Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Han, Won Bae | - |
dc.contributor.author | Kang, Dong-Hyun | - |
dc.contributor.author | Na, Jung-Hyun | - |
dc.contributor.author | Yu, Yeon Gyu | - |
dc.contributor.author | Kim, Tae Song | - |
dc.date.accessioned | 2024-01-19T19:30:22Z | - |
dc.date.available | 2024-01-19T19:30:22Z | - |
dc.date.created | 2021-09-05 | - |
dc.date.issued | 2019-09 | - |
dc.identifier.issn | 0956-5663 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/119611 | - |
dc.description.abstract | The 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.language | English | - |
dc.publisher | Pergamon Press Ltd. | - |
dc.title | Enhancement of membrane protein reconstitution on 3D free-standing lipid bilayer array in a microfluidic channel | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.bios.2019.111404 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | Biosensors and Bioelectronics, v.141 | - |
dc.citation.title | Biosensors and Bioelectronics | - |
dc.citation.volume | 141 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000486132800036 | - |
dc.identifier.scopusid | 2-s2.0-85067079998 | - |
dc.relation.journalWebOfScienceCategory | Biophysics | - |
dc.relation.journalWebOfScienceCategory | Biotechnology & Applied Microbiology | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Analytical | - |
dc.relation.journalWebOfScienceCategory | Electrochemistry | - |
dc.relation.journalWebOfScienceCategory | Nanoscience & Nanotechnology | - |
dc.relation.journalResearchArea | Biophysics | - |
dc.relation.journalResearchArea | Biotechnology & Applied Microbiology | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalResearchArea | Electrochemistry | - |
dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | UNILAMELLAR VESICLES | - |
dc.subject.keywordPlus | TRANSPORT | - |
dc.subject.keywordPlus | FUSION | - |
dc.subject.keywordPlus | RECORDINGS | - |
dc.subject.keywordPlus | STABILITY | - |
dc.subject.keywordPlus | RECEPTOR | - |
dc.subject.keywordPlus | BIOSENSOR | - |
dc.subject.keywordPlus | APERTURES | - |
dc.subject.keywordAuthor | Lipid | - |
dc.subject.keywordAuthor | 3-Dimensional lipid structure | - |
dc.subject.keywordAuthor | Free-standing lipid bilayer | - |
dc.subject.keywordAuthor | Protein reconstitution | - |
dc.subject.keywordAuthor | Membrane protein | - |
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