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dc.contributor.authorKim, Kyung Rim-
dc.contributor.authorAhn, Keum-Young-
dc.contributor.authorPark, Jin-Seung-
dc.contributor.authorLee, Kyung Eun-
dc.contributor.authorJeon, Hyesung-
dc.contributor.authorLee, Jeewon-
dc.date.accessioned2024-01-20T17:02:48Z-
dc.date.available2024-01-20T17:02:48Z-
dc.date.created2021-09-02-
dc.date.issued2011-05-06-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/130359-
dc.description.abstractProtein nanoparticles (PNPs) that are nanostructured biomaterials with intrinsic biological function have been widely employed as three-dimensional nanobiomaterials for sensitive bioassays, MRI contrast, semiconductor devices, template for hybrid materials, etc., and stable and long-term maintenance of PNPs seems to be of crucial importance. We evaluated the stability of PNPs and the efficacy of lyophilization for the long-term stability of PNPs, especially using green fluorescent protein nanoparticles (gFPNPs) as a model PNP. Fluorescence intensities and TEM images of gFPNPs were analyzed to monitor their functional and structural stabilities. Unlike the green fluorescent protein monomers (eGFP) that were gradually inactivated in aqueous solution, gFPNP in the same aqueous solution retained the initial fluorescence activity and spherical nanoparticle structure even for 2 weeks at 4 degrees C. To ensure stable and long-term maintenance of gFPNPs, gFPNPs in aqueous solution were converted to the dried solid forms through lyophilization. It is notable that fluorescence activity and nanoparticle structure of gFPNPs that were lyophilized with both Tween 80 and sucrose were very stably maintained even for 10 weeks at various storage temperatures (-20 degrees C, 4 degrees C, 25 degrees C, and 37 degrees C). During the period of 10 weeks, the fluorescence of gFPNP was always more than 80% level of initial fluorescence at a wide range of temperature. Although this stability study was focused on gFPNPs, the developed optimal lyophilization conditions for gFPNPs can be applied in general to stable and long-term maintenance of many other PNP-derived biomaterials. (C) 2011 Published by Elsevier Inc.-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectFERRITIN-
dc.subjectDENATURATION-
dc.subjectARRAY-
dc.subjectCAGE-
dc.titleLyophilization and enhanced stability of fluorescent protein nanoparticles-
dc.typeArticle-
dc.identifier.doi10.1016/j.bbrc.2011.03.123-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.408, no.2, pp.225 - 229-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume408-
dc.citation.number2-
dc.citation.startPage225-
dc.citation.endPage229-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000290606200006-
dc.identifier.scopusid2-s2.0-79955663272-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.type.docTypeArticle-
dc.subject.keywordPlusFERRITIN-
dc.subject.keywordPlusDENATURATION-
dc.subject.keywordPlusARRAY-
dc.subject.keywordPlusCAGE-
dc.subject.keywordAuthorFluorescent protein nanoparticles-
dc.subject.keywordAuthorLyophilization-
dc.subject.keywordAuthorStability-
dc.subject.keywordAuthorProtein nanoparticle structure-
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KIST Article > 2011
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