Unit

UNIT 23.2 The Isotope-Coded Affinity Tag Method for Quantitative Protein Profile Comparison and Relative Quantitation of Cysteine Redox Modifications

  1. James Chun Yip Chan1,
  2. Lei Zhou2,
  3. Eric Chun Yong Chan1

Published Online: 2 NOV 2015

DOI: 10.1002/0471140864.ps2302s82

Current Protocols in Protein Science

Current Protocols in Protein Science

How to Cite

Chan, J.C.Y., Zhou, L., and Chan, E.C.Y. 2015. The isotope-coded affinity tag method for quantitative protein profile comparison and relative quantitation of cysteine redox modifications. Curr. Protoc. Protein Sci. 82:23.2.1-23.2.19. doi: 10.1002/0471140864.ps2302s82

Author Information

  1. 1

    Department of Pharmacy, National University of Singapore, Singapore

  2. 2

    Singapore Eye Research Institute, Singapore

Publication History

  1. Published Online: 2 NOV 2015

Abstract

The isotope-coded affinity tag (ICAT) technique has been applied to measure pairwise changes in protein expression through differential stable isotopic labeling of proteins or peptides followed by identification and quantification using a mass spectrometer. Changes in protein expression are observed when the identical peptide from each of two biological conditions is identified and a difference is detected in the measurements comparing the peptide labeled with the heavy isotope to the one with a normal isotopic distribution. This approach allows the simultaneous comparison of the expression of many proteins between two different biological states (e.g., yeast grown on galactose versus glucose, or normal versus cancer cells). Due to the cysteine-specificity of the ICAT reagents, the ICAT technique has also been applied to perform relative quantitation of cysteine redox modifications such as oxidation and nitrosylation. This unit describes both protein quantitation and profiling of cysteine redox modifications using the ICAT technique. © 2015 by John Wiley & Sons, Inc.

Keywords:

  • isotope-coded affinity tag (ICAT);
  • quantitative protein profiling;
  • tandem mass spectrometry;
  • liquid chromatography;
  • cysteine thiol modification;
  • redox proteomics