Volgenau School of Engineering, Department of Bioengineering, George Mason University, Fairfax, VA 22030, USA.
Institute for Advanced Biomedical Research, George Mason University, Manassas, VA 20110, USA.
Molecules. 2020 Jul 26;25(15):3386. doi: 10.3390/molecules25153386.
DNA origami nanocarriers have emerged as a promising tool for many biomedical applications, such as biosensing, targeted drug delivery, and cancer immunotherapy. These highly programmable nanoarchitectures are assembled into any shape or size with nanoscale precision by folding a single-stranded DNA scaffold with short complementary oligonucleotides. The standard scaffold strand used to fold DNA origami nanocarriers is usually the M13mp18 bacteriophage's circular single-stranded DNA genome with limited design flexibility in terms of the sequence and size of the final objects. However, with the recent progress in automated DNA origami design-allowing for increasing structural complexity-and the growing number of applications, the need for scalable methods to produce custom scaffolds has become crucial to overcome the limitations of traditional methods for scaffold production. Improved scaffold synthesis strategies will help to broaden the use of DNA origami for more biomedical applications. To this end, several techniques have been developed in recent years for the scalable synthesis of single stranded DNA scaffolds with custom lengths and sequences. This review focuses on these methods and the progress that has been made to address the challenges confronting custom scaffold production for large-scale DNA origami assembly.
DNA 折纸纳米载体已成为许多生物医学应用的有前途的工具,例如生物传感、靶向药物输送和癌症免疫治疗。这些高度可编程的纳米结构可以通过用短互补寡核苷酸折叠单链 DNA 支架以纳米级精度组装成任何形状或大小。用于折叠 DNA 折纸纳米载体的标准支架链通常是 M13mp18 噬菌体的圆形单链 DNA 基因组,其在最终对象的序列和大小方面的设计灵活性有限。然而,随着自动化 DNA 折纸设计的最新进展(允许增加结构复杂性)和应用数量的增加,需要可扩展的方法来生产定制支架,以克服传统支架生产方法的局限性。改进的支架合成策略将有助于拓宽 DNA 折纸在更多生物医学应用中的使用。为此,近年来已经开发了几种技术来可扩展地合成具有自定义长度和序列的单链 DNA 支架。这篇综述重点介绍了这些方法以及为解决大规模 DNA 折纸组装的定制支架生产所面临的挑战而取得的进展。