Center for Cancer Research Nanobiology Program, NCI, Frederick, Maryland 21702, USA.
Nat Nanotechnol. 2013 Apr;8(4):296-304. doi: 10.1038/nnano.2013.44. Epub 2013 Mar 31.
Split-protein systems, an approach that relies on fragmentation of proteins with their further conditional re-association to form functional complexes, are increasingly used for various biomedical applications. This approach offers tight control of protein functions and improved detection sensitivity. Here we report a similar technique based on a pair of RNA-DNA hybrids that can be used generally for triggering different split functionalities. Individually, each hybrid is inactive but when two cognate hybrids re-associate, different functionalities are triggered inside mammalian cells. As a proof of concept, this work mainly focuses on the activation of RNA interference. However, the release of other functionalities (such as resonance energy transfer and RNA aptamer) is also shown. Furthermore, in vivo studies demonstrate a significant uptake of the hybrids by tumours together with specific gene silencing. This split-functionality approach presents a new route in the development of 'smart' nucleic acid-based nanoparticles and switches for various biomedical applications.
分裂蛋白系统是一种依赖于蛋白质的碎片化及其进一步的条件性重新组合以形成功能复合物的方法,越来越多地用于各种生物医学应用。这种方法可以对蛋白质功能进行严格的控制,并提高检测灵敏度。在这里,我们报告了一种基于 RNA-DNA 杂交体的类似技术,该技术可用于普遍触发不同的分裂功能。单独来看,每个杂交体都是不活跃的,但当两个同源杂交体重新组合时,不同的功能会在哺乳动物细胞内被触发。作为概念验证,这项工作主要集中在 RNA 干扰的激活上。然而,其他功能(如共振能量转移和 RNA 适体)的释放也有显示。此外,体内研究表明,这些杂交体被肿瘤大量摄取,并伴有特定的基因沉默。这种分裂功能方法为各种生物医学应用的“智能”基于核酸的纳米粒子和开关的开发提供了一条新途径。