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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorLE FER, Gaëlle
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorWIROTIUS, Anne-Laure
hal.structure.identifierGroupe Diffusion petits angles [GDPA]
dc.contributor.authorBRÛLET, Annie
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorGARANGER, Elisabeth
IDREF: 089451740
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorLECOMMANDOUX, Sebastien
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2019
dc.identifier.issn1525-7797
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/19853
dc.description.abstractEnThe synthesis and original thermoresponsive behavior of hybrid diblock copolypeptides composed of synthetic and recombinant polypeptides are herein reported. A thermoresponsive recombinant elastin-like polypeptide was used as a macroinitiator to synthesize a range of poly(L-glutamic acid)-block-elastin-like polypeptide (PGlu-b-ELP) diblock copoly-peptides with variable PGlu block lengths. Their temperature-triggered self-assembly in water and in phosphate-buffered saline (PBS) was investigated at the macroscopic scale using complementary techniques such as turbidimetry, dynamic and static light scattering, small-angle neutron scattering, and at the molecular scale by 1 H NMR and circular dichroism (CD). In deionized water, PGlu-b-ELP copolypeptides showed one transition from free soluble chains below the transition temperature (Tt) of the ELP block to macroscopic aggregates above the Tt. In contrast, in PBS, four successive regimes were observed upon increasing temperature: below the Tt , copolypeptides were soluble, above the Tt , large aggregates appeared and fell apart into discrete and defined spherical nanoparticles at a temperature named critical micellization temperature (CMT), before finally reaching an equilibrium. During the last regime, neutron scattering experiments revealed that the micelle-like structures underwent a densification step and expelled water from their core. In addition, 1H NMR and CD experiments revealed, in deionized water, the formation of type II β-turns into the ELP block upon temperature increase. These β-turns are known to participate in the intrinsic thermoresponsive behavior of the ELPs. In contrast, in PBS, circular dichroism measurements showed an attenuation of folded structure during the self-assembly phase, leading to less cohesive aggregates able to reorganize into nanoparticles at the CMT.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enRecombinant polypeptides
dc.subject.enSmall angle neutron scattering
dc.subject.enSynthetic polypeptides
dc.subject.enBiohybrids
dc.subject.enPoly(glutamic acid)
dc.subject.enelastin-like polypeptides
dc.subject.enpoly(L-glutamic acid)
dc.subject.enthermoresponsive diblock copolypeptides
dc.subject.enself-assembly
dc.subject.ennanoparticles
dc.title.enSelf-Assembly of Stimuli-Responsive Biohybrid Synthetic-b-Recombinant Block Copolypeptides
dc.typeArticle de revue
dc.identifier.doi10.1021/acs.biomac.8b01390
dc.subject.halChimie/Polymères
dc.subject.halChimie/Matériaux
dc.subject.halPhysique [physics]/Matière Condensée [cond-mat]/Matière Molle [cond-mat.soft]
bordeaux.journalBiomacromolecules
bordeaux.page254-272
bordeaux.volume20
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue1
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01948441
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01948441v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Biomacromolecules&rft.date=2019&rft.volume=20&rft.issue=1&rft.spage=254-272&rft.epage=254-272&rft.eissn=1525-7797&rft.issn=1525-7797&rft.au=LE%20FER,%20Ga%C3%ABlle&WIROTIUS,%20Anne-Laure&BR%C3%9BLET,%20Annie&GARANGER,%20Elisabeth&LECOMMANDOUX,%20Sebastien&rft.genre=article


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