Lipid Bilayer Modules as Determinants of K+ Channel Gating
被引:6
作者:
Syeda, Ruhma
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Univ Calif San Diego, Div Biol Sci, Neurobiol Sect, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol Sci, Neurobiol Sect, La Jolla, CA 92093 USA
Syeda, Ruhma
[1
]
Santos, Jose S.
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Univ Calif San Diego, Div Biol Sci, Neurobiol Sect, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol Sci, Neurobiol Sect, La Jolla, CA 92093 USA
Santos, Jose S.
[1
]
Montal, Mauricio
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Univ Calif San Diego, Div Biol Sci, Neurobiol Sect, La Jolla, CA 92093 USAUniv Calif San Diego, Div Biol Sci, Neurobiol Sect, La Jolla, CA 92093 USA
Montal, Mauricio
[1
]
机构:
[1] Univ Calif San Diego, Div Biol Sci, Neurobiol Sect, La Jolla, CA 92093 USA
Background: Lipid bilayer composition and asymmetry modulate K+ channel function by unknown mechanisms. Results: Lipid headgroups with exposed hydroxyls on the extracellular facing monolayer stabilize the channel open conformation irrespective of charge. Conclusion: Stabilization is mediated through a change of interfacial water structure. Significance: Lipid bilayer asymmetry and its individual monolayers emerge as crucial determinants of K+ channel gating. The crystal structure of the sensorless pore module of a voltage-gated K+ (Kv) channel showed that lipids occupy a crevice between subunits. We asked if individual lipid monolayers of the bilayer embody independent modules linked to channel gating modulation. Functional studies using single channel current recordings of the sensorless pore module reconstituted in symmetric and asymmetric lipid bilayers allowed us to establish the deterministic role of lipid headgroup on gating. We discovered that individual monolayers with headgroups that coat the bilayer-aqueous interface with hydroxyls stabilize the channel open conformation. The hydroxyl need not be at a terminal position and the effect is not dependent on the presence of phosphate or net charge on the lipid headgroup. Asymmetric lipid bilayers allowed us to determine that phosphoglycerides with glycerol or inositol on the extracellular facing monolayer stabilize the open conformation of the channel. This indirect effect is attributed to a change in water structure at the membrane interface. By contrast, inclusion of the positively charged lysyl-dioleoyl-phosphatidylglycerol exclusively on the cytoplasmic facing monolayer of the bilayer increases drastically the probability of finding the channel open. Such modulation is mediated by a -cation interaction between Phe-19 of the pore module and the lysyl moiety anchored to the phosphatidylglycerol headgroup. The new findings imply that the specific chemistry of the lipid headgroup and its selective location in either monolayer of the bilayer dictate the stability of the open conformation of a Kv pore module in the absence of voltage-sensing modules.
机构:
Stanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
Beckman Ctr Mol & Genet Med, Stanford, CA 94305 USA
Palo Alto VA Hlth Care Syst, Dept Vet Affairs, Palo Alto, CA 94304 USAStanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
Bertaccini, Edward J.
Trudell, James R.
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机构:
Stanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
Beckman Ctr Mol & Genet Med, Stanford, CA 94305 USAStanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
Trudell, James R.
Lindahl, Erik
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机构:
Stockholm Univ, Stockholm Bioinformat Ctr, S-10691 Stockholm, Sweden
Stockholm Univ, Ctr Biomembrane Res, Dept Biochem & Biophys, S-10691 Stockholm, SwedenStanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
Lindahl, Erik
ACS CHEMICAL NEUROSCIENCE,
2010,
1
(08):
: 552
-
558
机构:
Stanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
Beckman Ctr Mol & Genet Med, Stanford, CA 94305 USA
Palo Alto VA Hlth Care Syst, Dept Vet Affairs, Palo Alto, CA 94304 USAStanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
Bertaccini, Edward J.
Trudell, James R.
论文数: 0引用数: 0
h-index: 0
机构:
Stanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
Beckman Ctr Mol & Genet Med, Stanford, CA 94305 USAStanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
Trudell, James R.
Lindahl, Erik
论文数: 0引用数: 0
h-index: 0
机构:
Stockholm Univ, Stockholm Bioinformat Ctr, S-10691 Stockholm, Sweden
Stockholm Univ, Ctr Biomembrane Res, Dept Biochem & Biophys, S-10691 Stockholm, SwedenStanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
Lindahl, Erik
ACS CHEMICAL NEUROSCIENCE,
2010,
1
(08):
: 552
-
558