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首页> 外文期刊>Nature Communications >Quantifying quality in DNA self-assembly
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Quantifying quality in DNA self-assembly

机译:量化DNA自组装的质量

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Molecular self-assembly with DNA is an attractive route for building nanoscale devices. The development of sophisticated and precise objects with this technique requires detailed experimental feedback on the structure and composition of assembled objects. Here we report a sensitive assay for the quality of assembly. The method relies on measuring the content of unpaired DNA bases in self-assembled DNA objects using a fluorescent de-Bruijn probe for three-base 'codons', which enables a comparison with the designed content of unpaired DNA. We use the assay to measure the quality of assembly of several multilayer DNA origami objects and illustrate the use of the assay for the rational refinement of assembly protocols. Our data suggests that large and complex objects like multilayer DNA origami can be made with high strand integration quality up to 99%. Beyond DNA nanotechnology, we speculate that the ability to discriminate unpaired from paired nucleic acids in the same macromolecule may also be useful for analysing cellular nucleic acids.
机译:具有DNA的分子自组装是构建纳米级设备的诱人途径。利用这种技术开发精密精密的物体需要对组装物体的结构和组成进行详细的实验反馈。在这里,我们报告了一种对组装质量的敏感分析方法。该方法依靠使用用于三碱基“密码子”的荧光de-Bruijn探针测量自组装DNA对象中未配对DNA碱基的含量,从而可以与未配对DNA的设计含量进行比较。我们使用该检测方法来测量几个多层DNA折纸对象的组装质量,并举例说明该检测方法对组装方案的合理改进。我们的数据表明,可以制造高达99%的高链整合质量的大型复杂物体(如多层DNA折纸)。除了DNA纳米技术,我们推测在同一大分子中区分未配对的核酸与配对的核酸的能力也可能对分析细胞核酸有用。

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