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. 2017 Feb 24;114(11):E2156–E2165. doi: 10.1073/pnas.1610414114

Fig. 7.

Fig. 7.

hP2X7RG345C single-channel modifications by MTS reagents that were pipette applied to the intracellular side of outside-out patches. (A and B) The representative current traces were recorded from inside-out patches excised from hP2X7RG335C-expressing oocytes without MTSET+ (A) and with 0.025 mM MTSET+ (B) in the patch pipette. The horizontal bar indicates the period of ATP4− application. The corresponding single-channel currents were calculated from the adjacent amplitude histograms. (C–E) Effect of intracellularly applied MTSET+ on current noise kinetics. Shown are original traces recorded with pipette solutions without MTSET+ (C) or with 0.025 mM MTSET+ (D). The running average current Irunavg is shown as a white line. The corresponding time-dependent smoothed noise σ2runavg is shown in the adjacent panels. (E) Statistics for the relative noise (σ2/Imean,500) of the first 500 ms during the very first ATP4− application. The means from 16 and 7 patches excised without and with MTSET+ in the pipette, respectively, are significantly different. For details, see SI Appendix, SI Materials and Methods.