Cardoso Ana, Trabulo Sara, Moreira João Nuno, Düzgüneş Nejat, de Lima Maria C Pedroso
Department of Biochemistry, Faculty of Science and Technology, University of Coimbra, Coimbra, Portugal.
Methods Enzymol. 2009;465:267-87. doi: 10.1016/S0076-6879(09)65014-X.
RNA interference provides a powerful technology for silencing any single protein within a target cell. Therapeutic applications of small interfering RNAs (siRNAs), however, require vehicles for stable and efficient delivery of these nucleic acid molecules, both in vitro and in vivo. Targeted lipoplexes have been used as a promising system to mediate siRNA delivery and to achieve gene silencing. Electrostatic association of transferrin (Tf) to cationic liposomes enhances the transfection of siRNA. We describe the methods used for the preparation of Tf-lipoplexes and evaluation of their biocompatibility. Approaches to assess the complexation of siRNAs, the ability of Tf-lipoplexes to mediate siRNA protection, and intracellular delivery, as well as to achieve both mRNA and protein knockdown, are also described. We illustrate the efficiency of Tf-lipoplexes in mediating the knockdown of both green fluorescent protein (GFP) and luciferase in cell lines stably expressing these reporter genes.
RNA干扰为沉默靶细胞内的任何单一蛋白质提供了一项强大技术。然而,小干扰RNA(siRNA)的治疗应用需要载体,以便在体外和体内稳定且高效地递送这些核酸分子。靶向脂质体已被用作一种有前景的系统来介导siRNA递送并实现基因沉默。转铁蛋白(Tf)与阳离子脂质体的静电结合增强了siRNA的转染。我们描述了用于制备Tf-脂质体及其生物相容性评估的方法。还描述了评估siRNA复合、Tf-脂质体介导siRNA保护和细胞内递送的能力以及实现mRNA和蛋白质敲低的方法。我们举例说明了Tf-脂质体在稳定表达这些报告基因的细胞系中介导绿色荧光蛋白(GFP)和荧光素酶敲低的效率。