Ludmann K, Gergely C, Dér A, Váró G
Institute of Biophysics, Biological Research Centre of the Hungarian Academy of Sciences, Szeged H-6701, Hungary.
Biophys J. 1998 Dec;75(6):3120-6. doi: 10.1016/S0006-3495(98)77753-7.
From the electric signals measured after photoexcitation, the electrogenicity of the photocycle intermediates of bacteriorhodopsin were determined in a pH range of 4.5-9. Current measurements and absorption kinetic signals at five wavelengths were recorded in the time interval from 300 ns to 0.5 s. To fit the data, the model containing sequential intermediates connected by reversible first-order reactions was used. The electrogenicities were calculated from the integral of the current signal, by using the time-dependent concentrations of the intermediates, obtained from the fits. Almost all of the calculated electrogenicities were pH independent, suggesting that the charge motions occur inside the protein. Only the N intermediate exhibited pH-dependent electrogenicity, implying that the protonation of Asp96, from the intracellular part of the protein, is not from a well-determined proton donor. The calculated electrogenicities gave good approximations of all of the details of the measured electric signals.
通过光激发后测量的电信号,在4.5 - 9的pH范围内测定了细菌视紫红质光循环中间体的电活性。在300纳秒至0.5秒的时间间隔内记录了五个波长处的电流测量值和吸收动力学信号。为了拟合数据,使用了包含通过可逆一级反应连接的连续中间体的模型。通过使用从拟合中获得的中间体的时间依赖性浓度,从电流信号的积分计算电活性。几乎所有计算出的电活性都与pH无关,这表明电荷运动发生在蛋白质内部。只有N中间体表现出pH依赖性电活性,这意味着来自蛋白质细胞内部分的Asp96的质子化并非来自确定的质子供体。计算出的电活性很好地近似了测量的电信号的所有细节。