐segmentation AO-­‐TCSPC-­‐FLIM demonstrates improved
    signal-­‐to-­‐noise ratio (SNR) and resolution, permiting a more
    accurate determination of fluorescent lifetime in turbid media.
    Date of Award2015
    Original languageEnglish
    Awarding Institution
    • King's College London
    SupervisorSimon Ameer-Beg (Supervisor) & Frederic Festy (Supervisor)

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