The Journal of General Physiology
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Published online Feb 27 2006. doi:10.1085/jgp.200509421
The Rockefeller University Press, 0022-1295 $8.00
JGP, Volume 127, Number 3, 309-328
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ARTICLE

 Role of Charged Residues in the S1–S4 Voltage Sensor of BK Channels



Zhongming Ma, Xing Jian Lou, and Frank T. Horrigan

Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104

Correspondence to Frank T. Horrigan: Horrigan{at}mail.med.upenn.edu

The activation of large conductance Ca2+-activated (BK) potassium channels is weakly voltage dependent compared to Shaker and other voltage-gated K+ (KV) channels. Yet BK and KV channels share many conserved charged residues in transmembrane segments S1–S4. We mutated these residues individually in mSlo1 BK channels to determine their role in voltage gating, and characterized the voltage dependence of steady-state activation (Po) and IK kinetics ({tau}(IK)) over an extended voltage range in 0–50 µM [Ca2+]i. mSlo1 contains several positively charged arginines in S4, but only one (R213) together with residues in S2 (D153, R167) and S3 (D186) are potentially voltage sensing based on the ability of charge-altering mutations to reduce the maximal voltage dependence of PO. The voltage dependence of PO and {tau}(IK) at extreme negative potentials was also reduced, implying that the closed–open conformational change and voltage sensor activation share a common source of gating charge. Although the position of charged residues in the BK and KV channel sequence appears conserved, the distribution of voltage-sensing residues is not. Thus the weak voltage dependence of BK channel activation does not merely reflect a lack of charge but likely differences with respect to KV channels in the position and movement of charged residues within the electric field. Although mutation of most sites in S1–S4 did not reduce gating charge, they often altered the equilibrium constant for voltage sensor activation. In particular, neutralization of R207 or R210 in S4 stabilizes the activated state by 3–7 kcal mol–1, indicating a strong contribution of non–voltage-sensing residues to channel function, consistent with their participation in state-dependent salt bridge interactions. Mutations in S4 and S3 (R210E, D186A, and E180A) also unexpectedly weakened the allosteric coupling of voltage sensor activation to channel opening. The implications of our findings for BK channel voltage gating and general mechanisms of voltage sensor activation are discussed.

Abbreviations used in this paper: BK, large conductance Ca2+-activated; MES, methanesulfonic acid; WT, wild-type.

X.J. Lou's present address is Johnson & Johnson Pharmaceutical Research and Development, Spring House, PA 19477.


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