体外组装基于立方 RNA 的支架,该支架通过计算机设计。
In vitro assembly of cubic RNA-based scaffolds designed in silico.
机构信息
Department of Chemistry and Biochemistry, Biomolecular Science and Engineering Program, University of California, Santa Barbara, California 93106-9510, USA.
出版信息
Nat Nanotechnol. 2010 Sep;5(9):676-82. doi: 10.1038/nnano.2010.160. Epub 2010 Aug 29.
The organization of biological materials into versatile three-dimensional assemblies could be used to build multifunctional therapeutic scaffolds for use in nanomedicine. Here, we report a strategy to design three-dimensional nanoscale scaffolds that can be self-assembled from RNA with precise control over their shape, size and composition. These cubic nanoscaffolds are only approximately 13 nm in diameter and are composed of short oligonucleotides, making them amenable to chemical synthesis, point modifications and further functionalization. Nanocube assembly is verified by gel assays, dynamic light scattering and cryogenic electron microscopy. Formation of functional RNA nanocubes is also demonstrated by incorporation of a light-up fluorescent RNA aptamer that is optimally active only upon full RNA assembly. Moreover, we show that the RNA nanoscaffolds can self-assemble in isothermal conditions (37 degrees C) during in vitro transcription, which opens a route towards the construction of sensors, programmable packaging and cargo delivery systems for biomedical applications.
将生物材料组织成多功能的三维组装体,可以用于构建用于纳米医学的多功能治疗支架。在这里,我们报告了一种设计三维纳米支架的策略,该支架可以通过 RNA 自组装形成,对其形状、大小和组成具有精确的控制。这些立方纳米支架的直径仅约为 13nm,由短寡核苷酸组成,这使得它们易于化学合成、点修饰和进一步功能化。通过凝胶分析、动态光散射和低温电子显微镜验证了纳米立方的组装。通过掺入仅在完整 RNA 组装时才具有最佳活性的点亮荧光 RNA 适体,证明了功能性 RNA 纳米立方的形成。此外,我们还表明,RNA 纳米支架可以在等温条件(37°C)下在体外转录过程中自组装,这为构建用于生物医学应用的传感器、可编程包装和货物输送系统开辟了一条途径。