Brandén L J, Mohamed A J, Smith C I
Center for BioTechnology, Department of Biosciences, Karolinska Institutet, NOVUM, SE-14157, Huddinge, Sweden.
Nat Biotechnol. 1999 Aug;17(8):784-7. doi: 10.1038/11726.
We have combined a peptide nucleic acid (PNA) with the SV40 core nuclear localization signal (NLS), to create a bifunctional PNA-NLS peptide. The PNA-NLS peptide increased the nuclear uptake of oligonucleotides and enhanced the transfection efficacy of plasmids. Gene expression from an enhanced green fluorescent protein plasmid and a lacZ plasmid was preserved when hybridized to PNA-NLS. In combination with the transfection agent polyethyleneimine, we have improved both the nuclear translocation of fluorescence-marked oligonucleotides, and the efficacy of plasmid transfection, up to eightfold. The technique obviates the use of cumbersome coupling procedures of the vector due to DNA-PNA duplex formation or displacement of the antisense plasmid DNA strand by a PNA molecule.
我们将一种肽核酸(PNA)与SV40核心核定位信号(NLS)相结合,构建了一种双功能PNA-NLS肽。PNA-NLS肽增加了寡核苷酸的核摄取,并提高了质粒的转染效率。当与PNA-NLS杂交时,增强型绿色荧光蛋白质粒和lacZ质粒的基因表达得以保留。与转染试剂聚乙烯亚胺联合使用时,我们将荧光标记寡核苷酸的核转位以及质粒转染效率提高了多达八倍。该技术避免了由于DNA-PNA双链形成或PNA分子取代反义质粒DNA链而使用繁琐的载体偶联程序。