| Literature DB >> 35113480 |
Sydney L Rosenblum1, Amanda L Garner1,2.
Abstract
Increasing interest in studying and modulating the interactions between RNAs and their RNA-binding proteins has indicated the need for enabling technologies. Existing means of detecting RNA-protein interactions (RPIs) are often limited to biochemical or post-lysis methods or cell-based methods that require the addition of an RNA-based affinity tag, such as the MS2 hairpin, precluding them from use in detecting small or highly processed RNAs. Taking advantage of bioorthogonal chemistry- and split-luciferase-based technologies, we developed an assay for the detection of RPIs in live cells. This article details the protocol and design considerations for RiPCA, or RNA interaction with Protein-mediated Complementation Assay.Entities:
Keywords: RNA; RNA-binding protein; RNA-protein interaction; cellular assay; protein complementation assay
Mesh:
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Year: 2022 PMID: 35113480 PMCID: PMC8852372 DOI: 10.1002/cpz1.358
Source DB: PubMed Journal: Curr Protoc ISSN: 2691-1299