High-sensitivity in situ capture of endogenous RNA-protein interactions in fixed cells and primary tissues

RNA-binding proteins (RBPs) have pivotal functions in RNA metabolism, but current methods are limited in retrieving RBP-RNA interactions within endogenous biological contexts. Here, we develop INSCRIBE (IN situ Sensitive Capture of RNA-protein Interactions in Biological Environments), circumventing the challenges through in situ RNA labeling by precisely directing a purified APOBEC1-nanobody fusion to the RBP of interest. This method enables highly specific RNA-binding site identification across a diverse range of fixed biological samples such as HEK293T cells and mouse brain tissue and accurately identifies the canonical binding motifs of RBFOX2 (UGCAUG) and TDP-43 (UGUGUG) in native cellular environments. Applicable to any RBP with available primary antibodies, INSCRIBE enables sensitive capture of RBP-RNA interactions from ultra-low input equivalent to ~5 cells. The robust, versatile, and sensitive INSCRIBE workflow is particularly beneficial for precious tissues such as clinical samples, empowering the exploration of genuine RBP-RNA interactions in RNA-related disease contexts.

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Publication Details

Journal
Nature Communications
Published
2024-08-16
DOI
https://doi.org/10.1038/s41467-024-50363-4
Citations
7
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
1.64

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article

High-sensitivity in situ capture of endogenous RNA-protein interactions in fixed cells and primary tissues

Kevin D. Corbett, Brian A. Yee, Eric Kofman, Kevin Rhine et al.
7 citations
Nature Communications
RNA Research and Splicing
1.64
article

High-sensitivity in situ capture of endogenous RNA-protein interactions in fixed cells and primary tissues

Kevin D. Corbett, Brian A. Yee, Eric Kofman, Kevin Rhine, Pratibha Jagannatha, G Yeo, Qishan Liang, Tao Yu
article en
7 citations

Abstract

RNA-binding proteins (RBPs) have pivotal functions in RNA metabolism, but current methods are limited in retrieving RBP-RNA interactions within endogenous biological contexts. Here, we develop INSCRIBE (IN situ Sensitive Capture of RNA-protein Interactions in Biological Environments), circumventing the challenges through in situ RNA labeling by precisely directing a purified APOBEC1-nanobody fusion to the RBP of interest. This method enables highly specific RNA-binding site identification across a diverse range of fixed biological samples such as HEK293T cells and mouse brain tissue and accurately identifies the canonical binding motifs of RBFOX2 (UGCAUG) and TDP-43 (UGUGUG) in native cellular environments. Applicable to any RBP with available primary antibodies, INSCRIBE enables sensitive capture of RBP-RNA interactions from ultra-low input equivalent to ~5 cells. The robust, versatile, and sensitive INSCRIBE workflow is particularly beneficial for precious tissues such as clinical samples, empowering the exploration of genuine RBP-RNA interactions in RNA-related disease contexts.

Nature CommunicationsVol. 15(1)
University of California San Diego (US), Stem Cell Institute (PA)
U.S. Department of Defense, American Heart Association, Waitt Foundation, San Diego Supercomputer Center, National Institutes of Health, University of California, San Diego, National Cancer Institute
Openalex Percentile: Top 16%
RNA Research and Splicing
1.64
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