Hydrazone-modulated peptides for efficient gene transfection
| dc.contributor.affiliation | Universidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Moleculares | gl |
| dc.contributor.affiliation | Universidade de Santiago de Compostela. Departamento de Química Orgánica | gl |
| dc.contributor.author | Louzao Pernas, Iria | |
| dc.contributor.author | García Fandiño, Rebeca | |
| dc.contributor.author | Montenegro García, Javier | |
| dc.date.accessioned | 2017-04-03T07:32:39Z | |
| dc.date.available | 2018-02-22T02:00:10Z | |
| dc.date.issued | 2017-02-22 | |
| dc.description.abstract | Gene transfection continues to be a major challenge in chemistry, biology and materials sciences. New methodologies and recent breakthroughs have renewed the interest in the discovery and development of new tools for efficient gene transfection. Hydrazone formation between a cationic head and hydrophobic tails has emerged as one of the most promising techniques for nucleotide delivery. In this contribution, we have exploited hydrazone formation to modulate the transfection activity of a parent linear peptide in combination with a plasmid DNA cargo. This strategy allowed the straightforward preparation, under physiologically compatible conditions, of a discrete library of amphiphilic modulated penetrating peptides. Without the requirement of any isolation or purification steps, these modulated amphiphilic peptides were combined with a plasmid DNA and screened in transfection experiments of human HeLa cells. Three of these hydrazone-conjugated peptides were identified as excellent vectors for plasmid delivery with comparable, or even higher, efficiencies and lower toxicity than the commercial reagents employed in routine transfection assays | gl |
| dc.description.peerreviewed | SI | gl |
| dc.description.sponsorship | We are thankful to Dr. Irene Lostalé-Seijo for cell culture assistance and discussions. We acknowledge funding from the Spanish Government MINECO: [CTQ2014-59646-R] and [CTQ2015-74621-JIN], the Xunta de Galicia (ED431G/09), the ERDF and the CESGA. R. G.-F. received a FCT Investigator Grant from Portugal (IF/01133/2015). J.M. received a Ramon y Cajal (RYC-2013-13784) and an ERC Starting Investigator Grant (DYNAP-677786) | gl |
| dc.identifier.citation | Louzao, I., García-Fandiño, R. and Montenegro, J. (2017), Hydrazone-modulated peptides for efficient gene transfection. J. Mater. Chem. B. [doi: 10.1039/c7tb00179g]. Royal Society of Chemistry | gl |
| dc.identifier.doi | 10.1039/C7TB00179G | |
| dc.identifier.issn | 2050-750X | |
| dc.identifier.uri | http://hdl.handle.net/10347/15266 | |
| dc.language.iso | eng | gl |
| dc.publisher | Royal Society of Chemistry | gl |
| dc.relation.projectID | info:eu-repo/grantAgreement/EC/H2020/677786 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2014-59646-R/ES/NUEVOS DISEÑOS CON CONTROL TOPOLOGICO DE PEPTIDOS PENETRANTES EN CELULAS | |
| dc.relation.projectID | info:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/RYC-2013-13784/ES | |
| dc.relation.projectID | info:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2015-74621-JIN/ES/DISEÑO DE BIOCIDAS INNOVADORES A PARTIR DE LA ELUCIDACION DEL MECANISMO DE OLIGOMEROS CON PROPIEDADES ANTIMICROBIANAS | |
| dc.relation.publisherversion | http://dx.doi.org/10.1039/C7TB00179G | gl |
| dc.rights | © Royal Society of Chemistry | gl |
| dc.rights.accessRights | open access | gl |
| dc.subject | Gene transfection | |
| dc.subject | Hydrazone-modulated peptides | |
| dc.title | Hydrazone-modulated peptides for efficient gene transfection | gl |
| dc.type | journal article | gl |
| dc.type.hasVersion | AM | gl |
| dspace.entity.type | Publication | |
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| relation.isAuthorOfPublication | b645ce32-31f3-4ca4-9e9f-c1324ff0717e | |
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