Fraser Iain, Liu Wei, Rebres Robert, Roach Tamara, Zavzavadjian Joelle, Santat Leah, Liu Jamie, Wall Estelle, Mumby Marc
AfCS Molecular Biology Laboratory, Division of Biology, California Institute of Technology, Pasadena, CA, USA.
Methods Mol Biol. 2007;365:261-86. doi: 10.1385/1-59745-267-X:261.
The use of RNA interference to knock down protein phosphatases has proven to be a valuable approach to understanding the functions of these enzymes in mammalian cells. Many protein phosphatases exist as multisubunit and multigene families, which has made it difficult to assess their physiological functions using traditional approaches. The ability to selectively knock down specific subunits and individual isoforms with RNA interference has begun to make it possible to determine the contributions of individual phosphatase proteins to cellular signaling. This chapter describes methods for knocking down protein phosphatases with small interfering RNAs in easily transfectable cells and by the introduction of short-hairpin RNAs into less tractable cells using lentivirus vectors.
事实证明,利用RNA干扰来敲低蛋白磷酸酶是了解这些酶在哺乳动物细胞中功能的一种有价值的方法。许多蛋白磷酸酶以多亚基和多基因家族的形式存在,这使得使用传统方法评估它们的生理功能变得困难。通过RNA干扰选择性敲低特定亚基和单个同工型的能力,已开始使确定单个磷酸酶蛋白对细胞信号传导的作用成为可能。本章介绍了在易于转染的细胞中用小干扰RNA敲低蛋白磷酸酶的方法,以及使用慢病毒载体将短发夹RNA导入较难处理的细胞中的方法。