Synthesis of D-labeled naphthyliodoacetamide and application to quantitative peptide analysis by isotope differential mass spectrometry

Bioorg Med Chem Lett. 2006 Dec 1;16(23):6054-7. doi: 10.1016/j.bmcl.2006.08.112. Epub 2006 Sep 18.

Abstract

D-labeled and -unlabeled N-beta-naphthyliodoacetamides have been synthesized for specific modification of the sulfhydryl groups of cysteine residues in proteins or peptides, and have been applied to quantitative analysis of several peptides. A combination of these reagents, coupled with mass spectrometry, is anticipated to serve as a useful tool for quantitative analysis of peptides and hence proteins.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Iodoacetamide / chemical synthesis*
  • Iodoacetamide / chemistry
  • Isotopes
  • Molecular Structure
  • Naphthalenes / chemical synthesis*
  • Naphthalenes / chemistry
  • Peptides / analysis*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

  • Isotopes
  • Naphthalenes
  • Peptides
  • Iodoacetamide