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Rational Engineering of Dynamic DNA Systems

机译:动态DNA系统的合理工程

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摘要

During the past quarter of a century the application of DNA molecules as a scaffold material for constructions in the nanometer range has developed from the design of simple,yet ground-breaking four-armed double-helical junction motifs'11 to the self-assembly of complex structural motifs which serve as building blocks to form large supramolecular constructs.The key property of DNA that makes it so attractive for bottom-up nanotechnology is the extraordinary specificity of the hybridization of single-stranded nucleic acids with their Watson-Crick complements to form stable double helices.Thus,a set of carefully designed oligonucleotides can be programmed to self-assemble into a broad range of diverse superstructures.In addition,reversible transition mechanisms between various stable or metastable states,such as secondary structure conformations,can be engineered into DNA superstructures such that static scaffolds become dynamic nano-devices.Such devices may perform,for example,mechanical work,translate information aggregate and dissociate nanoparticles,or bind and release proteins.While the design of static DNA arrays nowadays increasingly follows systematic rules which allow the retrosynthetic analysis of desired superstructures to obtain suitable sets of oligonucleotides that will form these structures,dynamic DNA devices are usually prepared by individual approaches,which take advantage of various conformational states,transition reactions,and respective triggering stimuli,such as oligonucleotide displacement,changes in ionic strengths or pH values of buffers,or binding of small molecules.
机译:在过去的四分之一世纪中,DNA分子作为纳米结构支架材料的应用已经从简单但突破性的四臂双螺旋连接基序设计[11]发展到了自组装。复杂的结构基序可作为构成大型超分子构建体的基础.DNA使其对自下而上的纳米技术如此具有吸引力的关键特性是单链核酸与其Watson-Crick互补序列杂交形成的非凡特异性因此,可以对一组精心设计的寡核苷酸进行编程,以自组装成各种多样的超结构。此外,还可以将各种稳定或亚稳态之间的可逆转变机制(例如二级结构构象)工程化为DNA超结构,使静态支架变成动态的纳米设备。此类设备可以执行例如机械作用虽然当今静态DNA阵列的设计越来越遵循系统的规则,这些规则允许对所需的超结构进行反合成分析以获得适合的寡核苷酸组,这些寡核苷酸将形成这些结构,但动态DNA却可以工作,翻译信息,使纳米粒子聚集或解离或结合并释放蛋白质。装置通常是通过单独的方法制备的,这些方法利用各种构象状态,过渡反应和相应的触发刺激,例如寡核苷酸置换,离子强度或缓冲液的pH值变化或小分子结合。

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