School of Physics and Astronomy, Faculty of Engineering and Physical Sciences , University of Southampton , Southampton , SO17 1BJ , U.K.
Chemistry Research Laboratory, Department of Chemistry , University of Oxford , 12 Mansfield Road , Oxford , OX1 3TA , U.K.
ACS Nano. 2019 May 28;13(5):5771-5777. doi: 10.1021/acsnano.9b01294. Epub 2019 Apr 8.
DNA-mediated self-assembly of nanoparticles has been of great interest because it enables access to nanoparticle superstructures that cannot be synthesized otherwise. However, the programmability of higher order nanoparticle structures can be easily lost under DNA denaturing conditions. Here, we demonstrate that light can be employed as an external stimulus to master the stability of nanoparticle superlattices (SLs) via the promotion of a reversible photoligation of DNA in SLs. The oligonucleotides attached to the nanoparticles are encoded to ligate using 365 nm light, effectively locking the SLs and rendering them stable under DNA denaturing conditions. The reversible process of unlocking these structures is possible by irradiation with light at 315 nm, recovering the structures to their natural state. Our work inspires an alternative research direction toward postassembly manipulation of nanoparticle superstructures using external stimuli as a tool to enrich the library of additional material forms and their application in different media and environments.
DNA 介导的纳米粒子自组装引起了广泛关注,因为它使我们能够获得无法通过其他方法合成的纳米粒子超结构。然而,在 DNA 变性条件下,更高阶的纳米粒子结构的可编程性很容易丢失。在这里,我们证明可以利用光作为外部刺激,通过促进 SLs 中的 DNA 可逆光连接来控制纳米粒子超晶格(SLs)的稳定性。连接到纳米粒子上的寡核苷酸被编码为使用 365nm 光进行连接,有效地锁定 SLs,并使其在 DNA 变性条件下保持稳定。通过用 315nm 的光照射可以实现解锁这些结构的可逆过程,使结构恢复到其自然状态。我们的工作为使用外部刺激作为工具对纳米粒子超结构进行后组装操作提供了一个替代的研究方向,以丰富额外材料形式的库,并将其应用于不同的介质和环境中。