用于纳米技术教育的DNA和肽核酸的模块化、铰接模型

Caleigh M. Goodwin-Schoen, Rebecca E. Taylor
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引用次数: 0

摘要

动态和灵活的核酸模型可以为当前和未来的科学家提供DNA结构的物理直觉,以及DNA及其合成模拟物用于构建自组装结构和先进纳米机器的方法。随着越来越多的研究实验室和教室深入结构核酸纳米技术领域,学生和研究人员需要使用交互式、动态的手持模型。在此,我们提出了一种用于构建DNA和肽核酸(PNA)的3D可打印试剂盒。我们设计了以前的模块化DNA试剂盒,以降低成本,同时提高组装的容易性、灵活性和稳健性。我们还通过创建γPNA的第一个3D可打印模型扩大了可用的快速组装模型的范围,γPNA是一种用于核酸酶和蛋白酶抗性纳米技术的新兴材料。在先前研究的基础上,将具有代表性的核酸双链体拆分为逻辑单体片段,并使用原子坐标创建用于3D打印的实体模型。我们使用人为因素方法定制了3种类型的铰接式卡扣式连接器,这些连接器允许模型中每个接口的物理相关运动特性。模块易于手动连接和分离,但在操纵模型时会保持在一起。为了大大降低成本,我们将这些部分捆绑在一起进行打印,并创建了一个使用不到一半打印材料的小型化版本。我们的新型3D打印铰接式卡扣模型捕捉了DNA和γPNA纳米结构的灵活性和稳健性。由此产生的手持螺旋模型复制了已发表结构中的几何形状,现在可以弯曲形成交叉,并允许生物相关的拉链和拉链,以允许进行链置换反应的纳米机器的复杂演示。最后,用于创建这些模型的相同工具可以很容易地应用于其他类型的骨干和核基地,以实现无尽的研究和教育可能性。
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Modular, Articulated Models of DNA and Peptide Nucleic Acids for Nanotechnology Education
Dynamic and flexible nucleic acid models can provide current and future scientists with physical intuition for the structure of DNA and the ways that DNA and its synthetic mimics can be used to build self-assembling structures and advanced nanomachines. As more research labs and classrooms dive into the field of structural nucleic acid nanotechnology, students and researchers need access to interactive, dynamic, handheld models. Here, we present a 3D-printable kit for the construction of DNA and peptide nucleic acid (PNA). We have engineered a previous modular DNA kit to reduce costs while improving ease of assembly, flexibility, and robustness. We have also expanded the scope of available snap-together models by creating the first 3D-printable models of γPNA, an emerging material for nuclease- and protease-resistance nanotechnology. Building on previous research, representative nucleic acid duplexes were split into logical monomer segments, and atomic coordinates were used to create solid models for 3D printing. We used a human factors approach to customize 3 types of articulated snap-together connectors that allow for physically relevant motion characteristic of each interface in the model. Modules are easy to connect and separate manually but stay together when the model is manipulated. To greatly reduce cost, we bundled these segments for printing, and we created a miniaturized version that uses less than half the printing material to build. Our novel 3D-printed articulated snap-together models capture the flexibility and robustness of DNA and γPNA nanostructures. Resulting handheld helical models replicate the geometries in published structures and can now flex to form crossovers and allow biologically relevant zipping and unzipping to allow complex demonstrations of nanomachines undergoing strand displacement reactions. Finally, the same tools used to create these models can be readily applied to other types of backbones and nucleobases for endless research and education possibilities.
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