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Direct real-time molecular scale visualisation of the degradation of condensed DNA complexes exposed to DNase I

机译:直接实时分子规模可视化暴露于DNase I的浓缩DNA复合物的降解

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摘要

The need to protect DNA from in vivo degradation is one of the basic tenets of therapeutic gene delivery and a standard test for any proposed delivery vector. The currently employed in vitro tests, however, presently provide no direct link between the molecular structure of the vector complexes and their success in this role, thus hindering the rational design of successful gene delivery agents. Here we apply atomic force microscopy (AFM) in liquid to visualise at the molecular scale and in real time, the effect of DNase I on generation 4 polyamidoamine dendrimers (G4) complexed with DNA. These complexes are revealed to be dynamic in nature showing a degree of mobility, in some cases revealing the addition and loss of dendrimers to individual complexes. The formation of the G4–DNA complexes is observed to provide a degree of protection to the DNA. This protection is related to the structural morphology of the formed complex, which is itself shown to be dependent on the dendrimer loading and the time allowed for complex formation.
机译:保护DNA免受体内降解的需要是治疗性基因递送的基本原则之一,并且是任何提议的递送载体的标准测试。但是,目前使用的体外试验目前在载体复合物的分子结构与其在这种作用中的成功之间没有直接联系,因此阻碍了成功的基因递送剂的合理设计。在这里,我们在液体中应用原子力显微镜(AFM)以可视化的分子规模,并实时观察DNase I对与DNA结合的第4代聚酰胺酰胺树状聚合物(G4)的影响。这些复合物在性质上是动态的,显示出一定程度的迁移性,在某些情况下揭示了树枝状大分子向各个复合物中的添加和丢失。观察到G4-DNA复合物的形成为DNA提供了一定程度的保护。这种保护作用与所形成的复合物的结构形态有关,其本身显示出依赖于树枝状聚合物的负载量和复合物形成所需的时间。

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