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. 2006 Oct 6;92(1):76–86. doi: 10.1529/biophysj.106.088757

TABLE 2.

Kinetic and equilibrium parameters for wild-type, single-mutant, and double-mutant AChRs

AChR τo (ms) τc (ms) Popen β2 (s−1) α2 (s1) θ2 θ2 Ratio (mut/wt) n
Wild-type 0.5 ± 0.1 12 ± 5 0.04 ± 0.01 95 1910 0.05 1.0 10
αM1-F15′L 1.0 ± 0.2 0.7 ± 0.1 0.55 ± 0.07 1460 1150 1.3 26 8
αM2-L11′F 0.5 ± 0.1 122 ± 17 0.005 ± 0.001 10 2130 0.005 0.1 8
αM1-F15′L+αM2-L11′F 0.3 ± 0.1 14 ± 3 0.02 ± 0.01 80 4930 0.016 0.3 7
ɛL269F (bg) 2.3 ± 0.8 0.8 ± 0.3 0.86 ± 0.03 1030 150 6.9 138 3
bg+αM2-L11′F 1.7 ± 0.4 8.1 ± 0.3 0.21 ± 0.04 130 440 0.3 6 3
bg+αM1-F15′L+αM2-L11′F 2.2 ± 0.4 0.8 ± 0.1 0.78 ± 0.02 1460 350 4.2 84 3

The mean open (τo) and mean closed (τc) times were obtained from the corresponding histograms. Popen is the probability of channel opening within a cluster. For AChRs carrying the ɛL269F mutation, τc corresponds to the main closed component. The data correspond to the mean ± SD. Rate constants are results of a global fit of dwell times from the selected clusters at 20 mM choline by Scheme 1 (wild-type, αM1-F15′L, αM2-L11′F, and αM1-F15′L+αM2-L11′F) or by Scheme 2 for AChRs containing the background (bg) ɛL269F mutation (ɛL269F (bg), bg+αM2-L11′F, bg+αM1-F15′L+αM2-L11′F). The gating equilibrium constant, θ2, was calculated as β2/α2.