Fluorescein Redirects a Ruthenium−Octaarginine Conjugate to the Nucleus

Cindy A. Puckett and Jacqueline K. Barton*
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125
J. Am. Chem. Soc., 2009, 131 (25), pp 8738–8739
DOI: 10.1021/ja9025165
Publication Date (Web): June 8, 2009
Copyright © 2009 American Chemical Society

Abstract

Abstract Image

The cellular uptake and localization of a Ru−octaarginine conjugate with and without an appended fluorescein are compared. The inherent luminescence of the Ru(II) dipyridophenazine complex allows observation of its uptake without the addition of a fluorophore. Ru−octaarginine−fluorescein stains the cytosol, nuclei, and nucleoli of HeLa cells under conditions where the Ru−octaarginine conjugate without fluorescein shows only punctate cytoplasmic labeling. At higher concentrations, however, Ru−octaarginine without the fluorescein tag does exhibit cytoplasmic, nuclear, and nucleolar staining. Attaching fluorescein to Ru−octaarginine lowers the threshold concentration required for diffuse cytoplasmic labeling and nuclear entry. Hence, the localization of the fluorophore-bound peptide cannot serve as a proxy for that of the free peptide.

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History

  • Published In Issue July 01, 2009
  • Article ASAPJune 08, 2009
  • Received: March 30, 2009

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