Sasaki J, Yuzawa T, Kandori H, Maeda A, Hamaguchi H
Department of Biophysics, Faculty of Science, Kyoto University, Japan.
Biophys J. 1995 May;68(5):2073-80. doi: 10.1016/S0006-3495(95)80386-3.
The photochemical reaction process of bacteriorhodopsin in the nanosecond time range (-120-860 ns) was measured in the 1400-900 cm-1 region with an improved time resolved dispersive-type infrared spectrometer. The system is equipped with a newly developed detection unit whose instrumental response to a 5-ns laser pulse has a full width of the half-maximum of 60 ns. It provides highly accurate data that enabled us to extract a kinetic process one order of magnitude faster than the instrumental response. The spectral changes in the 1400-900 cm-1 region were analyzed by singular value decomposition and resolved into three components. These components were separated by fitting with 10- and 1000-ns exponential functions and a step function, which were convoluted with the instrumental response function. The components with decay time constants of 10 and 1000 ns are named K and KL, respectively, on the basis of previous visible spectroscopy. The spectral shapes of K and KL are distinguishable by their hydrogen-out-of-plane (HOOP) modes, at 958 and 984 cm-1, respectively. The former corresponds to the K intermediate recorded at 77 K and the latter to a K-like photoproduct at 135 K. On the basis of published data, these bands are assigned to the 15-HOOP mode, indicating that the K and KL differ in a twist around the C14-C15 bond.
使用改进的时间分辨色散型红外光谱仪,在1400 - 900 cm-1区域测量了细菌视紫红质在纳秒时间范围(-120 - 860 ns)内的光化学反应过程。该系统配备了新开发的检测单元,其对5 ns激光脉冲的仪器响应半高宽为60 ns。它提供了高精度的数据,使我们能够提取比仪器响应快一个数量级的动力学过程。通过奇异值分解分析了1400 - 900 cm-1区域的光谱变化,并将其分解为三个成分。通过与10 ns和1000 ns指数函数以及阶跃函数拟合来分离这些成分,这些函数与仪器响应函数进行卷积。根据先前的可见光谱,衰减时间常数为10 ns和1000 ns的成分分别命名为K和KL。K和KL的光谱形状可通过它们分别在958 cm-1和984 cm-1处的氢面外(HOOP)模式来区分。前者对应于在77 K记录的K中间体,后者对应于在135 K的类K光产物。根据已发表的数据,这些谱带被指定为15 - HOOP模式,表明K和KL在围绕C14 - C15键的扭转方面存在差异。