| Literature DB >> 27032044 |
David H Schaffert1,2, Anders H Okholm1,2, Rasmus S Sørensen1,2, Jesper S Nielsen1,2, Thomas Tørring2,3, Christian B Rosen2,3, Anne Louise B Kodal2,3, Michael R Mortensen2,3, Kurt V Gothelf2,3, Jørgen Kjems1,2.
Abstract
DNA origami provides rapid access to easily functionalized, nanometer-sized structures making it an intriguing platform for the development of defined drug delivery and sensor systems. Low cellular uptake of DNA nanostructures is a major obstacle in the development of DNA-based delivery platforms. Herein, significant strong increase in cellular uptake in an established cancer cell line by modifying a planar DNA origami structure with the iron transport protein transferrin (Tf) is demonstrated. A variable number of Tf molecules are coupled to the origami structure using a DNA-directed, site-selective labeling technique to retain ligand functionality. A combination of confocal fluorescence microscopy and quantitative (qPCR) techniques shows up to 22-fold increased cytoplasmic uptake compared to unmodified structures and with an efficiency that correlates to the number of transferrin molecules on the origami surface.Entities:
Keywords: DNA origami; cell uptake; drug delivery; nanoparticles; transferrin
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Year: 2016 PMID: 27032044 DOI: 10.1002/smll.201503934
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281