| Literature DB >> 31347109 |
Tobias Langrock1, Ralf Hoffmann2.
Abstract
Hydroxyproline (Hyp) is an imino acid posttranslationally formed by sequence-specific hydroxylases in the repeating collagen Gly-Xaa-Yaa triad present in all collagen types of all species. In both Xaa- and Yaa-positions, Pro is the most common residue, often oxidized to 4-Hyp in the Yaa- and rarely to 3-Hyp in the Xaa-positions. Here we describe the qualitative and quantitative analysis of 3- and 4-Hyp-isomers by separating the free imino acids either with hydrophilic interaction chromatography (HILIC) or after derivatization with reversed-phase chromatography (RPC). In both cases the compounds were detected by electrospray-ionization mass spectrometry.Entities:
Keywords: Amino acid analysis; Amino acid quantitation; Collagen; ESI-MS/MS; Hydrophilic interaction chromatography; Hydroxyproline; Hydroxyproline isomers; Mass spectrometry
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Year: 2019 PMID: 31347109 DOI: 10.1007/978-1-4939-9639-1_5
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745