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dc.rights.licenseopenen_US
hal.structure.identifierSoutien à la Recherche de l'Institut Européen de Chimie Biologique
dc.contributor.authorMORVAN, Estelle
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
dc.contributor.authorGRELARD, Axelle
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
hal.structure.identifierInstitut Européen de Chimie et Biologie [IECB]
dc.contributor.authorLOQUET, Antoine
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
hal.structure.identifierInstitut Européen de Chimie et Biologie [IECB]
dc.contributor.authorTAIB-MAAMAR, Nada
hal.structure.identifierChimie et Biologie des Membranes et des Nanoobjets [CBMN]
hal.structure.identifierInstitut Européen de Chimie et Biologie [IECB]
dc.contributor.authorDUFOURC, Erick
dc.date.accessioned2024-04-24T09:42:13Z
dc.date.available2024-04-24T09:42:13Z
dc.date.issued2023-02-07
dc.identifier.issn0003-2700en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/199301
dc.description.abstractEnUnderstanding the membrane dynamics of complex systems is essential to follow their function. As molecules in membranes can be in a rigid or mobile state depending on external (temperature, pressure) or internal (pH, domains, etc.) conditions, we propose an in-depth examination of NMR methods to filter highly mobile molecular parts from others that are in more restricted environments. We have thus developed a quantitative magic-angle spinning (MAS) 13C NMR approach coupled with cross-polarization (CP) and/or Insensitive Nuclei Enhanced by Polarization Transfer (INEPT) on rigid and fluid unlabeled model membranes. We demonstrate that INEPT can detect only very mobile lipid headgroups in gel (solid-ordered) phases; the remaining rigid parts are only detected with CP. A direct correlation is established between the normalized line intensity as obtained by CP and the C–H (C–D) order parameters measured by wide-line 2H NMR or extracted from molecular dynamics: ICP/IDPeq ≈ 5|SCH|, indicating that when the order is greater than 0.2–0.3 (maximum value of 0.5 for chain CH2), only rigid parts can be filtered and detected using CP techniques. In very fluid (liquid-disordered) membranes, where there are many more active motions, both INEPT and CP detect resonances, with, however, a clear propensity of each technique to detect mobile and restricted molecular parts, respectively. Interestingly, the 13C NMR chemical shift of lipid hydrocarbon chains can be used to monitor order–disorder phase transitions and calculate the fraction of chain defects (rotamers) and the part of the transition enthalpy due to bond rotations (6–7 kJ·mol–1 for dimyristolphosphatidylcholine, DMPC). Cholesterol-containing membranes (liquid-ordered phases) can be dynamically contrasted as the rigid-body sterol is mainly detected by the CP technique, with a contact time of 1 ms, and the phospholipid by INEPT. Our work opens up a straightforward, robust, and cost-effective route for the determination of membrane dynamics by taking advantage of well-resolved conventional 13C NMR experiments without the need of isotopic labeling
dc.language.isoENen_US
dc.subject.enlipid membrane dynamics
dc.subject.ensolid-state NMR
dc.subject.enrigid cholesterol
dc.subject.enorder parameters
dc.subject.enselective polarization transfer
dc.subject.enlipid membrane dynamics
dc.subject.enlipid membrane dynamics
dc.subject.enlipid membrane dynamics
dc.title.enDynamic Sorting of Mobile and Rigid Molecules in Biomembranes by Magic-Angle Spinning 13 C NMR
dc.typeArticle de revueen_US
dc.identifier.doi10.1021/acs.analchem.2c04185en_US
dc.subject.halChimie/Chimie théorique et/ou physiqueen_US
dc.subject.halSciences du Vivant [q-bio]/Biochimie, Biologie Moléculaire/Biologie structurale [q-bio.BM]en_US
bordeaux.journalAnalytical Chemistryen_US
bordeaux.page3596-3605en_US
bordeaux.volume95en_US
bordeaux.hal.laboratoriesCBMN : Chimie & de Biologie des Membranes & des Nano-objets - UMR 5248en_US
bordeaux.issue7en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcehal
hal.identifierhal-04308708
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=Analytical%20Chemistry&rft.date=2023-02-07&rft.volume=95&rft.issue=7&rft.spage=3596-3605&rft.epage=3596-3605&rft.eissn=0003-2700&rft.issn=0003-2700&rft.au=MORVAN,%20Estelle&GRELARD,%20Axelle&LOQUET,%20Antoine&TAIB-MAAMAR,%20Nada&DUFOURC,%20Erick&rft.genre=article


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