Einterz C M, Lewis J W, Kliger D S
Proc Natl Acad Sci U S A. 1987 Jun;84(11):3699-703. doi: 10.1073/pnas.84.11.3699.
Transient-absorption difference spectra from 320 nm to 700 nm were obtained at times ranging from 30 ns to 1200 ns after 532-nm photolysis of rhodopsin at room temperature. Kinetics on this time scale at various wavelengths are also presented. The isosbestic points between spectra acquired at successive times after photolysis shift from 510 nm to 530 nm. This shift is inconsistent with a simple process of one bathorhodopsin (BathoR) intermediate being transformed into one lumirhodopsin (LumiR) intermediate on this time scale. The kinetics at 425 nm, 515 nm, and 575 nm could not be fit well to a single-exponential expression. The data are consistent with the existence of two forms of BathoR (BathoR1 and BathoR2) that exhibit different spectra and decay kinetics. The BathoR1 absorption maximum lies near 565 nm, and the BathoR1/LumiR1 isosbestic point is near 430 nm. The BathoR2 absorption maximum lies near 535 nm, and the BathoR2/LumiR2 isosbestic point is near 480 nm. The kinetics at the isosbestic wavelengths were fit to single-exponential expressions corresponding to BathoR1 and BathoR2 lifetimes of 170 +/- 20 ns and 36 +/- 15 ns, respectively.
在室温下用532 nm光解视紫红质后,于30 ns至1200 ns的时间范围内获得了320 nm至700 nm的瞬态吸收差光谱。还给出了在不同波长下该时间尺度上的动力学数据。光解后连续时间获取的光谱之间的等吸收点从510 nm移至530 nm。这种位移与在该时间尺度上一个视紫红质中间体(BathoR)简单地转变为一个发光视紫红质中间体(LumiR)的过程不一致。在425 nm、515 nm和575 nm处的动力学不能很好地拟合为单指数表达式。数据与存在两种具有不同光谱和衰减动力学的BathoR形式(BathoR1和BathoR2)一致。BathoR1的最大吸收峰位于565 nm附近,BathoR1/LumiR1的等吸收点在430 nm附近。BathoR2的最大吸收峰位于535 nm附近,BathoR2/LumiR2的等吸收点在480 nm附近。在等吸收波长处的动力学拟合为单指数表达式,分别对应于BathoR1和BathoR2的寿命为170±20 ns和36±15 ns。