Faiad Sinan, Laurent Quentin, Asohan Jathavan, Brown Tyler, Prinzen Alexander, Sleiman Hanadi Farouk
Department of Chemistry McGill University 801 Sherbrooke St West Montreal Québec H3A 0B8 Canada.
Small Sci. 2024 Dec 12;5(4):2400471. doi: 10.1002/smsc.202400471. eCollection 2025 Apr.
The development of DNA nanotechnology has enabled the creation of diverse nanomaterials with significant potential in biological applications, such as sensing or drug delivery. From DNA origami to wireframe nanostructures, several strategies have been developed to deliver nucleic acid therapeutics into cells. However, these self-assembled structures suffer from poor stability in biological media due to low concentrations of divalent cations, degradation by nucleases, and thermal denaturation. Herein, a site-specific crosslinking method based on thiol-disulfide exchange to stabilize a wireframe DNA nanocube is developed. With nearly quantitative crosslinking yields, the structure retains its structural integrity in conditions that mimic physiological environments. This results in improved cellular uptake, likely due to more favorable interaction with cell-surface scavenger receptors, followed by endocytosis. This study paves the way for in vivo applications of DNA wireframe nanostructures by removing one of the major bottlenecks for their translation from in vitro to preclinical work.
DNA纳米技术的发展使得能够创建各种在生物应用中具有巨大潜力的纳米材料,如传感或药物递送。从DNA折纸到线框纳米结构,已经开发了几种策略将核酸治疗剂递送至细胞中。然而,由于二价阳离子浓度低、核酸酶降解和热变性,这些自组装结构在生物介质中稳定性较差。在此,开发了一种基于硫醇-二硫键交换的位点特异性交联方法来稳定线框DNA纳米立方体。交联产率接近定量,该结构在模拟生理环境的条件下保持其结构完整性。这导致细胞摄取改善,可能是由于与细胞表面清道夫受体的更有利相互作用,随后是内吞作用。这项研究通过消除DNA线框纳米结构从体外转化到临床前工作的主要瓶颈之一,为其体内应用铺平了道路。