Isolation and characterization of collagen type I crosslink from skin: high-resolution NMR reveals diastereomers of hydroxylysinonorleucine crosslink

Skin is made up of mainly Collagen type I and its structure is stabilised by the formation of covalent immature and mature crosslinks. In this study, Collagen immature crosslink hydroxylysinonorleucine (HLNL) was isolated from bovine skin in high purity using two sequential purification steps. These consisted of preparative fibrous cellulose and size exclusion chromatography. The purified crosslink was then analysed using tandem mass spectrometry and high-resolution nuclear magnetic resonance (NMR) spectroscopy. The mass of singly and doubly charged ions of HLNL was 292.1865 and 146.5970 m/z and their optimised fragmentation energy was 17 keV and 5 keV, respectively. The ¹³C NMR of HLNL showed a doubled-up peak at 67.84 and 67.91 ppm which corroborated a diastereomeric form of Collagen immature crosslink HLNL and both are chiroptically indistinguishable. The chemical structure was fully resolved using ¹H, ¹³C and DEPT-135 high-resolution NMR spectroscopy and compared with Other previous studies. We also obtained for the first time the 2D NMR spectra COSY and HSQC of HLNL. We therefore suggested that Collagen organization into specific fibrils' orientation may be affected by the different configuration of these diastereomers of HLNL.

Collagen type I; Hydroxylysinonorleucine crosslink; NMR; Preparative chromatography; Skin; Unusual amino acids.