Packaging DNA origami into viral protein cages

dc.contributorAalto-yliopistofi
dc.contributorAalto Universityen
dc.contributor.authorLinko, Veikkoen_US
dc.contributor.authorMikkilä, Joonaen_US
dc.contributor.authorKostiainen, Mauri A.en_US
dc.contributor.departmentDepartment of Bioproducts and Biosystemsen
dc.contributor.editorWege, Christinaen_US
dc.contributor.editorLomonossoff, George P.en_US
dc.contributor.groupauthorBiohybrid Materialsen
dc.date.accessioned2019-05-06T09:26:22Z
dc.date.available2019-05-06T09:26:22Z
dc.date.embargoinfo:eu-repo/date/embargoEnd/2019-01-02en_US
dc.date.issued2018-01-01en_US
dc.description.abstractThe DNA origami technique is a widely used method to create customized, complex, spatially well-defined two-dimensional (2D) and three-dimensional (3D) DNA nanostructures. These structures have huge potential to serve as smart drug-delivery vehicles and molecular devices in various nanomedical and biotechnological applications. However, so far only little is known about the behavior of these novel structures in living organisms or in cell culture/tissue models. Moreover, enhancing pharmacokinetic bioavailability and transfection properties of such structures still remains a challenge. One intriguing approach to overcome these issues is to coat DNA origami nanostructures with proteins or lipid membranes. Here, we show how cowpea chlorotic mottle virus (CCMV) capsid proteins (CPs) can be used for coating DNA origami nanostructures. We present a method for disassembling native CCMV particles and isolating the pure CP dimers, which can further bind and encapsulate a rectangular DNA origami shape. Owing to the highly programmable nature of DNA origami, packaging of DNA nanostructures into viral protein cages could find imminent uses in enhanced targeting and cellular delivery of various active nano-objects, such as enzymes and drug molecules.en
dc.description.versionPeer revieweden
dc.format.extent11
dc.format.extent267-277
dc.format.mimetypeapplication/pdfen_US
dc.identifier.citationLinko, V, Mikkilä, J & Kostiainen, M A 2018, Packaging DNA origami into viral protein cages . in C Wege & G P Lomonossoff (eds), Virus-Derived Nanoparticles for Advanced Technologies . vol. 1776, Methods in Molecular Biology, vol. 1776, Springer, pp. 267-277 . https://doi.org/10.1007/978-1-4939-7808-3_18en
dc.identifier.doi10.1007/978-1-4939-7808-3_18en_US
dc.identifier.isbn978-1-4939-7806-9
dc.identifier.isbn978-1-4939-7808-3
dc.identifier.issn1064-3745
dc.identifier.otherPURE UUID: eaf5dce7-8956-40dc-a2c1-d38b8af89aefen_US
dc.identifier.otherPURE ITEMURL: https://research.aalto.fi/en/publications/eaf5dce7-8956-40dc-a2c1-d38b8af89aefen_US
dc.identifier.otherPURE LINK: http://www.scopus.com/inward/record.url?scp=85048227687&partnerID=8YFLogxKen_US
dc.identifier.otherPURE FILEURL: https://research.aalto.fi/files/32914370/CHEM_Linko_et_al_OrigamiVirus_2018_Methods_in_Molecular_Biology.pdfen_US
dc.identifier.urihttps://aaltodoc.aalto.fi/handle/123456789/37796
dc.identifier.urnURN:NBN:fi:aalto-201905062914
dc.language.isoenen
dc.relation.ispartofseriesVirus-Derived Nanoparticles for Advanced Technologiesen
dc.relation.ispartofseriesVolume 1776en
dc.relation.ispartofseriesMethods in Molecular Biologyen
dc.rightsopenAccessen
dc.subject.keywordCCMVen_US
dc.subject.keywordDNA nanotechnologyen_US
dc.subject.keywordDNA origamien_US
dc.subject.keywordElectrostatic assemblyen_US
dc.subject.keywordNucleic acidsen_US
dc.subject.keywordSelf-assemblyen_US
dc.subject.keywordVirus capsid proteinen_US
dc.titlePackaging DNA origami into viral protein cagesen
dc.typeA3 Kirjan tai muun kokoomateoksen osafi
dc.type.versionacceptedVersion

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