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<dc:title>1D alignment of proteins and other nanoparticles by using reversible covalent bonds on cyclic peptide nanotubes</dc:title>
<dc:creator>Priegue Caamaño, Juan Manuel</dc:creator>
<dc:creator>Louzao Pernas, Iria</dc:creator>
<dc:creator>Gallego Gómez, Iván</dc:creator>
<dc:creator>Montenegro García, Javier</dc:creator>
<dc:creator>Granja Guillán, Juan Ramón</dc:creator>
<dc:contributor>Universidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Moleculares</dc:contributor>
<dc:contributor>Universidade de Santiago de Compostela. Departamento de Química Orgánica</dc:contributor>
<dc:description>Self-assembling cyclic peptide nanotubes are supramolecular structures whose diameter and external surface properties are precisely controlled. In this communication we describe a general strategy to align different molecules on top of the nanotube surface by using cyclic peptides bearing chemoreversible reactive groups. D,L-α-Cyclic peptides endowed with a hydrazide moiety were condensed with a pyrenecarboxyaldehyde to facilitate the nanotube formation and deposition on flat unfunctionalized surfaces. The hydrazide moieties can be liberated without affecting the tubular structure and then used to align on top of the nanotube other molecules bearing aldehyde functions. Additionally, the attachment of specific ligands allowed the supramolecular alignment of corresponding receptors, such as mannosyl aldehyde and concavaline-A, driven by the nanotube structure through complemetary protein–ligand interactions</dc:description>
<dc:description>This work was supported by the Spanish Agencia Estatal de Investigación (AEI) and the ERDF (PID2019 111126RB-100, SAF2017-89890-R, EIG_JC2018-054), and by the Xunta de Galicia and the ERDF (ED431C 2017/25 and Centro singular de Investigación de Galicia accreditation 2019-2022, ED431G 2019/03). We also thank the ORFEO-CINCA network and Mineco (RED2018-102331-T). J.M.P. thanks to the Ministerio de Educación y Cultura (MEC) for his FPI contract. J.M. received an ISCIII (COV20/00297), ERC - Stg (DYNAP-677786), ERC-PoC (TraffikGene, 838002),and a YIG from the HFSP (RGY0066/2017)</dc:description>
<dc:description>SI</dc:description>
<dc:date>2022-10-31T12:15:33Z</dc:date>
<dc:date>2022-12-20T02:00:09Z</dc:date>
<dc:date>2021</dc:date>
<dc:type>journal article</dc:type>
<dc:type>AM</dc:type>
<dc:identifier>Org. Chem. Front., 2022,9, 1226-1233 https://doi.org/10.1039/D1QO01349A</dc:identifier>
<dc:identifier>2052-4110</dc:identifier>
<dc:identifier>http://hdl.handle.net/10347/29370</dc:identifier>
<dc:identifier>10.1039/D1QO01349A</dc:identifier>
<dc:identifier>2052-4129</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>https://doi.org/10.1039/D1QO01349A</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-111126RB-100/ES</dc:relation>
<dc:relation>info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/SAF2017-89890-R/ES/PEPTIDOS HIBRIDOS PARA EL TRANSPORTE SELECTIVO Y ENTREGA DE PROTEINAS TERAPEUTICAS</dc:relation>
<dc:rights>© The Royal Society of Chemistry, 2021</dc:rights>
<dc:rights>embargoed access</dc:rights>
<dc:publisher>Royal Society of Chemistry</dc:publisher>
</oai_dc:dc>
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