Zhang Zhe, Zhao Yanjie, Meng Xianggao, Zhao Dan, Zhang Dan, Wang Li, Liu Changlin
Key Laboratory of Pesticide and Chemical Biology, Ministry of Education and School of Chemistry, Central China Normal University, Wuhan, 430079, China.
PLoS One. 2016 Jul 19;11(7):e0158766. doi: 10.1371/journal.pone.0158766. eCollection 2016.
Metal complexes might become a new type of promising gene delivery systems because of their low cytotoxicity, structural diversity, controllable aqua- and lipo-solubility, and appropriate density and distribution of positive charges. In this study, Zn2+ complexes (1-10) formed with a series of ligands contained benzimidazole(bzim)were prepared and characterized. They were observed to have different affinities for DNA, dependent on their numbers of positive charges, bzim groups, and coordination structures around Zn2+. The binding induced DNA to condensate into spherical nanoparticles with ~ 50 nm in diameter. The cell transfection efficiency of the DNA nanoparticles was poor, although they were low toxic. The sequential addition of the cell-penetrating peptide (CPP) TAT(48-60) and polyethylene glycol (PEG) resulted in the large DNA condensates (~ 100 nm in diameter) and the increased cellular uptake. The clathrin-mediated endocytosis was found to be a key cellular uptake pathway of the nanoparticles formed with or without TAT(48-60) or/and PEG. The DNA nanoparticles with TAT(48-60) and PEG was found to have the cell transfection efficiency up to 20% of the commercial carrier Lipofect. These results indicated that a simple Zn2+-bzim complex-based composite system can be developed for efficient and low toxic gene delivery through the combination with PEG and CPPs such as TAT.
金属配合物因其低细胞毒性、结构多样性、可控的水相和脂相溶解性以及合适的正电荷密度和分布,可能成为一类新型的有前景的基因递送系统。在本研究中,制备并表征了由一系列含苯并咪唑(bzim)的配体形成的Zn2+配合物(1-10)。观察到它们对DNA具有不同的亲和力,这取决于它们的正电荷数量、bzim基团以及Zn2+周围的配位结构。这种结合促使DNA凝聚成直径约50 nm的球形纳米颗粒。尽管这些DNA纳米颗粒毒性较低,但其细胞转染效率较差。依次添加细胞穿透肽(CPP)TAT(48-60)和聚乙二醇(PEG)会导致形成较大的DNA凝聚物(直径约100 nm)并增加细胞摄取。发现网格蛋白介导的内吞作用是无论有无TAT(48-60)或/和PEG形成的纳米颗粒的关键细胞摄取途径。发现含有TAT(48-60)和PEG的DNA纳米颗粒的细胞转染效率高达商业载体Lipofect的20%。这些结果表明,通过与PEG和诸如TAT的CPPs结合,可以开发一种基于简单的Zn2+-bzim配合物的复合系统用于高效低毒的基因递送。