Proximity labeling to detect RNA-protein interactions in live cells

FEBS Open Bio. 2019 Nov;9(11):1860-1868. doi: 10.1002/2211-5463.12706. Epub 2019 Sep 25.

Abstract

RNA biology is orchestrated by the dynamic interactions of RNAs and RNA-binding proteins (RBPs). In the present study, we describe a new method of proximity-dependent protein labeling to detect RNA-protein interactions [RNA-bound protein proximity labeling (RBPL)]. We selected the well-studied RNA-binding protein PUF to examine the current proximity labeling enzymes birA* and APEX2. A new version of birA*, BASU, was used to validate that the PUF protein binds its RNA motif. We further optimized the RBPL labeling system using an inducible expression system. The RBPL (λN-BASU) labeling experiments exhibited high signal-to-noise ratios. We subsequently determined that RBPL (λN-BASU) is more suitable than RBPL (λN-APEX2) for the detection of RNA-protein interactions in live cells. Interestingly, our results also reveal that proximity labeling is probably capable of biotinylating proximate nascent peptide.

Keywords: APEX2; RNA binding protein; RNA-protein interactions; birA*; nascent peptide; proximity labeling.

MeSH terms

  • Biotinylation
  • Cell Survival
  • Cells, Cultured
  • HEK293 Cells
  • Humans
  • RNA / chemistry*
  • RNA / metabolism
  • RNA-Binding Proteins / chemistry*
  • RNA-Binding Proteins / metabolism
  • Staining and Labeling*

Substances

  • RNA-Binding Proteins
  • RNA