| Literature DB >> 35583779 |
Fatih Demir1,2, Andreas Perrar1,3, Melissa Mantz1,3, Pitter F Huesgen4,5,6.
Abstract
Protein N-termini provide unique and distinguishing information on proteolytically processed or N-terminally modified proteoforms. Also splicing, use of alternative translation initiation sites, and a variety of co- and post-translational N-terminal modifications generate distinct proteoforms that are unambiguously identified by their N-termini. However, N-terminal peptides are only a small fraction among all peptides generated in a shotgun proteome digest, are often of low stoichiometric abundance, and therefore require enrichment. Various protocols for enrichment of N-terminal peptides have been established and successfully been used for protease substrate discovery and profiling of N-terminal modification, but often require large amounts of proteome. We have recently established the High-efficiency Undecanal-based N-Termini EnRichment (HUNTER) as a fast and sensitive method to enable enrichment of protein N-termini from limited sample sources with as little as a few microgram proteome. Here we present our current HUNTER protocol for sensitive plant N-terminome profiling, including sample preparation, enrichment of N-terminal peptides, and mass spectrometry data analysis.Entities:
Keywords: HUNTER; N-terminal protein modifications; N-termini; N-terminomics; Positional proteomics; Proteolysis; Proteomics
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Year: 2022 PMID: 35583779 DOI: 10.1007/978-1-0716-2079-3_12
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745