论文标题

一种简单的方法,用于重新编程结晶的DNA涂层胶体的结合特异性

A simple method to reprogram the binding specificity of DNA-coated colloids that crystallize

论文作者

Moerman, Pepijn G., Fang, Huang, Videbæk, Thomas E., Rogers, W. Benjamin, Schulman, Rebecca

论文摘要

涂DNA涂层的胶体可以结晶成多种晶格,范围从面部中心到钻石,从而有助于我们对结晶和开放途径的理解,从而产生具有有用光子特性的结构。尽管具有DNA涂层的胶体的潜在设计空间很广,但合成DNA涂层颗粒的设计周期很慢:用新型的DNA序列制备粒子需要一天以上的时间,并且需要定制和化学修改的DNA,通常将供应商在一个月内将供应商带到一个月以上才能合成。在这里,我们介绍了一种在环境条件下在一个小时内从单个进料库存中生成具有自定义序列的粒子的方法。我们的方法将新的DNA结构域附加到接枝到胶体颗粒的DNA上,该模板将供应商不到一周才能产生。所得的颗粒与直接化学合成产生的温度很容易地和相同的温度结晶。此外,我们表明,涂有单个序列的粒子可以通过将不同的DNA序列附加到它们的情况下,将其转换为具有不同特异性的各种构件。这种涂DNA涂层颗粒制备方法的方法将使确定最佳且复杂的粒子序列设计并将其涂DNA涂层胶体的使用扩展到更广泛的研究者和商业实体是实际的。

DNA-coated colloids can crystallize into a multitude of lattices, ranging from face-centered cubic to diamond and thereby contribute to our understanding of crystallization and open avenues to producing structures with useful photonic properties. Despite the broad potential design space of DNA-coated colloids, the design cycle for synthesizing DNA-coated particles is slow: preparing a particle with a new type of DNA sequence takes more than one day and requires custom-made and chemically modified DNA that typically takes the supplier over a month to synthesize. Here, we introduce a method to generate particles with custom sequences from a single feed stock in under an hour at ambient conditions. Our method appends new DNA domains onto the DNA grafted to colloidal particles based on a template that takes the supplier less than a week to produce. The resultant particles crystallize as readily and at the same temperature as those produced via direct chemical synthesis. Moreover, we show that particles coated with a single sequence can be converted into a variety of building blocks with differing specificities by appending different DNA sequences to them. This approach to DNA-coated particle preparation will make it practical to identify optimal and complex particle sequence designs and to expand the use of DNA-coated colloids to a much broader range of investigators and commercial entities.

扫码加入交流群

加入微信交流群

微信交流群二维码

扫码加入学术交流群,获取更多资源