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Glycoconj J ; 34(3): 405-410, 2017 06.
Article in English | MEDLINE | ID: mdl-27523650

ABSTRACT

Studying polysaccharide-protein interactions under physiological conditions by conventional techniques is challenging. Ideally, macromolecules could be followed by both in vitro spectroscopy experiments as well as in tissues using microscopy, to enable a proper comparison of results over these different scales but, often, this is not feasible. The cell surface and extracellular matrix polysaccharides, glycosaminoglycans (GAGs) lack groups that can be detected selectively in the biological milieu. The introduction of 19F labels into GAG polysaccharides is explored and the interaction of a labelled GAG with the heparin-binding protein, antithrombin, employing 19F NMR spectroscopy is followed. Furthermore, the ability of 19F labelled GAGs to be imaged using CARS microscopy is demonstrated. 19F labelled GAGs enable both 19F NMR protein-GAG binding studies in solution at the molecular level and non-linear microscopy at a microscopic scale to be conducted on the same material, essentially free of background signals.


Subject(s)
Fluorine-19 Magnetic Resonance Imaging/methods , Fluorine/chemistry , Glycosaminoglycans/chemistry , Molecular Probes/chemistry , Staining and Labeling/methods , Acetylation , Antithrombins/chemistry , Glycosaminoglycans/analysis , Halogenation , Magnetic Resonance Spectroscopy/methods , Molecular Probes/analysis , Protein Binding , Solutions , Spectrum Analysis, Raman/methods
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