Functional Gallic Acid-Based Dendrimers as Synthetic Nanotools to Remodel Amyloid-β-42 into Noncytotoxic Forms

dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Molecularesgl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Física Aplicadagl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánicagl
dc.contributor.authorRodrigues Araújo, Ana Rita
dc.contributor.authorCorrea Chinea, Juan Francisco
dc.contributor.authorDomínguez Arca, Vicente
dc.contributor.authorReis, Rui L.
dc.contributor.authorFernández Megía, Eduardo
dc.contributor.authorRodrigues Pires, Ricardo Alexandre
dc.date.accessioned2022-07-08T12:04:45Z
dc.date.available2022-07-08T12:04:45Z
dc.date.issued2021
dc.descriptionThe Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acsami.1c17823. Synthesis and characterization of dendrimers, studies of interference of dendrimers in the Aβ supramolecular assembly, and cell studiesgl
dc.description.abstractThe self-assembly of amyloid-β (Aβ) generates cytotoxic oligomers linked to the onset and progression of Alzheimer’s disease (AD). As many fundamental molecular pathways that control Aβ aggregation are yet to be unraveled, an important strategy to control Aβ cytotoxicity is the development of bioactive synthetic nanotools capable of interacting with the heterogeneous ensemble of Aβ species and remodel them into noncytotoxic forms. Herein, the synthesis of nanosized, functional gallic acid (Ga)-based dendrimers with a precise number of Ga at their surface is described. It is shown that these Ga-terminated dendrimers interact by H-bonding with monomeric/oligomeric Aβ species at their Glu, Ala, and Asp residues, promoting their remodeling into noncytotoxic aggregates in a process controlled by the Ga units. The multivalent presentation of Ga on the dendrimer surface enhances their ability to interact with Aβ, inhibiting the primary and secondary nucleation of Aβ fibrillization and disrupting the Aβ preformed fibrilsgl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThe authors acknowledge the financial support from the EC (FORECAST-668983), “Programa Operacional Regional do Norte”, “Fundo Social Europeu”, Norte2020 TERM&SC, for the PhD grant NORTE-08-5369-FSE-000044, the SpanishMinistry of Science and Innovation (RTI2018-102212-B-I00), the Xunta de Galicia (ED431C 2018/30; Centro singular de investigación de Galicia accreditation 2019−2022, ED431G 2019/03), European Regional Development Fund-ERDF, and the Galician Supercomputing Centre (CESGA) and the MAT2016-80266-R of the Spanish Ministry of Science and Innovationgl
dc.identifier.citationACS Appl. Mater. Interfaces 2021, 13, 50, 59673–59682gl
dc.identifier.doi10.1021/acsami.1c17823
dc.identifier.essn1944-8252
dc.identifier.issn1944-8244
dc.identifier.urihttp://hdl.handle.net/10347/28892
dc.language.isoenggl
dc.publisherACS Publicationsgl
dc.relation.publisherversionhttps://doi.org/10.1021/acsami.1c17823gl
dc.rights© 2021 American Chemical Society. This work is licenced under a Creative Commons Attribution 4.0 International licence (https://creativecommons.org/licenses/by/4.0/legalcode)gl
dc.rightsAtribución 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectDendrimersgl
dc.subjectGallic acidgl
dc.subjectAmyloid-βgl
dc.subjectSupramolecular assemblygl
dc.subjectAlzheimer’s diseasegl
dc.titleFunctional Gallic Acid-Based Dendrimers as Synthetic Nanotools to Remodel Amyloid-β-42 into Noncytotoxic Formsgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublication593e79f0-facf-4f5f-beda-56c5487bad01
relation.isAuthorOfPublicationfe5ace22-ce25-4507-aacf-a74fa1010319
relation.isAuthorOfPublication.latestForDiscovery593e79f0-facf-4f5f-beda-56c5487bad01

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