Young Olivia J, Dembele Hawa, Rajwar Anjali, Kwon Ick Chan, Ryu Ju Hee, Shih William M, Zeng Yang C
Department of Cancer Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.
Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, Massachusetts 02115, USA.
bioRxiv. 2024 Aug 27:2024.08.27.609963. doi: 10.1101/2024.08.27.609963.
In recent years, notable advances in nanotechnology-based drug delivery have emerged. A particularly promising platform in this field is DNA origami-based nanoparticles, which offer highly programmable surfaces, providing precise control over the nanoscale spacing and stoichiometry of various cargo. These versatile particles are finding diverse applications ranging from basic molecular biology to diagnostics and therapeutics. This growing interest creates the need for effective methods to quantify cargo on DNA origami nanoparticles. Our study consolidates several previously validated methods focusing on gel-based and fluorescence-based techniques, including multiplexed quantification of protein, peptide, and nucleic acid cargo on these nanoparticles. This work may serve as a valuable resource for groups researchers keen on utilizing DNA origami-based nanoparticles in therapeutic applications.
近年来,基于纳米技术的药物递送取得了显著进展。该领域一个特别有前景的平台是基于DNA折纸术的纳米颗粒,它具有高度可编程的表面,能够精确控制各种负载的纳米级间距和化学计量。这些多功能颗粒正被广泛应用,从基础分子生物学到诊断和治疗领域。这种日益增长的兴趣催生了对有效方法来量化DNA折纸术纳米颗粒上负载的需求。我们的研究整合了几种先前经过验证的方法,重点是基于凝胶和基于荧光的技术,包括对这些纳米颗粒上蛋白质、肽和核酸负载的多重定量。这项工作可能为热衷于在治疗应用中利用基于DNA折纸术纳米颗粒的研究团队提供宝贵的资源。