<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Martinez-Miguel M</submitter><funding>Centro de Investigaci?n Biom?dica en Red en Bioingenier?a, Biomateriales y Nanomedicina</funding><funding>H2020 Marie Sklodowska-Curie Actions</funding><funding>European Social Fund</funding><funding>Ministerio de Ciencia, Innovaci?n y Universidades</funding><funding>H2020 Leadership in Enabling and Industrial Technologies</funding><funding>European Cooperation in Science and Technology</funding><funding>Universitat Aut?noma de Barcelona</funding><funding>Generalitat de Catalunya</funding><funding>Instituto de Salud Carlos III</funding><funding>Fundaci? la Marat? de TV3</funding><funding>Ag?ncia de Gesti? d?Ajuts Universitaris i de Recerca</funding><funding>Max-Planck-Gesellschaft</funding><funding>Ministerio de Econom?a y Competitividad</funding><funding>European Regional Development Fund</funding><pagination>48179-48193</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9614722</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(42)</volume><pubmed_abstract>The synthesis and study of the tripeptide Arg-Gly-Asp (RGD), the binding site of different extracellular matrix proteins, e.g., fibronectin and vitronectin, has allowed the production of a wide range of cell adhesive surfaces. Although the surface density and spacing of the RGD peptide at the nanoscale have already shown a significant influence on cell adhesion, the impact of its hierarchical nanostructure is still rather unexplored. Accordingly, a versatile colloidal system named quatsomes, based on fluid nanovesicles formed by the self-assembling of cholesterol and surfactant molecules, has been devised as a novel template to achieve hierarchical nanostructures of the RGD peptide. To this end, RGD was anchored on the vesicle's fluid membrane of quatsomes, and the RGD-functionalized nanovesicles were covalently anchored to planar gold surfaces, forming a state of quasi-suspension, through a long poly(ethylene glycol) (PEG) chain with a thiol termination. An underlying self-assembled monolayer (SAM) of a shorter PEG was introduced for vesicle stabilization and to avoid unspecific cell adhesion. In comparison with substrates featuring a homogeneous distribution of RGD peptides, the resulting hierarchical nanoarchitectonic dramatically enhanced cell adhesion, despite lower overall RGD molecules on the surface. The new versatile platform was thoroughly characterized using a multitechnique approach, proving its enhanced performance. These findings open new methods for the hierarchical immobilization of biomolecules on surfaces using quatsomes as a robust and novel tissue engineering strategy.</pubmed_abstract><journal>ACS applied materials &amp; interfaces</journal><pubmed_title>Hierarchical Quatsome-RGD Nanoarchitectonic Surfaces for Enhanced Integrin-Mediated Cell Adhesion.</pubmed_title><pmcid>PMC9614722</pmcid><funding_grant_id>PID2020-115296RA-I00</funding_grant_id><funding_grant_id>CEX2019-000917-S</funding_grant_id><funding_grant_id>CA15126</funding_grant_id><funding_grant_id>CB/06/0074</funding_grant_id><funding_grant_id>SAF2014-60138-R</funding_grant_id><funding_grant_id>PDC2021-121481-I00</funding_grant_id><funding_grant_id>RYC-2017-22614</funding_grant_id><funding_grant_id>PID2019-105622RBI00</funding_grant_id><funding_grant_id>BBN20PIV02</funding_grant_id><funding_grant_id>201812</funding_grant_id><funding_grant_id>CTQ2015-66194-R</funding_grant_id><funding_grant_id>2017-SGR-1442</funding_grant_id><funding_grant_id>2017-SGR-229</funding_grant_id><funding_grant_id>RTI2018-093831-B-I00</funding_grant_id><funding_grant_id>801342</funding_grant_id><funding_grant_id>720942</funding_grant_id><funding_grant_id>2020FI_B2 00137</funding_grant_id><funding_grant_id>2017-SGR-1439</funding_grant_id><funding_grant_id>MAT2016-80826-R</funding_grant_id><funding_grant_id>2017-SGR-918</funding_grant_id><funding_grant_id>PID2019-111682RB-I00</funding_grant_id><funding_grant_id>101007804</funding_grant_id><funding_grant_id>953110</funding_grant_id><funding_grant_id>BBN18PI01</funding_grant_id><pubmed_authors>Vargas-Nadal G</pubmed_authors><pubmed_authors>Royo M</pubmed_authors><pubmed_authors>Giannotti MI</pubmed_authors><pubmed_authors>Cristobal-Lecina E</pubmed_authors><pubmed_authors>Pulido D</pubmed_authors><pubmed_authors>Martinez-Miguel M</pubmed_authors><pubmed_authors>Kober M</pubmed_authors><pubmed_authors>Mas-Torrent M</pubmed_authors><pubmed_authors>Tomsen-Melero J</pubmed_authors><pubmed_authors>Ratera I</pubmed_authors><pubmed_authors>Castellote-Borrell M</pubmed_authors><pubmed_authors>Munoz J</pubmed_authors><pubmed_authors>Ventosa N</pubmed_authors><pubmed_authors>Kyvik AR</pubmed_authors><pubmed_authors>Guasch J</pubmed_authors><pubmed_authors>Veciana J</pubmed_authors><pubmed_authors>Passemard S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hierarchical Quatsome-RGD Nanoarchitectonic Surfaces for Enhanced Integrin-Mediated Cell Adhesion.</name><description>The synthesis and study of the tripeptide Arg-Gly-Asp (RGD), the binding site of different extracellular matrix proteins, e.g., fibronectin and vitronectin, has allowed the production of a wide range of cell adhesive surfaces. Although the surface density and spacing of the RGD peptide at the nanoscale have already shown a significant influence on cell adhesion, the impact of its hierarchical nanostructure is still rather unexplored. Accordingly, a versatile colloidal system named quatsomes, based on fluid nanovesicles formed by the self-assembling of cholesterol and surfactant molecules, has been devised as a novel template to achieve hierarchical nanostructures of the RGD peptide. To this end, RGD was anchored on the vesicle's fluid membrane of quatsomes, and the RGD-functionalized nanovesicles were covalently anchored to planar gold surfaces, forming a state of quasi-suspension, through a long poly(ethylene glycol) (PEG) chain with a thiol termination. An underlying self-assembled monolayer (SAM) of a shorter PEG was introduced for vesicle stabilization and to avoid unspecific cell adhesion. In comparison with substrates featuring a homogeneous distribution of RGD peptides, the resulting hierarchical nanoarchitectonic dramatically enhanced cell adhesion, despite lower overall RGD molecules on the surface. The new versatile platform was thoroughly characterized using a multitechnique approach, proving its enhanced performance. These findings open new methods for the hierarchical immobilization of biomolecules on surfaces using quatsomes as a robust and novel tissue engineering strategy.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-22T02:01:41.26Z</modification><creation>2025-04-05T20:14:42.416Z</creation></dates><accession>S-EPMC9614722</accession><cross_references><pubmed>36251059</pubmed><doi>10.1021/acsami.2c10497</doi></cross_references></HashMap>