...
首页> 外文期刊>ACS nano >Multimodal characterization of a linear DNA-based nanostructure
【24h】

Multimodal characterization of a linear DNA-based nanostructure

机译:基于线性DNA的纳米结构的多峰表征

获取原文
获取原文并翻译 | 示例
           

摘要

Designer DNA structures have garnered much interest as a way of assembling novel nanoscale architectures with exquisite control over the positioning of discrete molecules or nanoparticles. Exploiting this potential for a variety of applications such as light-harvesting, molecular electronics, or biosensing is contingent on the degree to which various nanoarchitectures with desired molecular functionalizations can be realized, and this depends critically on characterization. Many techniques exist for analyzing DNA-organized nanostructures; however, these are almost never used in concert because of overlapping concerns about their differing character, measurement environments, and the disparity in DNA modification chemistries and probe structure or size. To assess these concerns and to see what might be gleaned from a multimodal characterization, we intensively study a single DNA nanostructure using a multiplicity of methods. Our test bed is a linear 100 base-pair double-stranded DNA that has been modified by a variety of chemical handles, dyes, semiconductor quantum dots, gold nanoparticles, and electroactive labels. To this we apply a combination of physical/optical characterization methods including electrophoresis, atomic force microscopy, transmission electron microscopy, dynamic light scattering, F?rster resonance energy transfer, voltammetry, and structural modeling. In general, the results indicate that the differences among the techniques are not so large as to prevent their effective use in combination, that the data tend to be corroborative, and that differences observed among them can actually be quite informative.
机译:设计者的DNA结构作为一种组装新颖的纳米级体系结构的方式引起了广泛的兴趣,这种体系结构对离散分子或纳米颗粒的位置进行了精确控制。在光收集,分子电子学或生物传感等各种应用中开发这种潜力取决于实现具有所需分子功能化的各种纳米结构的程度,而这在很大程度上取决于表征。存在许多分析DNA组织的纳米结构的技术。但是,由于对它们的不同特性,测量环境以及DNA修饰化学和探针结构或大小的差异的共同关注,几乎从未将它们一起使用。为了评估这些问题并查看多峰表征可能带来的好处,我们使用多种方法深入研究了单个DNA纳米结构。我们的测试床是线性的100个碱基对的双链DNA,已通过各种化学处理,染料,半导体量子点,金纳米颗粒和电活性标记进行了修饰。为此,我们结合了物理/光学表征方法,包括电泳,原子力显微镜,透射电子显微镜,动态光散射,费斯特共振能量转移,伏安法和结构建模。通常,结果表明,这些技术之间的差异并不大,以至于无法有效地组合使用;这些数据往往具有确凿的意义;而且观察到的差异实际上可以提供很多信息。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号