Jabbari Hosna, Aminpour Maral, Montemagno Carlo
Ingenuity Lab , 11421 Saskatchewan Drive, Edmonton, Alberta T6G 2M9, Canada.
Department of Chemical and Materials Engineering, University of Alberta , Edmonton T6G 2V4, Canada.
ACS Comb Sci. 2015 Oct 12;17(10):535-47. doi: 10.1021/acscombsci.5b00079. Epub 2015 Sep 17.
Recent advances in experimental DNA origami have dramatically expanded the horizon of DNA nanotechnology. Complex 3D suprastructures have been designed and developed using DNA origami with applications in biomaterial science, nanomedicine, nanorobotics, and molecular computation. Ribonucleic acid (RNA) origami has recently been realized as a new approach. Similar to DNA, RNA molecules can be designed to form complex 3D structures through complementary base pairings. RNA origami structures are, however, more compact and more thermodynamically stable due to RNA's non-canonical base pairing and tertiary interactions. With all these advantages, the development of RNA origami lags behind DNA origami by a large gap. Furthermore, although computational methods have proven to be effective in designing DNA and RNA origami structures and in their evaluation, advances in computational nucleic acid origami is even more limited. In this paper, we review major milestones in experimental and computational DNA and RNA origami and present current challenges in these fields. We believe collaboration between experimental nanotechnologists and computer scientists are critical for advancing these new research paradigms.
实验性DNA折纸技术的最新进展极大地拓展了DNA纳米技术的视野。利用DNA折纸技术设计并开发出了复杂的三维超结构,其在生物材料科学、纳米医学、纳米机器人技术和分子计算等领域都有应用。核糖核酸(RNA)折纸技术最近成为了一种新方法。与DNA类似,RNA分子可以通过互补碱基配对设计形成复杂的三维结构。然而,由于RNA的非经典碱基配对和三级相互作用,RNA折纸结构更加紧凑,热力学稳定性也更高。尽管具有所有这些优点,但RNA折纸技术的发展仍远远落后于DNA折纸技术。此外,虽然计算方法已被证明在设计DNA和RNA折纸结构及其评估方面有效,但计算核酸折纸技术的进展甚至更为有限。在本文中,我们回顾了实验性和计算性DNA与RNA折纸技术的主要里程碑,并介绍了这些领域当前面临的挑战。我们认为,实验性纳米技术专家与计算机科学家之间的合作对于推动这些新的研究范式至关重要。