Electrostatic potentials arising due to adsorption of Na+, K+-ATPase-containing membrane fragments on bilayer lipid membrane

被引:0
|
作者
Sokolov, V. S. [1 ]
Sokolenko, E. A.
Filinsky, D. V.
Ermakov, Yu. A.
Lopina, O. D.
Apell, H.-J.
机构
[1] Moscow MV Lomonosov State Univ, Dept Biol, Moscow, Russia
[2] Univ Konstanz, Dept Biol, D-7750 Constance, Germany
[3] Russian Acad Sci, Frumkin Inst Physc Chem & Electrochem, Moscow 119991, Russia
来源
BIOLOGICHESKIE MEMBRANY | 2007年 / 24卷 / 04期
关键词
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The adsorption of Na+,K+-ATPase-containing membrane fragments (MF) on the surface of planar bilayer membranes (BLM) was studied by the method of capacitive current second harmonic compensation extended to laterally heterogenic systems. The suspension of MF added to water solution adjacent to BLM creates the electrostatic potential measured by the method mentioned above and changes the BLM capacity and its conductivity induced by nonactine or pentachlorophenole. It is shown that the electrostatic potential can be caused by two different mechanisms. The first is the adsorption on BLM of charged molecules which can be either phospholipids dissolved in water, or detergent, sodium dodecyl sulfate, present in the sample as an impurity. The second mechanism is the adsorption of charged MF leading to the creation of an electric field inside the BLM in the contact region with the MF, if the distance between the membranes is comparable to the thickness of the diffuse electric double layer. To distinguish between both possibilities, experiments were carried out with ex-change of the aqueous solution adjacent to the BLM by perfusion of the cell. The perfusion leads to a potential drop due to washing of single molecules adsorbed on the membrane surface. The remaining potential (about 10 mV) is probably caused by irreversible adsorption of ME The surface charge of MF was about -10 mC/m(2), determined from their electrophoretic mobility in suspension. Most likely, this charge is caused by charged lipids present in ME It was confirmed by the experiments with liposomes made with the lipids extracted from ME The addition of these liposomes into the cell created the potential changes in BLM of the same sign as in the case of ME The electric field inside MF contacting with BLM was estimated using different values of unknown parameters of the system, namely, the thikness of water gap between BLM and MF, and the surface coverage of BLM by fragments. This field may be very large and has to be taken into account in studies of Na+, K+-ATPase functioning in such experimental systems.
引用
收藏
页码:333 / 347
页数:15
相关论文
共 50 条
  • [1] ORIENTATION OF MEMBRANE-FRAGMENTS CONTAINING (NA++K+)-ATPASE
    GERGELY, C
    DER, A
    SZARAZ, S
    KESZTHELYI, L
    BIOELECTROCHEMISTRY AND BIOENERGETICS, 1992, 28 (1-2): : 149 - 157
  • [2] NA+,K+-ATPASE-BASED BILAYER-LIPID MEMBRANE SENSOR FOR ADENOSINE 5'-TRIPHOSPHATE
    ADACHI, Y
    SUGAWARA, M
    TANIGUCHI, K
    UMEZAWA, Y
    ANALYTICA CHIMICA ACTA, 1993, 281 (03) : 577 - 584
  • [4] Aminophospholipid glycation causes lipid bilayer structure alterations and inhibition of membrane-bound Na+,K+-ATPase
    Obsil, T
    Amler, E
    Pavlicek, Z
    COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, 1998, 63 (07) : 1060 - 1073
  • [5] On the Na+,K+ pump in fluctuating membrane potentials
    Neagu, M
    Neagu, A
    EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2001, 30 (03): : 221 - 226
  • [6] On the Na+,K+ pump in fluctuating membrane potentials
    Monica Neagu
    Adrian Neagu
    European Biophysics Journal, 2001, 30 : 221 - 226
  • [7] Dipole potential drop due to RH-dye adsorption on the lipid bilayer and its influence on Na+/K+-ATPase activity
    Malkov, DY
    Pavlov, KV
    Sokolov, VS
    NA/K-ATPASE AND RELATED TRANSPORT ATPASES: STRUCTURE, MECHANISM, AND REGULATION, 1997, 834 : 357 - 360
  • [8] EXPRESSION AND PURIFICATION OF FUSION PROTEINS CONTAINING NA+, K+-ATPASE ALPHA-SUBUNIT FRAGMENTS THAT ARE LOCATED NEAR THE MEMBRANE
    LARIN, DI
    SHAKHPARONOV, MI
    ORTIZ, E
    KOSTINA, MB
    MODYANOV, NN
    BIOLOGICHESKIE MEMBRANY, 1994, 11 (05): : 469 - 475
  • [9] BIOCHEMICAL LOCALIZATION OF HEPATIC SURFACE-MEMBRANE NA+,K+-ATPASE ACTIVITY DEPENDS ON MEMBRANE LIPID FLUIDITY
    SUTHERLAND, E
    DIXON, BS
    LEFFERT, HL
    SKALLY, H
    ZACCARO, L
    SIMON, FR
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (22) : 8673 - 8677
  • [10] IS NA+,K+-ATPASE PRESENT ON THE CANALICULAR MEMBRANE DOMAIN
    SELLINGER, M
    BARRETT, C
    MALLE, P
    GORDON, ER
    BOYER, JL
    HEPATOLOGY, 1988, 8 (05) : 1420 - 1420