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Updated: Jun 13, 2026

Exploring Protein-Glycan Interactions: Advances in Nuclear Magnetic Resonance
Published on: August 26, 2025
The tridentate metal-binding sites of the common glycoses
Natascha Ghaschghaie1, Thomas Hoffmann, Martin Steinborn
1Department of Chemistry and Biochemistry of the Ludwig Maximilian University Munich, Butenandtstr. 5-13, D-81377, Munich, Germany.
Abstract:
Co(III)(tacn) and Ga(III)(tacn) fragments (tacn = 1,4,7-triazacyclononane) are suitable metal probes for the detection of the tridentate chelating sites of a glycose. Three moles of hydroxide per mole of cobalt or gallium support triple deprotonation of the chelating triol functions at a glycose's backbone. The individual chelating sites are detected using 1D and 2D NMR techniques. The metal-binding sites always include the hydroxy function at the anomeric carbon atom. Chelators are derived from both the pyranose and the furanose isomers while forming five- and six-membered chelate rings by the use of cis,cis-1,2,3-triol functions. The assignment of less frequently occurring ligand isomers are supported by a DFT approach. Crystal-structure analysis on Na(4)[Cr(beta-d-Manf1,2,3H(-3))(2)]NO(3).8.5H(2)O (Man = mannose) additionally upholds the NMR assignments.
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