Articles producció científica> Enginyeria Química

Conformationally-locked N -glycosides: Exploiting long-range non-glycone interactions in the design of pharmacological chaperones for Gaucher disease

  • Dades identificatives

    Identificador: PC:1094
    Handle: https://hdl.handle.net/20.500.11797/PC1094
    Autors:
    Castillón, S.García Fernández, J.M.Ortiz Mellet, C.Díaz, Y.Suzuki, Y.Ohno, K.Nanba, E.Higaki, K.Rísquez, R.Castilla, J.
    Resum:
    10.1016/j.ejmech.2014.11.002

  • Altres:

    Autor segons l'article: Castillón, S. García Fernández, J.M. Ortiz Mellet, C. Díaz, Y. Suzuki, Y. Ohno, K. Nanba, E. Higaki, K. Rísquez, R. Castilla, J.
    Departament: Enginyeria Química
    Resum: Pyranoid-type glycomimetics having a cis-1,2-fused glucopyranose-2-alkylsulfanyl-1,3-oxazoline (Glc-PSO) structure exhibit an unprecedented specificity as inhibitors of mammalian ß-glucosidase. Notably, their inhibitory potency against human ß-glucocerebrosidase (GCase) was found to be strongly dependent on the nature of aglycone-type moieties attached at the sulfur atom. In the particular case of ?-substituted hexadecyl chains, an amazing influence of the terminal group was observed. A comparative study on a series of Glc-PSO derivatives suggests that hydrogen bond acceptor functionalities, e.g. fluoro or methyloxycarbonyl, significantly stabilize the Glc-PSO:GCase complex. The S-(16-fluorohexadecyl)-PSO glycomimetic turned out to be a more potent GCase competitive inhibitor than ambroxol, a non glycomimetic drug currently in pilot trials as a pharmacological chaperone for Gaucher disease. Moreover, the inhibition constant increased by one order of magnitude when shifting from neutral (pH 7) to acidic (pH 5) media, a favorable characteristic for a chaperone candidate. Indeed, the fluoro-PSO derivative also proved superior to ambroxol in mutant GCase activity enhancement assays in N370S/N370S Gaucher fibroblasts. The results presented here represent a proof of concept of the potential of exploiting long-range non-glycone interactions for the optimization of glycosidase inhibitors with chaperone activity.
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 0223-5234
    Pàgina final: 266
    Volum de revista: 90
    Versió de l'article dipositat: info:eu-repo/semantics/submittedVersion
    Enllaç font original: http://www.sciencedirect.com/science/article/pii/S0223523414010241
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    DOI de l'article: 10.1016/j.ejmech.2014.11.002
    Entitat: Universitat Rovira i Virgili.
    Any de publicació de la revista: 2015
    Pàgina inicial: 258