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DNA Condensation by Partially Acetylated Poly(amido amine) Dendrimers: Effects of Dendrimer Charge Density on Complex Formation

机译:部分乙酰化的聚(酰胺胺)树枝状大分子的DNA缩合:树枝状大分子电荷密度对复合物形成的影响。

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摘要

The ability of poly(amido amine) (or PAMAM) dendrimers to condense semiflexible dsDNA and penetrate cell membranes gives them great potential in gene therapy and drug delivery but their high positive surface charge makes them cytotoxic. Here, we describe the effects of partial neutralization by acetylation on DNA condensation using light scattering, circular dichroism, and single molecule imaging of dendrimer-DNA complexes combed onto surfaces and tethered to those surfaces under flow. We find that DNA can be condensed by generation-five (G5) dendrimers even when the surface charges are more than 65% neutralized, but that such dendrimers bind negligibly when an end-tethered DNA is stretched in flow. We also find that when fully charged dendrimers are introduced by flow to end-tethered DNA, all DNA molecules become equally highly coated with dendrimers at a rate that becomes very fast at high dendrimer concentration, and that dendrimers remain bound during subsequent flow of dendrimer-free buffer. These results suggest that the presence of dendrimer-free DNA coexisting with dendrimer-bound DNA after bulk mixing of the two in solution may result from diffusion-limited irreversible dendrimer-DNA binding, rather than, or in addition to, the previously proposed cooperative binding mechanism of dendrimers to DNA.
机译:聚(酰胺基胺)(或PAMAM)树状大分子凝聚半柔性dsDNA并穿透细胞膜的能力为它们提供了基因治疗和药物递送的巨大潜力,但它们的高正表面电荷使它们具有细胞毒性。在这里,我们描述了使用光散射,圆二色性和通过树状聚合物-DNA复合物在表面上梳理并束缚在流动下的那些表面的乙酰化,通过乙酰化对DNA缩合进行的部分中和作用。我们发现,即使表面电荷被中和超过65%,DNA仍可被第五代(G5)树枝状聚合物缩合,但是当末端束缚的DNA在流动中伸展时,这种树枝状聚合物的结合可以忽略不计。我们还发现,当通过流动将完全带电的树状聚合物引入末端连接的DNA时,所有DNA分子都被树状聚合物同样高度地覆盖,并且其速率在高树状聚合物浓度下变得非常快,并且在随后的树状聚合物流动过程中树状聚合物保持结合状态。可用缓冲区。这些结果表明,在溶液中两者大量混合后,与树状体结合的DNA共存的无树状体DNA的存在可能是由扩散受限的不可逆的树状体-DNA结合引起的,而不是先前提出的协同结合,或除此以外的结果。树枝状分子对DNA的作用机理。

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