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. 2016 May 23;113(23):E3290–E3299. doi: 10.1073/pnas.1606348113

Fig. 5.

Fig. 5.

SMIT1 plus myo-inositol enhances IP3 production and calcium release from intracellular stores. (A) Diagram of IP3 detection by FRET of the LIBRAvIII probe, which has a FRET pair flanking an IP3 binding domain from the rat IP3 receptor. (B) Representative control time course of the photometric FRET ratio change of LIBRAvIII induced by IP3 generation after application of Oxo-M. (C) Same as B after SMIT1/myo-inositol treatment. (D) Negative control using an IP3-insensitive LIBRA version N. The FRET ratio of LIBRAvN showed more fluctuations but was not responsive to Oxo-M. (E) Summary of time constants (τ) of the recoveries of LIBRA FRET ratios for experiments as in B and C (n = 5). (F) The effects of SMIT1/myo-inositol on the increase of intracellular calcium concentration after applying Oxo-M. The orange trace illustrates an example with Ca2+ oscillation in the same condition as the red trace. (G) Summary of Ca2+ release elicited by Oxo-M as in F; bars show the integral of the Ca2+ rise (n = 5–6). Means ± SEM, *P < 0.05.