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Intracellular mRNA Regulation with Self-Assembled Locked Nucleic Acid Polymer Nanoparticles

[Image: see text] 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...

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Detalles Bibliográficos
Autores principales: Rush, Anthony M., Nelles, David A., Blum, Angela P., Barnhill, Sarah A., Tatro, Erick T., Yeo, Gene W., Gianneschi, Nathan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046771/
https://www.ncbi.nlm.nih.gov/pubmed/24827740
http://dx.doi.org/10.1021/ja503598z
Descripción
Sumario:[Image: see text] 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.