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Essential but sparse collagen hydroxylysyl post-translational modifications detected by DNP NMR.

Accepted version
Peer-reviewed

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Type

Article

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Authors

Li, Rui 
Rajan, Rakesh 

Abstract

The sparse but functionally essential post-translational collagen modification 5-hydroxylysine can undergo further transformations, including crosslinking, O-glycosylation, and glycation. Dynamic nuclear polarization (DNP) and stable isotope enriched lysine incorporation provide sufficient solid-state NMR sensitivity to identify these adducts directly in skin and vascular smooth muscle cell extracellular matrix (ECM), without extraction procedures, by comparison with chemical shifts of model compounds. Thus, DNP provides access to the elucidation of structural consequences of collagen modifications in intact tissue.

Description

Keywords

0601 Biochemistry and Cell Biology, Basic Science, 1.1 Normal biological development and functioning

Journal Title

Chem Commun (Camb)

Conference Name

Journal ISSN

1359-7345
1364-548X

Volume Title

54

Publisher

Royal Society of Chemistry (RSC)
Sponsorship
EPSRC (1652492)
Medical Research Council (MR/M01066X/1)
Biotechnology and Biological Sciences Research Council (BB/G021392/1)
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