Phosphine quenching of cyanine dyes as a versatile tool for fluorescence microscopy

J Am Chem Soc. 2013 Jan 30;135(4):1197-200. doi: 10.1021/ja3105279. Epub 2013 Jan 17.

Abstract

We report that the cyanine dye Cy5 and several of its structural relatives are reversibly quenched by the phosphine tris(2-carboxyethyl)phosphine (TCEP). Using Cy5 as a model, we show that the quenching reaction occurs by 1,4-addition of the phosphine to the polymethine bridge of Cy5 to form a covalent adduct. Illumination with UV light dissociates the adduct and returns the dye to the fluorescent state. We demonstrate that TCEP quenching can be used for super-resolution imaging as well as for other applications, such as differentiating between molecules inside and outside the cell.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Carbocyanines / chemistry*
  • Carbocyanines / pharmacokinetics
  • Cell Line
  • Humans
  • Microscopy, Fluorescence
  • Molecular Structure
  • Phosphines / chemistry*
  • Phosphines / pharmacokinetics
  • Temperature

Substances

  • Carbocyanines
  • Phosphines
  • cyanine dye 5
  • tris(2-carboxyethyl)phosphine