The positively charged S4 transmembrane segment of voltage-gated channels is thought to function as the voltage sensor by moving charge through the membrane electric field in response to depolarization. Here we studied S4 movements in the mammalian HCN pacemaker channels. Unlike most voltage-gated channel family members that are activated by depolarization, HCN channels are activated by hyperpolarization. We determined the reactivity of the charged sulfhydryl-modifying reagent, MTSET, with substituted cysteine (Cys) residues along the HCN1 S4 segment. Using an HCN1 channel engineered to be MTS resistant except for the chosen S4 Cys substitution, we determined the reactivity of 12 S4 residues to external or internal MTSET application in either the closed or open state of the channel. Cys substitutions in the NH2-terminal half of S4 only reacted with external MTSET; the rates of reactivity were rapid, regardless of whether the channel was open or closed. In contrast, Cys substitutions in the COOH-terminal half of S4 selectively reacted with internal MTSET when the channel was open. In the open state, the boundary between externally and internally accessible residues was remarkably narrow (∼3 residues). This suggests that S4 lies in a water-filled gating canal with a very narrow barrier between the external and internal solutions, similar to depolarization-gated channels. However, the pattern of reactivity is incompatible with either classical gating models, which postulate a large translational or rotational movement of S4 within a gating canal, or with a recent model in which S4 forms a peripheral voltage-sensing paddle (with S3b) that moves within the lipid bilayer (the KvAP model). Rather, we suggest that voltage sensing is due to a rearrangement in transmembrane segments surrounding S4, leading to a collapse of an internal gating canal upon channel closure that alters the shape of the membrane field around a relatively static S4 segment.
Skip Nav Destination
Article navigation
1 January 2004
Article Contents
Article|
December 15 2003
Changes in Local S4 Environment Provide a Voltage-sensing Mechanism for Mammalian Hyperpolarization–activated HCN Channels
Damian C. Bell,
Damian C. Bell
Center for Neurobiology and Behavior, Howard Hughes Medical Institute, Columbia University, New York, NY 10032
Search for other works by this author on:
Huan Yao,
Huan Yao
Center for Neurobiology and Behavior, Howard Hughes Medical Institute, Columbia University, New York, NY 10032
Search for other works by this author on:
Renee C. Saenger,
Renee C. Saenger
Center for Neurobiology and Behavior, Howard Hughes Medical Institute, Columbia University, New York, NY 10032
Search for other works by this author on:
John H. Riley,
John H. Riley
Center for Neurobiology and Behavior, Howard Hughes Medical Institute, Columbia University, New York, NY 10032
Search for other works by this author on:
Steven A. Siegelbaum
Steven A. Siegelbaum
Center for Neurobiology and Behavior, Howard Hughes Medical Institute, Columbia University, New York, NY 10032
Search for other works by this author on:
Damian C. Bell
Center for Neurobiology and Behavior, Howard Hughes Medical Institute, Columbia University, New York, NY 10032
Huan Yao
Center for Neurobiology and Behavior, Howard Hughes Medical Institute, Columbia University, New York, NY 10032
Renee C. Saenger
Center for Neurobiology and Behavior, Howard Hughes Medical Institute, Columbia University, New York, NY 10032
John H. Riley
Center for Neurobiology and Behavior, Howard Hughes Medical Institute, Columbia University, New York, NY 10032
Steven A. Siegelbaum
Center for Neurobiology and Behavior, Howard Hughes Medical Institute, Columbia University, New York, NY 10032
Address correspondence to Steven A. Siegelbaum, Center for Neurobiology & Behavior, Columbia University, 722 West 168th Street, New York, NY 10032. Fax: (212) 795-7997; email: [email protected]
Abbreviations used in this paper: HCN1-R, methane thiosulfonate–resistant mHCN1 channel; IO, inside-out; mHCN1, mouse hyperpolarization–activated, cyclic nucleotide–modulated, cation-nonselective; MTS, methane thiosulfonate; MTSET, [2-(trimethylammonium) ethyl] methane thiosulfonate; TEVC, two-electrode voltage clamp.
Received:
August 11 2003
Accepted:
October 16 2003
Online ISSN: 1540-7748
Print ISSN: 0022-1295
The Rockefeller University Press
2004
J Gen Physiol (2004) 123 (1): 5–20.
Article history
Received:
August 11 2003
Accepted:
October 16 2003
Citation
Damian C. Bell, Huan Yao, Renee C. Saenger, John H. Riley, Steven A. Siegelbaum; Changes in Local S4 Environment Provide a Voltage-sensing Mechanism for Mammalian Hyperpolarization–activated HCN Channels . J Gen Physiol 1 January 2004; 123 (1): 5–20. doi: https://doi.org/10.1085/jgp.200308918
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
A Cysteine Scan of the Inner Vestibule of Cyclic Nucleotide–gated Channels Reveals Architecture and Rearrangement of the Pore
J Gen Physiol (May,2003)
Allosteric Voltage Gating of Potassium Channels I : Mslo Ionic Currents in the Absence of Ca2+
J Gen Physiol (August,1999)
Fast and Slow Voltage Sensor Movements in HERG Potassium Channels
J Gen Physiol (February,2002)
Email alerts
Advertisement