Department of Frontier Materials, Nagoya Institute of Technology, Showa-ku, Nagoya 466-8555, Japan.
Biochemistry. 2012 Feb 14;51(6):1126-33. doi: 10.1021/bi201676y. Epub 2012 Feb 2.
Protein-bound water molecules play crucial roles in the structure and function of proteins. The functional role of water molecules has been discussed for rhodopsin, the light sensor for twilight vision, on the basis of X-ray crystallography, Fourier transform infrared (FTIR) spectroscopy, and a radiolytic labeling method, but nothing is known about the protein-bound waters in our color visual pigments. Here we apply low-temperature FTIR spectroscopy to monkey red (MR)- and green (MG)-sensitive color pigments at 77 K and successfully identify water vibrations using D(2)O and D(2)(18)O in the whole midinfrared region. The observed water vibrations are 6-8 for MR and MG, indicating that several water molecules are present near the retinal chromophore and change their hydrogen bonds upon retinal photoisomerization. In this sense, color visual pigments possess protein-bound water molecules essentially similar to those of rhodopsin. The absence of strongly hydrogen-bonded water molecules (O-D stretch at <2400 cm(-1)) is common between rhodopsin and color pigments, which greatly contrasts with the case of proton-pumping microbial rhodopsins. On the other hand, two important differences are observed in water signal between rhodopsin and color pigments. First, the water vibrations are identical between the 11-cis and 9-cis forms of rhodopsin, but different vibrational bands are observed at >2550 cm(-1) for both MR and MG. Second, strongly hydrogen-bonded water molecules (2303 cm(-1) for MR and 2308 cm(-1) for MG) are observed for the all-trans form after retinal photoisomerization, which is not the case for rhodopsin. These specific features of MR and MG can be explained by the presence of water molecules in the Cl(-)-biding site, which are located near positions C11 and C9 of the retinal chromophore. The averaged frequencies of the observed water O-D stretching vibrations for MR and MG are lower as the λ(max) is red-shifted, suggesting that water molecules are involved in the color tuning of our vision.
蛋白质结合水分子在蛋白质的结构和功能中起着至关重要的作用。基于 X 射线晶体学、傅里叶变换红外(FTIR)光谱和放射化学标记方法,已经讨论了视紫红质( twilight vision 的光传感器)中水分子的功能作用,但我们的颜色视觉色素中的蛋白质结合水尚不清楚。在这里,我们将低温 FTIR 光谱应用于猴红(MR)和绿(MG)敏感的颜色色素,在 77 K 下成功地使用 D2O 和 D2(18)O 在整个中红外区域识别水振动。观察到的水振动为 6-8 对于 MR 和 MG,表明在视黄醛光异构化时,几个水分子存在于视黄醛发色团附近并改变它们的氢键。从这个意义上说,颜色视觉色素具有与视紫红质基本相似的蛋白质结合水分子。在视紫红质和颜色色素之间,强烈氢键结合的水分子(O-D 伸展低于 2400 cm-1)的缺失是常见的,这与质子泵微生物视紫红质的情况形成鲜明对比。另一方面,在视紫红质和颜色色素之间的水信号中观察到两个重要差异。首先,视紫红质的 11-cis 和 9-cis 形式之间的水振动是相同的,但在 >2550 cm-1 处观察到 MR 和 MG 的不同振动带。其次,在视黄醛光异构化后,观察到全反式形式的强氢键结合水分子(MR 为 2303 cm-1,MG 为 2308 cm-1),而视紫红质则没有。MR 和 MG 的这些特定特征可以通过在视黄醛发色团的 C11 和 C9 位置附近存在水分子来解释。对于 MR 和 MG,观察到的水 O-D 伸缩振动的平均频率随着 λ(max)的红移而降低,这表明水分子参与了我们视觉的颜色调谐。