Fig. 3: Photochemical characterization of cPlk1i. | Nature Communications

Fig. 3: Photochemical characterization of cPlk1i.

From: Spatio-temporal control of mitosis using light via a Plk1 inhibitor caged for activity and cellular permeability

Fig. 3

a Absorption and emission spectra of cPlk1i. b Uncaging reaction of cPlk1i releasing the active Plk1 inhibitor Plk1i. c Uncaging of cPlk1i monitored by 1H NMR. The NMR sample (CH3CN:D2O) was illuminated with 455 nm light at 8.3 mW/cm2 for the indicated times. The reference spectrum of Plk1i without the coumarin cage is below in red. Orange boxes: signals of protons a and b used to quantify uncaging, shown in (d). The assigned spectra are shown in Supplementary Fig. 2a and b. e Uncaging of cPlk1i monitored by LC-MS. Absorption chromatogram at 260 nm (top) and 450 nm (bottom). Source data are provided as a Source Data file.

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