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Detection of Nα-terminally formylated native proteins by a pan-N-formyl methionine-specific antibody

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dc.contributor.authorKim, Dasom-
dc.contributor.authorSeok, Ok-Hee-
dc.contributor.authorJu, Shinyeong-
dc.contributor.authorKim, Sang-Yoon-
dc.contributor.authorKim, Jeong-Mok-
dc.contributor.authorLee, Cheolju-
dc.contributor.authorHwang, Cheol-Sang-
dc.date.accessioned2023-10-10T03:05:42Z-
dc.date.available2023-10-10T03:05:42Z-
dc.date.created2023-05-03-
dc.date.issued2023-05-
dc.identifier.issn0021-9258-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/192037-
dc.description.abstractN-formyl methionine (fMet)-containing proteins are produced in bacteria, eukaryotic organelles mitochondria and plastids, and even in cytosol. However, Nα-terminally formylated proteins have been poorly characterized because of the lack of appropriate tools to detect fMet independently of downstream proximal sequences. Using a fMet-Gly-Ser-Gly-Cys peptide as an antigen, we generated a pan-fMet-specific rabbit polyclonal antibody called anti-fMet. The raised anti-fMet recognized universally and sequence context–independently Nt-formylated proteins in bacterial, yeast, and human cells as determined by a peptide spot array, dot blotting, and immunoblotting. We anticipate that the anti-fMet antibody will be broadly used to enable an understanding of the poorly explored functions and mechanisms of Nt-formylated proteins in various organisms.-
dc.language영어-
dc.language.isoen-
dc.publisherAmerican Society for Biochemistry and Molecular Biology Inc.-
dc.titleDetection of Nα-terminally formylated native proteins by a pan-N-formyl methionine-specific antibody-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jeong-Mok-
dc.identifier.doi10.1016/j.jbc.2023.104652-
dc.identifier.scopusid2-s2.0-85153089298-
dc.identifier.wosid001009526700001-
dc.identifier.bibliographicCitationJournal of Biological Chemistry, v.299, no.5, pp.1 - 11-
dc.relation.isPartOfJournal of Biological Chemistry-
dc.citation.titleJournal of Biological Chemistry-
dc.citation.volume299-
dc.citation.number5-
dc.citation.startPage1-
dc.citation.endPage11-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.subject.keywordPlusPEPTIDE DEFORMYLASE-
dc.subject.keywordPlusTRANSFER-RNA-
dc.subject.keywordPlusSOLUBLE-RNA-
dc.subject.keywordPlusRECEPTORS-
dc.subject.keywordPlusINITIATOR-
dc.subject.keywordPlusFORMYLTRANSFERASE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusRIBOSOME-
dc.subject.keywordPlusPLATFORM-
dc.subject.keywordAuthoranti-fMet antibody-
dc.subject.keywordAuthorfMet/N-degron-
dc.subject.keywordAuthormitochondrial methionyl-tRNA formyltransferase-
dc.subject.keywordAuthorN-formyl methionine-
dc.subject.keywordAuthorpeptide deformylase-
dc.subject.keywordAuthorprotein synthesis-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0021925823002946?via%3Dihub-
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