Department of Biomedical Science, College of Life Science, CHA University, Seongnam 463-836, Republic of Korea.
Biochem Biophys Res Commun. 2010 Jul 30;398(3):542-6. doi: 10.1016/j.bbrc.2010.06.115. Epub 2010 Jul 1.
The efficient delivery of nucleic acids into mammalian cells is a central aspect of research involving cell biology and medical applications, including the clinical treatment of genetic disorders. We report an efficient small hairpin RNA (shRNA) delivery system that utilizes a single species of gold nanoparticle-DNA oligonucleotide conjugate (AuNP-DNA oligo) as a universal carrier. In vitro synthesized shRNA that is specific to the p53 gene was efficiently delivered into HEK293 and HeLa human cell lines using an AuNP-DNA oligo. The delivery resulted in an 80-90% knockdown of p53 expression. The same AuNP-DNA oligo was also efficient for the delivery of another shRNA, which is specific to the Mcl-1 gene, as well as the repression of MCL-1 expression. The knockdown efficiency of shRNA that was delivered using an AuNP-DNA oligo was comparable with that of a liposome-based shRNA delivery method. Our results offer an alternate delivery system for shRNA that can be used on any gene of interest.
金纳米粒子-DNA 寡核苷酸缀合物作为通用载体高效递送小发夹 RNA
将核酸高效递送入哺乳动物细胞是细胞生物学和医学应用研究的核心方面,包括遗传疾病的临床治疗。我们报告了一种高效的小发夹 RNA(shRNA)递送系统,该系统利用单一物种的金纳米粒子-DNA 寡核苷酸缀合物(AuNP-DNA oligo)作为通用载体。使用 AuNP-DNA oligo 将体外合成的针对 p53 基因的特异性 shRNA 高效递送至 HEK293 和 HeLa 人细胞系。递送导致 p53 表达降低 80-90%。相同的 AuNP-DNA oligo 也可有效递送至另一种针对 Mcl-1 基因的 shRNA,并抑制 MCL-1 表达。使用 AuNP-DNA oligo 递送的 shRNA 的敲低效率可与基于脂质体的 shRNA 递送方法相媲美。我们的结果提供了一种替代的 shRNA 递送系统,可用于任何感兴趣的基因。