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Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification
Published on: November 15, 2017
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Progress and pitfalls of using isobaric mass tags for proteome profiling
Loïc Dayon1,2, Michael Affolter1
1Proteomics, Nestlé Institute of Food Safety & Analytical Sciences, Nestlé Research, Lausanne, Switzerland.
Expert Review of Proteomics
|February 19, 2020
Summary
Isobaric mass tags enable simultaneous comparison of multiple protein samples in proteomic research. This technology enhances sample throughput and quantitative accuracy for pre-clinical and clinical studies.
Area of Science:
- Proteomics
- Mass Spectrometry
- Analytical Chemistry
Background:
- Quantitative proteomics utilizes label-free or label-based methods.
- Labeling strategies involve incorporating stable isotopes.
- Isobaric labeling allows relative quantification of peptides/proteins by mass spectrometry.
Purpose of the Study:
- Systematic review of isobaric mass tag use in proteomic research since 2003.
- Focus on quantitative performance, multiplexing evolution, and applications.
- Discussion of limitations and solutions for quantitative ratio distortion.
Main Methods:
- Systematic literature review.
- Analysis of quantitative performances and multiplexing capabilities.
- Evaluation of applications in pre-clinical and clinical studies.
Main Results:
- Isobaric mass tags facilitate simultaneous comparison of multiple protein samples.
- Technology improves sample throughput and internal relative quantification.
- Applications demonstrated in pre-clinical models and clinical studies.
Conclusions:
- Isobaric mass tag technology offers high sample throughput and improved quantitative accuracy.
- Well-suited for proteome profiling in discovery studies.
- Use of shared reference samples enables large-scale studies.
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