Real-time monitoring of serotonin with highly selective aptamer-functionalized conducting polymer nanohybrids

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dc.contributor.authorSeong Gi Lim-
dc.contributor.authorSung Eun Seo-
dc.contributor.authorSeon Joo Park-
dc.contributor.authorJinyeong Kim-
dc.contributor.authorYejin Kim-
dc.contributor.authorKyung Ho Kim-
dc.contributor.authorJai Eun An-
dc.contributor.authorOh Seok Kwon-
dc.date.accessioned2022-07-21T07:51:43Z-
dc.date.available2022-07-21T07:51:43Z-
dc.date.issued2022-
dc.identifier.issn2196-5404-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/30070-
dc.description.abstractAdequate serotonin levels are pivotal to human well-being; thus, serotonin can be used as a biomarker because it regulates a wide range of physical and psychological functions. As an imbalance of serotonin is highly likely to initiate the pathogenesis of various disorders, monitoring serotonin levels in real time is in high demand for the early detection of disease. We fabricated a field-effect transistor (FET) biosensor based on aptamer-immobilized conducting polymer nanohybrids, which showed an instantaneous response toward serotonin in solution. The mechanism of serotonin detection was based on aptamer deformation after aptamer-ligand interaction and the consequential decrease in the charge carrier density of the FET template. Docking simulations with AutoDock/Vina and PyMOL were successfully used to investigate the binding site of serotonin in the loop structure of the aptamer. The fabricated FET template showed high sensitivity toward serotonin in the range of 10 fM to 100 nM, and the limit of detection (LOD) was exceptionally low at 10 fM. Moreover, the selectivity toward serotonin was confirmed by observing no signal after the injection of structural analogs, functional analogs and excess physiological biomolecules. The potential clinical application of this sensor was confirmed because it remained consistent when the buffer solution was exchanged for artificial serum or artificial cerebrospinal fluid (CSF). † S.G.L. and S.E.S. contributed equally to this work.-
dc.publisherSpringer-
dc.titleReal-time monitoring of serotonin with highly selective aptamer-functionalized conducting polymer nanohybrids-
dc.title.alternativeReal-time monitoring of serotonin with highly selective aptamer-functionalized conducting polymer nanohybrids-
dc.typeArticle-
dc.citation.titleNano Convergence-
dc.citation.number0-
dc.citation.endPage31-
dc.citation.startPage31-
dc.citation.volume9-
dc.contributor.affiliatedAuthorSeong Gi Lim-
dc.contributor.affiliatedAuthorSung Eun Seo-
dc.contributor.affiliatedAuthorSeon Joo Park-
dc.contributor.affiliatedAuthorJinyeong Kim-
dc.contributor.affiliatedAuthorYejin Kim-
dc.contributor.affiliatedAuthorKyung Ho Kim-
dc.contributor.affiliatedAuthorJai Eun An-
dc.contributor.affiliatedAuthorOh Seok Kwon-
dc.contributor.alternativeName임성지-
dc.contributor.alternativeName서성은-
dc.contributor.alternativeName박선주-
dc.contributor.alternativeName김진영-
dc.contributor.alternativeName김예진-
dc.contributor.alternativeName김경호-
dc.contributor.alternativeName안재은-
dc.contributor.alternativeName권오석-
dc.identifier.bibliographicCitationNano Convergence, vol. 9, pp. 31-31-
dc.identifier.doi10.1186/s40580-022-00325-7-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Infectious Disease Research Center > 1. Journal Articles
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