Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA.
Langmuir. 2010 Oct 5;26(19):15445-52. doi: 10.1021/la1025203.
A new method to study substrate-mediated gene delivery was developed using a hexahistidine-tagged polymeric gene delivery vehicle (His-tagged polyplex) and nickel nitrilotriacetic acid (Ni-NTA) self-assembled monolayers (SAMs) on gold surfaces. The His-tagged polyplexes showed specific interaction with Ni-NTA surfaces compared to control surfaces, with increasing NTA content in SAM formulations corresponding to increasing amounts of immobilized His-tagged polypexes on the surface. Cells seeded on NTA SAMs demonstrated uptake of His-tagged polyplexes in the presence of imidazole and EDTA with low cytotoxicity. Cells seeded on NTA SAMs without imidazole and EDTA showed minimal a amount of His-tagged polyplex uptake. This showed that the release of polyplexes from the surface by imidazole and EDTA was necessary for cell uptake. Thus, this system provides potential spatial specificity for polyplex delivery controlled by location of NTA surfaces and temporal specificity for polyplex delivery controlled by the addition of imidazole and EDTA.
一种新的研究方法,以研究衬底介导的基因传递,使用六组氨酸标记的聚合物基因传递载体(His-标记的多聚物)和镍氮三乙酸(Ni-NTA)自组装单层(SAM)在金表面上。与对照表面相比,His-标记的多聚物与 Ni-NTA 表面表现出特异性相互作用,随着 SAM 配方中 NTA 含量的增加,相应地固定在表面上的 His-标记的多聚物的量也增加。在有咪唑和 EDTA 的情况下,接种在 NTA SAM 上的细胞摄取 His-标记的多聚物,细胞毒性低。没有咪唑和 EDTA 的 NTA SAM 上接种的细胞显示出最小量的 His-标记的多聚物摄取。这表明多聚物通过咪唑和 EDTA 从表面的释放是细胞摄取所必需的。因此,该系统提供了多聚物传递的空间特异性,由 NTA 表面的位置控制,以及多聚物传递的时间特异性,由添加咪唑和 EDTA 控制。