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The effect of cell penetrating peptides on transfection activity and cytotoxicity of polyallylamine

机译:细胞穿透肽对聚烯丙胺转染活性和细胞毒性的影响

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摘要

>Introduction: Cationic polymers have the potential to be modified to achieve an ideal gene vector lacking viral vector defects. The aim of the present study was to improve polyallylamine (PAA) transfection efficiency and to reduce cytotoxicity by incorporating of cell-penetrating peptides (CPPs). >Methods: To prepare the peptide-based polyplexes, PAA (15 kDa) was modified with 2 peptides (TAT and CyLoP-1) by covering the 0.5% and 1% of amines. Buffer capacity and DNA condensation ability of modified polymer, particle size and zeta potential of nanoparticles, cell viability, and transfection activity of vectors were evaluated. >Results: In low carrier to plasmid (C/P) weight ratios such as 0.5 and 1, the unmodified polymer was more capable to condense the DNA compared to the synthesized vectors. In C/P ratio of 2, the plasmid was fully condensed in all vectors. The size of polyplexes ranged from 195 to 240 nm. The zeta potential was almost as the same as PAA and varied from 25 to 27 mV. All polyplexes increased the buffer capacity compared to PAA. The transfection efficiency was improved compared to unmodified polymer especially in the vectors modified with 1% of TAT or CyLoP-1 peptides in C/P ratio of 2. The cytotoxicity of prepared vectors was less than PAA. In most ratios, the cytotoxicity of the CyLoP-1 modified samples was less than the TAT modified ones. >Conclusion: Modification of PAA with CPPs improved the transfection activity of vector.
机译:>简介:阳离子聚合物具有被修饰的潜力,可以实现理想的基因载体,而该载体没有病毒载体缺陷。本研究的目的是通过掺入细胞穿透肽(CPP)来提高聚烯丙胺(PAA)的转染效率并降低细胞毒性。 >方法:为了制备基于肽的多链体,用2种肽(TAT和CyLoP-1)修饰PAA(15 kDa),覆盖0.5%和1%的胺。评估了改性聚合物的缓冲液容量和DNA缩合能力,纳米粒子的粒径和Zeta电位,细胞活力以及载体的转染活性。 >结果:在低的载体与质粒(C / P)重量比(例如0.5和1)下,与合成载体相比,未修饰的聚合物更能浓缩DNA。在C / P比为2的情况下,质粒在所有载体中被完全浓缩。多链体的大小范围为195至240 nm。 zeta电位几乎与PAA相同,范围为25至27 mV。与PAA相比,所有多链体均增加了缓冲容量。与未修饰的聚合物相比,转染效率得到了改善,尤其是在以1%的TAT或CyLoP-1肽以2的C / P比修饰的载体中。制备的载体的细胞毒性小于PAA。在大多数比率中,CyLoP-1修饰的样品的细胞毒性小于TAT修饰的样品。 >结论:用CPP修饰PAA可改善载体的转染活性。

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