Wang C C, Bruner L J
Biophys J. 1978 Dec;24(3):749-64. doi: 10.1016/S0006-3495(78)85418-6.
A high amplitude voltage step technique has been used to meausre the surface density of dipicrylamine anions adsorbed at the surfaces of lipid bilayer membranes. Accompanying low amplitude measurements have determined the relaxation time for transient current flow across the membranes, a parameter governed by the height of the central energy barrier which dipicrylamine anions must cross in moving from one membrane surface to the other. Measured relaxation times and surface charge densities have been related by a quasi-continuum model of the discrete charge effect, which predicts that the membrane central barrier height will increase with increasing density of adsorbed surface charge. The experimentally determined relationship is in satisfactory agreement with the predictions of the model. The model does not provide a complete description of the membrane/solution interface, however, because it cannot be applied to the description of previously measured isotherms for the adsorption of dipicrylamine anions onto bilayer membranes surfaces. Possible reasons for this discrepancy are discussed.
一种高振幅电压阶跃技术已被用于测量吸附在脂质双分子层膜表面的二苦胺阴离子的表面密度。同时进行的低振幅测量确定了跨膜瞬态电流流动的弛豫时间,该参数由二苦胺阴离子从一个膜表面移动到另一个膜表面时必须跨越的中心能垒高度决定。测量得到的弛豫时间和表面电荷密度已通过离散电荷效应的准连续模型建立了关联,该模型预测膜中心势垒高度将随着吸附表面电荷密度的增加而增加。实验确定的关系与模型预测结果吻合良好。然而,该模型并未对膜/溶液界面提供完整描述,因为它无法用于描述先前测量的二苦胺阴离子在双分子层膜表面吸附的等温线。文中讨论了这种差异可能的原因。