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eCRUIS captures RNA-protein interaction in vitro and in vivo.
Zhang, Ziheng; Zhang, Yuanbing; Liu, Ji-Long.
Afiliação
  • Zhang Z; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
  • Zhang Y; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China.
  • Liu JL; School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, China; Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, OX1 3PT, United Kingdom; Shanghai Clinical Research and Trial Center, Shanghai, 201210, China. Electronic address: liujl3@shanghaitech.edu.cn.
Exp Cell Res ; 438(1): 114051, 2024 May 01.
Article em En | MEDLINE | ID: mdl-38631547
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Ligação a RNA / Sistemas CRISPR-Cas Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Ligação a RNA / Sistemas CRISPR-Cas Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article