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通过转铁蛋白受体内化途径实现平面 DNA 折纸结构的细胞内递送。

Intracellular Delivery of a Planar DNA Origami Structure by the Transferrin-Receptor Internalization Pathway.

机构信息

Department of Molecular Biology and Genetics, University of Aarhus, C. F. Møllers Allé 3, 8000, Aarhus C, Denmark.

Center for DNA Nanotechnology and Interdisciplinary Nanoscience Center (iNANO), University of Aarhus, Gustav Wieds Vej 14, 8000, Aarhus C, Denmark.

出版信息

Small. 2016 May;12(19):2634-40. doi: 10.1002/smll.201503934. Epub 2016 Mar 31.

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.

摘要

DNA 折纸术为功能化的纳米级结构提供了快速通道,使其成为开发明确的药物输送和传感器系统的诱人平台。DNA 纳米结构的细胞摄取率低是基于 DNA 的输送平台发展的主要障碍。本文通过用铁转运蛋白转铁蛋白(Tf)修饰平面 DNA 折纸结构,证明了在已建立的癌细胞系中细胞摄取率显著增加。使用 DNA 定向、位点选择性标记技术将可变数量的 Tf 分子偶联到折纸结构上,以保持配体的功能。共聚焦荧光显微镜和定量(qPCR)技术的组合表明,与未修饰的结构相比,细胞质摄取增加了 22 倍,并且效率与折纸表面上转铁蛋白分子的数量相关。

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