Dickopf S, Mielke T, Heyn M P
Biophysics Group, Department of Physics, Freie Universität Berlin, Arnimallee 14, D-14195 Berlin, Germany.
Biochemistry. 1998 Dec 1;37(48):16888-97. doi: 10.1021/bi981879m.
The kinetics of the formation of the metaII (MII) state of bovine rhodopsin was investigated by time-resolved electrical and absorption measurements with rod outer segment (ROS) fragments. Photoexcitation leads to proton transfer in the direction from the cytosolic to the intradiscal side of the membrane, probably from the Schiff base to the acceptor glutamate 113. Two components of comparable amplitude are required to describe the charge movement with exponential times of 1.1 (45%) and 3.0 ms (55%) (pH 7.8, 22 degreesC, 150 mM KCl). The corresponding activation energies are 86 and 123 kJ/mol, respectively (150 mM KCl). The time constants and amplitudes depend strongly on pH. Between pH 7.1 and 3.8 the kinetics becomes much faster, with the faster and slower components accelerating by factors of about 8 and 2, respectively. Complementary single-flash absorption experiments at 380 nm and 10 degreesC show that the formation of MII also occurs with two components with similar time constants and pH dependence. This suggests that both signals monitor the same molecular events. The pH dependence of the two apparent time constants and amplitudes of the optical data can be described well over the pH range 4-7.5 by two coupled equilibria between MI and two isochromic MII species MIIa and MIIb: MI MIIa(380) MIIb(380), with k0 proportional to the proton concentration. This model implies that deprotonation of the Schiff base and proton uptake are tightly coupled in ROS membranes. Models with k2 proportional to the proton concentration cannot describe the data. Photoreversal of MII by blue flashes (420 nm) leads to proton transfer in a direction opposite to that of the signal associated with MII formation. In this transition the Schiff base is reprotonated, most likely from glutamate 113. At pH 7.3, 150 mM KCl, 22 degreesC, this electrical charge reversal has an exponential time constant of about 30 ms and is about 10 times slower than the forward charge motion.
通过对杆状外段(ROS)片段进行时间分辨电学和吸收测量,研究了牛视紫红质亚稳态II(MII)状态的形成动力学。光激发导致质子从膜的胞质侧转移到盘内侧面,可能是从席夫碱转移到受体谷氨酸113。需要两个幅度相当的成分来描述电荷移动,其指数时间分别为1.1(45%)和3.0毫秒(55%)(pH 7.8,22℃,150 mM KCl)。相应的活化能分别为86和123 kJ/mol(150 mM KCl)。时间常数和幅度强烈依赖于pH值。在pH 7.1和3.8之间,动力学变得快得多,较快和较慢的成分分别加速约8倍和2倍。在380 nm和10℃下进行的互补单闪光吸收实验表明,MII的形成也由两个具有相似时间常数和pH依赖性的成分组成。这表明两个信号监测的是相同的分子事件。在pH范围4 - 7.5内,光学数据的两个表观时间常数和幅度的pH依赖性可以通过MI与两个同色MII物种MIIa和MIIb之间的两个耦合平衡很好地描述:MI⇌MIIa(380)⇌MIIb(380),其中k0与质子浓度成正比。该模型意味着席夫碱的去质子化和质子摄取在ROS膜中紧密耦合。k2与质子浓度成正比的模型无法描述这些数据。蓝色闪光(420 nm)使MII光逆转,导致质子转移方向与MII形成相关信号的方向相反。在这个转变过程中,席夫碱重新质子化,最有可能是从谷氨酸113获得质子。在pH 7.3、150 mM KCl、22℃下,这种电荷反转的指数时间常数约为30毫秒,比正向电荷移动慢约10倍。