Literature DB >> 31347109

Analysis of Hydroxyproline in Collagen Hydrolysates.

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


  1 in total

1.  Collagen-derived dipeptide Pro-Hyp administration accelerates muscle regenerative healing accompanied by less scarring after wounding on the abdominal wall in mice.

Authors:  Shiro Jimi; Seiko Koizumi; Kenji Sato; Motoyasu Miyazaki; Arman Saparov
Journal:  Sci Rep       Date:  2021-09-21       Impact factor: 4.379

  1 in total

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