Skip to main content
. 2018 May;17(5):889–900. doi: 10.1074/mcp.RA117.000382

Fig. 1.

Fig. 1.

General workflow for isotope-coded dimedone/iododimedone labeling of proteins. In the case of recombinant protein assays, prereduced protein was removed of reductant, exposed to varying concentrations of H2O2, and coincubated with d6-dimedone to label sulfenic acids. Additionally, microsomes were incubated with d6-dimedone. After incubation, samples were then reduced with TCEP and free thiols were counter-alkylated with (d0)-iododimedone. Samples were then subjected to LC-MS/MS analysis.