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• W2020191788 abstract "Abstract NMR spectroscopy and isothermal titration calorimetry (ITC) are powerful methods to investigate ligand–protein interactions. Here, we present a versatile and sensitive fluorine NMR spectroscopic approach that exploits the 19 F nucleus of 19 F‐labeled carbohydrates as a sensor to study glycan binding to lectins. Our approach is illustrated with the 11 kDa Cyanovirin‐N, a mannose binding anti‐HIV lectin. Two fluoro‐deoxy sugar derivatives, methyl 2‐deoxy‐2‐fluoro‐α‐ D ‐mannopyranosyl‐(1→2)‐α‐ D ‐mannopyranoside and methyl 2‐deoxy‐2‐fluoro‐α‐ D ‐mannopyranosyl‐(1→2)‐α‐ D ‐mannopyranosyl‐(1→2)‐α‐ D ‐mannopyranoside were utilized. Binding was studied by 19 F NMR spectroscopy of the ligand and 1 H– 15 N HSQC NMR spectroscopy of the protein. The NMR data agree well with those obtained from the equivalent reciprocal and direct ITC titrations. Our study shows that the strategic design of fluorinated ligands and fluorine NMR spectroscopy for ligand screening holds great promise for easy and fast identification of glycan binding, as well as for their use in reporting structural and/or electronic perturbations that ensue upon interaction with a cognate lectin." @default.
• W2020191788 created "2016-06-24" @default.
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• W2020191788 date "2013-02-28" @default.
• W2020191788 modified "2023-10-18" @default.
• W2020191788 title "Fluorinated Carbohydrates as Lectin Ligands: Dissecting Glycan-Cyanovirin Interactions by Using¹⁹F NMR Spectroscopy" @default.
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• W2020191788 doi "https://doi.org/10.1002/chem.201204070" @default.
• W2020191788 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3796943" @default.
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