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. 2018 Nov 20;19(24):2575–2583. doi: 10.1002/cbic.201800525

Table 2.

Mass transitions of 7‐methylguanosine isotopomers in pulse‐chase NAIL‐MS for RNA repair observation.

Nucleoside Labeling[a] Precursor[b] Product[c] t R [min]
guanosine unlabeled[d] 284 152 3.7
15N‐label[e] 289 157 3.7
SIL‐IS[f] 299 162 3.7
7‐methylguanosine unlabeled 298 166 2.0
CD3‐label[g] 301 169 2.0
15N/CD3‐label[e] 306 174 2.0
SIL‐IS 314 177 2.0

[a] Used labeling technique. [b] Precursor ion m/z. [c] Product ion m/z. [d] No labeled metabolites, original nucleosides. [e] tRNA transcribed in the presence of 15N, de novo nucleosides. [f] SIL‐IS: stable isotope labeled internal standard prepared from a complete 13C/15N‐labeled E. coli culture. [g] Labeling with CD3‐methionine to detect enzymatic methylation of original nucleoside, methylated after stress.