Oncotarget

Research Papers:

Isothermal approach to assemble spatial DNA nanotubes for drug delivery

Xiaolong Shi _, Haiyan Zhao, Xin Li and Tao Song

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DOI pending

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Abstract

Xiaolong Shi1, Haiyan Zhao1, Xin Li2 and Tao Song3,4

1Key Laboratory of Image Information Processing and Intelligent Control, School of Automation, Huazhong University of Science and Technology, Wuhan 430074, Hubei, China

2Department of Gynecology 2, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei, China

3College of Computer and Communication Engineering, China University of Petroleum, Qingdao 266580, Shandong, China

4Departamento de Inteligencia Artificial, Universidad Politécnica de Madrid, Campus de Montegancedo, Boadilla del Monte 28660, Madrid, Spain

Correspondence to:

Tao Song, email: [email protected], [email protected]

Keywords: DNA nanotechnology; DNA origami; DNA nanotube; drug cargo

Received: October 09, 2017     Accepted: November 13, 2017     Published: January 04, 2018

ABSTRACT

DNA Nanostructures assembled from artificial single stranded DNA provided an engineering method to fabricate highly biocompatible spatial objects, which have potentials applications as drug delivery vehicles and templates for the patterning of biological molecules as biosensor for active hepatic targeting drug delivery. Most DNA nanostructures are constructed by annealing process, which means some thermal sensitive drugs and biosensors made from peptides or proteins in the structure will be denatured during fabrication. Fabrication of DNA nanostructure under isothermal condition remains challenging. Herein we report a simple and cost-effective method to form DNA nanotubes in the presence of urea with only two single-stranded tiles (SST) at room temperature. The constructed DNA nanotubes were observed and analyzed by atomic force microscopy (AFM). Experimental results show the feasibility and stability of our method. This method avoids traditional annealing procedure and will provide possibility to further assembly nano-scale structures in vivo.


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