2. Academic Validation
  3. SpyCLIP: an easy-to-use and high-throughput compatible CLIP platform for the characterization of protein-RNA interactions with high accuracy

SpyCLIP: an easy-to-use and high-throughput compatible CLIP platform for the characterization of protein-RNA interactions with high accuracy

  • Nucleic Acids Res. 2019 Apr 8;47(6):e33. doi: 10.1093/nar/gkz049.
Ya Zhao 1 2 3,  Yao Zhang 1 4,  Yilan Teng 1,  Kai Liu 1 5,  Yanqing Liu 6,  Weihua Li 7,  Ligang Wu 1
Affiliations

Affiliations

  • 1 State Key Laboratory of Molecular Biology, Shanghai Key Laboratory of Molecular Andrology, CAS Center for Excellence in Molecular Cell Science, Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences; University of Chinese Academy of Sciences, Shanghai, China.
  • 2 Institute of Translational Medicine, School of Medicine, Yangzhou University, Yangzhou, China.
  • 3 Jiangsu Key Laboratory of Experimental & Translational Non-coding RNA Research, Yangzhou University, Yangzhou, China.
  • 4 NHC key Laboratory of Reproduction Regulation (Shanghai Institute of Planned Parenthood Research), pharmacy school, Fudan University, Shanghai, China.
  • 5 School of Life Sciences, Shanghai University, Shanghai, China.
  • 6 Institute of Integrated Traditional Chinese and Western Medicine, School of Medicine, Yangzhou University, Yangzhou, China.
  • 7 NHC key Laboratory of Reproduction Regulation (Shanghai Institute of Planned Parenthood Research), Fudan University, Shanghai, China.
PMID: 30715466 DOI: 10.1093/nar/gkz049
Abstract

UV crosslinking and immunoprecipitation (CLIP) coupled with high-throughput sequencing is the most state-of-the-art technology to characterize protein-RNA interactions, yet only a small portion of RNA-binding proteins (RBPs) have been studied by CLIP due to its complex procedures and high level of false-positive signals. Herein, we report a SpyCLIP method that employs a covalent linkage formed between the RBP-fused SpyTag and SpyCatcher, which can withstand the harshest washing conditions for removing nonspecific interactions. Moreover, SpyCLIP circumvents the radioactive labeling and PAGE-membrane purification steps, and the whole procedure can be performed on beads and is readily amenable to automation. We investigated multiple RBPs by SpyCLIP and generated high-quality RNA binding maps with significantly improved reproductivity and accuracy. Therefore, the small tag size and convenient protocol of SpyCLIP provides a robust method for both routine characterization and high-throughput studies of protein-RNA interactions.

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