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. 2018 Feb 26;9:825. doi: 10.1038/s41467-018-03062-w

Fig. 1.

Fig. 1

The Stormorken R304W STIM1 mutant is constitutively active. All experiments performed with HEK 293 cells. a Patch clamp recordings of CFP-STIM1 + YFP-Orai1 (black) and Stormorken mutant CFP-STIM1 R304W + YFP-Orai1 (red). b Representative images of co-localization experiments using confocal fluorescence imaging of CFP-Orai1 + YFP-STIM1 (left) and CFP-Orai1 + YFP-STIM1 R304W (right), both in resting (−TG) as well as store depleted (+TG) state. Length of scale bars correspond to 5 µm. c Representative images of localization experiments using confocal fluorescence imaging of YFP-STIM1 (top) and YFP-STIM1 R304W (bottom), both in resting (−TG) as well as store depleted (+TG) state. Length of scale bars correspond to 5 µm. d FRET homomerization experiments of YFP- + CFP- labeled STIM1 (black) and YFP- + CFP-labeled STIM1 R304W (red) in response to stored depletion using 2 µM TG. e Expression levels of STIM1 wt and STIM1 R304W, respectively, in HEK 293 cells. f FRET homomerization experiments of YFP-OASF + CFP-OASF (black) and YFP-OASF R304W + CFP-OASF R304W (red), respectively. *Significant difference (p < 0.05). Error bars are defined as SEM. Statistics are Student’s t‐test