Department of Chemistry and Biochemistry and the Biodesign Institute, Arizona State University , Tempe, Arizona 85287, United States.
Acc Chem Res. 2014 Jun 17;47(6):1861-70. doi: 10.1021/ar5000665. Epub 2014 May 22.
DNA nanotechnology is one of the most flourishing interdisciplinary research fields. DNA nanostructures can be designed to self-assemble into a variety of periodic or aperiodic patterns of different shapes and length scales. They can be used as scaffolds for organizing other nanoparticles, proteins, and chemical groups, leveraging their functions for creating complex bioinspired materials that may serve as smart drug delivery systems, in vitro or in vivo biomolecular computing platforms, and diagnostic devices. Achieving optimal structural features, efficient assembly protocols, and precise functional group positioning and modification requires a thorough understanding of the thermodynamics and kinetics of the DNA nanostructure self-assembly process. The most common real-time measurement strategies include monitoring changes in UV absorbance based on the hyperchromic effect of DNA, and the emission signal changes of DNA intercalating dyes or covalently conjugated fluorescent dyes/pairs that accompany temperature dependent structural changes. Thermodynamic studies of a variety of DNA nanostructures have been performed, from simple double stranded DNA formation to more complex origami assembly. The key parameters that have been evaluated in terms of stability and cooperativity include the overall dimensions, the folding path of the scaffold, crossover and nick point arrangement, length and sequence of single strands, and salt and ion concentrations. DNA tile-tile interactions through sticky end hybridization have also been analyzed, and the steric inhibition and rigidity of tiles turn out to be important factors. Many kinetic studies have also been reported, and most are based on double stranded DNA formation. A two-state assumption and the hypothesis of several intermediate states have been applied to determine the rate constant and activation energy of the DNA hybridization process. A few simulated models were proposed to represent the structural, mechanical, and kinetic properties of DNA hybridization. The kinetics of strand displacement reactions has also been studied as a special case of DNA hybridization. The thermodynamic and kinetic characteristics of DNA nanostructures have been exploited to develop rapid and isothermal annealing protocols. It is conceivable that a more thorough understanding of the DNA assembly process could be used to guide the structural design process and optimize the conditions for assembly, manipulation, and functionalization, thus benefiting both upstream design and downstream applications.
DNA 纳米技术是最繁荣的跨学科研究领域之一。DNA 纳米结构可以设计为自组装成各种具有不同形状和长度尺度的周期性或非周期性图案。它们可以用作组织其他纳米粒子、蛋白质和化学基团的支架,利用它们的功能来创建复杂的仿生材料,这些材料可用作智能药物输送系统、体外或体内生物分子计算平台以及诊断设备。实现最佳的结构特征、高效的组装方案以及精确的功能基团定位和修饰需要对 DNA 纳米结构自组装过程的热力学和动力学有透彻的了解。最常见的实时测量策略包括监测基于 DNA 增色效应的 UV 吸光度变化,以及伴随温度相关结构变化的 DNA 嵌入染料或共价连接荧光染料/对的发射信号变化。已经对各种 DNA 纳米结构进行了热力学研究,从简单的双链 DNA 形成到更复杂的折纸组装。已经评估了稳定性和协同性的关键参数包括整体尺寸、支架的折叠路径、交叉和缺口点排列、单链的长度和序列以及盐和离子浓度。还分析了 DNA 瓦片-瓦片通过粘性末端杂交的相互作用,并且瓦片的空间位阻和刚性被证明是重要的因素。已经报道了许多动力学研究,并且大多数都是基于双链 DNA 的形成。已经应用两态假设和几个中间态假设来确定 DNA 杂交过程的速率常数和活化能。已经提出了一些模拟模型来表示 DNA 杂交的结构、力学和动力学特性。作为 DNA 杂交的特殊情况,也研究了链置换反应的动力学。已经利用 DNA 纳米结构的热力学和动力学特性来开发快速和等温退火方案。可以想象,对 DNA 组装过程的更透彻理解可以用于指导结构设计过程并优化组装、操作和功能化的条件,从而使上游设计和下游应用都受益。