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Accessible Mannitol-Based Amphiphiles (MNAs) for Membrane Protein Solubilisation and Stabilisation

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dc.contributor.authorHussain, Hazrat-
dc.contributor.authorDu, Yang-
dc.contributor.authorScull, Nicola J.-
dc.contributor.authorMortensen, Jonas S.-
dc.contributor.authorTarrasch, Jeffrey-
dc.contributor.authorBae, Hyoung Eun-
dc.contributor.authorLoland, Claus J.-
dc.contributor.authorByrne, Bernadette-
dc.contributor.authorKobilka, Brian K.-
dc.contributor.authorChae, Pil Seok-
dc.date.accessioned2021-06-22T16:43:54Z-
dc.date.available2021-06-22T16:43:54Z-
dc.date.created2021-01-21-
dc.date.issued2016-05-
dc.identifier.issn0947-6539-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/13658-
dc.description.abstractIntegral membrane proteins are amphipathic molecules crucial for all cellular life. The structural study of these macromolecules starts with protein extraction from the native membranes, followed by purification and crystallisation. Detergents are essential tools for these processes, but detergent-solubilised membrane proteins often denature and aggregate, resulting in loss of both structure and function. In this study, a novel class of agents, designated mannitol-based amphiphiles (MNAs), were prepared and characterised for their ability to solubilise and stabilise membrane proteins. Some of MNAs conferred enhanced stability to four membrane proteins including a G protein-coupled receptor (GPCR), the beta(2) adrenergic receptor (beta(2)AR), compared to both n-dodecyl-D-maltoside (DDM) and the other MNAs. These agents were also better than DDM for electron microscopy analysis of the beta(2)AR. The ease of preparation together with the enhanced membrane protein stabilisation efficacy demonstrates the value of these agents for future membrane protein research.-
dc.language영어-
dc.language.isoen-
dc.publisherJohn Wiley & Sons Ltd.-
dc.titleAccessible Mannitol-Based Amphiphiles (MNAs) for Membrane Protein Solubilisation and Stabilisation-
dc.typeArticle-
dc.contributor.affiliatedAuthorChae, Pil Seok-
dc.identifier.doi10.1002/chem.201600533-
dc.identifier.scopusid2-s2.0-84981763964-
dc.identifier.wosid000377604100011-
dc.identifier.bibliographicCitationChemistry - A European Journal, v.22, no.21, pp.7068 - 7073-
dc.relation.isPartOfChemistry - A European Journal-
dc.citation.titleChemistry - A European Journal-
dc.citation.volume22-
dc.citation.number21-
dc.citation.startPage7068-
dc.citation.endPage7073-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusGLYCOL GNG AMPHIPHILES-
dc.subject.keywordPlusCRYSTAL-STRUCTURE-
dc.subject.keywordPlusFACIAL AMPHIPHILES-
dc.subject.keywordPlusMNG AMPHIPHILES-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusCRYSTALLIZATION-
dc.subject.keywordPlusINSIGHTS-
dc.subject.keywordPlusOVEREXPRESSION-
dc.subject.keywordPlusSURFACTANTS-
dc.subject.keywordPlusDETERGENTS-
dc.subject.keywordAuthoramphiphile design-
dc.subject.keywordAuthorelectron microscopy-
dc.subject.keywordAuthormembrane proteins-
dc.subject.keywordAuthornovel detergents-
dc.subject.keywordAuthorprotein stabilization-
dc.identifier.urlhttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/chem.201600533-
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