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Biotechnological mass production of DNA origami

机译:DNA折纸的生物技术大规模生产

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摘要

DNA nanotechnology, in particular DNA origami, enables the bottom-up self-assembly of micrometre-scale, three-dimensional structures with nanometre-precise features(1-12). These structures are customizable in that they can be site-specifically functionalized(13) or constructed to exhibit machine-like(14,15) or logic-gating behaviour(16). Their use has been limited to applications that require only small amounts of material (of the order of micrograms), owing to the limitations of current production methods. But many proposed applications, for example as therapeutic agents or in complex materials(3,16-22), could be realized if more material could be used. In DNA origami, a nanostructure is assembled from a very long single-stranded scaffold molecule held in place by many short single-stranded staple oligonucleotides. Only the bacteriophage-derived scaffold molecules are amenable to scalable and efficient mass production(23); the shorter staple strands are obtained through costly solid-phase synthesis(24) or enzymatic processes(25). Here we show that single strands of DNA of virtually arbitrary length and with virtually arbitrary sequences can be produced in a scalable and cost-efficient manner by using bacteriophages to generate single-stranded precursor DNA that contains target strand sequences interleaved with self-excising 'cassettes', with each cassette comprising two Zn2+-dependent DNA-cleaving DNA enzymes. We produce all of the necessary single strands of DNA for several DNA origami using shaker-flask cultures, and demonstrate end-to-end production of macroscopic amounts of a DNA origami nanorod in a litre-scale stirred-tank bioreactor. Our method is compatible with existing DNA origami design frameworks and retains the modularity and addressability of DNA origami objects that are necessary for implementing custom modifications using functional groups. With all of the production and purification steps amenable to scaling, we expect that our method will expand the scope of DNA nanotechnology in many areas of science and technology.
机译:DNA纳米技术,尤其是DNA折纸,可以实现具有纳米级精确特征的微米级,三维结构的自下而上的自组装(1-12)。这些结构是可定制的,因为它们可以在特定位置进行功能化(13)或构造为具有类似机器的功能(14,15)或逻辑门操作(16)。由于当前生产方法的局限性,它们的使用仅限于仅需要少量材料(微克数量级)的应用。但是,如果可以使用更多的材料,则可以实现许多建议的应用,例如作为治疗剂或用于复杂的材料(3,16-22)。在DNA折纸中,纳米结构是由很长的单链支架分子组装而成的,该分子由许多短的单链钉寡核苷酸固定在适当的位置。只有来自噬菌体的支架分子才能够进行可扩展且有效的大规模生产(23);较短的短链是通过昂贵的固相合成(24)或酶促工艺(25)获得的。在这里,我们表明,通过使用噬菌体产生单链前体DNA,可以以可扩展且具有成本效益的方式生产几乎任意长度和具有几乎任意序列的DNA单链DNA,该单链前体DNA包含与自我切割'盒式磁带交错的目标链序列,每个盒包含两个依赖Zn2 +的DNA切割DNA酶。我们使用摇瓶培养法生产几种DNA折纸的所有必需的DNA单链,并证明了升量搅拌罐生物反应器中宏观量的DNA折纸纳米棒的端到端生产。我们的方法与现有的DNA折纸设计框架兼容,并保留了DNA折纸对象的模块性和可寻址性,而这对于使用功能组实现自定义修饰是必需的。通过所有适合规模化的生产和纯化步骤,我们希望我们的方法将在许多科学和技术领域扩展DNA纳米技术的范围。

著录项

  • 来源
    《Nature》 |2017年第7683期|84-87|共4页
  • 作者单位

    Techn Univ Munich, Dept Phys, Coulombwall 4a, D-85748 Garching, Germany|Techn Univ Munich, Inst Adv Study, Coulombwall 4a, D-85748 Garching, Germany;

    Techn Univ Munich, Dept Phys, Coulombwall 4a, D-85748 Garching, Germany|Techn Univ Munich, Inst Adv Study, Coulombwall 4a, D-85748 Garching, Germany|Tech Univ Munich, Inst Biochem Engn, Boltzmannstr 15, D-85748 Garching, Germany;

    Tech Univ Munich, Inst Biochem Engn, Boltzmannstr 15, D-85748 Garching, Germany;

    Techn Univ Munich, Dept Phys, Coulombwall 4a, D-85748 Garching, Germany|Techn Univ Munich, Inst Adv Study, Coulombwall 4a, D-85748 Garching, Germany;

    Tech Univ Munich, Inst Biochem Engn, Boltzmannstr 15, D-85748 Garching, Germany;

    Techn Univ Munich, Dept Phys, Coulombwall 4a, D-85748 Garching, Germany|Techn Univ Munich, Inst Adv Study, Coulombwall 4a, D-85748 Garching, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 02:52:00

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