Plasmonic-assisted thermocyclizations in living cells using metal−organic framework based nanoreactors

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 de Partículasgl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánicagl
dc.contributor.authorCarrillo Carrión, Carolina
dc.contributor.authorMartínez González, Raquel
dc.contributor.authorPolo Tobajas, Ester
dc.contributor.authorTomás Gamasa, María
dc.contributor.authorDestito, Paolo
dc.contributor.authorCeballos Guzmán, Manuel
dc.contributor.authorPelaz García, Beatriz
dc.contributor.authorLópez García, Fernando
dc.contributor.authorMascareñas Cid, José Luis
dc.contributor.authorPino González de la Higuera, Pablo Alfonso del
dc.date.accessioned2021-10-27T06:39:41Z
dc.date.available2021-10-27T06:39:41Z
dc.date.issued2021
dc.description.abstractWe describe a microporous plasmonic nanoreactor to carry out designed near-infrared (NIR)-driven photothermal cyclizations inside living cells. As a proof of concept, we chose an intramolecular cyclization that is based on the nucleophilic attack of a pyridine onto an electrophilic carbon, a process that requires high activation energies and is typically achieved in bulk solution by heating at ∼90 °C. The core–shell nanoreactor (NR) has been designed to include a gold nanostar core, which is embedded within a metal–organic framework (MOF) based on a polymer-stabilized zeolitic imidazole framework-8 (ZIF-8). Once accumulated inside living cells, the MOF-based cloak of NRs allows an efficient diffusion of reactants into the plasmonic chamber, where they undergo the transformation upon near-IR illumination. The photothermal-driven reaction enables the intracellular generation of cyclic fluorescent products that can be tracked using fluorescence microscopy. The strategy may find different type of applications, such as for the spatio-temporal activation of prodrugsgl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThe authors thank the financial support of the MCIN/AEI (PID2020-119206RB-I00, PID2019-108624RB-I00, CTQ2017-84767-P, RYC-2017-23457, RYC-2019-028238-I, RTI2018-093813-J-I00), the Xunta de Galicia (ED431F 2017/02, 2021-CP054, ED431C-2021/25, Centro Singular de Investigación de Galicia Accreditation 2019−2022, and ED431G 2019/03), the European Union (European Regional Development Fund − ERDF; H2020-MSCA-IF grant agreement no. 749667; H2020-MSCA-ITN grant agreement no. 860942; H2020-FET-Open grant agreement No. 899612; and INTERREG V-A Spain−Portugal, project 0624_2IQBIONEURO_6_E), and the European Research Council (starting grant no. 950421, advanced grant no. 340055). The support of the orfeo-cinqa network (CTQ2016-81797-REDC) is also kindly acknowledgedgl
dc.identifier.citationACS Nano 2021, 15, 16924−16933gl
dc.identifier.doi10.1021/acsnano.1c07983
dc.identifier.essn1936-086X
dc.identifier.issn1936-0851
dc.identifier.urihttp://hdl.handle.net/10347/27035
dc.language.isoenggl
dc.publisherACSgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-119206RB-I00/ESgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-108624RB-I00/ES/HERRAMIENTAS BASADAS EN METALES PARA SU USO EN QUIMICA BIOLOGICA Y BIOMEDICINA. DESARROLLO DE NUEVAS ESTRATEGIAS ANTICANCERgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/CTQ2017-84767-P/ES/METODOS SINTETICOS EFICIENTES BASADOS EN CATALISIS METALICA. DESARROLLOS ENANTIOSELECTIVOS Y ACCESO A MOLECULAS BIOACTIVAS Y/O DE ALTO INTERES SINTETICOgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RYC-2017-23457/ESgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RYC-2019-028238-I/ESgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-093813-J-I00 /ES/FOTOCATALISIS BIOORTOGONAL MEDIADA POR LUZ VISIBLEgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020-MSCA-IF/749667gl
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020-MSCA-ITN/860942gl
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020-FET-Open/899612gl
dc.relation.publisherversionhttps://doi.org/10.1021/acsnano.1c07983gl
dc.rights© 2021 The Authors. Published by American Chemical Society. This document is licensed under a Creative Commons Attribution 4.0 International license (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.subjectBio-orthogonal chemistrygl
dc.subjectNanocompositesgl
dc.subjectThermoplasmonicsgl
dc.subjectIntracellular thermocyclizationgl
dc.subjectThermolabile protecting groupsgl
dc.titlePlasmonic-assisted thermocyclizations in living cells using metal−organic framework based nanoreactorsgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
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