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Single-molecule DNA visualization using AT-specific red and non-specific green DNA-binding fluorescent proteins

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dc.contributor.authorPark, Jihyun-
dc.contributor.authorLee, Seonghyun-
dc.contributor.authorWon, Nabin-
dc.contributor.authorShin, Eunji-
dc.contributor.authorKim, Soo-Hyun-
dc.contributor.authorChun, Min-Young-
dc.contributor.authorGu, Jungyeun-
dc.contributor.authorJung, Gun-Young-
dc.contributor.authorLim, Kwang-Il-
dc.contributor.authorJo, Kyubong-
dc.date.available2021-02-22T06:46:06Z-
dc.date.issued2019-02-
dc.identifier.issn0003-2654-
dc.identifier.issn1364-5528-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/3835-
dc.description.abstractThe recent advances in the single cell genome analysis are generating a considerable amount of novel insights into complex biological systems. However, there are still technical challenges because each cell has a single copy of DNA to be amplified in most single cell genome analytical methods. In this paper, we present a novel approach to directly visualize a genomic map on a large DNA molecule instantly stained with red and green DNA-binding fluorescent proteins without DNA amplification. For this visualization, we constructed a few types of fluorescent protein-fused DNA-binding proteins: H-NS (histone-like nucleoid-structuring protein), DNA-binding domain of BRCA1 (breast cancer 1), high mobility group-1 (HMG), and lysine tryptophan (KW) repeat motif. Because H-NS and HMG preferentially bind A/T-rich regions, we combined A/T specific binder (H-NS-mCherry and HMG-mCherry as red color) and a non-specific complementary DNA binder (BRCA1-eGFP and 2(KW)(2)-eGFP repeat as green color) to produce a sequence-specific two-color DNA physical map for efficient optical identification of single DNA molecules.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleSingle-molecule DNA visualization using AT-specific red and non-specific green DNA-binding fluorescent proteins-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/c8an01426d-
dc.identifier.scopusid2-s2.0-85060618103-
dc.identifier.wosid000457394400013-
dc.identifier.bibliographicCitationANALYST, v.144, no.3, pp 921 - 927-
dc.citation.titleANALYST-
dc.citation.volume144-
dc.citation.number3-
dc.citation.startPage921-
dc.citation.endPage927-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.subject.keywordPlusNUCLEOTIDE-SEQUENCE-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusGENOME-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2019/AN/C8AN01426D#!divAbstract-
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