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 (τ(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 τ(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.
Skip Nav Destination
Article navigation
1 March 2006
Article|
February 27 2006
Role of Charged Residues in the S1–S4 Voltage Sensor of BK Channels
Zhongming Ma,
Zhongming Ma
Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104
Search for other works by this author on:
Xing Jian Lou,
Xing Jian Lou
Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104
Search for other works by this author on:
Frank T. Horrigan
Frank T. Horrigan
Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104
Search for other works by this author on:
Zhongming Ma
Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104
Xing Jian Lou
Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104
Frank T. Horrigan
Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104
Correspondence to Frank T. Horrigan: [email protected]
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.
Received:
October 03 2005
Accepted:
February 07 2006
Online ISSN: 1540-7748
Print ISSN: 0022-1295
The Rockefeller University Press
2006
J Gen Physiol (2006) 127 (3): 309–328.
Article history
Received:
October 03 2005
Accepted:
February 07 2006
Citation
Zhongming Ma, Xing Jian Lou, Frank T. Horrigan; Role of Charged Residues in the S1–S4 Voltage Sensor of BK Channels . J Gen Physiol 1 March 2006; 127 (3): 309–328. doi: https://doi.org/10.1085/jgp.200509421
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
An Extracellular Cu2+ Binding Site in the Voltage Sensor of BK and Shaker Potassium Channels
J Gen Physiol (April,2008)
Mg2+ Enhances Voltage Sensor/Gate Coupling in BK Channels
J Gen Physiol (December,2007)
Mg2+ binding to open and closed states can activate BK channels provided that the voltage sensors are elevated
J Gen Physiol (November,2011)
Email alerts
Advertisement