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Virus-Inspired Membrane Encapsulation of DNA Nanostructures To Achieve In Vivo Stability

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Wyss Institute for Biologically Inspired Engineering and Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, United States,
§ Department of Cancer Biology, Dana Farber Cancer Institute, Boston, Massachusetts 02115, United States
*Address correspondence to [email protected]
Cite this: ACS Nano 2014, 8, 5, 5132–5140
Publication Date (Web):April 2, 2014
https://doi.org/10.1021/nn5011914
Copyright © 2014 American Chemical Society
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Abstract

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DNA nanotechnology enables engineering of molecular-scale devices with exquisite control over geometry and site-specific functionalization. This capability promises compelling advantages in advancing nanomedicine; nevertheless, instability in biological environments and innate immune activation remain as obstacles for in vivo application. Natural particle systems (i.e., viruses) have evolved mechanisms to maintain structural integrity and avoid immune recognition during infection, including encapsulation of their genome and protein capsid shell in a lipid envelope. Here we introduce virus-inspired enveloped DNA nanostructures as a design strategy for biomedical applications. Achieving a high yield of tightly wrapped unilamellar nanostructures, mimicking the morphology of enveloped virus particles, required precise control over the density of attached lipid conjugates and was achieved at 1 per ∼180 nm2. Envelopment of DNA nanostructures in PEGylated lipid bilayers conferred protection against nuclease digestion. Immune activation was decreased 2 orders of magnitude below controls, and pharmacokinetic bioavailability improved by a factor of 17. By establishing a design strategy suitable for biomedical applications, we have provided a platform for the engineering of sophisticated, translation-ready DNA nanodevices.

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Methods, additional data, and a nanostructure design schematic and oligonucleotide sequences are available as Supporting Information. This material is available free of charge via the Internet at http://pubs.acs.org.

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