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4‐Thiouridine‐Enhanced Peroxidase‐Generated Biotinylation of RNA

10

Citations

23

References

2020

Year

Abstract

Peroxidase-generated proximity labeling is in widespread use to study subcellular proteomes and the protein interaction networks in living cells, but the development of subcellular RNA labeling is limited. APEX-seq has emerged as a new method to study subcellular RNA in living cells, but the labeling of RNA still has room to improve. In this work, we describe 4-thiouridine (s<sup>4</sup> U)-enhanced peroxidase-generated biotinylation of RNA with high efficiency. The incorporation of s<sup>4</sup> U could introduce additional sites for RNA labeling, enhanced biotinylation was observed on monomer, model oligo RNA and total RNA. Through the s<sup>4</sup> U metabolic approach, the in vivo RNA biotinylation efficiency by peroxidase catalysis was also dramatically increased, which will benefit RNA isolation and study for the spatial transcriptome.

References

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