Lipid nanoparticle-mediated CRISPR-Cas13a delivery for the control of bacterial infection

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dc.contributor.authorBookun Kim-
dc.contributor.authorHwi Won Seo-
dc.contributor.authorK Lee-
dc.contributor.authorD Yong-
dc.contributor.authorY K Park-
dc.contributor.authorYujin Lee-
dc.contributor.authorSolip Lee-
dc.contributor.authorDo Wan Kim-
dc.contributor.authorDajeong Kim-
dc.contributor.authorChoong-Min Ryu-
dc.date.accessioned2025-03-18T16:32:30Z-
dc.date.available2025-03-18T16:32:30Z-
dc.date.issued2025-
dc.identifier.issn2192-2640-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/37352-
dc.description.abstractLipid nanoparticles (LNPs) can assist in the delivery of nucleic acid inside animal cells, as demonstrated by their use in COVID-19 vaccine development. However, LNPs applicable to bacteria have not been reported. Here, the screening of 511 LNPs containing random combinations of different lipid components identified two LNPs, LNP 496 and LNP 470, that efficiently delivered plasmids into Escherichia coli BW25113. Since Gram-negative bacteria have lipid bilayers, the bacteria are pretreated with LNP-helper that weakens the bacterial membrane. The cationic lipid DOTAP improved delivery of LNP-encapsulated plasmid DNA when present at a molar ratio of 10?25 mol% in the LNP. LNP encapsulation of the Cas13a/gRNA expression vector controlled infection by a clinical Escherichia strain in Galleria mellonela larvae and mouse infection models when used in combination with non-cytotoxic concentrations of polymyxin B, a bacterial membrane disruptor. Together, the results show that LNPs can be useful as a delivery platform for agents that counteract pathogenic bacterial infections.-
dc.publisherWiley-
dc.titleLipid nanoparticle-mediated CRISPR-Cas13a delivery for the control of bacterial infection-
dc.title.alternativeLipid nanoparticle-mediated CRISPR-Cas13a delivery for the control of bacterial infection-
dc.typeArticle-
dc.citation.titleAdvanced Healthcare Materials-
dc.citation.number7-
dc.citation.endPage2403281-
dc.citation.startPage2403281-
dc.citation.volume14-
dc.contributor.affiliatedAuthorBookun Kim-
dc.contributor.affiliatedAuthorHwi Won Seo-
dc.contributor.affiliatedAuthorYujin Lee-
dc.contributor.affiliatedAuthorSolip Lee-
dc.contributor.affiliatedAuthorDo Wan Kim-
dc.contributor.affiliatedAuthorDajeong Kim-
dc.contributor.affiliatedAuthorChoong-Min Ryu-
dc.contributor.alternativeName김부건-
dc.contributor.alternativeName서휘원-
dc.contributor.alternativeName이규리-
dc.contributor.alternativeName용동은-
dc.contributor.alternativeName박윤경-
dc.contributor.alternativeName이유진-
dc.contributor.alternativeName이소립-
dc.contributor.alternativeName김도완-
dc.contributor.alternativeName김다정-
dc.contributor.alternativeName류충민-
dc.identifier.bibliographicCitationAdvanced Healthcare Materials, vol. 14, no. 7, pp. 2403281-2403281-
dc.identifier.doi10.1002/adhm.202403281-
dc.description.journalClassY-
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Division of Research on National Challenges > Infectious Disease Research Center > 1. Journal Articles
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