Lansac Yves, Degrouard Jeril, Renouard Madalena, Toma Adriana C, Livolant Françoise, Raspaud Eric
GREMAN, Université François Rabelais, CNRS UMR 7347, 37200 Tours, France.
Laboratoire de Physique des Solides, CNRS, Université Paris-Sud, Université Paris Saclay, 91405 Orsay cedex, France.
Sci Rep. 2016 Feb 25;6:21995. doi: 10.1038/srep21995.
Highly charged polyelectrolytes can self-assemble in presence of condensing agents such as multivalent cations, amphiphilic molecules or proteins of opposite charge. Aside precipitation, the formation of soluble micro- and nano-particles has been reported in multiple systems. However a precise control of experimental conditions needed to achieve the desired structures has been so far hampered by the extreme sensitivity of the samples to formulation pathways. Herein we combine experiments and molecular modelling to investigate the detailed microscopic dynamics and the structure of self-assembled hexagonal bundles made of short dsDNA fragments complexed with small basic proteins. We suggest that inhomogeneous mixing conditions are required to form and stabilize charged self-assembled nano-aggregates in large excess of DNA. Our results should help re-interpreting puzzling behaviors reported for a large class of strongly charged polyelectrolyte systems.
高电荷聚电解质在诸如多价阳离子、两亲分子或带相反电荷的蛋白质等凝聚剂存在的情况下能够自组装。除了沉淀之外,在多个系统中都报道了可溶性微米和纳米颗粒的形成。然而,由于样品对配方途径极其敏感,迄今为止,实现所需结构所需的实验条件的精确控制受到了阻碍。在此,我们结合实验和分子建模,研究由与小碱性蛋白质复合的短双链DNA片段制成的自组装六边形束的详细微观动力学和结构。我们认为,需要不均匀的混合条件来形成并稳定大量过量DNA中的带电自组装纳米聚集体。我们的结果应该有助于重新解释一大类强电荷聚电解质系统所报道的令人困惑的行为。