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. Author manuscript; available in PMC: 2007 Sep 25.
Published in final edited form as: Biochim Biophys Acta. 2006 Dec 15;1768(4):772–793. doi: 10.1016/j.bbamem.2006.12.002

Fig. 11.

Fig. 11

(A) Activation and de-activation of muscarinic inwardly rectifying K+ channels is accelerated by the GTPase activating protein RGS4. The effect of a pulse of acetylcholine on the development of K+ currents was measured by the two electrode voltage clamp method. Top trace, K+ currents evoked by addition of acetylcholine (ACh) during the time-span shown, were recorded in an oocyte that that had been injected with cRNAs encoding the M2 muscarinic receptor and the Kir3.1 and Kir3.2 K+ channel subunits. Bottom trace, K+ currents evoked by acetylcholine in an oocyte that had been injected in addition with cRNA encoding mammalian RGS4. Note faster response to ACh addition and faster deactivation upon ACh wash-out. (Adapted from Doupnik et al., 1997 [98]). (B) Simulation of HR complex formation [p=f(t)] from H and R as a function of time using the formulas and rate constants shown. (C) Same as (B) but calculated for koff values spanning from 0.01 to 30 s−1. Note that at increasing koff equilibrium is reached faster and also, that the p(eq) values decrease. (D) Same as (C) but normalizing by expressing p(t) as a function of its value at equilibrium.