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Synthesis and Structure Elucidation of Glutamyl-Queuosine

[Image: see text] Queuosine is one of the most complex hypermodified RNA nucleosides found in the Wobble position of tRNAs. In addition to Queuosine itself, several further modified derivatives are known, where the cyclopentene ring structure is additionally modified by a galactosyl-, a mannosyl-, o...

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Detalles Bibliográficos
Autores principales: Pichler, Alexander, Hillmeier, Markus, Heiss, Matthias, Peev, Elsa, Xefteris, Stylianos, Steigenberger, Barbara, Thoma, Ines, Müller, Markus, Borsò, Marco, Imhof, Axel, Carell, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690763/
https://www.ncbi.nlm.nih.gov/pubmed/37967838
http://dx.doi.org/10.1021/jacs.3c10075
Descripción
Sumario:[Image: see text] Queuosine is one of the most complex hypermodified RNA nucleosides found in the Wobble position of tRNAs. In addition to Queuosine itself, several further modified derivatives are known, where the cyclopentene ring structure is additionally modified by a galactosyl-, a mannosyl-, or a glutamyl-residue. While sugar-modified Queuosine derivatives are found in the tRNAs of vertebrates, glutamylated Queuosine (gluQ) is only known in bacteria. The exact structure of gluQ, particularly with respect to how and where the glutamyl side chain is connected to the Queuosine cyclopentene side chain, is unknown. Here we report the first synthesis of gluQ and, using UHPLC-MS-coinjection and NMR studies, we show that the isolated natural gluQ is the α-allyl-connected gluQ compound.