Fluorescence ratio imaging of cyclic AMP in single cells

Nature. 1991 Feb 21;349(6311):694-7. doi: 10.1038/349694a0.

Abstract

Fluorescence imaging is perhaps the most powerful technique currently available for continuously observing the dynamic intracellular biochemistry of single living cells. However, fluorescent indicator dyes have been available only for simple inorganic ions such as Ca2+, H+, Na+, K+, Mg2+ and Cl-. We now report a fluorescent indicator for the adenosine 3',5'-cyclic monophosphate (cAMP) signalling pathway. The sensor consists of cAMP-dependent protein kinase in which the catalytic (C) and regulatory (R) subunits are each labelled with a different fluorescent dye such as fluorescein or rhodamine capable of fluorescence resonance energy transfer in the holoenzyme complex R2C2. When cAMP molecules bind to the R subunits, the C subunits dissociate, thereby eliminating energy transfer. The change in shape of the fluorescence emission spectrum allows cAMP concentrations and the activation of the kinase to be nondestructively visualized in single living cells microinjected with the labelled holoenzyme.

Publication types

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

MeSH terms

  • Animals
  • Biosensing Techniques*
  • Cell Line
  • Cyclic AMP / analysis*
  • Fluorescein-5-isothiocyanate
  • Fluoresceins
  • Fluorescence
  • Fluorescent Dyes
  • Macromolecular Substances
  • Protein Kinases*
  • Recombinant Proteins
  • Rhodamines
  • Thiocyanates

Substances

  • Fluoresceins
  • Fluorescent Dyes
  • Macromolecular Substances
  • Recombinant Proteins
  • Rhodamines
  • Thiocyanates
  • tetramethylrhodamine isothiocyanate
  • Cyclic AMP
  • Protein Kinases
  • Fluorescein-5-isothiocyanate