Nanostructured Polyelectrolyte Complexes Based on Water-Soluble Thiacalix[4]Arene and Pillar[5]Arene: Self-Assembly in Micelleplexes and Polyplexes at Packaging DNA

被引:3
|
作者
Yakimova, Luidmila S. [1 ]
Nugmanova, Aigul R. [1 ]
Mostovaya, Olga A. [1 ]
Vavilova, Alena A. [1 ]
Shurpik, Dmitriy N. [1 ]
Mukhametzyanov, Timur A. [1 ]
Stoikov, Ivan I. [1 ]
机构
[1] Kazan Fed Univ, AM Butlerov Chem Inst, Kremlevskaya St 18, Kazan 420008, Russia
基金
俄罗斯科学基金会;
关键词
nanomaterials; thiacalix[4]arene; pillar [5]arene; interpolyelectrolyte; co-assembly; selective recognition; DNA packing; MOLECULAR RECOGNITION; BINDING; GUEST; NANOPARTICLES; MEMBRANES; DAPI; NANOFILTRATION; CONVERSION; CHEMISTRY; CAPSULES;
D O I
10.3390/nano10040777
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Controlling the self-assembly of polyfunctional compounds in interpolyelectrolyte aggregates is an extremely challenging task. The use of macrocyclic compounds offers new opportunities in design of a new generation of mixed nanoparticles. This approach allows creating aggregates with multivalent molecular recognition, improved binding efficiency and selectivity. In this paper, we reported a straightforward approach to the synthesis of interpolyelectrolytes by co-assembling of the thiacalix[4]arene with four negatively charged functional groups on the one side of macrocycle, and pillar[5]arene with 10 ammonium groups located on both sides. Nanostructured polyelectrolyte complexes show effective packaging of high-molecular DNA from calf thymus. The interaction of co-interpolyelectrolytes with the DNA is completely different from the interaction of the pillar [5]arene with the DNA. Two different complexes with DNA, i.e., micelleplex- and polyplex-type, were formed. The DNA in both cases preserved its secondary structure in native B form without distorting helicity. The presented approach provides important advantage for the design of effective biomolecular gene delivery systems.
引用
收藏
页数:15
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