Lipid Bilayer Modules as Determinants of K+ Channel Gating

被引:6
|
作者
Syeda, Ruhma [1 ]
Santos, Jose S. [1 ]
Montal, Mauricio [1 ]
机构
[1] Univ Calif San Diego, Div Biol Sci, Neurobiol Sect, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
Gating; Lipid Structure; Membrane Bilayer; Phospholipid; Potassium Channels; Asymmetric Lipid Bilayers; Gating Modifiers; Phosphoglycerides; Voltage-gated Channels; PHOSPHOLIPID SURFACE-CHARGE; VOLTAGE-SENSOR DOMAIN; MOLECULAR TEMPLATE; CRYSTAL-STRUCTURE; MEMBRANE-LIPIDS; FORCE-FIELD; PORE MODULE; INACTIVATION; BINDING; PIP2;
D O I
10.1074/jbc.M113.530055
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:4233 / 4243
页数:11
相关论文
共 50 条
  • [1] Crucial Points within the Pore as Determinants of K+ Channel Conductance and Gating
    Shi, Ning
    Zeng, Weizhong
    Ye, Sheng
    Li, Yang
    Jiang, Youxing
    JOURNAL OF MOLECULAR BIOLOGY, 2011, 411 (01) : 27 - 35
  • [2] TASK-2 K2P K+ channel: thoughts about gating and its fitness to physiological function
    Lopez-Cayuqueo, Karen I.
    Pena-Muenzenmayer, Gaspar
    Isabel Niemeyer, Maria
    Sepulveda, Francisco V.
    Pablo Cid, L.
    PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2015, 467 (05): : 1043 - 1053
  • [3] The gating cycle of a K+ channel at atomic resolution
    Cuello, Luis G.
    Cortes, D. Marien
    Perozo, Eduardo
    ELIFE, 2017, 6
  • [4] MAGNESIUM GATING OF THE INWARDLY RECTIFYING K+ CHANNEL
    MATSUDA, H
    ANNUAL REVIEW OF PHYSIOLOGY, 1991, 53 : 289 - 298
  • [5] Molecular Determinants of Interactions between the N-Terminal Domain and the Transmembrane Core That Modulate hERG K+ Channel Gating
    Fernandez-Trillo, Jorge
    Barros, Francisco
    Machin, Angeles
    Carretero, Luis
    Dominguez, Pedro
    de la Pena, Pilar
    PLOS ONE, 2011, 6 (09):
  • [6] Gating energetics of a voltage-dependent K+ channel pore domain
    Starek, Greg
    Freites, J. Alfredo
    Berneche, Simon
    Tobias, Douglas J.
    JOURNAL OF COMPUTATIONAL CHEMISTRY, 2017, 38 (16) : 1472 - 1478
  • [7] Mechanism of activation gating in the full-length KcsA K+ channel
    Uysal, Serdar
    Cuello, Luis G.
    Cortes, D. Marien
    Koide, Shohei
    Kossiakoff, Anthony A.
    Perozo, Eduardo
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (29) : 11896 - 11899
  • [8] A Gating Model for the Archeal Voltage-Dependent K+ Channel KvAP in DPhPC and POPE:POPG Decane Lipid Bilayers
    Schmidt, Daniel
    Cross, Samuel R.
    MacKinnon, Roderick
    JOURNAL OF MOLECULAR BIOLOGY, 2009, 390 (05) : 902 - 912
  • [9] Structural Basis for pH-gating of the K+ channel TWIK1 at the selectivity filter
    Turney, Toby S.
    Li, Vivian
    Brohawn, Stephen G.
    NATURE COMMUNICATIONS, 2022, 13 (01)
  • [10] Intrinsic aqueduct orifices facilitate K+ channel gating
    Zhong, Wenyu
    Guo, Wanlin
    Ma, Shaojie
    FEBS LETTERS, 2008, 582 (23-24): : 3320 - 3324