Topological Effects and Binding Modes Operating with Multivalent Iminosugar-Based Glycoclusters and Mannosidases

• Published in: Journal of the American Chemical Society Vol. 135; no. 49; pp. 18427 - 18435
• Main Authors: Brissonnet, Yoan, Ortiz Mellet, Carmen, Morandat, Sandrine, Garcia Moreno, M. Isabel, Deniaud, David, Matthews, Susan E, Vidal, Sébastien, Šesták, Sergej, El Kirat, Karim, Gouin, Sébastien G
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 11.12.2013; Amer Chemical Soc
• Subjects: Animals; Binding Sites; Chemical Sciences; Chemistry; Chemistry, Multidisciplinary; Drosophila melanogaster; Imino Sugars - chemistry; Mannosidases - chemistry; Microscopy, Atomic Force; Organic chemistry; Physical Sciences; Science & Technology; CATALYSIS; CLICK CLUSTERS; LECTIN; GLYCOSIDASE INHIBITION; LIGANDS; BIOLOGICAL EVALUATION; HIGH-AFFINITY; PORPHYRIN; SELECTIVITY; EFFICIENT
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja406931w

Multivalent iminosugars have been recently explored for glycosidase inhibition. Affinity enhancements due to multivalency have been reported for specific targets, which are particularly appealing when a gain in enzyme selectivity is achieved but raise the question of the binding mode operating with this new class of inhibitors. Here we describe the development of a set of tetra- and octavalent iminosugar probes with specific topologies and an assessment of their binding affinities toward a panel of glycosidases including the Jack Bean α-mannosidase (JBαMan) and the biologically relevant class II α-mannosidases from Drosophila melanogaster belonging to glycohydrolase family 38, namely Golgi α-mannosidase ManIIb (GM) and lysosomal α-mannosidase LManII (LM). Very different inhibitory profiles were observed for compounds with identical valencies, indicating that the spatial distribution of the iminosugars is critical to fine-tune the enzymatic inhibitory activity. Compared to the monovalent reference, the best multivalent compound showed a dramatic 800-fold improvement in the inhibitory potency for JBαMan, which is outstanding for just a tetravalent ligand. The compound was also shown to increase both the inhibitory activity and the selectivity for GM over LM. This suggests that multivalency could be an alternative strategy in developing therapeutic GM inhibitors not affecting the lysosomal mannosidases. Dynamic light scattering experiments and atomic force microscopy performed with coincubated solutions of the compounds with JBαMan shed light on the multivalent binding mode. The multivalent compounds were shown to promote the formation of JBαMan aggregates with different sizes and shapes. The dimeric nature of the JBαMan allows such intermolecular cross-linking mechanisms to occur.