Facile analysis of protein-protein interactions in living cells by enriched visualization of the p-body = p-body를 활용한 손쉬운 세포기반 protein-protein interaction 평가법

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dc.contributor.authorMiri Choi-
dc.contributor.authorJiyeon Baek-
dc.contributor.authorS B Han-
dc.contributor.authorSungchan Cho-
dc.date.accessioned2019-01-23T16:30:27Z-
dc.date.available2019-01-23T16:30:27Z-
dc.date.issued2018-
dc.identifier.issn1225-8687-
dc.identifier.uri10.5483/BMBRep.2018.51.10.051ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/18159-
dc.description.abstractProtein-Protein Interactions (PPIs) play essential roles in diverse biological processes and their misregulations are associated with a wide range of diseases. Especially, the growing attention to PPIs as a new class of therapeutic target is increasing the need for an efficient method of cell-based PPI analysis. Thus, we newly developed a robust PPI assay (SeePPI) based on the co-translocation of interacting proteins to the discrete subcellular compartment 'processing body' (p-body) inside living cells, enabling a facile analysis of PPI by the enriched fluorescent signal. The feasibility and strength of SeePPI (Signal enhancement exclusively on P-body for Protein-protein Interaction) assay was firmly demonstrated with FKBP12/FRB interaction induced by rapamycin within seconds in real-time analysis of living cells, indicating its recapitulation of physiological PPI dynamics. In addition, we applied p53/MDM2 interaction and its dissociation by Nutlin-3 to SeePPI assay and further confirmed that SeePPI was quantitative and well reflected the endogenous PPI. Our SeePPI assay will provide another useful tool to achieve an efficient analysis of PPIs and their modulators in cells.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleFacile analysis of protein-protein interactions in living cells by enriched visualization of the p-body = p-body를 활용한 손쉬운 세포기반 protein-protein interaction 평가법-
dc.title.alternativeFacile analysis of protein-protein interactions in living cells by enriched visualization of the p-body-
dc.typeArticle-
dc.citation.titleBMB Reports-
dc.citation.number10-
dc.citation.endPage531-
dc.citation.startPage526-
dc.citation.volume51-
dc.contributor.affiliatedAuthorMiri Choi-
dc.contributor.affiliatedAuthorJiyeon Baek-
dc.contributor.affiliatedAuthorSungchan Cho-
dc.contributor.alternativeName최미리-
dc.contributor.alternativeName백지연-
dc.contributor.alternativeName한상배-
dc.contributor.alternativeName조성찬-
dc.identifier.bibliographicCitationBMB Reports, vol. 51, no. 10, pp. 526-531-
dc.identifier.doi10.5483/BMBRep.2018.51.10.051-
dc.subject.keywordP-body-
dc.subject.keywordPPI modulator-
dc.subject.keywordProtein-Protein interaction-
dc.subject.keywordTranslocation-based PPI assay-
dc.subject.localP-body-
dc.subject.localPPI modulator-
dc.subject.localProtein-protein interaction-
dc.subject.localProteinprotein interactions-
dc.subject.localProtein-Protein Interaction-
dc.subject.localProtein-Protein interaction-
dc.subject.localprotein-protein interaction-
dc.subject.localProtein-protein interactions-
dc.subject.localTranslocation-based PPI assay-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Nucleic Acid Therapeutics Research Center > 1. Journal Articles
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