重复使用多余的主食寡核苷酸,经济地制作 DNA 折纸

Giorgia Isinelli, Christopher Wintersinger, Pascal Lill, Olivia Young, Jie Deng, William Shih, Yang Zeng
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引用次数: 0

摘要

DNA 折纸使我们能够开发出具有精确特征的响应性给药载体,而这在以前的仿生技术中是无法实现的。为了降低制作治疗级 DNA 折纸的成本,我们重新利用折叠过程中剩余的主寡核苷酸来折叠更多的 DNA 折纸。我们确定,通过循环回收和重复使用多余的主链,可以成功折叠出 DNA 折纸,并节省高达 80% 的成本。我们发现有证据表明,质量较高的主链会优先融入折纸中,这与过去的报告一致,因此会优先从自由链池中耗尽。用重复使用多达 11 次的主链折叠 DNA 折纸,与用新链折叠的对照组相比,在我们的检测小组中没有区别,只要在每个周期用少量过量的新鲜链补充重复使用的寡核苷酸即可。我们还观察到客体在 DNA 折纸上的高度结合。通过回收、重复使用和补充多余的主链寡核苷酸,可以大大降低制作成型良好的折纸的生产成本,这有助于测试更多的治疗设计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reusing excess staple oligonucleotides for economical production of DNA origami
DNA origami has enabled the development of responsive drug-delivery vehicles with precision features that were previously not attainable in bionanotechnology. To reduce the costs of creating therapeutics-scale amounts of DNA origami that need to bear costly modifications with high occupancy, we reused the excess staple oligonucleotides that are leftover from the folding process to fold additional origami. We determined that a DNA origami can be successfully folded with up to 80% cost savings by cyclic recovery and reuse of excess staple strands. We found evidence that higher quality staple strands are preferentially incorporated into origami, consistent with past reports, and therefore are preferentially depleted from the free-strand pool. The folding of DNA origami with staple strands that were reused up to eleven times was indistinguishable by our panel of assays versus a control folded with new strands, so long as the reused oligonucleotides were replenished each cycle with a small excess of fresh strands. We also observed a high degree of incorporation of guests on the DNA origami. By recovering, reusing, and replenishing excess staple oligonucleotides, it is possible to significantly lessen production costs to create well-formed origami, which is useful to allow more therapeutic designs to be tested.
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