A Photoactivatable Push−Pull Fluorophore for Single-Molecule Imaging in Live Cells

Samuel J. Lord, Nicholas R. Conley, Hsiao-lu D. Lee, Reichel Samuel, Na Liu, Robert J. Twieg and W. E. Moerner
Department of Chemistry, Stanford University, Stanford, California 94305-5080, and Department of Chemistry, Kent State University, Kent, Ohio 44240
J. Am. Chem. Soc., 2008, 130 (29), pp 9204–9205
DOI: 10.1021/ja802883k
Publication Date (Web): June 24, 2008
Copyright © 2008 American Chemical Society
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Stanford University.

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Kent State University.

Abstract

Abstract Image

We have reengineered a red-emitting dicyanomethylenedihydrofuran push−pull fluorophore so that it is dark until photoactivated with a short burst of low-intensity violet light. Photoactivation of the dark fluorogen leads to conversion of an azide to an amine, which shifts the absorption to long wavelengths. After photoactivation, the fluorophore is bright and photostable enough to be imaged on the single-molecule level in living cells. This proof-of-principle demonstration provides a new class of bright photoactivatable fluorophores, as are needed for super-resolution imaging schemes that require active control of single molecule emission.

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History

  • Published In Issue July 23, 2008
  • Article ASAPJune 24, 2008
  • Received: April 18, 2008

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