Figure 4
From: Activation Stoichiometry and Pore Architecture of TRPA1 Probed with Channel Concatemers

The block of D918H and WT-DH does not require the permeation of Zn2+. (A–C): Effect of Zn2+ on currents from TRPA1 dimers measured with a stable holding potential of either +80 mV or −80 mV throughout the duration of the solution exchange. Traces were recorded sequentially but are shown on the same axes for illustrative purposes. Currents were activated by pretreatment with cinnamaldehyde (100 µM). (D) Summary of fraction change of TRPA1 WT, D918H and WT-D918H currents in response to Zn2+ (40 nM). IZn2+/Iinitial was calculated from the current magnitude measured 5 seconds after application of Zn2+, relative to that before Zn2+ application. n.s. P > 0.05, ****P < 0.0001 (Sidak’s multiple comparison following two-way ANOVA); N ≥ 4. (E,F): Average data from experiments as in A-C showing the magnitude of the currents in the presence of Zn2+, at the concentration indicated, relative to the starting current level IZn2+/Iinitial with a holding potential of +80 mV (E) or −80 mV (F). Note that while the potentiation of WT channels by Zn2+ is very sensitive to membrane potential, the inhibition of the D918H and WT-D918H channels is not very sensitive to membrane potential.