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Assembly of RNA nanostructures on supported lipid bilayers

机译:组装的RNA在支持脂质纳米结构影响

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The assembly of nucleic acid nanostructures with controlled size and shape has large impact in the fields of nanotechnology, nanomedicine and synthetic biology. The directed arrangement of nano-structures at interfaces is important for many applications. In spite of this, the use of laterally mobile lipid bilayers to control RNA three-dimensional nanostructure formation on surfaces remains largely unexplored. Here, we direct the self-assembly of RNA building blocks into three-dimensional structures of RNA on fluid lipid bilayers composed of cationic 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) or mixtures of zwitterionic 1,2-dioleoyl-sn-glycero-3-phosphatidylcholine (DOPC) and cationic sphingosine. We demonstrate the stepwise supramolecular assembly of discrete building blocks through specific and selective RNA-RNA interactions, based on results from quartz crystal microbalance with dissipation (QCM-D), ellipsometry, fluorescence recovery after photobleaching (FRAP) and total internal reflection fluorescence microscopy (TIRF) experiments. The assembly can be controlled to give a densely packed single layer of RNA polyhedrons at the fluid lipid bilayer surface. We show that assembly of the 3D structure can be modulated by sequence specific interactions, surface charge and changes in the salt composition and concentration. In addition, the tertiary structure of the RNA polyhedron can be controllably switched from an extended structure to one that is dense and compact. The versatile approach to building up three-dimensional structures of RNA does not require modification of the surface or the RNA molecules, and can be used as a bottom-up means of nanofabrication of functionalized bio-mimicking surfaces.
机译:核酸纳米结构的组装控制尺寸和形状有较大的影响纳米技术、纳米医学和合成生物学。纳米结构的接口是非常重要的许多应用程序。横向移动控制RNA的脂质影响三维纳米结构形成表面基本上仍是无人涉足。直接RNA的自组装构建块流体三维结构的RNA脂质阳离子组成的影响1,2-dioleoyl-3-trimethylammonium-propane (DOTAP)或两性离子的混合物1, 2-dioleoyl-sn-glycero-3-phosphatidylcholine(DOPC)和阳离子鞘氨醇。离散的逐步超分子组装构建块通过特定的和选择性RNA-RNA交互,基于结果石英晶体微量天平与耗散(QCM-D),椭圆光度法,荧光恢复光漂白后(收紧)和全内反射荧光显微镜(TIRF)实验。密集的单层的RNA多面体的流体脂质双分子层的表面。我们表明,装配的三维结构调制序列具体的交互,表面电荷和盐的变化成分和浓度。三级结构的RNA多面体控制从一个扩展结构一个密集的和紧凑。建立三维的方法RNA结构不需要修改的表面或RNA分子,可以作为奈米制造的自底向上的方法功能化bio-mimicking表面。

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