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J Biol Chem
2013 Oct 25;28843:31154-64. doi: 10.1074/jbc.M113.496117.
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Identification of novel cholesterol-binding regions in Kir2 channels.
Rosenhouse-Dantsker A
,
Noskov S
,
Durdagi S
,
Logothetis DE
,
Levitan I
.
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Inwardly rectifying potassium (Kir) channels play an important role in setting the resting membrane potential and modulating membrane excitability. We have recently shown that cholesterol regulates representative members of the Kir family and that in the majority of the cases, cholesterol suppresses channel function. Furthermore, recent data indicate that cholesterol regulates Kir channels by specific sterol-protein interactions, yet the location of the cholesterol binding site in Kir channels is unknown. Using a combined computational-experimental approach, we show that cholesterol may bind to two nonanular hydrophobic regions in the transmembrane domain of Kir2.1 located between adjacent subunits of the channel. The location of the binding regions suggests that cholesterol modulates channel function by affecting the hinging motion at the center of the pore-lining transmembrane helix that underlies channel gating either directly or through the interface between the N and C termini of the channel.
Addona,
Where does cholesterol act during activation of the nicotinic acetylcholine receptor?
1998, Pubmed
Addona,
Where does cholesterol act during activation of the nicotinic acetylcholine receptor?
1998,
Pubmed
Addona,
Low chemical specificity of the nicotinic acetylcholine receptor sterol activation site.
2003,
Pubmed
Baier,
Disclosure of cholesterol recognition motifs in transmembrane domains of the human nicotinic acetylcholine receptor.
2011,
Pubmed
Barrantes,
Structural basis for lipid modulation of nicotinic acetylcholine receptor function.
2004,
Pubmed
Bichet,
Merging functional studies with structures of inward-rectifier K(+) channels.
2003,
Pubmed
Brooks,
CHARMM: the biomolecular simulation program.
2009,
Pubmed
Bukiya,
Specificity of cholesterol and analogs to modulate BK channels points to direct sterol-channel protein interactions.
2011,
Pubmed
Chanda,
Gating charge displacement in voltage-gated ion channels involves limited transmembrane movement.
2005,
Pubmed
Covey,
ent-Steroids: novel tools for studies of signaling pathways.
2009,
Pubmed
D'Avanzo,
Enantioselective protein-sterol interactions mediate regulation of both prokaryotic and eukaryotic inward rectifier K+ channels by cholesterol.
2011,
Pubmed
Deol,
Lipid-protein interactions of integral membrane proteins: a comparative simulation study.
2004,
Pubmed
Domene,
Lipid/protein interactions and the membrane/water interfacial region.
2003,
Pubmed
Epand,
Cholesterol and the interaction of proteins with membrane domains.
2006,
Pubmed
Epshtein,
Identification of a C-terminus domain critical for the sensitivity of Kir2.1 to cholesterol.
2009,
Pubmed
Fantini,
How cholesterol interacts with membrane proteins: an exploration of cholesterol-binding sites including CRAC, CARC, and tilted domains.
2013,
Pubmed
Hanson,
A specific cholesterol binding site is established by the 2.8 A structure of the human beta2-adrenergic receptor.
2008,
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
Hibino,
Inwardly rectifying potassium channels: their structure, function, and physiological roles.
2010,
Pubmed
Hilgemann,
The complex and intriguing lives of PIP2 with ion channels and transporters.
2001,
Pubmed
Jiang,
The open pore conformation of potassium channels.
2002,
Pubmed
Jin,
The (beta)gamma subunits of G proteins gate a K(+) channel by pivoted bending of a transmembrane segment.
2002,
Pubmed
,
Xenbase
Jo,
CHARMM-GUI Membrane Builder for mixed bilayers and its application to yeast membranes.
2009,
Pubmed
Jo,
PBEQ-Solver for online visualization of electrostatic potential of biomolecules.
2008,
Pubmed
Jones,
Annular and nonannular binding sites for cholesterol associated with the nicotinic acetylcholine receptor.
1988,
Pubmed
Joy,
Detailed comparison of the protein-ligand docking efficiencies of GOLD, a commercial package and ArgusLab, a licensable freeware.
2006,
Pubmed
Klauda,
Update of the CHARMM all-atom additive force field for lipids: validation on six lipid types.
2010,
Pubmed
Levitan,
Cholesterol and Kir channels.
2009,
Pubmed
Levitan,
Cholesterol and ion channels.
2010,
Pubmed
Li,
Peripheral-type benzodiazepine receptor function in cholesterol transport. Identification of a putative cholesterol recognition/interaction amino acid sequence and consensus pattern.
1998,
Pubmed
Lim,
Update of the cholesterol force field parameters in CHARMM.
2012,
Pubmed
Logothetis,
Phosphoinositide-mediated gating of inwardly rectifying K(+) channels.
2007,
Pubmed
Lopatin,
Inward rectifiers in the heart: an update on I(K1).
2001,
Pubmed
Lopes,
Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies.
2002,
Pubmed
,
Xenbase
Maguy,
Involvement of lipid rafts and caveolae in cardiac ion channel function.
2006,
Pubmed
Marsh,
Immobilized lipid in acetylcholine receptor-rich membranes from Torpedo marmorata.
1978,
Pubmed
Meng,
The molecular mechanism by which PIP(2) opens the intracellular G-loop gate of a Kir3.1 channel.
2012,
Pubmed
Minor,
Transmembrane structure of an inwardly rectifying potassium channel.
1999,
Pubmed
Nishida,
Crystal structure of a Kir3.1-prokaryotic Kir channel chimera.
2007,
Pubmed
Noskov,
Importance of hydration and dynamics on the selectivity of the KcsA and NaK channels.
2007,
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
Picazo-Juárez,
Identification of a binding motif in the S5 helix that confers cholesterol sensitivity to the TRPV1 ion channel.
2011,
Pubmed
Romanenko,
Cholesterol sensitivity and lipid raft targeting of Kir2.1 channels.
2004,
Pubmed
Romanenko,
Modulation of endothelial inward-rectifier K+ current by optical isomers of cholesterol.
2002,
Pubmed
Rosenhouse-Dantsker,
Comparative analysis of cholesterol sensitivity of Kir channels: role of the CD loop.
2010,
Pubmed
,
Xenbase
Rosenhouse-Dantsker,
Regulation of ion channels by membrane lipids.
2012,
Pubmed
Rosenhouse-Dantsker,
Cholesterol sensitivity of KIR2.1 depends on functional inter-links between the N and C termini.
2013,
Pubmed
Rosenhouse-Dantsker,
New roles for a key glycine and its neighboring residue in potassium channel gating.
2006,
Pubmed
,
Xenbase
Rosenhouse-Dantsker,
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)).
2012,
Pubmed
,
Xenbase
Rosenhouse-Dantsker,
Molecular characteristics of phosphoinositide binding.
2007,
Pubmed
Rosenhouse-Dantsker,
Cholesterol sensitivity of KIR2.1 is controlled by a belt of residues around the cytosolic pore.
2011,
Pubmed
,
Xenbase
Roux,
Influence of the membrane potential on the free energy of an intrinsic protein.
1997,
Pubmed
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
Setny,
How Can Hydrophobic Association Be Enthalpy Driven?
2010,
Pubmed
Singh,
Direct regulation of prokaryotic Kir channel by cholesterol.
2009,
Pubmed
Singh,
Cholesterol regulates prokaryotic Kir channel by direct binding to channel protein.
2011,
Pubmed
Singh,
Multiple cholesterol recognition/interaction amino acid consensus (CRAC) motifs in cytosolic C tail of Slo1 subunit determine cholesterol sensitivity of Ca2+- and voltage-gated K+ (BK) channels.
2012,
Pubmed
Swanson,
Revisiting free energy calculations: a theoretical connection to MM/PBSA and direct calculation of the association free energy.
2004,
Pubmed
Tai,
Ion-blocking sites of the Kir2.1 channel revealed by multiscale modeling.
2009,
Pubmed
Tikku,
Relationship between Kir2.1/Kir2.3 activity and their distributions between cholesterol-rich and cholesterol-poor membrane domains.
2007,
Pubmed