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The Multivalent Effect in Glycosidase Inhibition: Probing the Influence of Valency, Peripheral Ligand Structure, and Topology with Cyclodextrin-Based Iminosugar Click Clusters

Abstract : In view of recent reports of a strong multivalent effect in glycosidase inhibition, a library of β‐CD‐based multivalent iminosugars has been efficiently synthesized by way of CuI‐catalyzed azide–alkyne cycloaddition (CuAAC). In combination with the first application of isothermal titration calorimetry (ITC) experiments to the study of multivalent iminosugar–enzyme interactions, the inhibition properties of these click clusters were evaluated on a panel of glycosidases. The structural parameters that were varied include valency, peripheral ligand structure, and topology. The inhibition results obtained with the iminosugar clusters further highlight the importance of multivalency in the inhibition of α‐mannosidase. Generally, the evaluated multivalent iminosugars displayed comparable thermodynamic signatures of binding towards α‐mannosidase (Jack bean): that is, large negative enthalpies of complexation coupled with small entropies of either sign. In addition, the enthalpy–entropy compensation observed in all tested cases may be attributed to a common mechanism of dissociation for the enzyme–multivalent iminosugar interactions. The measured binding stoichiometries indicated that each iminosugar cluster interacts with no more than one protein molecule.
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https://hal-normandie-univ.archives-ouvertes.fr/hal-02548562
Contributor : Madeleine Roux-Merlin <>
Submitted on : Monday, April 20, 2020 - 5:28:09 PM
Last modification on : Tuesday, April 21, 2020 - 2:03:30 AM

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Camille Decroocq, Antoine Joosten, Raphaël Sergent, Teresa Mena Barragán, Carmen Ortiz Mellet, et al.. The Multivalent Effect in Glycosidase Inhibition: Probing the Influence of Valency, Peripheral Ligand Structure, and Topology with Cyclodextrin-Based Iminosugar Click Clusters. ChemBioChem, Wiley-VCH Verlag, 2013, 14 (15), pp.2038-2049. ⟨10.1002/cbic.201300283⟩. ⟨hal-02548562⟩

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