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dc.contributor.authorHan, Won Bae-
dc.contributor.authorKang, Dong-Hyun-
dc.contributor.authorNa, Jung-Hyun-
dc.contributor.authorYu, Yeon Gyu-
dc.contributor.authorKim, Tae Song-
dc.date.accessioned2024-01-19T19:30:22Z-
dc.date.available2024-01-19T19:30:22Z-
dc.date.created2021-09-05-
dc.date.issued2019-09-
dc.identifier.issn0956-5663-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/119611-
dc.description.abstractThe bio-sensory organs of living creatures have evolved to have the best sensing performance. They have 3-dimensional protrusions that have large surface areas to accommodate a large number of membrane proteins such as ion channels and G-protein coupled receptors, resulting in high sensitivity and specificity to target molecules. From the perspective of mimicking this system, BLM, which has been used extensively as a platform for a single nanopore-based sensing systems, has some limitations, i.e., some residual solvent, low mechanical stability, small surface area for appropriate stability, and difficulty in high-throughput fabrication. Herein, to eliminate these limitations, a solvent-free, size-controllable, 3-dimensional free-standing lipid bilayer (3DFLB) structure array with high stability (similar to 130 h) and high density (similar to 300,000 cm(-2)) is proposed, and its structural advantages for efficient and rapid protein reconstitution, compared to BLM, is demonstrated by human 5-HT3A receptor assay as well as alpha-hemolysin assay. A continuous process of 3DFLB array fabrication, 5-HT3A reconstitution, and 5-HT detections in a microfluidic channel proves the applicability of the proposed structures as a highly-sensitive sensing platform mimicking bio-sensory organs.-
dc.languageEnglish-
dc.publisherPergamon Press Ltd.-
dc.titleEnhancement of membrane protein reconstitution on 3D free-standing lipid bilayer array in a microfluidic channel-
dc.typeArticle-
dc.identifier.doi10.1016/j.bios.2019.111404-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBiosensors and Bioelectronics, v.141-
dc.citation.titleBiosensors and Bioelectronics-
dc.citation.volume141-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000486132800036-
dc.identifier.scopusid2-s2.0-85067079998-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryElectrochemistry-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaElectrochemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.type.docTypeArticle-
dc.subject.keywordPlusUNILAMELLAR VESICLES-
dc.subject.keywordPlusTRANSPORT-
dc.subject.keywordPlusFUSION-
dc.subject.keywordPlusRECORDINGS-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusBIOSENSOR-
dc.subject.keywordPlusAPERTURES-
dc.subject.keywordAuthorLipid-
dc.subject.keywordAuthor3-Dimensional lipid structure-
dc.subject.keywordAuthorFree-standing lipid bilayer-
dc.subject.keywordAuthorProtein reconstitution-
dc.subject.keywordAuthorMembrane protein-
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KIST Article > 2019
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