(B) Schematic illustration of one-step functionalization of Direct Blue 71 dye via electrooxidation

of amine. In order to compare the gatekeeping efficiency of two different functional ABT-737 ic50 chemistries, transmembrane ionic rectification was measured on DWCNT-dye membranes. Figure 4 illustrates the schematic mechanism of ionic rectification on the DWCNT-dye membrane. With a negative applied bias across the membrane, the dye molecules are repelled away from CNT entrance, resulting in an open state, and potassium ions can go through the CNT channel, giving easily measured current. However, at a positive bias, anionic gatekeepers will be dragged into the pore entrance, thus blocking or reducing the ionic current. The rectification experiment

setup is diagrammed in Additional file 1: Figure 4EGI-1 ic50 S1. The DWCNT membrane coated with a layer of 30-nm-thick Au/Pd film (working electrode) was placed in U-tube filled with potassium ferricyanide. Ag/AgCl electrode was used as reference/counter electrode. Constant potential was provided using a Princeton Applied Research (Oak Ridge, TN, USA) model 263A potentiostat. Linear scan was ranged from −0.60 to +0.60 V with the scan rate as 50 mV/s. The rectification factor was calculated by the ratio of ionic transport current at ±0.6-V bias. Figure 4 Schematic mechanism of ionic rectification on DWCNT-dye membrane (A, B). Gray, C; blue, N; red, O; yellow, S; light green, Fe(CN)6 3−; dark green, K+. Non-faradic EIS measurements were carried out to prove the effectiveness of the one-step electrochemical reaction on DWCNT membranes and demonstrate the conformational changes of tethered dye molecules [42]. The Nyquist plots of EIS

are shown in Figure 5A,B, with the frequency ranging from 100 kHz to 0.2 Hz. Platinum wire, Ag/AgCl, and DWCNT-dye membranes were used as counter, reference, and working electrodes, respectively (Additional file 2: Figure S2). By switching Glycogen branching enzyme the bias from 0 to + 0.6 V, charge transfer resistance was increased (R ct) 2.3 times in 20 mM KCl (Figure 5A). It indicated that positive bias can draw the negatively charged dye to the CNT entrance, resulting in the blocking of the CNT, reducing ionic current, and increasing R ct. By applying negative applied bias, R ct was Daporinad in vitro reduced two times since the dye molecules can be repelled away from the tip. Under higher concentration at 100 mM KCl, R ct was increased only 1.2 times, switching the bias from 0 to + 0.6 V, and a factor of 1.7 times, switching the bias from 0 to −0.6 V (Figure 5B). The slower R ct changing rate was due to the ionic screening effect. The results of non-faradic EIS indicated that the gatekeeper can be actuated to mimic the protein channel under bias. Figure 5 Nyquist plots of dye-modified membrane in (a) 20 mM KCl (b) 100 mM KCl.