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. 2003 Oct;122(4):459–469. doi: 10.1085/jgp.200308818

Figure 8.

Figure 8.

State-dependent modification of KAT1 cysteine mutants currents induced by external MTSET. (A) Voltage protocol for the assay of closed channels. The time course of channel modification was followed by recording every 6 s the ionic current responses to 300 ms or 1 s −160-mV pulses maintaining a constant holding potential during the intervals. Holding potential was 0 mV. (B) For the open-closed protocol the holding potential was −140 mV and the test pulse as in A. MTSET was superfused continuously in the assay of extracellular accessibility during cut-open oocyte voltage clamping. (C) MTSET modification of the macroscopic currents induced by the G163C mutant using the closed protocol. (D) Macroscopic currents induced by the G163C mutant before and after MTSET using the open/closed protocol.