Beach Dale L, Keene Jack D
University of North Carolina, Chapel Hill, USA.
Methods Mol Biol. 2008;419:69-91. doi: 10.1007/978-1-59745-033-1_5.
Many elegant methodologies have been devised to explore RNA-protein as well as RNA-RNA interactions. Although the characterization of messages targeted by a specific RNA-binding protein (RBP) has been accelerated by the application of microarray technologies, reliable methods to describe the endogenous assembly of ribonucleoproteins (RNPs) are needed. However, this approach requires the targeted purification of a select mRNA under conditions favorable for the copurification of associated factors including RNA and protein components of the RNP. This chapter describes previous methods used to characterize RNPs in the context of in vitro approaches and presents the Ribotrap methodology, an in vivo protocol for message-specific purification of a target RNP. The method was developed in a yeast model system, yet is amenable to other in vivo cell systems including mammalian cell culture.
人们已经设计出许多精巧的方法来探索RNA与蛋白质以及RNA与RNA之间的相互作用。尽管微阵列技术的应用加速了对特定RNA结合蛋白(RBP)靶向的信使RNA的表征,但仍需要可靠的方法来描述核糖核蛋白(RNP)的内源性组装。然而,这种方法需要在有利于共纯化相关因子(包括RNP的RNA和蛋白质成分)的条件下对选定的mRNA进行靶向纯化。本章介绍了以前在体外方法中用于表征RNP的方法,并介绍了Ribotrap方法,这是一种用于在体内对目标RNP进行信使特异性纯化的方案。该方法是在酵母模型系统中开发的,但也适用于包括哺乳动物细胞培养在内的其他体内细胞系统。