| Literature DB >> 26965255 |
Xuexiu Zheng1, Sunghee Cho1, Heegyum Moon1, Tiing Jen Loh1, Ha Na Jang1, Haihong Shen2.
Abstract
RNA-protein interaction can be detected by RNA pull-down and immunoblotting methods. Here, we describe a method to detect RNA-protein interaction using RNA pull down and to identify the proteins that are pulled-down by the RNA using immunoblotting. In this protocol, RNAs with specific sequences are biotinylated and immobilized onto Streptavidin beads, which are then used to pull down interacting proteins from cellular extracts. The presence of a specific protein is subsequently verified by SDS- polyacrylamide gel electrophoresis and immunoblotting with antibodies. Interactions between the SMN RNA and the PSF protein and between the caspase-2 RNA and the SRSF3 protein (SRp20) in nuclear extract prepared from HeLa cells are illustrated as examples.Entities:
Keywords: Biotinylation; Immunoblotting; RNA binding protein; RNA pull-down; RNA–protein interaction; Spliceosome; Streptavidin
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Year: 2016 PMID: 26965255 DOI: 10.1007/978-1-4939-3591-8_4
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745