Dynamic and quantitative Ca2+ measurements using improved cameleons

Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2135-40. doi: 10.1073/pnas.96.5.2135.

Abstract

Cameleons are genetically-encoded fluorescent indicators for Ca2+ based on green fluorescent protein variants and calmodulin (CaM). Because cameleons can be targeted genetically and imaged by one- or two-photon excitation microscopy, they offer great promise for monitoring Ca2+ in whole organisms, tissues, organelles, and submicroscopic environments in which measurements were previously impossible. However, the original cameleons suffered from significant pH interference, and their Ca2+-buffering and cross-reactivity with endogenous CaM signaling pathways was uncharacterized. We have now greatly reduced the pH-sensitivity of the cameleons by introducing mutations V68L and Q69K into the acceptor yellow green fluorescent protein. The resulting new cameleons permit Ca2+ measurements despite significant cytosolic acidification. When Ca2+ is elevated, the CaM and CaM-binding peptide fused together in a cameleon predominantly interact with each other rather than with free CaM and CaM-dependent enzymes. Therefore, if cameleons are overexpressed, the primary effect is likely to be the unavoidable increase in Ca2+ buffering rather than specific perturbation of CaM-dependent signaling.

Publication types

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

MeSH terms

  • 3',5'-Cyclic-AMP Phosphodiesterases / metabolism*
  • Adenoviridae
  • Amino Acid Substitution
  • Animals
  • Calcium / analysis
  • Calcium / metabolism*
  • Calmodulin / analysis
  • Calmodulin / metabolism*
  • Cytosol / metabolism
  • Green Fluorescent Proteins
  • HeLa Cells
  • Hippocampus / metabolism
  • Histamine / pharmacology
  • Humans
  • Hydrogen-Ion Concentration
  • Kinetics
  • Luminescent Proteins / analysis
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism*
  • Mutagenesis, Site-Directed
  • Neurons / metabolism*
  • Recombinant Proteins / analysis
  • Recombinant Proteins / metabolism
  • Signal Transduction
  • Spectrometry, Fluorescence / methods
  • Transfection

Substances

  • Calmodulin
  • Luminescent Proteins
  • Recombinant Proteins
  • Green Fluorescent Proteins
  • Histamine
  • 3',5'-Cyclic-AMP Phosphodiesterases
  • Calcium