A proximity-dependent assay for specific RNA–protein interactions in intact cells
Year: 2016
Type: article
Abstract: The proximity ligation assay (PLA) is an immune staining method that detects protein-protein interactions in fixed cells. We describe here RNA-PLA, a simple adaptation of this technology that allows the detection of specific RNA-protein interactions in fixed cells by using a DNA oligonucleotide that hybridizes to a target RNA in combination with an antibody that recognizes the protein bound to the target RNA. Stable and transient RNA-protein interactions can be readily detected by generation of a fluorescent signal in discrete compartments in intact fixed cells with high specificity. We demonstrate that this approach requires the colocalization of the binding protein and its RNA target in the same cellular compartment, use of an oligonucleotide complementary to the target RNA, and the presence of a binding site for the protein in the target RNA.
Source: RNA
Language: English
Topic: RNA Research and Splicing
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Awards: The essential role of gamma-secretase in human papillomavirus infection, Noncanonical microRNA biogenesis and function in a gamma herpesvirus and mammals, Role of Retromer-mediated Retrograde Transport in HPV Entry, Molecular Basis of Cancer Virus Replication, Transformation, and Innate Defense, Viral Non-Coding RNAs and Cell Transformation, G9000132752, Yale Clinical and Translational Science Award, Noncanonical microRNA biogenesis and function in a gamma herpesvirus and mammals
OpenAlex ID: W2522773523
