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Informatics for protein identification by mass spectrometry
Richard S Johnson1, Michael T Davis, J Alex Taylor
1Amgen Corporation, Molecular Sciences, 1201 Amgen Court West, Seattle, WA 98119, USA. jsrichar@amgen.com
Methods (San Diego, Calif.)
|February 22, 2005
Summary
High-throughput proteomics enables protein identification in complex mixtures using mass spectrometry. This review discusses challenges with modified peptides and introduces automated de novo sequencing and homology searches for accurate protein identification and validation.
Area of Science:
- Biochemistry
- Proteomics
- Mass Spectrometry
Background:
- High-throughput protein analysis (proteomics) advanced with peptide mass mapping and tandem mass spectrometry.
- Identifying proteins in complex mixtures became feasible, but challenges remain with modified or variant peptides.
Purpose of the Study:
- To review advancements in proteomics, focusing on challenges and solutions for protein identification.
- To discuss automated de novo sequencing and homology search modifications for mass spectrometry data.
- To highlight the critical aspect of validating protein identifications.
Main Methods:
- Peptide mass mapping and tandem mass spectrometry for protein identification.
- Automated de novo sequencing to derive peptide sequences independently of databases.
- Homology-based database searches (e.g., BLAST, FASTA) adapted for mass spectrometry data.
Main Results:
- Development of sensitive techniques enabling large-scale protein identification.
- Introduction of de novo sequencing and modified homology searches to address peptide modification and sequence variations.
- Emphasis on the necessity of rigorous validation for protein identifications.
Conclusions:
- Proteomics has evolved significantly, allowing identification of proteins in complex biological samples.
- Addressing challenges like peptide modifications requires advanced computational approaches.
- Robust validation is crucial to ensure the reliability of protein identification results.