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The Escherichia coli endoribonucleases RNase E (Rne) and RNase G (Rng) have sequence similarity and broadly similar sequence specificity. Whereas the absence of Rne normally is lethal, we show here that E. coli bacteria that lack the rne gene can be made viable by overexpression of Rng. Rng-compleme...
ORGANISM(S): Escherichia coli 
Four open-source software suites for the analysis of oligonucleotide data from tandem MS have been reported. These tools are all based on matching theoretical spectral libraries generated by silico digestion. While some software publications have included simple comparisons with previously published...
ORGANISM(S): Escherichia coli 
2026-03-09 | PXD075396 | Pride
The Escherichia coli endoribonucleases RNase E (Rne) and RNase G (Rng) have sequence similarity and broadly similar sequence specificity. Whereas the absence of Rne normally is lethal, we show here that E. coli bacteria that lack the rne gene can be made viable by overexpression of Rng. Rng-compleme...
ORGANISM(S): Escherichia coli 
Here, we establish a sequence-resolved mouse liver small-RNA epitranscriptomic database by integrating nucleoside-level modification discovery with complementary RNase T1 and RNase A LC–MS/MS oligonucleotide mapping, enabling high-confidence modification-site annotation across tRNAs, 5S and 5.8S rRN...
ORGANISM(S): Mus musculus (Mouse) 
2026-08-31 | PXD082484 | Pride
RNA modifications play crucial roles in regulating cellular processes, but comprehensive mapping of the human RNome still remains limited by technological challenges. Mass spectrometry is a valuable tool to analyse RNA modifications and complementing sequencing-based analysis. Current MS-based oligo...
ORGANISM(S): Escherichia coli 
2026-09-07 | PXD070755 | Pride
With the rapid growth of synthetic messenger RNA (mRNA)-based therapeutics and vaccines, the development of analytical tools for characterization of long, complex RNAs has become essential. Tandem liquid chromatography-mass spectrometry (LC-MS/MS) permits direct assessment of the mRNA primary sequen...
ORGANISM(S): synthetic RNA 
2022-07-26 | PXD033334 | Pride
We immunoprecipitate (IP) RSRC2 from HCT116 cells in the presence or absence of RNase A/T1 mix to identify RNA-mediated and RNA-independent RSRC2 protein-protein interaction networks. Four biological replicates were performed for each IP-MS in cells +/- RNase A/T1 Mix (EN0551, ThermoFisher) using Ig...
ORGANISM(S): Homo sapiens (Human) 
2026-03-12 | PXD059507 | Pride
We developed native elongating transcript sequencing (NET-seq, Churchman and Weissman Nature 2011, PMID: 21248844) combined with RNase footprinting of nascent transcripts (RNET-seq) to visualize translocation dynamics and nascent transcript errors in paused RNA polymerases in E. coli. We employed R...
ORGANISM(S): Escherichia coli 
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