Flow cytometric analysis of genetic FRET detectors containing variable substrate sequences

A genetic Fluorescence Resonance Energy Transfer (FRET) detector undergoes a post‐translational modification (PTM)‐induced conformational change that results in increased FRET. To test if the PTM‐dependent FRET change can be quantified by flow cytometry, we purified and immobilized a genetic detector on microbeads and used flow cytometry to measure its FRET efficiency before and after Erk‐2–mediated phosphorylation. The fluorescence ratio R between the acceptor and donor fluorescence, which was obtained by fitting a straight line through the data points in linear space, increases following phosphorylation, thus demonstrating that flow cytometry is capable of detecting a PTM‐dependent FRET response. Furthermore, when Erk‐2 and a genetic detector are coexpressed in bacteria, the measured R value changes with the substrate sequence with near single residue resolution. Similarly, the cells coexpressing the glycosylating enzyme O‐GlcNAc transferase (OGT) and a genetic detector specific for OGT exhibit a PTM‐induced change in FRET efficiency. Therefore, the combination of flow cytometry and a genetic detector may be useful to characterize the substrate specificity of a PTM enzyme and identify the sequences that are preferentially targeted for PTM in vivo. © 2010 American Institute of Chemical Engineers Biotechnol. Prog., 2010