Delange F, Merkx M, Bovee-Geurts P H, Pistorius A M, Degrip W J
Department of Biochemistry F.M.W., Institute of Cellular Signalling, University of Nijmegen, The Netherlands.
Eur J Biochem. 1997 Jan 15;243(1-2):174-80. doi: 10.1111/j.1432-1033.1997.0174a.x.
The effects of ionic strength on formation and decay of metarhodopsin II (MII), the active photointermediate of bovine rhodopsin, were studied in the native membrane environment by means of ultraviolet/ visible and Fourier-transform infrared (FTIR) spectroscopy. By increasing the concentration of KCl in the range from hypotonic to 4 M, the apparent pKa of the metarhodopsin I(MI)/MII equilibrium is shifted by approximately pH three, in favor of the MII intermediate. In addition, the apparent rate of MII formation is enhanced by an increase in ionic strength (about twofold in the presence of 2 M KCl). MIII decay is independent of the salt concentration. Attenuated-total-reflectance/FTIR data show that the high-salt conditions have no effect on the rigidity of the membrane matrix and do not induce structural changes in the intermediates themselves. Different salts were tested for their ability to shift the MI/MII equilibrium; however, no clear ion dependence was observed. We interpret these results as an indication for direct involvement of the cytosolic surface charge in the regulation of the photochemical activity of bovine rhodopsin.
通过紫外/可见光谱和傅里叶变换红外(FTIR)光谱,在天然膜环境中研究了离子强度对牛视紫红质的活性光中间体——变视紫红质II(MII)形成和衰变的影响。通过将KCl浓度从低渗增加到4 M,变视紫红质I(MI)/MII平衡的表观pKa大约偏移了三个pH单位,有利于MII中间体。此外,离子强度的增加会提高MII的形成速率(在2 M KCl存在下约提高两倍)。MIII衰变与盐浓度无关。衰减全反射/FTIR数据表明,高盐条件对膜基质的刚性没有影响,也不会诱导中间体本身的结构变化。测试了不同盐类使MI/MII平衡发生偏移的能力;然而,未观察到明显的离子依赖性。我们将这些结果解释为胞质表面电荷直接参与牛视紫红质光化学活性调节的一个迹象。