APEX2 proximity labeling of RNA in bacteria

Rapid, spatially controlled methods are needed to investigate RNA localization in bacterial cells. APEX2 proximity labeling was shown to be adaptable to rapid RNA labeling in eukaryotic cells and, through the fusion of APEX2 to different proteins targeted to diverse subcellular locations, has been useful to identify RNA localization in these cells. Therefore, we adapted APEX2 proximity labeling of RNA to bacterial cells by generating an APEX2 fusion to the ribonuclease (RNase) E gene, which is necessary and sufficient for bacterial ribonucleoprotein (BR)-body formation. APEX2 fusion is minimally perturbative, and RNA can be rapidly labeled on the sub-minute timescale with alkyne-phenol, outpacing the rapid speed of mRNA decay in bacteria. Alkyne-phenol provides flexibility in the overall application with copper-catalyzed click chemistry for downstream processes, such as fluorescent dye azides or biotin-azides for purification. Altogether, APEX2 proximity labeling of RNA provides a useful method for studying RNA localization in bacteria.

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Publication Details

Journal
Cell Reports Methods
Published
2025-10-21
DOI
https://doi.org/10.1016/j.crmeth.2025.101206
Citations
1
Primary Topic
Biotin and Related Studies
Type
article
Field-Weighted Citation Impact
1.15
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article

APEX2 proximity labeling of RNA in bacteria

Jared M. Schrader, E. Sirotkin, Hadi Mohamad Yassine, Daniel B. Kearns et al.
1 citations
Cell Reports Methods
Biotin and Related Studies
1.15
article

APEX2 proximity labeling of RNA in bacteria

Jared M. Schrader, E. Sirotkin, Hadi Mohamad Yassine, Daniel B. Kearns, Orna Amster‐Choder, Omer Goldberger, Vincent A Lawal
article en
1 citations

Abstract

Rapid, spatially controlled methods are needed to investigate RNA localization in bacterial cells. APEX2 proximity labeling was shown to be adaptable to rapid RNA labeling in eukaryotic cells and, through the fusion of APEX2 to different proteins targeted to diverse subcellular locations, has been useful to identify RNA localization in these cells. Therefore, we adapted APEX2 proximity labeling of RNA to bacterial cells by generating an APEX2 fusion to the ribonuclease (RNase) E gene, which is necessary and sufficient for bacterial ribonucleoprotein (BR)-body formation. APEX2 fusion is minimally perturbative, and RNA can be rapidly labeled on the sub-minute timescale with alkyne-phenol, outpacing the rapid speed of mRNA decay in bacteria. Alkyne-phenol provides flexibility in the overall application with copper-catalyzed click chemistry for downstream processes, such as fluorescent dye azides or biotin-azides for purification. Altogether, APEX2 proximity labeling of RNA provides a useful method for studying RNA localization in bacteria.

Cell Reports MethodsVol. 5(11)
Wayne State University (US), Hebrew University of Jerusalem (IL), Indiana University Bloomington (US)
Openalex Percentile: Top 19%
Biotin and Related Studies
1.15
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