Department of Materials Science and Engineering, Northwestern University, 2220 Campus Drive, Evanston, IL, 60208, USA.
Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL, 60208, USA.
Adv Mater. 2019 Jan;31(1):e1805480. doi: 10.1002/adma.201805480. Epub 2018 Oct 29.
A postsynthetic method for stabilizing colloidal crystals programmed from DNA is developed. The method relies on Ag ions to stabilize the particle-connecting DNA duplexes within the crystal lattice, essentially transforming them from loosely bound structures to ones with very strong interparticle links. Such crystals do not dissociate as a function of temperature like normal DNA or DNA-interconnected superlattices, and they can be moved from water to organic media or the solid state, and stay intact. The Ag -stabilization of the DNA bonds is accompanied by a nondestructive ≈25% contraction of the lattice, and both the stabilization and contraction are reversible with the chemical extraction of the Ag ions, by AgCl precipitation with NaCl. This synthetic tool is important, since it allows scientists and engineers to study such crystals in environments that are incompatible with structures made by conventional DNA programmable methods and without the influence of a matrix such as silica.
一种用于稳定由 DNA 编程的胶体晶体的后合成方法被开发出来。该方法依赖于 Ag 离子来稳定晶格内的连接颗粒的 DNA 双链体,实质上将其从松散结合的结构转变为具有很强的颗粒间连接的结构。这样的晶体不像普通 DNA 或 DNA 互联超晶格那样随温度解离,并且它们可以从水转移到有机介质或固态,并且保持完整。Ag 对 DNA 键的稳定伴随着晶格的 ≈25%的非破坏性收缩,并且稳定和收缩都是可逆的,可以通过 AgCl 与 NaCl 的沉淀来提取 Ag 离子。这个合成工具非常重要,因为它允许科学家和工程师在与传统 DNA 可编程方法不兼容的环境中研究这些晶体,而不会受到硅石等基质的影响。