Hou Sen, Trochimczyk Piotr, Sun Lili, Wisniewska Agnieszka, Kalwarczyk Tomasz, Zhang Xuzhu, Wielgus-Kutrowska Beata, Bzowska Agnieszka, Holyst Robert
Institute of Physical Chemistry PAS, Kasprzaka 44/52, 01-224 Warsaw, Poland.
Division of Biophysics, Institute of Experimental Physics, Faculty of Physics, University of Warsaw, al. Zwirki i Wigury 93, 02-089 Warsaw, Poland.
Sci Rep. 2016 Feb 23;6:22033. doi: 10.1038/srep22033.
In contrast to the already known effect that macromolecular crowding usually promotes biological reactions, solutions of PEG 6k at high concentrations stop the cleavage of DNA by HindIII enzyme, due to the formation of DNA nanoparticles. We characterized the DNA nanoparticles and probed the prerequisites for their formation using multiple techniques such as fluorescence correlation spectroscopy, dynamic light scattering, fluorescence analytical ultracentrifugation etc. In >25% PEG 6k solution, macromolecular crowding promotes the formation of DNA nanoparticles with dimensions of several hundreds of nanometers. The formation of DNA nanoparticles is a fast and reversible process. Both plasmid DNA (2686 bp) and double-stranded/single-stranded DNA fragment (66 bp/nt) can form nanoparticles. We attribute the enhanced nanoparticle formation to the depletion effect of macromolecular crowding. This study presents our idea to enhance the formation of DNA nanoparticles by macromolecular crowding, providing the first step towards a final solution to efficient gene therapy.
与已知的大分子拥挤通常促进生物反应的效应相反,高浓度的聚乙二醇6000(PEG 6k)溶液会阻止HindIII酶对DNA的切割,这是由于DNA纳米颗粒的形成。我们对DNA纳米颗粒进行了表征,并使用多种技术,如荧光相关光谱、动态光散射、荧光分析超速离心等,探究了其形成的先决条件。在大于25%的PEG 6k溶液中,大分子拥挤促进了尺寸达数百纳米的DNA纳米颗粒的形成。DNA纳米颗粒的形成是一个快速且可逆的过程。质粒DNA(2686 bp)和双链/单链DNA片段(66 bp/nt)均可形成纳米颗粒。我们将纳米颗粒形成的增强归因于大分子拥挤的耗尽效应。本研究提出了通过大分子拥挤增强DNA纳米颗粒形成的想法,为高效基因治疗最终解决方案迈出了第一步。