<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Idiago-Lopez J</submitter><funding>Ministerio de Universidades</funding><funding>Ministerio de Asuntos Econ?micos y Transformaci?n Digital, Gobierno de Espa?a</funding><funding>Gobierno de Arag?n</funding><funding>Ministerio de Ciencia, Innovaci?n y Universidades</funding><funding>Eusko Jaurlaritza</funding><funding>Agencia Estatal de Investigaci?n</funding><funding>European Commission</funding><funding>Ministerio de Econom?a y Competitividad</funding><funding>Fondos Feder</funding><funding>Operativo Fondo Social Europeo de  Arag?n</funding><pagination>1620-1633</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9501912</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(9)</volume><pubmed_abstract>In this work, we report the use of bioorthogonal chemistry, specifically the strain-promoted click azide-alkyne cycloaddition (SPAAC) for the covalent attachment of magnetic nanoparticles (MNPs) on living cell membranes. Four types of MNPs were prepared, functionalized with two different stabilizing/passivation agents (a polyethylene glycol derivative and a glucopyranoside derivative, respectively) and two types of strained alkynes with different reactivities: a cyclooctyne (CO) derivative and a dibenzocyclooctyne (DBCO) derivative. The MNPs were extensively characterized in terms of physicochemical characteristics, colloidal stability, and click reactivity in suspension. Then, the reactivity of the MNPs toward azide-modified surfaces was evaluated as a closer approach to their final appli</pubmed_abstract><journal>Bioconjugate chemistry</journal><pubmed_title>From Bench to Cell: A Roadmap for Assessing the Bioorthogonal "Click" Reactivity of Magnetic Nanoparticles for Cell Surface Engineering.</pubmed_title><pmcid>PMC9501912</pmcid><funding_grant_id>DGA 2017-2021</funding_grant_id><funding_grant_id>RYC-2015-17640</funding_grant_id><funding_grant_id>FPU17/02024</funding_grant_id><funding_grant_id>PCIN-2017-060</funding_grant_id><funding_grant_id>PGC2018-096016-B-I00</funding_grant_id><funding_grant_id>GIC-2015_IT-1033-16</funding_grant_id><funding_grant_id>E15_20R</funding_grant_id><funding_grant_id>BIO 2017-84246-C2-1R</funding_grant_id><pubmed_authors>Eceiza M</pubmed_authors><pubmed_authors>Fratila RM</pubmed_authors><pubmed_authors>Grazu V</pubmed_authors><pubmed_authors>Idiago-Lopez J</pubmed_authors><pubmed_authors>Moreno-Antolin E</pubmed_authors><pubmed_authors>de la Fuente JM</pubmed_authors><pubmed_authors>Aizpurua JM</pubmed_authors></additional><is_claimable>false</is_claimable><name>From Bench to Cell: A Roadmap for Assessing the Bioorthogonal "Click" Reactivity of Magnetic Nanoparticles for Cell Surface Engineering.</name><description>In this work, we report the use of bioorthogonal chemistry, specifically the strain-promoted click azide-alkyne cycloaddition (SPAAC) for the covalent attachment of magnetic nanoparticles (MNPs) on living cell membranes. Four types of MNPs were prepared, functionalized with two different stabilizing/passivation agents (a polyethylene glycol derivative and a glucopyranoside derivative, respectively) and two types of strained alkynes with different reactivities: a cyclooctyne (CO) derivative and a dibenzocyclooctyne (DBCO) derivative. The MNPs were extensively characterized in terms of physicochemical characteristics, colloidal stability, and click reactivity in suspension. Then, the reactivity of the MNPs toward azide-modified surfaces was evaluated as a closer approach to their final appli</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-19T14:23:13.831Z</modification><creation>2024-11-12T22:01:37.427Z</creation></dates><accession>S-EPMC9501912</accession><cross_references><pubmed>35857350</pubmed><doi>10.1021/acs.bioconjchem.2c00230</doi></cross_references></HashMap>