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Quantitative kinetic analysis of DNA nanocomplex self-assembly with Quantum Dots FRET in a microfluidic device

机译:微流体装置中用量子点褶的DNA纳米麦基麦络合物自组装的定量动力学分析

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The demand for safer and more efficient non-viral gene vectors has increased with the recent progress of genetic medicine. Appropriate nanocomplex assembly of DNA and gene carriers is critical for successful cellular entry and transfection. However, there is a lack of knowledge on this self-assembly process, let alone the controllability of monodisperse nanocomplexes. This paper describes a novel platform integrating nanobiophotonics (Quantum Dots-mediated FRET) and microfluidic technology to determine binding kinetics that govern the structural and chemical properties of DNA nanocomplexes. We anticipate that this method will elucidate mechanistic and kinetic insights into the self-assembly process of nanocomplexes which may facilitate the rational design of more efficient gene carriers. In addition, a microfluidic platform offers many advantages, including small volume, fast response to external stimulations, continuous monitoring and real-time control of reaction environments, which may be potentially used to generate more monodisperse complexes.
机译:随着遗传医学的近期进展,对更安全和更高效的非病毒基因载体的需求增加。 DNA和基因载体的适当纳米键合组件对于成功的细胞入口和转染至关重要。然而,对这种自组装过程缺乏了解,更不用说单分散纳米复合的可控性。本文介绍了一种新的平台,整合纳米双胞腔体(量子点介导的FRET)和微流体技术,以确定控制DNA纳米键合的结构和化学性质的结合动力学。我们预计该方法将阐明机械和动力学洞察进入纳米复合物的自组装过程,这可以促进更有效的基因载体的合理设计。此外,微流体平台提供了许多优点,包括小体积,对外部刺激的快速响应,连续监测和反应环境的实时控制,这可能是可能用于产生更多单分散的复合物。

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