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Fluorinated Carbohydrates as Lectin Ligands: Simultaneous Screening of a Monosaccharide Library and Chemical Mapping by 19F NMR Spectroscopy
Author(s) -
José Daniel Martínez,
Ana I. Manzano,
Eva Calviño,
Ana de Diego,
Borja Rodríguez de Francisco,
Cecilia Romanò,
Stefan Oscarson,
Óscar Millet,
HansJoachim Gabius,
Jesús JiménezBarbero,
F. Javier Cañada
Publication year - 2020
Publication title -
the journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.2
H-Index - 228
eISSN - 1520-6904
pISSN - 0022-3263
DOI - 10.1021/acs.joc.0c01830
Subject(s) - chemistry , monosaccharide , galactose , lectin , carbohydrate , nuclear magnetic resonance spectroscopy , anomer , mannose , stereochemistry , organic chemistry , biochemistry
Molecular recognition of carbohydrates is a key step in essential biological processes. Carbohydrate receptors can distinguish monosaccharides even if they only differ in a single aspect of the orientation of the hydroxyl groups or harbor subtle chemical modifications. Hydroxyl-by-fluorine substitution has proven its merits for chemically mapping the importance of hydroxyl groups in carbohydrate-receptor interactions. 19 F NMR spectroscopy could thus be adapted to allow contact mapping together with screening in compound mixtures. Using a library of fluorinated glucose (Glc), mannose (Man), and galactose (Gal) derived by systematically exchanging every hydroxyl group by a fluorine atom, we developed a strategy combining chemical mapping and 19 F NMR T 2 filtering-based screening. By testing this strategy on the proof-of-principle level with a library of 13 fluorinated monosaccharides to a set of three carbohydrate receptors of diverse origin, i.e. the human macrophage galactose-type lectin, a plant lectin, Pisum sativum agglutinin, and the bacterial Gal-/Glc-binding protein from Escherichia coli , it became possible to simultaneously define their monosaccharide selectivity and identify the essential hydroxyls for interaction.

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