Hydroxide Ion Mechanism for Long-Range Proton Pumping in the Third Proton Transfer of Bacteriorhodopsin

被引:4
|
作者
Ono, Junichi [1 ,2 ]
Okada, Chika [3 ]
Nakai, Hiromi [1 ,2 ,3 ]
机构
[1] Kyoto Univ, Elements Strategy Initiat Catalysts & Batteries E, Nishikyo Ku, 1-30 Goryo Ohara, Kyoto 6158245, Japan
[2] Waseda Univ, Waseda Res Inst Sci & Engn WISE, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
[3] Waseda Univ, Sch Adv Sci & Engn, Dept Chem & Biochem, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
基金
日本学术振兴会;
关键词
proteins; proton transport; quantum chemistry; molecular dynamics; reaction mechanisms; SERIAL FEMTOSECOND CRYSTALLOGRAPHY; MOLECULAR-DYNAMICS SIMULATIONS; FUNCTIONAL TIGHT-BINDING; DIVIDE-AND-CONQUER; SCHIFF-BASE; STRUCTURAL-CHANGES; WATER-MOLECULES; CHAIN; MODEL;
D O I
10.1002/cphc.202200109
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In bacteriorhodopsin, representative light-driven proton pump, five proton transfers yield vectorial active proton translocation, resulting in a proton gradient in microbes. Third proton transfer occurs from Asp96 to the Schiff base on the photocycle, which is expected to be a long-range proton transfer via the Grotthuss mechanism through internal water molecules. Here, large-scale quantum molecular dynamics simulations are performed for the third proton transfer, where all the atoms (similar to 50000 atoms) are treated quantum-mechanically. The simulations demonstrate that two reaction paths exist along the water wire, namely, via hydronium and via hydroxide ions. The free energy analysis confirms that the path via hydroxide ions is considerably favorable and consistent with the observed lifetime of the transient water wire. Therefore, the proposed hydroxide ion mechanism, as in the first proton transfer, is responsible for the third long-range proton transfer.
引用
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页数:11
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