Protons migrate along interfacial water without significant contributions from jumps between ionizable groups on the membrane surface

被引:103
作者
Springer, Andreas [1 ]
Hagen, Volker [2 ]
Cherepanov, Dmitry A. [3 ]
Antonenko, Yuri N. [4 ]
Pohl, Peter [1 ]
机构
[1] Johannes Kepler Univ Linz, Inst Biophys, A-4040 Linz, Austria
[2] Leibniz Inst Mol Pharmacol, Berlin, Germany
[3] Frumkin Inst Phys Chem & Electrochem, Moscow, Russia
[4] Belozersky Inst Physicochem Biol, Moscow, Russia
关键词
chemiosmotic theory; fluorimetry; planar bilayer; proton-collecting antenna; CARBONIC-ANHYDRASE-II; DIFFUSION; TRANSPORT; BILAYERS; PERMEATION; MECHANISM; DYNAMICS; IONS;
D O I
10.1073/pnas.1107476108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proton diffusion along membrane surfaces is thought to be essential for many cellular processes such as energy transduction. Commonly, it is treated as a succession of jumps between membrane-anchored proton-binding sites. Our experiments provide evidence for an alternative model. We released membrane-bound caged protons by UV flashes and monitored their arrival at distant sites by fluorescence measurements. The kinetics of the arrival is probed as a function of distance for different membranes and for different water isotopes. We found that proton diffusion along the membrane is fast even in the absence of ionizable groups in the membrane, and it decreases strongly in D(2)O as compared to H(2)O. We conclude that the fast proton transport along the membrane is dominated by diffusion via interfacial water, and not via ionizable lipid moieties.
引用
收藏
页码:14461 / 14466
页数:6
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