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. Author manuscript; available in PMC: 2019 Apr 8.
Published in final edited form as: Nat Chem Biol. 2018 Oct 8;14(11):1032–1042. doi: 10.1038/s41589-018-0136-y

Figure 2. The methyl oxoacetate ester of DMOG is rapidly hydrolysed in cell culture media to yield MOG.

Figure 2

a) LC-MS base-peak chromatogram and corresponding mass spectrum of 10 µM DMOG in water, with peak and ion annotated.

b) LC-MS base-peak chromatogram and corresponding mass spectrum of 10 µM NOG in water, with peak and ion annotated.

c) LC-MS base-peak chromatogram demonstrating the MOG peak formed after incubation in water for 20 h at room temperature. Right: mass spectrum of MOG peak, with ion corresponding to MOG annotated.

d) 1D-1H-NMR spectra of DMOG freshly resuspended in RPMI medium, or after incubation in RPMI medium overnight, with and without the addition of a synthesised MOG standard. Signals annotated according to the labelled structure of DMOG in (e), DMOG peaks with blue numbers and MOG peaks with red numbers.

e) 2D-1H,13C-HMBC-NMR spectrum of DMOG incubated in RPMI media, DMOG peaks with blue numbers and MOG peaks with red numbers, overlapping cross-peak shown in purple. Right: DMOG structure annotated with the relevant 13C signal shifts.

Data are representative of more than 3 independent experiments each with similar results.