Mechanistic Insight into the Binding of Multivalent Pyrrolidines to alpha-Mannosidases
Anno: 2017
Autori: Mirabella S., D’Adamio G., Matassini C., Goti A., Delgado S., Gimeno A., Robina I., Moreno-Vargas AJ., Sestak S., Jimenez-Barbero J., Cardona F.
Affiliazione autori: Univ Firenze, Dipartimento Chim Ugo Schiff, Via Lastruccia 3-13, I-50019 Sesto Fiorentino, FI, Italy; Univ Seville, Dept Quim Organ, Fac Quim, C Prof Garcia Gonzalez 1, E-41012 Seville, Spain; Slovak Acad Sci, Inst Chem, Ctr Glyc, Dubravska Cesta 9, Bratislava 84538, Slovakia; CIC bioGUNE, Bizkaia Sci & Technol Pk,Bldg 801A, Derio 48160, Spain; Basque Fdn Sci, Ikerbasque, Maria Diaz de Haro 5, Bilbao 48005, Spain; EHU UPV, Dept Organ Chem 2, Leioa 48040, Spain; CNR INO, Via N Carrara 1, Sesto Fiorentino, FI, Italy
Abstract: Novel pyrrolidine-based multivalent iminosugars, synthesized by a CuAAC approach, have shown remarkable multivalent effects towards jack bean alpha-mannosidase and a Golgi alpha-mannosidase from Drosophila melanogaster, as well as a good selectivity with respect to a lysosomal alpha-mannosidase, which is important for anticancer applications. STD NMR and molecular modeling studies supported a multivalent mechanism with specific interactions of the bioactive iminosugars with Jack bean alpha-mannosidase. TEM studies suggested a binding mode that involves the formation of aggregates, which result from the intermolecular cross-linked network of interactions between the multivalent inhibitors and two or more dimers of JBMan heterodimeric subunits.
Giornale/Rivista: CHEMISTRY-A EUROPEAN JOURNAL
Volume: 23 (58) Da Pagina: 14585 A: 14596
Parole chiavi: enzymes; iminosugars; inhibitors; multivalency; pyrrolidineDOI: 10.1002/chem.201703011Citazioni: 29dati da “WEB OF SCIENCE” (of Thomson Reuters) aggiornati al: 2024-03-24Riferimenti tratti da Isi Web of Knowledge: (solo abbonati) Link per visualizzare la scheda su IsiWeb: Clicca quiLink per visualizzare la citazioni su IsiWeb: Clicca qui