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dc.contributor.authorPark, Seon Joo
dc.contributor.authorSong, Hyun Seok
dc.contributor.authorKwon, Oh Seok
dc.contributor.authorChung, Ji Hyun
dc.contributor.authorLee, Seung Hwan
dc.contributor.authorAn, Ji Hyun
dc.contributor.authorAhn, Sae Ryun
dc.contributor.authorLee, Ji Eun
dc.contributor.authorYoon, Hyeonseok
dc.contributor.authorPark, Tai Hyun
dc.contributor.authorJang, Jyongsik
dc.date.accessioned2014-07-08T20:39:41Z
dc.date.available2014-07-08T20:39:41Z
dc.date.issued2014-03
dc.date.submitted2013-12
dc.identifier.issn2045-2322
dc.identifier.urihttp://hdl.handle.net/1721.1/88219
dc.description.abstractThe development of molecular detection that allows rapid responses with high sensitivity and selectivity remains challenging. Herein, we demonstrate the strategy of novel bio-nanotechnology to successfully fabricate high-performance dopamine (DA) biosensor using DA Receptor-containing uniform-particle-shaped Nanovesicles-immobilized Carboxylated poly(3,4-ethylenedioxythiophene) (CPEDOT) NTs (DRNCNs). DA molecules are commonly associated with serious diseases, such as Parkinson's and Alzheimer's diseases. For the first time, nanovesicles containing a human DA receptor D1 (hDRD1) were successfully constructed from HEK-293 cells, stably expressing hDRD1. The nanovesicles containing hDRD1 as gate-potential modulator on the conducting polymer (CP) nanomaterial transistors provided high-performance responses to DA molecule owing to their uniform, monodispersive morphologies and outstanding discrimination ability. Specifically, the DRNCNs were integrated into a liquid-ion gated field-effect transistor (FET) system via immobilization and attachment processes, leading to high sensitivity and excellent selectivity toward DA in liquid state. Unprecedentedly, the minimum detectable level (MDL) from the field-induced DA responses was as low as 10 pM in real- time, which is 10 times more sensitive than that of previously reported CP based-DA biosensors. Moreover, the FET-type DRNCN biosensor had a rapid response time (<1 s) and showed excellent selectivity in human serum.en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/srep04342en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0en_US
dc.sourceNature Publishing Groupen_US
dc.titleHuman dopamine receptor nanovesicles for gate-potential modulators in high-performance field-effect transistor biosensorsen_US
dc.typeArticleen_US
dc.identifier.citationPark, Seon Joo, Hyun Seok Song, Oh Seok Kwon, Ji Hyun Chung, Seung Hwan Lee, Ji Hyun An, Sae Ryun Ahn, et al. “Human Dopamine Receptor Nanovesicles for Gate-Potential Modulators in High-Performance Field-Effect Transistor Biosensors.” Sci. Rep. 4 (March 11, 2014).en_US
dc.contributor.departmentInstitute for Medical Engineering and Scienceen_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorSong, Hyun Seoken_US
dc.contributor.mitauthorKwon, Oh Seoken_US
dc.relation.journalScientific Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsPark, Seon Joo; Song, Hyun Seok; Kwon, Oh Seok; Chung, Ji Hyun; Lee, Seung Hwan; An, Ji Hyun; Ahn, Sae Ryun; Lee, Ji Eun; Yoon, Hyeonseok; Park, Tai Hyun; Jang, Jyongsiken_US
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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