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Updated: Feb 15, 2026

Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification
Published on: November 15, 2017
A Sulfoxide-Based Isobaric Labelling Reagent for Accurate Quantitative Mass Spectrometry
Michael Stadlmeier1, Jana Bogena1, Miriam Wallner1
1Center for Integrated Protein Science at the Department of Chemistry, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, 81377, Munich, Germany.
Researchers developed a new isobaric labeling reagent for precise peptide quantification in proteomics. This novel reagent, utilizing sulfoxide pyrolysis, enhances fragmentation for more accurate relative quantification across multiple samples.
Area of Science:
- Proteomics
- Analytical Chemistry
- Mass Spectrometry
Background:
- Accurate peptide quantification is crucial for modern proteomics.
- Isobaric tags are commonly used for relative quantification, enabling multiplexed sample analysis.
- Existing isobaric tags rely on gas-phase separation of balancer and reporter elements.
Purpose of the Study:
- To develop a novel isobaric labeling reagent with improved fragmentation characteristics.
- To enhance the sensitivity and accuracy of relative peptide quantification in complex mixtures.
- To enable more robust complementary ion analysis in mass spectrometry.
Main Methods:
- Design and synthesis of a new isobaric labeling reagent featuring a sulfoxide linkage.
- Utilizing sulfoxide pyrolysis for controlled and asymmetric cleavage.
- Employing mass spectrometry for fragmentation analysis and signal detection.
Main Results:
- The new reagent demonstrates significantly improved fragmentation compared to existing methods.
- Enhanced intensity of complementary ion signals was observed.
- The reagent facilitates easier and asymmetric cleavage at low fragmentation energy.
- The findings support complementary ion cluster analysis for improved quantification.
Conclusions:
- The novel sulfoxide-linked isobaric tag offers superior fragmentation efficiency for proteomics.
- This advancement improves the accuracy and sensitivity of relative peptide quantification.
- The reagent design facilitates more reliable complementary ion analysis in mass spectrometry.
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