Two-Photon Fluorescence Microscopy Imaging of Cellular Oxidative Stress Using Profluorescent Nitroxides

Authors

    Authors

    H. Y. Ahn; K. E. Fairfull-Smith; B. J. Morrow; V. Lussini; B. Kim; M. V. Bondar; S. E. Bottle;K. D. Belfield

    Comments

    Authors: contact us about adding a copy of your work at STARS@ucf.edu

    Abbreviated Journal Title

    J. Am. Chem. Soc.

    Keywords

    RADICAL HYBRID COMPOUNDS; ISOINDOLINE NITROXIDES; FLUORENE DERIVATIVES; PROBES; CELLS; MYELOPEROXIDASE; NEUROTOXICITY; ANISOTROPY; SYSTEMS; TEMPOL; Chemistry, Multidisciplinary

    Abstract

    A range of varying chromophore nitroxide free radicals and their nonradical methoxyamine analogues were synthesized and their linear photophysical properties examined. The presence of the proximate free radical masks the chromophore's usual fluorescence emission, and these species are described as profluorescent. Two nitroxides incorporating anthracene and fluorescein chromophores (compounds 7 and 19, respectively) exhibited two-photon absorption (2PA) cross sections of approximately 400 G.M. when excited at wavelengths greater than 800 nm. Both of these profluorescent nitroxides demonstrated low cytotoxicity toward Chinese hamster ovary (CHO) cells. Imaging colocalization experiments with the commercially available CellROX Deep Red oxidative stress monitor demonstrated good cellular uptake of the nitroxide probes. Sensitivity of the nitroxide probes to H2O2-induced damage was also demonstrated by both one- and two-photon fluorescence microscopy. These profluorescent nitroxide probes are potentially powerful tools for imaging oxidative stress in biological systems, and they essentially "light up" in the presence of certain species generated from oxidative stress. The high ratio of the fluorescence quantum yield between the profluorescent nitroxide species and their nonradical adducts provides the sensitivity required for measuring a range of cellular redox environments. Furthermore, their reasonable 2PA cross sections provide for the option of using two-photon fluorescence microscopy, which circumvents commonly encountered disadvantages associated with one-photon imaging such as photobleaching and poor tissue penetration.

    Journal Title

    Journal of the American Chemical Society

    Volume

    134

    Issue/Number

    10

    Publication Date

    1-1-2012

    Document Type

    Article

    Language

    English

    First Page

    4721

    Last Page

    4730

    WOS Identifier

    WOS:000301990600048

    ISSN

    0002-7863

    Share

    COinS