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原子力显微镜揭示了聚-L-鸟氨酸对潜在DNA“纳米载体”的组装过程。

Atomic force microscopy reveals the assembly of potential DNA "nanocarriers" by poly-L-ornithine.

作者信息

Mann Anita, Khan Meraj Alam, Shukla Vasundhara, Ganguli Munia

机构信息

Institute of Genomics and Integrative Biology, Mall Road (near Jubilee Hall), Delhi 110 007, India.

出版信息

Biophys Chem. 2007 Sep;129(2-3):126-36. doi: 10.1016/j.bpc.2007.05.012. Epub 2007 May 31.

Abstract

Atomic force microscopy (AFM) has been used to visualize the process of condensation of plasmid DNA by poly-L-ornithine on mica surface. AFM images reveal that the transition of negatively charged DNA to condensed nanoparticles on addition of increasing amounts of positively charged poly-L-ornithine (charge ratio (Z+/Z-) varied between 0.1 and 1) at a wide range of DNA concentrations (3-20 ng/microl) occurs through formation of several distinct morphologies. The nature of the complexes is strongly dependent on both the charge ratio and the DNA concentration. Initiation of condensation when the concentration of DNA is low (approximately 3-7 ng/microl) occurs possibly through formation of monomolecular complexes which are thick rod-like in shape. On the contrary, when condensation is carried out at DNA concentrations of 13-20 ng/microl, multimolecular structures are also formed even at low charge ratios. This difference in pathway seems to result in differences in the extent of condensation as well as size and aggregation of the nanoparticles formed at the high charge ratios. To the best of our knowledge, this is the first direct single molecule elucidation of the mechanism of DNA condensation by poly-L-ornithine. Cationic poly-aminoacids like poly-L-ornithine are known to be efficient in delivery of plasmid DNA containing therapeutic genes in a variety of mammalian cell lines by forming condensed "nanocarriers" with DNA. Single molecule insight into the mechanism by which such nanocarriers are packaged during the condensation process could be helpful in predicting efficacy of intracellular delivery and release of DNA from them and also provide important inputs for design of new gene delivery vectors.

摘要

原子力显微镜(AFM)已被用于观察聚-L-鸟氨酸在云母表面使质粒DNA凝聚的过程。AFM图像显示,在广泛的DNA浓度范围(3 - 20 ng/微升)内,随着带正电荷的聚-L-鸟氨酸添加量增加(电荷比(Z⁺/Z⁻)在0.1至1之间变化),带负电荷的DNA向凝聚的纳米颗粒转变是通过形成几种不同的形态实现的。复合物的性质强烈依赖于电荷比和DNA浓度。当DNA浓度较低(约3 - 7 ng/微升)时,凝聚的起始可能是通过形成单分子复合物,其形状为粗棒状。相反,当在13 - 20 ng/微升的DNA浓度下进行凝聚时,即使在低电荷比下也会形成多分子结构。这种途径上的差异似乎导致了凝聚程度以及在高电荷比下形成的纳米颗粒的大小和聚集方面的差异。据我们所知,这是首次对聚-L-鸟氨酸使DNA凝聚的机制进行直接的单分子阐释。像聚-L-鸟氨酸这样的阳离子聚氨基酸已知可通过与DNA形成凝聚的“纳米载体”,有效地将含有治疗性基因的质粒DNA递送至多种哺乳动物细胞系中。对这种纳米载体在凝聚过程中如何包装的单分子深入了解,有助于预测细胞内递送和DNA从其中释放的效率,也为设计新的基因递送载体提供重要信息。

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