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Inducible site-selective bottom-up assembly of virus-derived nanotube arrays on RNA-equipped wafers

机译:配备RNA的晶圆上病毒衍生的纳米管阵列的诱导位点选择性自下而上装配

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Tobacco mosaic virus (TMV) is a tube-shaped, exceptionally stable plant virus, which is among the biomolecule complexes offering most promising perspectives for nanotechnology applications. Every viral nanotube self-assembles from a single RNA strand and numerous identical coat protein (CP) subunits. Here we demonstrate that biotechnologically engineered RNA species containing the TMV origin of assembly can be selectively attached to solid surfaces via one end and govern the bottom-up growth of surface-linked TMV-like nanotubes in situ on demand. SiO_2 wafers patterned by polymer blend lithography were modified in a chemically selective manner, which allowed positioning of in vitro produced RNA scaffolds into predefined patches on the 100-500 nm scale. The RNA operated as guiding strands for the self-assembly of spatially ordered nanotube 3D arrays on the micrometer scale. This novel approach may promote technically applicable production routes toward a controlled integration of multivalent biotemplates into miniaturized devices to functionalize poorly accessible components prior to use. Furthermore, the results mark a milestone in the experimental verification of viral nucleoprotein complex self-assembly mechanisms.
机译:烟草花叶病毒(TMV)是一种管状,异常稳定的植物病毒,是生物分子复合物中的一种,为纳米技术的应用提供了最有希望的前景。每个病毒纳米管都由一条RNA链和许多相同的外壳蛋白(CP)亚基自组装。在这里,我们证明了包含TMV装配起点的生物技术工程化RNA物种可以通过一端选择性地附着到固体表面,并按需控制表面连接的TMV状纳米管的自下而上的生长。通过化学共混光刻技术对通过聚合物共混光刻法图案化的SiO_2晶圆进行了修饰,从而可以将体外产生的RNA支架定位在100-500 nm范围内的预定斑点中。 RNA充当导向链,用于在微米尺度上自组装空间有序的纳米管3D阵列。这种新颖的方法可以促进技术上适用的生产路线,朝着将多价生物模板可控制地集成到小型化装置中,以在使用前使难以接近的组件功能化的目的。此外,该结果标志着病毒核蛋白复合物自组装机制实验验证的里程碑。

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