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Updated: May 29, 2026

Quantitative Proteomics Using Reductive Dimethylation for Stable Isotope Labeling
Published on: July 1, 2014
Quantification of tryptic peptides in quadrupole ion trap using high-mass signals derived from isotope-coded N-acetyl
Jongcheol Seo1, Hye-Joo Yoon, Seung Koo Shin
1Department of Chemistry, Bio-Nanotechnology Center, Pohang University of Science and Technology, Pohang, Kyungbuk, 790-784, Korea.
Abstract:
Isotope-labeled N-acetyl dipeptides (Ac-Xxx-Ala) are coupled to the primary amines of tryptic peptides and then analyzed by tandem mass spectrometry. Amide bond cleavage between Xxx and Ala provides both low- and high-mass isotope-coded signals for quantification of peptides. Especially, facile cleavage at the modified lysine side chain yields very strong high-mass quantitation signals in a noise-free region. Tagging tryptic peptides with isobaric N-acetyl dipeptides is a viable strategy for accurate quantification of proteins, which can be used with most quadrupole ion trap mass spectrometers carrying the 1/3 mass cut-off problem.
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