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Chemical Amination/Imination of Carbonothiolated Nucleosides During RNA Hydrolysis
Author(s) -
Jora Manasses,
Borland Kayla,
Abernathy Scott,
Zhao Ruoxia,
Kelley Melissa,
Kellner Stefanie,
Addepalli Balasubrahmanyam,
Limbach Patrick A.
Publication year - 2021
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202010793
Subject(s) - ribonucleoside , rna , chemistry , mass spectrometry , hydrolysate , nucleic acid , hydrolysis , chromatography , combinatorial chemistry , biochemistry , gene
Liquid chromatography‐tandem mass spectrometry (LC‐MS/MS) has become the gold‐standard technique to study RNA and its various modifications. While most research on RNA nucleosides has been focused on their biological roles, discovery of new modifications remains of interest. With state‐of‐the‐art technology, the presence of artifacts can confound the identification of new modifications. Here, we report the characterization of a non‐natural mcm 5 isoC ribonucleoside in S. cerevisiae total tRNA hydrolysate by higher‐energy collisional dissociation (HCD)‐based fingerprints and isotope labeling of RNA. Its discovery revealed a class of amino/imino ribonucleoside artifacts that are generated during RNA hydrolysis under ammonium‐buffered mild basic conditions. We then identified digestion conditions that can reduce or eliminate their formation. These finding and method enhancements will improve the accurate detection of new RNA modifications.