| Literature DB >> 31515919 |
Joshua K G Karlsson1, Alex Laude2, Michael J Hall3, Anthony Harriman1.
Abstract
Cyanine dyes, as used in super-resolution fluorescence microscopy, undergo light-induced "blinking", enabling localization of fluorophores with spatial resolution beyond the optical diffraction limit. Despite a plethora of studies, the molecular origins of this blinking are not well understood. Here, we examine the photophysical properties of a bio-conjugate cyanine dye (AF-647), used extensively in dSTORM imaging. In the absence of a potent sacrificial reductant, light-induced electron transfer and intermediates formed via the metastable, triplet excited state are considered unlikely to play a significant role in the blinking events. Instead, it is found that, under conditions appropriate to dSTORM microscopy, AF-647 undergoes reversible photo-induced isomerization to at least two long-lived dark species. These photo-isomers are characterized spectroscopically and their interconversion probed by computational means. The first-formed isomer is light sensitive and transforms to a longer-lived species in modest yield that could be involved in dSTORM related blinking. Permanent photobleaching of AF-647 occurs with very low quantum yield and is partially suppressed by the anaerobic redox buffer.Entities:
Keywords: cyanine dyes; dSTORM microscopy; isomerisation; molecular photophysics; rotational barriers
Year: 2019 PMID: 31515919 DOI: 10.1002/chem.201904117
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236