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Immunopeptidomics: Isolation of Mouse and Human MHC Class I- and II-Associated Peptides for Mass Spectrometry Analysis
Published on: October 15, 2021
A mouse plasma peptide atlas as a resource for disease proteomics
Qing Zhang1, Rajasree Menon, Eric W Deutsch
1Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. qing@fhcrc.org
Genome Biology
|June 5, 2008
Summary
This study analyzed mouse plasma using mass spectrometry, creating a public database of peptides and proteins. Novel protein isoforms and transcript variants were discovered, expanding our understanding of plasma proteomes.
Area of Science:
- Proteomics
- Biochemistry
- Genomics
Background:
- Plasma proteome analysis is crucial for understanding biological functions and disease.
- Existing mouse plasma proteomic data is limited, hindering comprehensive research.
Purpose of the Study:
- To create a comprehensive, publicly accessible repository of mouse plasma proteomic data.
- To identify novel peptides, proteins, isoforms, and transcript variants in mouse plasma.
- To establish a high-confidence dataset for future research and biomarker discovery.
Main Methods:
- Liquid chromatography-tandem mass spectrometry (LC-MS/MS) was employed for high-throughput proteomic analysis.
- Extensive data processing and high-confidence peptide/protein identification were performed.
- A repository of 568 LC-MS/MS runs was established, containing data for 13,779 distinct peptides and ~3,000 proteins.
Main Results:
- Identification of 13,779 high-confidence distinct peptides and approximately 3,000 proteins.
- Quantification revealed a 7-logarithmic range of protein abundance in mouse plasma.
- Discovery of novel protein isoforms and transcript variants not predicted by prior genome analysis.
Conclusions:
- The developed mouse plasma proteomic repository significantly enhances available research resources.
- The identified novel isoforms and variants offer new avenues for investigating gene regulation and function.
- This work provides a foundation for future studies in mouse physiology, disease, and drug development.
