Journal
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume 24, Issue 4, Pages -Publisher
MDPI
DOI: 10.3390/ijms24043718
Keywords
galectin; lactoside; isothermal titration calorimetry (ITC); X-ray
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Lactose and N-Acetyllactosamine have been widely used ligands for galectins, but with limited selectivity. In this study, simultaneous modifications at the anomeric position, C-2, and O-3' of each sugar were performed, leading to a 3'-O-sulfated N-Acetyllactosamine analog with a significantly increased affinity of 14.7 μM against human Gal-3. The three best compounds contained sulfate groups at the O-3' position, which are in line with the highly cationic character of the Gal-3 binding site.
Galectins constitute a family of galactose-binding lectins overly expressed in the tumor microenvironment as well as in innate and adaptive immune cells, in inflammatory diseases. Lactose ((beta-D-galactopyranosyl)-(1 -> 4)-beta-D-glucopyranose, Lac) and N-Acetyllactosamine (2-acetamido-2-deoxy-4-O-beta-D-galactopyranosyl-D-glucopyranose, LacNAc) have been widely exploited as ligands for a wide range of galectins, sometimes with modest selectivity. Even though several chemical modifications at single positions of the sugar rings have been applied to these ligands, very few examples combined the simultaneous modifications at key positions known to increase both affinity and selectivity. We report herein combined modifications at the anomeric position, C-2, and O-3 ' of each of the two sugars, resulting in a 3 '-O-sulfated LacNAc analog having a Kd of 14.7 mu M against human Gal-3 as measured by isothermal titration calorimetry (ITC). This represents a six-fold increase in affinity when compared to methyl beta-D-lactoside having a Kd of 91 mu M. The three best compounds contained sulfate groups at the O-3 ' position of the galactoside moieties, which were perfectly in line with the observed highly cationic character of the human Gal-3 binding site shown by the co-crystal of one of the best candidates of the LacNAc series.
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