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Cited 47 time in webofscience Cited 52 time in scopus
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dc.contributor.authorAyyadurai, N-
dc.contributor.authorPrabhu, NS-
dc.contributor.authorDeepankumar, K-
dc.contributor.authorJang, YJ-
dc.contributor.authorChitrapriya, N-
dc.contributor.authorSong, E-
dc.contributor.authorLee, N-
dc.contributor.authorKim, SK-
dc.contributor.authorKim, BG-
dc.contributor.authorSoundrarajan, N-
dc.contributor.authorLee, S-
dc.contributor.authorCha, HJ-
dc.contributor.authorBudisa, N-
dc.contributor.authorYun, H-
dc.date.accessioned2016-03-31T09:39:26Z-
dc.date.available2016-03-31T09:39:26Z-
dc.date.created2011-06-07-
dc.date.issued2011-04-
dc.identifier.issn1043-1802-
dc.identifier.other2011-OAK-0000023604-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/17447-
dc.description.abstractWe describe the simple bioconjugation strategy in combination of periodate chemistry and unnatural amino acid incorporation. The residue specific incorporation of 3,4-dihydroxy-L-phenylalanine can alter the properties of protein to conjugate into the polymers. The homogeneously modified protein will yield quinone residues that are covalently conjugated to nucleophilic groups of the amino polysaccharide. This novel approach holds great promise for widespread use to prepare protein conjugates and synthetic biology applications.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.relation.isPartOfBIOCONJUGATE CHEMISTRY-
dc.subjectIN-VIVO-
dc.subjectCHEMISTRY-
dc.subjectVACCINES-
dc.subjectBIOLOGY-
dc.subjectCELLS-
dc.titleBioconjugation of L-3,4-Dihydroxyphenylalanine Containing Protein with a Polysaccharide-
dc.typeArticle-
dc.contributor.college화학공학과-
dc.identifier.doi10.1021/BC2000066-
dc.author.googleAyyadurai, N-
dc.author.googlePrabhu, NS-
dc.author.googleDeepankumar, K-
dc.author.googleJang, YJ-
dc.author.googleChitrapriya, N-
dc.author.googleSong, E-
dc.author.googleLee, N-
dc.author.googleKim, SK-
dc.author.googleKim, BG-
dc.author.googleSoundrarajan, N-
dc.author.googleLee, S-
dc.author.googleCha, HJ-
dc.author.googleBudisa, N-
dc.author.googleYun, H-
dc.relation.volume22-
dc.relation.issue4-
dc.relation.startpage551-
dc.relation.lastpage555-
dc.contributor.id10057405-
dc.relation.journalBIOCONJUGATE CHEMISTRY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOCONJUGATE CHEMISTRY, v.22, no.4, pp.551 - 555-
dc.identifier.wosid000289613400006-
dc.date.tcdate2019-01-01-
dc.citation.endPage555-
dc.citation.number4-
dc.citation.startPage551-
dc.citation.titleBIOCONJUGATE CHEMISTRY-
dc.citation.volume22-
dc.contributor.affiliatedAuthorCha, HJ-
dc.identifier.scopusid2-s2.0-79954999145-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc26-
dc.description.scptc25*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-

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차형준CHA, HYUNG JOON
Dept. of Chemical Enginrg
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