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J Biol Chem
2012 Nov 23;28748:40266-78. doi: 10.1074/jbc.M111.336339.
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Distant cytosolic residues mediate a two-way molecular switch that controls the modulation of inwardly rectifying potassium (Kir) channels by cholesterol and phosphatidylinositol 4,5-bisphosphate (PI(4,5)P(2)).
Rosenhouse-Dantsker A
,
Noskov S
,
Han H
,
Adney SK
,
Tang QY
,
Rodríguez-Menchaca AA
,
Kowalsky GB
,
Petrou VI
,
Osborn CV
,
Logothetis DE
,
Levitan I
.
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BACKGROUND: Cholesterol modulates inwardly rectifying potassium (Kir) channels.
RESULTS: A two-way molecular cytosolic switch controls channel modulation by cholesterol and PI(4,5)P(2).
CONCLUSION: Cholesterol and PI(4,5)P(2) induce a common gating pathway of Kir2.1 despite their opposite impact on channel function.
SIGNIFICANCE: These findings provide insights into structure-function relationship of ion channels and contribute to understanding of the mechanisms underlying their regulation by lipids. Inwardly rectifying potassium (Kir) channels play an important role in setting the resting membrane potential and modulating membrane excitability. An emerging feature of several Kir channels is that they are regulated by cholesterol. However, the mechanism by which cholesterol affects channel function is unclear. Here we show that mutations of two distant Kir2.1 cytosolic residues, Leu-222 and Asn-251, form a two-way molecular switch that controls channel modulation by cholesterol and affects critical hydrogen bonding. Notably, these two residues are linked by a residue chain that continues from Asn-251 to connect adjacent subunits. Furthermore, our data indicate that the same switch also regulates the sensitivity of the channels to phosphatidylinositol 4,5-bisphosphate, a phosphoinositide that is required for activation of Kir channels. Thus, although cholesterol and phosphatidylinositol 4,5-bisphosphate do not interact with the same region of Kir2.1, these different modulators induce a common gating pathway of the channel.
Ambudkar,
Cellular domains that contribute to Ca2+ entry events.
2004, Pubmed
Ambudkar,
Cellular domains that contribute to Ca2+ entry events.
2004,
Pubmed
Bolotina,
Variations of membrane cholesterol alter the kinetics of Ca2(+)-dependent K+ channels and membrane fluidity in vascular smooth muscle cells.
1989,
Pubmed
Bowles,
Hypercholesterolemia inhibits L-type calcium current in coronary macro-, not microcirculation.
2004,
Pubmed
Brooks,
CHARMM: the biomolecular simulation program.
2009,
Pubmed
D'Avanzo,
Enantioselective protein-sterol interactions mediate regulation of both prokaryotic and eukaryotic inward rectifier K+ channels by cholesterol.
2011,
Pubmed
Du,
Characteristic interactions with phosphatidylinositol 4,5-bisphosphate determine regulation of kir channels by diverse modulators.
2004,
Pubmed
,
Xenbase
Epshtein,
Identification of a C-terminus domain critical for the sensitivity of Kir2.1 to cholesterol.
2009,
Pubmed
Fang,
Functional expression of Kir2.x in human aortic endothelial cells: the dominant role of Kir2.2.
2005,
Pubmed
Hansen,
Structural basis of PIP2 activation of the classical inward rectifier K+ channel Kir2.2.
2011,
Pubmed
He,
Identification of critical residues controlling G protein-gated inwardly rectifying K(+) channel activity through interactions with the beta gamma subunits of G proteins.
2002,
Pubmed
Heaps,
Hypercholesterolemia abolishes voltage-dependent K+ channel contribution to adenosine-mediated relaxation in porcine coronary arterioles.
2005,
Pubmed
Hilgemann,
The complex and intriguing lives of PIP2 with ion channels and transporters.
2001,
Pubmed
Huang,
Direct activation of inward rectifier potassium channels by PIP2 and its stabilization by Gbetagamma.
1998,
Pubmed
,
Xenbase
Humphrey,
VMD: visual molecular dynamics.
1996,
Pubmed
HUTTER,
Rectifying properties of heart muscle.
1960,
Pubmed
Jo,
CHARMM-GUI Membrane Builder for mixed bilayers and its application to yeast membranes.
2009,
Pubmed
Levitan,
Membrane cholesterol content modulates activation of volume-regulated anion current in bovine endothelial cells.
2000,
Pubmed
Levitan,
Cholesterol and ion channels.
2010,
Pubmed
Levitan,
Cholesterol and Kir channels.
2009,
Pubmed
Lockwich,
Assembly of Trp1 in a signaling complex associated with caveolin-scaffolding lipid raft domains.
2000,
Pubmed
Logothetis,
Phosphoinositide-mediated gating of inwardly rectifying K(+) channels.
2007,
Pubmed
Lopes,
Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies.
2002,
Pubmed
,
Xenbase
Lundbaek,
Membrane stiffness and channel function.
1996,
Pubmed
Lundbaek,
Regulation of sodium channel function by bilayer elasticity: the importance of hydrophobic coupling. Effects of Micelle-forming amphiphiles and cholesterol.
2004,
Pubmed
Martens,
Differential targeting of Shaker-like potassium channels to lipid rafts.
2000,
Pubmed
Martens,
Isoform-specific localization of voltage-gated K+ channels to distinct lipid raft populations. Targeting of Kv1.5 to caveolae.
2001,
Pubmed
McDonald,
Satisfying hydrogen bonding potential in proteins.
1994,
Pubmed
Mirshahi,
Hydrogen-bonding dynamics between adjacent blades in G-protein beta-subunit regulates GIRK channel activation.
2006,
Pubmed
,
Xenbase
Nishida,
Crystal structure of a Kir3.1-prokaryotic Kir channel chimera.
2007,
Pubmed
Noskov,
Control of ion selectivity in potassium channels by electrostatic and dynamic properties of carbonyl ligands.
2004,
Pubmed
Olesen,
Haemodynamic shear stress activates a K+ current in vascular endothelial cells.
1988,
Pubmed
Pegan,
Cytoplasmic domain structures of Kir2.1 and Kir3.1 show sites for modulating gating and rectification.
2005,
Pubmed
,
Xenbase
Phillips,
Scalable molecular dynamics with NAMD.
2005,
Pubmed
Romanenko,
Cholesterol sensitivity and lipid raft targeting of Kir2.1 channels.
2004,
Pubmed
Romanenko,
Sensitivity of volume-regulated anion current to cholesterol structural analogues.
2004,
Pubmed
Romanenko,
Modulation of endothelial inward-rectifier K+ current by optical isomers of cholesterol.
2002,
Pubmed
Rosenhouse-Dantsker,
Cholesterol sensitivity of KIR2.1 is controlled by a belt of residues around the cytosolic pore.
2011,
Pubmed
,
Xenbase
Rosenhouse-Dantsker,
Regulation of ion channels by membrane lipids.
2012,
Pubmed
Rosenhouse-Dantsker,
A sodium-mediated structural switch that controls the sensitivity of Kir channels to PtdIns(4,5)P(2).
2008,
Pubmed
Rosenhouse-Dantsker,
Molecular characteristics of phosphoinositide binding.
2007,
Pubmed
Rosenhouse-Dantsker,
New roles for a key glycine and its neighboring residue in potassium channel gating.
2006,
Pubmed
,
Xenbase
Rosenhouse-Dantsker,
Comparative analysis of cholesterol sensitivity of Kir channels: role of the CD loop.
2010,
Pubmed
,
Xenbase
Santiago,
Probing the effects of membrane cholesterol in the Torpedo californica acetylcholine receptor and the novel lipid-exposed mutation alpha C418W in Xenopus oocytes.
2001,
Pubmed
,
Xenbase
Singh,
Cholesterol regulates prokaryotic Kir channel by direct binding to channel protein.
2011,
Pubmed
Singh,
Direct regulation of prokaryotic Kir channel by cholesterol.
2009,
Pubmed
Soom,
Multiple PIP2 binding sites in Kir2.1 inwardly rectifying potassium channels.
2001,
Pubmed
,
Xenbase
Tai,
Ion-blocking sites of the Kir2.1 channel revealed by multiscale modeling.
2009,
Pubmed
Tao,
Crystal structure of the eukaryotic strong inward-rectifier K+ channel Kir2.2 at 3.1 A resolution.
2009,
Pubmed
,
Xenbase
Tikku,
Relationship between Kir2.1/Kir2.3 activity and their distributions between cholesterol-rich and cholesterol-poor membrane domains.
2007,
Pubmed
Toselli,
Caveolin-1 expression and membrane cholesterol content modulate N-type calcium channel activity in NG108-15 cells.
2005,
Pubmed
Wu,
The effect of hypercholesterolemia on the sodium inward currents in cardiac myocyte.
1995,
Pubmed
Yin,
Phosphoinositide regulation of the actin cytoskeleton.
2003,
Pubmed
Yokogawa,
NMR analyses of the Gbetagamma binding and conformational rearrangements of the cytoplasmic pore of G protein-activated inwardly rectifying potassium channel 1 (GIRK1).
2011,
Pubmed
Zaritsky,
Targeted disruption of Kir2.1 and Kir2.2 genes reveals the essential role of the inwardly rectifying K(+) current in K(+)-mediated vasodilation.
2000,
Pubmed
Zerangue,
A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels.
1999,
Pubmed
,
Xenbase
Zhang,
Activation of inwardly rectifying K+ channels by distinct PtdIns(4,5)P2 interactions.
1999,
Pubmed
,
Xenbase
Zidovetzki,
Use of cyclodextrins to manipulate plasma membrane cholesterol content: evidence, misconceptions and control strategies.
2007,
Pubmed