Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
J Biol Chem
2011 May 27;28621:19065-75. doi: 10.1074/jbc.M111.238899.
Show Gene links
Show Anatomy links
Demonstration of physical proximity between the N terminus and the S4-S5 linker of the human ether-a-go-go-related gene (hERG) potassium channel.
de la Peña P, Alonso-Ron C, Machín A, Fernández-Trillo J, Carretero L, Domínguez P, Barros F.
???displayArticle.abstract???
Potassium channels encoded by the human ether-à-go-go-related gene (hERG) contribute to cardiac repolarization as a result of their characteristic gating properties. The hERG channel N terminus acts as a crucial determinant in gating. It is also known that the S4-S5 linker couples the voltage-sensing machinery to the channel gate. Moreover, this linker has been repeatedly proposed as an interaction site for the distal portion of the N terminus controlling channel gating, but direct evidence for such an interaction is still lacking. In this study, we used disulfide bond formation between pairs of engineered cysteines to demonstrate the close proximity between the beginning of the N terminus and the S4-S5 linker. Currents from channels with introduced cysteines were rapidly and strongly attenuated by an oxidizing agent, this effect being maximal for cysteine pairs located around amino acids 3 and 542 of the hERG sequence. The state-dependent modification of the double-mutant channels, but not the single-cysteine mutants, and the ability to readily reverse modification with the reducing agent dithiothreitol indicate that a disulfide bond is formed under oxidizing conditions, locking the channels in a non-conducting state. We conclude that physical interactions between the N-terminal-most segment of the N terminus and the S4-S5 linker constitute an essential component of the hERG gating machinery, thus providing a molecular basis for previous data and indicating an important contribution of these cytoplasmic domains in controlling its unusual gating and hence determining its physiological role in setting the electrical behavior of cardiac and other cell types.
Alonso-Ron,
Thermodynamic and kinetic properties of amino-terminal and S4-S5 loop HERG channel mutants under steady-state conditions.
2008, Pubmed,
Xenbase
Alonso-Ron,
Thermodynamic and kinetic properties of amino-terminal and S4-S5 loop HERG channel mutants under steady-state conditions.
2008,
Pubmed
,
Xenbase Alonso-Ron,
Participation of HERG channel cytoplasmic structures on regulation by the G protein-coupled TRH receptor.
2009,
Pubmed
,
Xenbase Al-Owais,
Role of intracellular domains in the function of the herg potassium channel.
2009,
Pubmed Barghaan,
Dynamic coupling of voltage sensor and gate involved in closed-state inactivation of kv4.2 channels.
2009,
Pubmed
,
Xenbase Bass,
Use of site-directed cysteine and disulfide chemistry to probe protein structure and dynamics: applications to soluble and transmembrane receptors of bacterial chemotaxis.
2007,
Pubmed Bell,
Probing S4 and S5 segment proximity in mammalian hyperpolarization-activated HCN channels by disulfide bridging and Cd2+ coordination.
2009,
Pubmed
,
Xenbase Brown,
A highly conserved alanine in the S6 domain of the hERG1 K+ channel is required for normal gating.
2008,
Pubmed
,
Xenbase Chen,
Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation.
1999,
Pubmed
,
Xenbase Chiang,
The long QT syndromes: genetic basis and clinical implications.
2000,
Pubmed Choveau,
KCNQ1 channels voltage dependence through a voltage-dependent binding of the S4-S5 linker to the pore domain.
2011,
Pubmed Falke,
Structure of a bacterial sensory receptor. A site-directed sulfhydryl study.
1988,
Pubmed Ferrer,
The S4-S5 linker directly couples voltage sensor movement to the activation gate in the human ether-a'-go-go-related gene (hERG) K+ channel.
2006,
Pubmed
,
Xenbase Finlayson,
Acquired QT interval prolongation and HERG: implications for drug discovery and development.
2004,
Pubmed Gómez-Varela,
Influence of amino-terminal structures on kinetic transitions between several closed and open states in human erg K+ channels.
2002,
Pubmed
,
Xenbase Gómez-Varela,
Relevance of the proximal domain in the amino-terminus of HERG channels for regulation by a phospholipase C-coupled hormone receptor.
2003,
Pubmed
,
Xenbase Gustina,
A recombinant N-terminal domain fully restores deactivation gating in N-truncated and long QT syndrome mutant hERG potassium channels.
2009,
Pubmed
,
Xenbase Horenstein,
Protein mobility and GABA-induced conformational changes in GABA(A) receptor pore-lining M2 segment.
2001,
Pubmed
,
Xenbase Ju,
The pore domain outer helix contributes to both activation and inactivation of the HERG K+ channel.
2009,
Pubmed Keating,
Molecular and cellular mechanisms of cardiac arrhythmias.
2001,
Pubmed Kolbe,
Cysteine 723 in the C-linker segment confers oxidative inhibition of hERG1 potassium channels.
2010,
Pubmed Li,
NMR solution structure of the N-terminal domain of hERG and its interaction with the S4-S5 linker.
2010,
Pubmed Liu,
Negative charges in the transmembrane domains of the HERG K channel are involved in the activation- and deactivation-gating processes.
2003,
Pubmed
,
Xenbase Liu,
Structural and functional role of the extracellular s5-p linker in the HERG potassium channel.
2002,
Pubmed
,
Xenbase Lu,
Effects of premature stimulation on HERG K(+) channels.
2001,
Pubmed Miranda,
FRET with multiply labeled HERG K(+) channels as a reporter of the in vivo coarse architecture of the cytoplasmic domains.
2008,
Pubmed Morais Cabral,
Crystal structure and functional analysis of the HERG potassium channel N terminus: a eukaryotic PAS domain.
1998,
Pubmed
,
Xenbase Muskett,
Mechanistic insight into human ether-à-go-go-related gene (hERG) K+ channel deactivation gating from the solution structure of the EAG domain.
2011,
Pubmed Ng,
The N-terminal tail of hERG contains an amphipathic α-helix that regulates channel deactivation.
2011,
Pubmed Piper,
Gating currents associated with intramembrane charge displacement in HERG potassium channels.
2003,
Pubmed
,
Xenbase Redfern,
Relationships between preclinical cardiac electrophysiology, clinical QT interval prolongation and torsade de pointes for a broad range of drugs: evidence for a provisional safety margin in drug development.
2003,
Pubmed Roden,
Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.
1996,
Pubmed Saenen,
Modulation of HERG gating by a charge cluster in the N-terminal proximal domain.
2006,
Pubmed Sanguinetti,
Mutations of the S4-S5 linker alter activation properties of HERG potassium channels expressed in Xenopus oocytes.
1999,
Pubmed
,
Xenbase Sanguinetti,
A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel.
1995,
Pubmed
,
Xenbase Schönherr,
Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel.
1996,
Pubmed
,
Xenbase Schwartz,
Management of long QT syndrome.
2005,
Pubmed Smith,
Fast and slow voltage sensor movements in HERG potassium channels.
2002,
Pubmed
,
Xenbase Smith,
The inward rectification mechanism of the HERG cardiac potassium channel.
1996,
Pubmed Spector,
Fast inactivation causes rectification of the IKr channel.
1996,
Pubmed
,
Xenbase Subbiah,
Molecular basis of slow activation of the human ether-a-go-go related gene potassium channel.
2004,
Pubmed
,
Xenbase Subbiah,
Tryptophan scanning mutagenesis of the HERG K+ channel: the S4 domain is loosely packed and likely to be lipid exposed.
2005,
Pubmed
,
Xenbase Thomas,
Regulation of HERG potassium channel activation by protein kinase C independent of direct phosphorylation of the channel protein.
2003,
Pubmed
,
Xenbase Trudeau,
HERG, a human inward rectifier in the voltage-gated potassium channel family.
1995,
Pubmed Van Slyke,
Mutations within the S4-S5 linker alter voltage sensor constraints in hERG K+ channels.
2010,
Pubmed
,
Xenbase Viloria,
Differential effects of amino-terminal distal and proximal domains in the regulation of human erg K(+) channel gating.
2000,
Pubmed
,
Xenbase Viskin,
Long QT syndromes and torsade de pointes.
1999,
Pubmed Wang,
Dynamic control of deactivation gating by a soluble amino-terminal domain in HERG K(+) channels.
2000,
Pubmed
,
Xenbase Wang,
Regulation of deactivation by an amino terminal domain in human ether-à-go-go-related gene potassium channels.
1998,
Pubmed
,
Xenbase Zhang,
Gating charges in the activation and inactivation processes of the HERG channel.
2004,
Pubmed
,
Xenbase Zhang,
Interactions between charged residues in the transmembrane segments of the voltage-sensing domain in the hERG channel.
2005,
Pubmed
,
Xenbase