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Core-Shell and Layer-by-Layer Assembly of 3D DNA Crystals

机译:3D DNA晶体的核-壳层和逐层组装

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摘要

A long-standing goal of DNA nanotechnology has been to assemble 3D crystals to be used as molecular scaffolds. The DNA 13-mer, BET66, self-assembles via Crick-Watson and noncanonical base pairs to form crystals. The crystals contain solvent channels that run through them in multiple directions, allowing them to accommodate tethered guest molecules. Here, the first example of biomacromolecular core-shell crystal growth is described, by showing that these crystals can be assembled with two or more discrete layers. This approach leads to structurally identical layers on the DNA level, but with each layer differentiated based on the presence or absence of conjugated guest molecules. The crystal solvent channels also allow layer-specific postcrystallization covalent attachment of guest molecules. Through controlling the guest-molecule identity, concentration, and layer thickness, this study opens up a new method for using DNA to create multifunctional periodic biomaterials with tunable optical, chemical, and physical properties.
机译:DNA纳米技术的长期目标是组装3D晶体以用作分子支架。 DNA 13-mer BET66通过Crick-Watson和非规范碱基对自组装形成晶体。晶体包含沿多个方向贯穿它们的溶剂通道,从而使它们能够容纳束缚的客体分子。在此,通过显示生物大分子核-壳晶体的生长可以与两个或多个不连续的层组装在一起,来描述它们的第一个例子。这种方法导致了DNA层在结构上相同的层,但是每一层都根据是否存在共轭客体分子而有所区别。晶体溶剂通道还允许客体分子进行层特定的结晶后共价连接。通过控制客体分子的身份,浓度和层厚度,本研究开辟了一种新的方法来使用DNA来创建具有可调的光学,化学和物理特性的多功能周期性生物材料。

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