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Biophys J
2007 May 15;9210:3524-40. doi: 10.1529/biophysj.106.097360.
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Probing the outer mouth structure of the HERG channel with peptide toxin footprinting and molecular modeling.
Tseng GN
,
Sonawane KD
,
Korolkova YV
,
Zhang M
,
Liu J
,
Grishin EV
,
Guy HR
.
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Previous studies have shown that the unusually long S5-P linker lining human ether a-go-go related gene's (hERG's) outer vestibule is critical for its channel function: point mutations at high-impact positions here can interfere with the inactivation process and, in many cases, also reduce the pore's K+ selectivity. Because no data are available on the equivalent region in the available K channel crystal structures to allow for homology modeling, we used alternative approaches to model its three-dimensional structure. The first part of this article describes mutant cycle analysis used to identify residues on hERG's outer vestibule that interact with specific residues on the interaction surface of BeKm-1, a peptide toxin with known NMR structure and a high binding affinity to hERG. The second part describes molecular modeling of hERG's pore domain. The transmembrane region was modeled after the crystal structure of KvAP pore domain. The S5-P linker was docked to the transmembrane region based on data from previous NMR and mutagenesis experiments, as well as a set of modeling criteria. The models were further restrained by contact points between hERG's outer vestibule and the bound BeKm-1 toxin molecule deduced from the mutant cycle analysis. Based on these analyses, we propose a working model for the open conformation of the outer vestibule of the hERG channel, in which the S5-P linkers interact with the pore loops to influence ion flux through the pore.
Bauer,
HERG K(+) currents in human prolactin-secreting adenoma cells.
2003, Pubmed
Bauer,
HERG K(+) currents in human prolactin-secreting adenoma cells.
2003,
Pubmed
Clarke,
Effect of S5P alpha-helix charge mutants on inactivation of hERG K+ channels.
2006,
Pubmed
,
Xenbase
Crociani,
Cell cycle-dependent expression of HERG1 and HERG1B isoforms in tumor cells.
2003,
Pubmed
Doyle,
The structure of the potassium channel: molecular basis of K+ conduction and selectivity.
1998,
Pubmed
Dun,
Allosteric effects of mutations in the extracellular S5-P loop on the gating and ion permeation properties of the hERG potassium channel.
1999,
Pubmed
,
Xenbase
Durell,
Models of the structure and voltage-gating mechanism of the shaker K+ channel.
2004,
Pubmed
Emmi,
Do glia have heart? Expression and functional role for ether-a-go-go currents in hippocampal astrocytes.
2000,
Pubmed
Fan,
Effects of outer mouth mutations on hERG channel function: a comparison with similar mutations in the Shaker channel.
1999,
Pubmed
,
Xenbase
Faravelli,
A HERG-like K+ channel in rat F-11 DRG cell line: pharmacological identification and biophysical characterization.
1996,
Pubmed
Gang,
Na+ permeation and block of hERG potassium channels.
2006,
Pubmed
Gross,
Agitoxin footprinting the shaker potassium channel pore.
1996,
Pubmed
,
Xenbase
Guy,
Molecular model of the action potential sodium channel.
1986,
Pubmed
Hidalgo,
Revealing the architecture of a K+ channel pore through mutant cycles with a peptide inhibitor.
1995,
Pubmed
,
Xenbase
Hol,
Effects of the alpha-helix dipole upon the functioning and structure of proteins and peptides.
1985,
Pubmed
Imredy,
Energetic and structural interactions between delta-dendrotoxin and a voltage-gated potassium channel.
2000,
Pubmed
,
Xenbase
Jiang,
The open pore conformation of potassium channels.
2002,
Pubmed
Jiang,
X-ray structure of a voltage-dependent K+ channel.
2003,
Pubmed
Jiang,
Dynamic conformational changes of extracellular S5-P linkers in the hERG channel.
2005,
Pubmed
Kiss,
Contribution of the selectivity filter to inactivation in potassium channels.
1999,
Pubmed
Korolkova,
New binding site on common molecular scaffold provides HERG channel specificity of scorpion toxin BeKm-1.
2002,
Pubmed
Korolkova,
An ERG channel inhibitor from the scorpion Buthus eupeus.
2001,
Pubmed
Kuo,
Crystal structure of the potassium channel KirBac1.1 in the closed state.
2003,
Pubmed
Liu,
Structural and functional role of the extracellular s5-p linker in the HERG potassium channel.
2002,
Pubmed
,
Xenbase
Long,
Crystal structure of a mammalian voltage-dependent Shaker family K+ channel.
2005,
Pubmed
López-Barneo,
Effects of external cations and mutations in the pore region on C-type inactivation of Shaker potassium channels.
1993,
Pubmed
,
Xenbase
Miller,
The charybdotoxin family of K+ channel-blocking peptides.
1995,
Pubmed
Milnes,
Preferential closed channel blockade of HERG potassium currents by chemically synthesised BeKm-1 scorpion toxin.
2003,
Pubmed
Overholt,
HERG-Like potassium current regulates the resting membrane potential in glomus cells of the rabbit carotid body.
2000,
Pubmed
Pardo-Lopez,
Mapping the binding site of a human ether-a-go-go-related gene-specific peptide toxin (ErgTx) to the channel's outer vestibule.
2002,
Pubmed
Ranganathan,
Spatial localization of the K+ channel selectivity filter by mutant cycle-based structure analysis.
1996,
Pubmed
Rosati,
Glucose- and arginine-induced insulin secretion by human pancreatic beta-cells: the role of HERG K(+) channels in firing and release.
2000,
Pubmed
Rost,
The PredictProtein server.
2004,
Pubmed
Sali,
Comparative protein modelling by satisfaction of spatial restraints.
1993,
Pubmed
Sanguinetti,
A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel.
1995,
Pubmed
,
Xenbase
Schreiber,
Energetics of protein-protein interactions: analysis of the barnase-barstar interface by single mutations and double mutant cycles.
1995,
Pubmed
Shrivastava,
A model of voltage gating developed using the KvAP channel crystal structure.
2004,
Pubmed
Smith,
The inward rectification mechanism of the HERG cardiac potassium channel.
1996,
Pubmed
Starkus,
Ion conduction through C-type inactivated Shaker channels.
1997,
Pubmed
,
Xenbase
Swartz,
Mapping the receptor site for hanatoxin, a gating modifier of voltage-dependent K+ channels.
1997,
Pubmed
Thompson,
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.
1994,
Pubmed
Torres,
Structure of the HERG K+ channel S5P extracellular linker: role of an amphipathic alpha-helix in C-type inactivation.
2003,
Pubmed
Tseng,
I(Kr): the hERG channel.
2001,
Pubmed
Tseng-Crank,
Molecular cloning and functional expression of a potassium channel cDNA isolated from a rat cardiac library.
1990,
Pubmed
,
Xenbase
Tytgat,
A unified nomenclature for short-chain peptides isolated from scorpion venoms: alpha-KTx molecular subfamilies.
1999,
Pubmed
Wang,
The seizure locus encodes the Drosophila homolog of the HERG potassium channel.
1997,
Pubmed
Wang,
A high-Na(+) conduction state during recovery from inactivation in the K(+) channel Kv1.5.
2000,
Pubmed
Wang,
A quantitative analysis of the activation and inactivation kinetics of HERG expressed in Xenopus oocytes.
1997,
Pubmed
,
Xenbase
Wang,
HERG K+ channel, a regulator of tumor cell apoptosis and proliferation.
2002,
Pubmed
Winterfield,
A hot spot for the interaction of gating modifier toxins with voltage-dependent ion channels.
2000,
Pubmed
Yao,
Estimation of potency of HERG channel blockers: impact of voltage protocol and temperature.
2005,
Pubmed
Zhang,
BeKm-1 is a HERG-specific toxin that shares the structure with ChTx but the mechanism of action with ErgTx1.
2003,
Pubmed
,
Xenbase
Zhou,
HERG-like K+ channels in microglia.
1998,
Pubmed