Abstract
Fluorescent molecular switches have widespread potential for use as sensors, material applications in electro-optical data storages and displays, and superresolution fluorescence microscopy. We demonstrate that adjustment of fluorophore properties and environmental conditions allows the use of ordinary fluorescent dyes as efficient single-molecule switches that report sensitively on their local redox condition. Adding or removing reductant or oxidant, switches the fluorescence of oxazine dyes between stable fluorescent and non-fluorescent states. At low oxygen concentrations, the off-state that we ascribe to a radical anion is thermally stable with a lifetime in the minutes range. The molecular switches show a remarkable reliability with intriguing fatigue resistance at the single-molecule level: Depending on the switching rate, between 400 and 3,000 switching cycles are observed before irreversible photodestruction occurs. A detailed picture of the underlying photoinduced and redox reactions is elaborated. In the presence of both reductant and oxidant, continuous switching is manifested by ‘‘blinking’’ with independently controllable on- and off-state lifetimes in both deoxygenated and oxygenated environments. This ‘‘continuous switching mode’’ is advantageously used for imaging actin filament and actin filament bundles in fixed cells with subdiffraction-limited resolution.
Original language | English |
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Pages (from-to) | 8107-8112 |
Number of pages | 6 |
Journal | Proceedings of the National Academy of Sciences of the United States of America |
Volume | 106 |
Issue number | 20 |
DOIs | |
Publication status | Published - 2009 |
Externally published | Yes |
Keywords
- single-molecule spectroscopy
- sensor
- molecular switch
- electron transfer
- INTERFACIAL ELECTRON-TRANSFER
- PHOTOCHROMISM
- NANOSCOPY
- SPECTROSCOPY
- KINETICS
- BLINKING
- PROTEIN
- SYSTEM
- DRONPA