Detection of 3'-end RNA uridylation with a protein nanopore.
basic_science · Level V
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- Record sourced from PubMed, PMID 24369707.
- Also identified by DOI 10.1021/nn4050479 and PMC identifier 3936189.
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Abstract
Post-transcriptional modifications of the 3'-ends of RNA molecules have a profound impact on their stability and processing in the cell. Uridylation, the addition of uridines to 3'-ends, has recently been found to be an important regulatory signal to stabilize the tagged molecules or to direct them toward degradation. Simple and cost-effective methods for the detection of this post-transcriptional modification are not yet available. Here, we demonstrate the selective and transient binding of 3'-uridylated ssRNAs inside the β barrel of the staphylococcal α-hemolysin (αHL) nanopore and investigate the molecular basis of uridine recognition by the pore. We show the discrimination of 3'-oligouridine tails on the basis of their lengths and propose the αHL nanopore as a useful sensor for this biologically relevant RNA modification.
Medical subject headings
- 3' Untranslated Regions
- Nanopores
- Proteins
- RNA
- Uridine