Kinetics of proton release and uptake by channelrhodopsin-2

被引:27
|
作者
Nack, Melanie [1 ]
Radu, Ionela [1 ]
Schultz, Bernd-Joachim [1 ]
Resler, Tom [1 ]
Schlesinger, Ramona [1 ]
Bondar, Ana-Nicoleta [1 ]
del Val, Coral [2 ]
Abbruzzetti, Stefania [3 ]
Viappiani, Cristiano [3 ]
Bamann, Christian [4 ]
Bamberg, Ernst [4 ]
Heberle, Joachim [1 ]
机构
[1] Free Univ Berlin, Inst Expt Phys, D-14195 Berlin, Germany
[2] Univ Granada, Dept Comp Sci & Artificial Intelligence, E-18071 Granada, Spain
[3] Univ Parma, Dipartimento Fis, I-43100 Parma, Italy
[4] Max Planck Inst Biophys, D-60438 Frankfurt, Germany
关键词
Bacteriorhodopsin; Proton transfer; Optogenetics; Rhodopsin; Ion channel; BACTERIORHODOPSIN; PHOTOCYCLE; TRANSLOCATION; SURFACE; PUMP; DYNAMICS; CHLORIDE; SITES; CHAIN;
D O I
10.1016/j.febslet.2012.03.047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Electrophysiological experiments showed that the light-activated cation channel channelrhodopsin-2 (ChR2) pumps protons in the absence of a membrane potential. We determined here the kinetics of transient pH change using a water-soluble pH-indicator. It is shown that ChR2 released protons prior to uptake with a stoichiometry of 0.3 protons per ChR2. Comparison to the photocycle kinetics revealed that proton release and uptake match rise and decay of the P-3(520) intermediate. As the P-3(520) state also represents the conductive state of cation channeling, the concurrence of proton pumping and channel gating implies an intimate mechanistic link of the two functional modes. Studies on the E123T and S245E mutants show that these residues are not critically involved in proton translocation. (C) 2012 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:1344 / 1348
页数:5
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