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Photocatalytic Chemical Crosslinking for Profiling RNA-Protein Interactions in Living Cells #MMPMID35451177
Luo H; Tang W; Liu H; Zeng X; Ngai WSC; Gao R; Li H; Li R; Zheng H; Guo J; Qin F; Wang G; Li K; Fan X; Zou P; Chen PR
Angew Chem Int Ed Engl 2022[Jul]; 61 (27): e202202008 PMID35451177show ga
The dynamic interactions between RNAs and proteins play crucial roles in regulating diverse cellular processes. Proteome-wide characterization of these interactions in their native cellular context remains desirable but challenging. Herein, we developed a photocatalytic crosslinking (PhotoCAX) strategy coupled with mass spectrometry (PhotoCAX-MS) and RNA sequencing (PhotoCAX-seq) for the study of the composition and dynamics of protein-RNA interactions. By integrating the blue light-triggered photocatalyst with a dual-functional RNA-protein crosslinker (RP-linker) and the phase separation-based enrichment strategy, PhotoCAX-MS revealed a total of 2044 RBPs in human HEK293 cells. We further employed PhotoCAX to investigate the dynamic change of RBPome in macrophage cells upon LPS-stimulation, as well as the identification of RBPs interacting directly with the 5' untranslated regions of SARS-CoV-2 RNA.