Sokolov V S, Stukolov S M, Darmostuk A S, Apell H J
Frumkin Institute of Electrochemistry, Russian Academy of Sciences, Moscow, Russia.
Membr Cell Biol. 1998;11(5):653-78.
The goal of work was to investigate the electrogenic transport of Na ions by Na+,K(+)-ATPase in membrane fragments absorbed on a planar bilayer lipid membrane. The photorelease of ATP from an inactive precursor, caged ATP, induced a transient current and changes in the net system capacitance measured during the application of an alternating voltage. The increments of capacitance (delta c) decreased with the increase in the frequency of the applied voltage. The characteristic frequency F0 of the steepest slope of the curve significantly decreased in solutions with high ionic strength (either NaCl or choline chloride), in which Na+ transport is decelerated. The value of delta c correlated with the total charge delta q transported across the membrane. The capacitance increments decreased when the Na+ concentration in solution decreased. At a concentration below 2 mM the increment became negative. The increase in membrane capacitance can be attributed to the charge relaxation process inside the protein, as discovered in the cells by other methods. The characteristic frequency F0 depends on the time constants of charge redistribution. The nonlinear dependences of delta c on delta q were explained by a voltage bias across the membrane fragments resulting from pumping. The potentials corresponding to the maximum capacitance change were similar to the midpoint potentials of the equilibrium charge distribution and depended on the Na+ concentrations in solution. The model enabled also the determination of the total capacitance of the active region of a lipid membrane with the adsorbed protein containing membrane fragments.
本研究的目的是研究在平面双层脂质膜上吸附的膜片段中,Na⁺,K⁺-ATP酶对Na离子的电转运。从无活性前体笼形ATP光释放ATP,在施加交流电压期间诱导了瞬态电流和净系统电容的变化。电容增量(δc)随着施加电压频率的增加而减小。在高离子强度(NaCl或氯化胆碱)溶液中,Na⁺转运减速,曲线最陡斜率的特征频率F0显著降低。δc值与跨膜转运的总电荷δq相关。当溶液中Na⁺浓度降低时,电容增量减小。在浓度低于2 mM时,增量变为负值。膜电容的增加可归因于蛋白质内部的电荷弛豫过程,这是通过其他方法在细胞中发现的。特征频率F0取决于电荷重新分布的时间常数。δc对δq的非线性依赖性是由泵送导致的膜片段上的电压偏置解释的。对应于最大电容变化的电位类似于平衡电荷分布的中点电位,并取决于溶液中的Na⁺浓度。该模型还能够确定含有吸附蛋白质的膜片段的脂质膜活性区域的总电容。