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dc.rights.licenseopenen_US
dc.contributor.authorMENKE, Friedericke
dc.contributor.authorMAZZIER, Daniela
dc.contributor.authorWICHER, Barbara
dc.contributor.authorALLMENDINGER, Lars
hal.structure.identifierImagerie Moléculaire et Nanobiotechnologies - Institut Européen de Chimie et Biologie [IECB]
dc.contributor.authorKAUFFMANN, Brice
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorMAURIZOT, Victor
dc.contributor.authorHUC, Ivan
dc.date.accessioned2024-04-30T09:25:49Z
dc.date.available2024-04-30T09:25:49Z
dc.date.issued2023
dc.identifier.issn1477-0520en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/199528
dc.description.abstractEnThe first abiotic foldamer tertiary structures have been recently reported in the form of aromatic helix–turn–helix motifs based on oligo-quinolinecarboxamides held together by intramolecular hydrogen bonds. Tertiary folds were predicted by computational modelling of the hydrogen-bonding interfaces between helices and later verified by X-ray crystallography. However, the prognosis of how the conformational preference inherent to each helix influences the tertiary structure warranted further investigation. Several new helix–turn–helix sequences were synthesised in which some hydrogen bonds have been removed. Contrary to expectations, this change did not strongly destabilise the tertiary folds. On closer inspection, a new crystal structure revealed that helices adopt their natural curvature when some hydrogen bonds are missing and undergo some spring torsion upon forming the said hydrogen bonds, thus potentially giving rise to a conformational frustration. This phenomenon sheds light on the aggregation behaviour of the helices when they are not linked by a turn unit..
dc.language.isoENen_US
dc.title.enMolecular torsion springs: alteration of helix curvature in frustrated tertiary folds
dc.typeArticle de revueen_US
dc.identifier.doi10.1039/d2ob02109aen_US
dc.subject.halChimie/Chimie organiqueen_US
dc.subject.halChimie/Cristallographieen_US
bordeaux.journalOrganic & Biomolecular Chemistryen_US
bordeaux.page1275-1283en_US
bordeaux.volume21en_US
bordeaux.hal.laboratoriesCBMN : Chimie & de Biologie des Membranes & des Nano-objets - UMR 5248en_US
bordeaux.issue6en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcehal
hal.identifierhal-04274841
hal.version1
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Organic%20&%20Biomolecular%20Chemistry&rft.date=2023&rft.volume=21&rft.issue=6&rft.spage=1275-1283&rft.epage=1275-1283&rft.eissn=1477-0520&rft.issn=1477-0520&rft.au=MENKE,%20Friedericke&MAZZIER,%20Daniela&WICHER,%20Barbara&ALLMENDINGER,%20Lars&KAUFFMANN,%20Brice&rft.genre=article


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