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Cryo-EM structure of a 3D DNA-origami object

机译:3D DNA折纸对象的Cryo-EM结构

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摘要

A key goal for nanotechnology is to design synthetic objects that may ultimately achieve functionalities known today only from natural macromolecular complexes. Molecular self-assembly with DNA has shown potential for creating user-defined 3D scaffolds, but the level of attainable positional accuracy has been unclear. Here we report the cryo-EM structure and a full pseudoatomic model of a discrete DNA object that is almost twice the size of a prokaryotic ribosome. The structure provides a variety of stable, previously undescribed DNA topologies for future use in nanotechnology and experimental evidence that discrete 3D DNA scaffolds allow the positioning of user-defined structural motifs with an accuracy that is similar to that observed in natural macromole-cules. Thereby, our results indicate an attractive route to fabricate nanoscale devices that achieve complex functionalities by DNA-templated design steered by structural feedback.
机译:纳米技术的一个关键目标是设计合成对象,这些对象最终可能仅通过天然高分子复合物才能实现当今已知的功能。具有DNA的分子自组装已显示出创建用户定义的3D支架的潜力,但尚不清楚可达到的位置准确性水平。在这里,我们报告了冷冻-EM结构和离散的DNA对象的完整假原子模型,该对象几乎是原核糖体大小的两倍。该结构提供了多种稳定的,以前未描述的DNA拓扑结构,可用于未来的纳米技术和实验证据,即离散的3D DNA支架可以定位用户定义的结构基序,其准确性与在自然大分子中观察到的精度相似。因此,我们的结果表明,通过结构反馈指导的DNA模板设计,可以制造出可实现复杂功能的纳米级器件的诱人途径。

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    Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 OQH, United Kingdom;

    Physics Department, Walter Schottky Institute,Technische Universitat Miinchen, 85748 Garching near Munich, Germany;

    Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 OQH, United Kingdom;

    Physics Department, Walter Schottky Institute,Technische Universitat Miinchen, 85748 Garching near Munich, Germany;

  • 收录信息 美国《科学引文索引》(SCI);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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