Department of Chemical and Biological Engineering, 1415 Engineering Drive, and §Department of Chemistry, 1101 University Avenue, University of Wisconsin-Madison , Madison, Wisconsin 53706, United States.
ACS Appl Mater Interfaces. 2013 Sep 11;5(17):8283-8. doi: 10.1021/am402594z. Epub 2013 Aug 28.
We report principles for active, user-defined control over the locations and timing with which DNA is expressed in cells. Our approach exploits unique properties of a ferrocenyl cationic lipid that is inactive when oxidized, but active when chemically reduced. We show that methods that exert spatial control over the administration of reducing agents can lead to local activation of lipoplexes and spatial control over gene expression. The versatility of this approach is demonstrated using both soluble and solid-phase reducing agents. These methods provide control over cell transfection, including methods for remote activation and the patterning of expression using solid-phase redox agents, that are difficult to achieve using conventional lipoplexes.
我们报告了一种主动的、用户定义的控制方法,可以控制 DNA 在细胞中的表达位置和时间。我们的方法利用了一种二茂铁阳离子脂质的独特性质,当它被氧化时是无活性的,但被化学还原时是有活性的。我们表明,通过对还原剂的施加进行空间控制的方法,可以导致脂质体的局部激活和基因表达的空间控制。使用可溶性和固相还原剂证明了这种方法的多功能性。这些方法提供了对细胞转染的控制,包括使用固相氧化还原试剂进行远程激活和表达模式化的方法,这是使用传统脂质体难以实现的。