| Literature DB >> 30366097 |
Peter A Lobue1, Ningxi Yu1, Manasses Jora1, Scott Abernathy1, Patrick A Limbach2.
Abstract
Research into post-transcriptional processing and modification of RNA continues to speed forward, as their ever-emerging role in the regulation of gene expression in biological systems continues to unravel. Liquid chromatography tandem mass spectrometry (LC-MS/MS) has proven for over two decades to be a powerful ally in the elucidation of RNA modification identity and location, but the technique has not proceeded without its own unique technical challenges. The throughput of LC-MS/MS modification mapping experiments continues to be impeded by tedious and time-consuming spectral interpretation, particularly during for the analysis of complex RNA samples. RNAModMapper was recently developed as a tool to improve the interpretation and annotation of LC-MS/MS data sets from samples containing post-transcriptionally modified RNAs. Here, we delve deeper into the methodology and practice of RNAModMapper to provide greater insight into its utility, and remaining hurdles, in current RNA modification mapping experiments.Entities:
Keywords: Bioinformatics; Modification placement; Modified nucleosides; Sequence analysis; Transfer RNA
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Year: 2018 PMID: 30366097 PMCID: PMC6397789 DOI: 10.1016/j.ymeth.2018.10.012
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608