Iioka Hidekazu, Macara Ian G
Department of Cell and Developmental Biology, Vanderbilt University Medical Center, 465 21st Avenue S., Nashville, TN, 37232, USA.
Methods Mol Biol. 2015;1316:67-73. doi: 10.1007/978-1-4939-2730-2_6.
Recent progress in large-scale nucleic acid analysis technology has revealed the presence of vast numbers of RNA species in cells, and extensive processing. To investigate the functions of these transcripts highly efficient methods are needed to analyze their interactions with RNA-binding proteins (RNBPs), and to understand the binding mechanisms. Many methods have been described to identify RNBPs, but none are wholly satisfactory, in part because RNAs are flexible macromolecules that adopt multiple conformations only some of which might bind to specific proteins. Here we describe a novel in vitro RNA-pull-down assay using tRNA scaffolded Streptavidin Aptamer (tRSA), to identify transcript specific RNA binding protein from mammalian cell lysates. The tRNA scaffold functions to stabilize the structure of the aptamer and the attached RNA, increasing the efficiency of the affinity purification.
大规模核酸分析技术的最新进展揭示了细胞中存在大量的RNA种类以及广泛的加工过程。为了研究这些转录本的功能,需要高效的方法来分析它们与RNA结合蛋白(RNBPs)的相互作用,并了解结合机制。已经描述了许多鉴定RNBPs的方法,但没有一种是完全令人满意的,部分原因是RNA是灵活的大分子,会采取多种构象,其中只有一些可能与特定蛋白质结合。在这里,我们描述了一种使用tRNA支架化链霉亲和素适体(tRSA)的新型体外RNA下拉分析方法,用于从哺乳动物细胞裂解物中鉴定转录本特异性RNA结合蛋白。tRNA支架起到稳定适体和附着RNA结构的作用,提高了亲和纯化的效率。