Proton transport via the membrane surface

被引:58
|
作者
Georgievskii, Y
Medvedev, ES
Stuchebrukhov, AA
机构
[1] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
[2] Russian Acad Sci, Inst Problems Chem Phys, Chernogolovka 142432, Moscow, Russia
基金
俄罗斯基础研究基金会; 美国国家卫生研究院;
关键词
D O I
10.1016/S0006-3495(02)75626-9
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Some proton pumps, such as cytochrome c oxidase (CcO), translocate protons across biological membranes at a rate that considerably exceeds the rate of proton transport to the entrance of the proton-conducting channel via bulk diffusion. This effect is usually ascribed to a proton-collecting antenna surrounding the channel entrance. In this paper, we consider a realistic phenomenological model of such an antenna. In our model, a homogeneous membrane surface, which can mediate proton diffusion toward the channel entrance, is populated with protolytic groups that are in dynamic equilibrium with the solution. Equations that describe coupled surface-bulk proton diffusion are derived and analyzed. A general expression for the rate constant of proton transport via such a coupled surface-bulk diffusion mechanism is obtained. A rigorous criterion is formulated of when proton diffusion along the surface enhances the transport. The enhancement factor is found to depend on the ratio of the surface and bulk diffusional constants, pK(a) values of surface protolytic groups, and their concentration. A capture radius for a proton on the surface and an effective size of the antenna are found. The theory also predicts the effective distance that a proton can migrate on the membrane surface between a source (such as CcO) and a sink (such as ATIP synthase) without fully equilibrating with the bulk. In pure aqueous solutions, protons can travel over long distances (microns). In buffered solutions, the travel distance is much shorter (nanometers); still the enhancement effect of the surface diffusion on the proton flow to a target on the surface can be tens to hundreds at physiological buffer concentrations. These results are discussed in a general context of chemiosmotic theory.
引用
收藏
页码:2833 / 2846
页数:14
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