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Proc Natl Acad Sci U S A
2011 May 31;10822:9095-100. doi: 10.1073/pnas.1100872108.
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KCNE1 enhances phosphatidylinositol 4,5-bisphosphate (PIP2) sensitivity of IKs to modulate channel activity.
Li Y, Zaydman MA, Wu D, Shi J, Guan M, Virgin-Downey B, Cui J.
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Phosphatidylinositol 4,5-bisphosphate (PIP(2)) is necessary for the function of various ion channels. The potassium channel, I(Ks), is important for cardiac repolarization and requires PIP(2) to activate. Here we show that the auxiliary subunit of I(Ks), KCNE1, increases PIP(2) sensitivity 100-fold over channels formed by the pore-forming KCNQ1 subunits alone, which effectively amplifies current because native PIP(2) levels in the membrane are insufficient to activate all KCNQ1 channels. A juxtamembranous site in the KCNE1 C terminus is a key structural determinant of PIP(2) sensitivity. Long QT syndrome associated mutations of this site lower PIP(2) affinity, resulting in reduced current. Application of exogenous PIP(2) to these mutants restores wild-type channel activity. These results reveal a vital role of PIP(2) for KCNE1 modulation of I(Ks) channels that may represent a common mechanism of auxiliary subunit modulation of many ion channels.
Abbott,
MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia.
1999, Pubmed,
Xenbase
Abbott,
MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia.
1999,
Pubmed
,
Xenbase Abbott,
MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis.
2001,
Pubmed
,
Xenbase Abbott,
Disease-associated mutations in KCNE potassium channel subunits (MiRPs) reveal promiscuous disruption of multiple currents and conservation of mechanism.
2002,
Pubmed Angelo,
KCNE5 induces time- and voltage-dependent modulation of the KCNQ1 current.
2002,
Pubmed
,
Xenbase Barhanin,
K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current.
1996,
Pubmed
,
Xenbase Bian,
HERG K(+) channel activity is regulated by changes in phosphatidyl inositol 4,5-bisphosphate.
2001,
Pubmed Cui,
Gating of IsK expressed in Xenopus oocytes depends on the amount of mRNA injected.
1994,
Pubmed
,
Xenbase Deschênes,
Modulation of Kv4.3 current by accessory subunits.
2002,
Pubmed Ding,
Regulation of cardiac IKs potassium current by membrane phosphatidylinositol 4,5-bisphosphate.
2004,
Pubmed Grunnet,
KCNE4 is an inhibitory subunit to the KCNQ1 channel.
2002,
Pubmed
,
Xenbase Grunnet,
KCNQ1 channels sense small changes in cell volume.
2003,
Pubmed
,
Xenbase Habuchi,
Endothelin enhances delayed potassium current via phospholipase C in guinea pig ventricular myocytes.
1992,
Pubmed Hedley,
The genetic basis of long QT and short QT syndromes: a mutation update.
2009,
Pubmed Heitzmann,
Heteromeric KCNE2/KCNQ1 potassium channels in the luminal membrane of gastric parietal cells.
2004,
Pubmed Kang,
Structure of KCNE1 and implications for how it modulates the KCNQ1 potassium channel.
2008,
Pubmed Kapplinger,
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
2009,
Pubmed Kurokawa,
Requirement of subunit expression for cAMP-mediated regulation of a heart potassium channel.
2003,
Pubmed Lai,
Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms.
2005,
Pubmed Lo,
Independent and exclusive modulation of cardiac delayed rectifying K+ current by protein kinase C and protein kinase A.
1998,
Pubmed
,
Xenbase Lopes,
Protein kinase A modulates PLC-dependent regulation and PIP2-sensitivity of K+ channels.
2007,
Pubmed
,
Xenbase Loussouarn,
Phosphatidylinositol-4,5-bisphosphate, PIP2, controls KCNQ1/KCNE1 voltage-gated potassium channels: a functional homology between voltage-gated and inward rectifier K+ channels.
2003,
Pubmed Lvov,
Identification of a protein-protein interaction between KCNE1 and the activation gate machinery of KCNQ1.
2010,
Pubmed Marx,
Requirement of a macromolecular signaling complex for beta adrenergic receptor modulation of the KCNQ1-KCNE1 potassium channel.
2002,
Pubmed Matavel,
PKC activation and PIP(2) depletion underlie biphasic regulation of IKs by Gq-coupled receptors.
2009,
Pubmed
,
Xenbase McCrossan,
MinK-related peptide 2 modulates Kv2.1 and Kv3.1 potassium channels in mammalian brain.
2003,
Pubmed McDonald,
A minK-HERG complex regulates the cardiac potassium current I(Kr).
1997,
Pubmed
,
Xenbase Murata,
Phosphoinositide phosphatase activity coupled to an intrinsic voltage sensor.
2005,
Pubmed
,
Xenbase Nakajo,
Stoichiometry of the KCNQ1 - KCNE1 ion channel complex.
2010,
Pubmed
,
Xenbase Oliver,
Functional conversion between A-type and delayed rectifier K+ channels by membrane lipids.
2004,
Pubmed
,
Xenbase Park,
Impaired KCNQ1-KCNE1 and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT syndrome.
2005,
Pubmed Pian,
Regulation of gating and rundown of HCN hyperpolarization-activated channels by exogenous and endogenous PIP2.
2006,
Pubmed
,
Xenbase Rocheleau,
Secondary structure of a KCNE cytoplasmic domain.
2006,
Pubmed
,
Xenbase Romey,
Molecular mechanism and functional significance of the MinK control of the KvLQT1 channel activity.
1997,
Pubmed Rosenhouse-Dantsker,
Molecular characteristics of phosphoinositide binding.
2007,
Pubmed Rudy,
Computational biology in the study of cardiac ion channels and cell electrophysiology.
2006,
Pubmed Sanguinetti,
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.
1996,
Pubmed
,
Xenbase Schroeder,
A constitutively open potassium channel formed by KCNQ1 and KCNE3.
2000,
Pubmed
,
Xenbase Sesti,
Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome.
1998,
Pubmed
,
Xenbase Shamgar,
Calmodulin is essential for cardiac IKS channel gating and assembly: impaired function in long-QT mutations.
2006,
Pubmed Suh,
PIP2 is a necessary cofactor for ion channel function: how and why?
2008,
Pubmed Takumi,
Alteration of channel activities and gating by mutations of slow ISK potassium channel.
1991,
Pubmed
,
Xenbase Tapper,
MinK subdomains that mediate modulation of and association with KvLQT1.
2000,
Pubmed
,
Xenbase Thomas,
Characterization of a binding site for anionic phospholipids on KCNQ1.
2011,
Pubmed Tinel,
KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel.
2000,
Pubmed
,
Xenbase Tinel,
M-type KCNQ2-KCNQ3 potassium channels are modulated by the KCNE2 subunit.
2000,
Pubmed Wang,
MinK-KvLQT1 fusion proteins, evidence for multiple stoichiometries of the assembled IsK channel.
1998,
Pubmed Winks,
Relationship between membrane phosphatidylinositol-4,5-bisphosphate and receptor-mediated inhibition of native neuronal M channels.
2005,
Pubmed Xie,
Phosphatidylinositol-4,5-bisphosphate (PIP2) regulation of strong inward rectifier Kir2.1 channels: multilevel positive cooperativity.
2008,
Pubmed
,
Xenbase Yang,
Single-channel properties of IKs potassium channels.
1998,
Pubmed
,
Xenbase Yasuda,
Regulation of the muscarinic K+ channel by extracellular ATP through membrane phosphatidylinositol 4,5-bisphosphate in guinea-pig atrial myocytes.
2005,
Pubmed Yu,
MinK-related peptide 1: A beta subunit for the HCN ion channel subunit family enhances expression and speeds activation.
2001,
Pubmed
,
Xenbase Zhang,
PIP(2) activates KCNQ channels, and its hydrolysis underlies receptor-mediated inhibition of M currents.
2003,
Pubmed
,
Xenbase Zhang,
minK-related peptide 1 associates with Kv4.2 and modulates its gating function: potential role as beta subunit of cardiac transient outward channel?
2001,
Pubmed
,
Xenbase