Quantitative protein analysis using (13)C7-labeled iodoacetanilide and d5-labeled N-ethylmaleimide by nano liquid chromatography/nanoelectrospray ionization ion trap mass spectrometry

Bioorg Med Chem Lett. 2013 May 15;23(10):3111-8. doi: 10.1016/j.bmcl.2013.02.112. Epub 2013 Mar 14.

Abstract

We have developed a methodology for quantitative analysis and concurrent identification of proteins by the modification of cysteine residues with a combination of iodoacetanilide (IAA, 1) and (13)C7-labeled iodoacetanilide ((13)C7-IAA, 2), or N-ethylmaleimide (NEM, 3) and d5-labeled N-ethylmaleimide (d5-NEM, 4), followed by mass spectrometric analysis using nano liquid chromatography/nanoelectrospray ionization ion trap mass spectrometry (nano LC/nano-ESI-IT-MS). The combinations of these stable isotope-labeled and unlabeled modifiers coupled with LC separation and ESI mass spectrometric analysis allow accurate quantitative analysis and identification of proteins, and therefore are expected to be a useful tool for proteomics research.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetanilides / chemistry*
  • Animals
  • Carbon Isotopes
  • Cattle
  • Chromatography, Liquid
  • Ethylmaleimide / chemistry*
  • Lactalbumin / analysis*
  • Molecular Structure
  • Nanotechnology*
  • Ovalbumin / analysis*
  • Serum Albumin, Bovine / analysis*
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Acetanilides
  • Carbon Isotopes
  • iodoacetanilide
  • Serum Albumin, Bovine
  • Ovalbumin
  • Lactalbumin
  • Ethylmaleimide