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Enhanced Cellular Transfection by Ternary Non-Viral Gene Vectors Coupled with Adeno-Associated Virus-Derived Peptides

机译:三元非病毒基因载体与腺相关病毒衍生肽结合增强的细胞转染。

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摘要

The establishment of efficient and safe gene delivery systems is crucial for biomedical applications. To address this objective, novel, ternary hybrid gene vectors are designed with viral capsid peptides in non-viral gene carriers. The viral peptide, TQVGQKT, is coupled with a membrane active peptide, LK15. Which acts as a linker to tag peptide with plasmid DNA. Additionally, polyethylenimine (PEI) is employed to condense the complexes further, thereby forming ternary DNA/TQVGQKT-LK15/PEI complexes. The ternary complexes result in rapid internalization leading to significantly enhanced cellular transfection. The new moiety, TQVGQKT, as well as enhanced cellular transfection, will certainly provide crucial insights for the design of novel non-viral gene carriers with efficient and safe properties.
机译:建立有效和安全的基因递送系统对于生物医学应用至关重要。为了实现该目的,设计了在非病毒基因载体中具有病毒衣壳肽的新颖的三元杂种基因载体。病毒肽TQVGQKT与膜活性肽LK15偶联。用作标记质粒DNA的肽的接头。另外,使用聚乙烯亚胺(PEI)进一步浓缩复合物,从而形成三元DNA / TQVGQKT-LK15 / PEI复合物。三元复合物导致快速内在化,导致细胞转染显着增强。新的部分,TQVGQKT,以及增强的细胞转染,必将为设计具有高效和安全特性的新型非病毒基因载体提供至关重要的见解。

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