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从甲醛交联的哺乳动物细胞中亲和纯化长链非编码RNA-蛋白质复合物

Affinity purification of long noncoding RNA-protein complexes from formaldehyde cross-linked mammalian cells.

作者信息

Gong Chenguang, Maquat Lynne E

机构信息

Department of Biochemistry and Biophysics, School of Medicine and Dentistry, University of Rochester, 601 Elmwood Ave., Rochester, NY, 14642, USA.

出版信息

Methods Mol Biol. 2015;1206:81-6. doi: 10.1007/978-1-4939-1369-5_7.

Abstract

Long noncoding RNAs (lncRNAs) are a class of recently identified untranslated RNA molecules that have been shown to function in diverse cellular processes. The purification and analysis of lncRNA-protein (lncRNP) complexes is critical toward understanding the normal physiological function of these molecules. Here, we describe the purification of lncRNP complexes from human cells using a FLAG-tagged MS2-phage coat protein (MS2 CP) that binds in sequence-specific fashion to MS2-phage coat protein-binding sites (MS2bs) with high affinity. In these experiments, a FLAG-tagged MS2 CP is transiently co-expressed with a version of the lncRNA into which 12 copies of the MS2bs have been inserted near its 3'-end. The lncRNA-FLAG-tagged MS2 CP complex is then isolated using an anti-FLAG antibody, allowing for characterization of associated cellular proteins and RNAs.

摘要

长链非编码RNA(lncRNAs)是一类最近才被发现的非翻译RNA分子,已被证明在多种细胞过程中发挥作用。lncRNA-蛋白质(lncRNP)复合物的纯化和分析对于理解这些分子的正常生理功能至关重要。在此,我们描述了使用带有FLAG标签的MS2噬菌体外壳蛋白(MS2 CP)从人细胞中纯化lncRNP复合物的方法,该蛋白以序列特异性方式与MS2噬菌体外壳蛋白结合位点(MS2bs)高亲和力结合。在这些实验中,带有FLAG标签的MS2 CP与一个lncRNA版本瞬时共表达,该lncRNA在其3'端附近插入了12个MS2bs拷贝。然后使用抗FLAG抗体分离lncRNA-带有FLAG标签的MS2 CP复合物,以便对相关的细胞蛋白质和RNA进行表征。

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