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Proteolytic disassembly of peptide-mediated graphene oxide assemblies for turn-on fluorescence sensing of proteases

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dc.contributor.authorYang, Jin-Kyoung-
dc.contributor.authorKwak, Seon-Yeong-
dc.contributor.authorJeon, Su-Ji-
dc.contributor.authorLee, Eunjin-
dc.contributor.authorJu, Jong-Min-
dc.contributor.authorKim, Hye-In-
dc.contributor.authorLee, Yoon-Sik-
dc.contributor.authorKim, Jong-Ho-
dc.date.accessioned2021-06-22T18:23:01Z-
dc.date.available2021-06-22T18:23:01Z-
dc.date.created2021-01-21-
dc.date.issued2016-05-
dc.identifier.issn2040-3364-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/16028-
dc.description.abstractMolecule-induced assembly of nanomaterials can alter their unique chemical and physical properties, which can be a promising approach for sensing. Herein, we demonstrate an optical 'turn-on' biosensor for the detection of matrix metalloproteinase-2 (MMP-2), fabricated by means of a peptide-induced assembly of fluorescent graphene oxide (GO). Functionalization of GO with a peptide substrate for MMP-2 bearing a thiol group leads to its self-assembly via disulfide bonding, accompanied by self-quenching of GO's strong fluorescence. This peptide-induced GO assembly is then disassembled by proteolytic cleavage in the presence of MMP-2, thereby restoring the level of self-quenched GO fluorescence. With this approach, we are able to detect MMP-2 and to investigate the kinetic parameters of MMP-2 activity. The GO-peptide assembly is successfully applied to the selective and sensitive detection of MMP-2 secreted by living cells, human hepatocytes HepG2, at a concentration of 2 ng mL(-1).-
dc.language영어-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.titleProteolytic disassembly of peptide-mediated graphene oxide assemblies for turn-on fluorescence sensing of proteases-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jong-Ho-
dc.identifier.doi10.1039/c6nr02815b-
dc.identifier.scopusid2-s2.0-84975462036-
dc.identifier.wosid000378244900021-
dc.identifier.bibliographicCitationNanoscale, v.8, no.24, pp.12272 - 12281-
dc.relation.isPartOfNanoscale-
dc.citation.titleNanoscale-
dc.citation.volume8-
dc.citation.number24-
dc.citation.startPage12272-
dc.citation.endPage12281-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.subject.keywordPlusRESONANCE ENERGY-TRANSFER-
dc.subject.keywordPlusHIGHLY SENSITIVE DETECTION-
dc.subject.keywordPlusMATRIX METALLOPROTEINASES-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusOPTICAL-DETECTION-
dc.subject.keywordPlusSENSOR-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusGELATINASE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusBIOSENSOR-
dc.subject.keywordAuthorRESONANCE ENERGY-TRANSFER-
dc.subject.keywordAuthorHIGHLY SENSITIVE DETECTION-
dc.subject.keywordAuthorMATRIX METALLOPROTEINASE-2-
dc.subject.keywordAuthorIN-VIVO-
dc.subject.keywordAuthorOPTICAL-DETECTION-
dc.subject.keywordAuthorCARCINOMA CELLS-
dc.subject.keywordAuthorQUANTUM DOTS-
dc.subject.keywordAuthorBIOSENSOR-
dc.subject.keywordAuthorSENSOR-
dc.subject.keywordAuthorPROBE-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2016/NR/C6NR02815B-
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ERICA 공학대학 (DEPARTMENT OF MATERIALS SCIENCE AND CHEMICAL ENGINEERING)
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