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从最小数量的未修饰链设计 DNA 纳米管:快速、室温组装和易于调节的结构。

Simple design for DNA nanotubes from a minimal set of unmodified strands: rapid, room-temperature assembly and readily tunable structure.

机构信息

Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, QC H3A 0B8 Canada.

出版信息

ACS Nano. 2013 Apr 23;7(4):3022-8. doi: 10.1021/nn4006329. Epub 2013 Mar 19.

Abstract

DNA nanotubes have great potential as nanoscale scaffolds for the organization of materials and the templation of nanowires and as drug delivery vehicles. Current methods for making DNA nanotubes either rely on a tile-based step-growth polymerization mechanism or use a large number of component strands and long annealing times. Step-growth polymerization gives little control over length, is sensitive to stoichiometry, and is slow to generate long products. Here, we present a design strategy for DNA nanotubes that uses an alternative, more controlled growth mechanism, while using just five unmodified component strands and a long enzymatically produced backbone. These tubes form rapidly at room temperature and have numerous, orthogonal sites available for the programmable incorporation of arrays of cargo along their length. As a proof-of-concept, cyanine dyes were organized into two distinct patterns by inclusion into these DNA nanotubes.

摘要

DNA 纳米管作为纳米级支架,在材料的组织和纳米线的模板以及药物输送载体方面具有巨大的潜力。目前制造 DNA 纳米管的方法要么依赖于基于瓦片的逐步聚合机制,要么使用大量的组件链和长时间的退火。逐步聚合对长度的控制很小,对化学计量敏感,而且生成长产物的速度很慢。在这里,我们提出了一种 DNA 纳米管的设计策略,该策略使用了一种替代的、更可控的生长机制,同时只使用了五条未经修饰的组件链和一条长的酶促产生的骨架。这些纳米管在室温下迅速形成,并且在其长度上有许多可供可编程掺入货物阵列的正交位点。作为概念验证,通过将花青染料包含在这些 DNA 纳米管中,将其组织成两种不同的模式。

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