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C-terminal de novo sequencing of peptides using oxazolone-based derivatization with bromine signature

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dc.contributor.authorKim, Jong-Seo-
dc.contributor.authorShin, Mansup-
dc.contributor.authorSong, Jin-Su-
dc.contributor.authorAn, Songhie-
dc.contributor.authorKim, Hie-Joon-
dc.date.accessioned2024-05-14T06:49:25Z-
dc.date.available2024-05-14T06:49:25Z-
dc.date.created2021-11-03-
dc.date.issued2011-12-
dc.identifier.citationAnalytical Biochemistry, Vol.419 No.2, pp.211-216-
dc.identifier.issn0003-2697-
dc.identifier.urihttps://hdl.handle.net/10371/201903-
dc.description.abstractDue to almost identical chemical properties of C-terminal and side-chain carboxylic groups, selective C-terminal derivatization has been difficult. Although oxazolone-based C-terminal derivatization is the only selective C-terminal modification available, it has not been used widely because of its low derivatization efficiency. In this paper, an improved oxazolone chemistry for incorporation of Br signature to C-terminus is reported. MS/MS analysis of the brominated peptides led to a series of y ions with Br signature, facilitating de novo C-terminal sequencing. (C) 2011 Elsevier Inc. All rights reserved.-
dc.language영어-
dc.publisherAcademic Press-
dc.titleC-terminal de novo sequencing of peptides using oxazolone-based derivatization with bromine signature-
dc.typeArticle-
dc.identifier.doi10.1016/j.ab.2011.08.011-
dc.citation.journaltitleAnalytical Biochemistry-
dc.identifier.wosid000296119400021-
dc.identifier.scopusid2-s2.0-80054063140-
dc.citation.endpage216-
dc.citation.number2-
dc.citation.startpage211-
dc.citation.volume419-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorKim, Jong-Seo-
dc.contributor.affiliatedAuthorKim, Hie-Joon-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusDESORPTION/IONIZATION MASS-SPECTROMETRY-
dc.subject.keywordPlusPROTEIN N-TERMINI-
dc.subject.keywordPlusACETIC-ANHYDRIDE-
dc.subject.keywordPlusCYANOGEN-BROMIDE-
dc.subject.keywordPlusCLEAVAGE SITES-
dc.subject.keywordPlusPROTEOMIC ERA-
dc.subject.keywordPlusSULFONATION-
dc.subject.keywordPlusFRAGMENTS-
dc.subject.keywordPlusACID-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordAuthorBr signature-
dc.subject.keywordAuthorDe novo sequencing-
dc.subject.keywordAuthorC-terminal-
dc.subject.keywordAuthorDerivatization-
dc.subject.keywordAuthorOxazolone-
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  • College of Natural Sciences
  • School of Biological Sciences
Research Area Molecular Interactomics, Proteomics, Systems Biology, 단백체학, 분자상호작용체학, 시스템생물학

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