Quantitative Analysis of Complex Protein Mixtures Using Isotope-Coded Affinity Tags

Nat Biotechnol. 1999 Oct;17(10):994-9. doi: 10.1038/13690.

Abstract

We describe an approach for the accurate quantification and concurrent sequence identification of the individual proteins within complex mixtures. The method is based on a class of new chemical reagents termed isotope-coded affinity tags (ICATs) and tandem mass spectrometry. Using this strategy, we compared protein expression in the yeast Saccharomyces cerevisiae, using either ethanol or galactose as a carbon source. The measured differences in protein expression correlated with known yeast metabolic function under glucose-repressed conditions. The method is redundant if multiple cysteinyl residues are present, and the relative quantification is highly accurate because it is based on stable isotope dilution techniques. The ICAT approach should provide a widely applicable means to compare quantitatively global protein expression in cells and tissues.

Publication types

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

MeSH terms

  • Affinity Labels*
  • Amino Acid Sequence
  • Chromatography, Liquid
  • Isotope Labeling*
  • Mass Spectrometry
  • Proteins / chemistry*

Substances

  • Affinity Labels
  • Proteins