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Spot arrays on modified glass surfaces for efficient SPOT synthesis and on-chip bioassay of peptides

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dc.contributor.authorKim, DH-
dc.contributor.authorShin, DS-
dc.contributor.authorLee, YS-
dc.date.accessioned2022-04-19T11:07:12Z-
dc.date.available2022-04-19T11:07:12Z-
dc.date.issued2007-10-
dc.identifier.issn1075-2617-
dc.identifier.issn1099-1387-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/148350-
dc.description.abstractTo make SPOT synthesis of peptides and their assays on glass surfaces more convenient, a simple method for making spot arrays on a slide glass was designed through patterning with a photoresist and perfluorination followed by amination with various silane compounds and polymers. With these spot-arrayed glass surfaces, we could measure the coupling completion of each Fmoc amino acid on the glass surface by direct fluorescence analysis after fluorescence-labeling the amino groups on the surface of each spot. Then we synthesized several types of decapeptides and HPQ-pentapeptides on the spot-arrayed glasses and identified the optimal surface condition for stepwise peptide coupling and on-chip bioassay. After optimizing the surface conditions, we synthesized a model library of biotin-Gly-Ala-P-1-Gly (P-1: one of 19 amino acids) and successfully replicated the well-known a-chymotrypsin subsite specificities through Cy5-streptavidin binding to the remaining biotin on the surface after the enzymatic digestion. Copyright (C) 2007 European Peptide Society and John Wiley & Sons, Ltd.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherJOHN WILEY & SONS LTD-
dc.titleSpot arrays on modified glass surfaces for efficient SPOT synthesis and on-chip bioassay of peptides-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1002/psc.884-
dc.identifier.scopusid2-s2.0-35348917245-
dc.identifier.wosid000250348600001-
dc.identifier.bibliographicCitationJOURNAL OF PEPTIDE SCIENCE, v.13, no.10, pp 625 - 633-
dc.citation.titleJOURNAL OF PEPTIDE SCIENCE-
dc.citation.volume13-
dc.citation.number10-
dc.citation.startPage625-
dc.citation.endPage633-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/psc.884-
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