Biodesign Center for Molecular Design and Biomimetics (at the Biodesign Institute) at Arizona State University, Tempe, AZ, United States of America.
Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, United States of America.
PLoS One. 2023 Jul 19;18(7):e0283134. doi: 10.1371/journal.pone.0283134. eCollection 2023.
DNA origami purification is essential for many fields, including biophysics, molecular engineering, and therapeutics. The increasing interest in DNA origami has led to the development of rate-zonal centrifugation (RZC) as a scalable, high yield, and contamination-free method for purifying DNA origami nanostructures. RZC purification uses a linear density gradient of viscous media, such as glycerol or sucrose, to separate molecules according to their mass and shape. However, many methods for creating density gradients are time-consuming because they rely on slow passive diffusion. To expedite the preparation time, we used a LEGO gradient mixer to generate rotational motion and rapidly create a quasi-continuous density gradient with a minimal layering of the viscous media. Rotating two layers of differing concentrations at an angle decreases the time needed to form the density gradient from a few hours to minutes. In this study, the density gradients created by the LEGO gradient mixer were used to purify 3 DNA origami shapes that have different aspect ratios and numbers of components, with an aspect ratio ranging from 1:1 to 1:100 and the number of components up to 2. The gradient created by our LEGO gradient mixer is sufficient to purify folded DNA origami nanostructures from excess staple strands, regardless of their aspect ratios. Moreover, the gradient was able to separate DNA origami dimers from DNA origami monomers. In light of recent advances in large-scale DNA origami production, our method provides an alternative for purifying DNA origami nanostructures in large (gram) quantities in resource-limited settings.
DNA 折纸纯化对于包括生物物理、分子工程和治疗学在内的许多领域都至关重要。人们对 DNA 折纸的兴趣日益浓厚,促使速率区带离心(RZC)成为一种可扩展、高产且无污染的纯化 DNA 折纸纳米结构的方法。RZC 纯化利用粘性介质(如甘油或蔗糖)的线性密度梯度,根据分子的质量和形状分离分子。然而,许多创建密度梯度的方法都很耗时,因为它们依赖于缓慢的被动扩散。为了加快准备时间,我们使用乐高梯度混合器产生旋转运动,快速创建具有最小粘性介质分层的准连续密度梯度。以一定角度旋转两层不同浓度的溶液可以将形成密度梯度的时间从数小时缩短至数分钟。在这项研究中,乐高梯度混合器创建的密度梯度用于纯化 3 种具有不同纵横比和组件数量的 DNA 折纸形状,纵横比范围从 1:1 到 1:100,组件数量最多可达 2。我们的乐高梯度混合器创建的梯度足以从多余的订书钉链中纯化折叠的 DNA 折纸纳米结构,而与纵横比无关。此外,该梯度还能够将 DNA 折纸二聚体与 DNA 折纸单体分离。鉴于大规模 DNA 折纸生产的最新进展,我们的方法为在资源有限的环境中以大(克)量纯化 DNA 折纸纳米结构提供了一种替代方法。