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Intracellular mRNA regulation with self-assembled locked nucleic acid polymer nanoparticles.

Journal of the American Chemical Society · 2014 · Vol. 136 (21) · pp. 7615-8

Abstract

We present an untemplated, single-component antisense oligonucleotide delivery system capable of regulating mRNA abundance in live human cells. While most approaches to nucleic acid delivery rely on secondary carriers and complex multicomponent charge-neutralizing formulations, we demonstrate efficient delivery using a simple locked nucleic acid (LNA)-polymer conjugate that assembles into spherical micellar nanoparticles displaying a dense shell of nucleic acid at the surface. Cellular uptake of soft LNA nanoparticles occurs rapidly within minutes as evidenced by flow cytometry and fluorescence microscopy. Importantly, these LNA nanoparticles knockdown survivin mRNA, an established target for cancer therapy, in a sequence-specific fashion as analyzed by RT-PCR.

Publication Types

["Journal Article", "Research Support, N.I.H., Extramural", "Research Support, Non-U.S. Gov't", "Research Support, U.S. Gov't, Non-P.H.S."]

Keywords

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MeSH Terms

["Flow Cytometry", "Gene Expression Regulation", "HeLa Cells", "Humans", "Nanoparticles", "Oligonucleotides", "Polymers", "RNA, Messenger"]

Funding

R01 HG004659 NHGRI NIH HHS (United States)
P30 CA023100 NCI NIH HHS (United States)
P30 NS047101 NINDS NIH HHS (United States)
R01 NS075449 NINDS NIH HHS (United States)
R21 DA036423 NIDA NIH HHS (United States)
DP2 OD008724 NIH HHS (United States)
R21DA036423 NIDA NIH HHS (United States)
P0 NS047101 NINDS NIH HHS (United States)
P30 NS076411 NINDS NIH HHS (United States)
1DP2OD008724 NIH HHS (United States)