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As an information bridge between DNA and protein, RNA regulates cellular processes and gene expression in various ways. From its synthesis to degradation, RNA is associated with a range of RNA-binding proteins. Therefore, it is necessary to develop innovative methods to study the interaction between RNA and proteins. Previously, we developed an RNA-centric method, called CRISPR-based RNA-United Interacting System (CRUIS), to capture RNA-protein interaction in cells. On this basis, here we develop an enhanced CRUIS (eCRUIS) by combining the power of dCas13d and the engineered promiscuous ligase TurboID. The current version allows us to rapidly label RNA-binding proteins on the target RNA within 30 minutes, potentially for in vivo use. By introducing bait-assay with exogenous RNA, we confirm that eCRUIS can effectively label RNA-binding proteins on bait RNA in a short time. eCRUIS provides a broader range of in vitro and in vivo applications for studying RNA-protein interactions.

Original publication

DOI

10.1016/j.yexcr.2024.114051

Type

Journal article

Journal

Exp Cell Res

Publication Date

01/05/2024

Volume

438

Keywords

CRISPR, RNA-Protein interaction, TurboID, eCRUIS, Humans, CRISPR-Cas Systems, HEK293 Cells, Protein Binding, RNA, RNA-Binding Proteins