Controlling the fluorescence of ordinary oxazine dyes for single-molecule switching and superresolution microscopy

Jan Vogelsang, Thorben Cordes, Carsten Forthmann, Christian Steinhauer, Philip Tinnefeld

Research output: Contribution to journalArticleAcademicpeer-review

229 Citations (Scopus)
278 Downloads (Pure)

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 languageEnglish
Pages (from-to)8107-8112
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume106
Issue number20
DOIs
Publication statusPublished - 2009
Externally publishedYes

Keywords

  • single-molecule spectroscopy
  • sensor
  • molecular switch
  • electron transfer
  • INTERFACIAL ELECTRON-TRANSFER
  • PHOTOCHROMISM
  • NANOSCOPY
  • SPECTROSCOPY
  • KINETICS
  • BLINKING
  • PROTEIN
  • SYSTEM
  • DRONPA

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