Barth C, Bihler H, Wilhelm M, Stark G
Fakultät für Biologie, Universität Konstanz, Germany.
Biophys Chem. 1995 Apr;54(2):127-36. doi: 10.1016/0301-4622(94)00112-w.
We report on a modified charge-pulse relaxation technique applied at planar lipid membranes. The method has an improved time resolution of 20-30 ns. It is based on the capacitive coupling of a voltage-jump to the membrane. The method was used to study the fast relaxation processes induced by valinomycin/K+ in the presence of 2,4-dichlorophenoxyacetic acid (2,4-D). The change of the rate constants of the ion carrier valinomycin was analysed as a consequence of the adsorption of the dipolar substance 2,4-D to the membrane/water interface of monoolein membranes. The effect of 2,4-D can be explained solely via the influence of the introduced dipole potential, VD. The latter was found to act (primarily) on the inner membrane barrier experienced by the positively charged carrier-ion complex and on the interfacial barriers responsible for complex formation and dissociation. No evidence for a change of the microviscosity of the membrane interior was obtained.
我们报道了一种应用于平面脂质膜的改进型电荷脉冲弛豫技术。该方法具有20 - 30纳秒的改进时间分辨率。它基于电压阶跃与膜的电容耦合。该方法用于研究在2,4 - 二氯苯氧乙酸(2,4 - D)存在下缬氨霉素/K⁺诱导的快速弛豫过程。分析了离子载体缬氨霉素速率常数的变化,这是由于偶极物质2,4 - D吸附到单油酸膜的膜/水界面所致。2,4 - D的作用仅可通过引入的偶极电位VD的影响来解释。发现后者(主要)作用于带正电的载体 - 离子复合物所经历的内膜屏障以及负责复合物形成和解离的界面屏障。未获得膜内部微粘度变化的证据。