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质子沿脂质双层的结构扩散。

Structural proton diffusion along lipid bilayers.

作者信息

Serowy Steffen, Saparov Sapar M, Antonenko Yuri N, Kozlovsky Wladas, Hagen Volker, Pohl Peter

机构信息

Forschungsinstitut fuer Molekulare Pharmakologie, Campus Berlin-Buch, Robert-Rössle-Strasse 10, D-13125 Berlin, Germany.

出版信息

Biophys J. 2003 Feb;84(2 Pt 1):1031-7. doi: 10.1016/S0006-3495(03)74919-4.

Abstract

For H(+) transport between protein pumps, lateral diffusion along membrane surfaces represents the most efficient pathway. Along lipid bilayers, we measured a diffusion coefficient of 5.8 x 10(-5) cm(2) s(-1). It is too large to be accounted for by vehicle diffusion, considering proton transport by acid carriers. Such a speed of migration is accomplished only by the Grotthuss mechanism involving the chemical exchange of hydrogen nuclei between hydrogen-bonded water molecules on the membrane surface, and the subsequent reorganization of the hydrogen-bonded network. Reconstitution of H(+)-binding sites on the membrane surface decreased the velocity of H(+) diffusion. In the absence of immobile buffers, structural (Grotthuss) diffusion occurred over a distance of 100 micro m as shown by microelectrode aided measurements of the spatial proton distribution in the immediate membrane vicinity and spatially resolved fluorescence measurements of interfacial pH. The efficiency of the anomalously fast lateral diffusion decreased gradually with an increase in mobile buffer concentration suggesting that structural diffusion is physiologically important for distances of approximately 10 nm.

摘要

对于蛋白质泵之间的H(+)转运,沿膜表面的横向扩散是最有效的途径。沿着脂质双层,我们测得扩散系数为5.8×10(-5) cm(2) s(-1)。考虑到酸载体进行的质子转运,该系数太大,无法用载体扩散来解释。这种迁移速度只能通过Grotthuss机制实现,该机制涉及膜表面氢键结合水分子之间氢核的化学交换以及随后氢键网络的重组。膜表面H(+)结合位点的重建降低了H(+)扩散速度。在没有固定缓冲剂的情况下,通过微电极辅助测量膜附近空间质子分布以及界面pH的空间分辨荧光测量表明,结构(Grotthuss)扩散发生在100μm的距离上。异常快速横向扩散的效率随着移动缓冲剂浓度的增加而逐渐降低,这表明结构扩散对于大约10nm的距离在生理上很重要。

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