Faculty of Advanced Life Science, Hokkaido University, Sapporo, Japan; Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Biophys J. 2010 Apr 7;98(7):1353-63. doi: 10.1016/j.bpj.2009.12.4288.
Sensory rhodopsin II (HsSRII, also called phoborhodopsin) is a negative phototaxis receptor of Halobacterium salinarum, a bacterium that avoids blue-green light. In this study, we expressed the protein in Escherichia coli cells, and reconstituted the purified protein with phosphatidylcholine. The reconstituted HsSRII was stable. We examined the photocycle by flash-photolysis spectroscopy in the time range of milliseconds to seconds, and measured proton uptake/release using a transparent indium-tin oxide electrode. The pKa of the counterion of the Schiff base, Asp(73), was 3.0. Below pH 3, the depleted band was observed on flash illumination, but the positive band in the difference spectra was not found. Above pH 3, the basic photocycle was HsSRII (490) --> M (350) --> O (520) --> Y (490) --> HsSRII, where the numbers in parentheses are the maximum wavelengths. The decay rate of O-intermediate and Y-intermediate were pH-independent, whereas the M-intermediate decay was pH-dependent. For 3 < pH < 4.5, the M-decay was one phase, and the rate decreased with an increase in pH. For 4.5 < pH < 6.5, the decay was one phase with pH-independent rates, and azide markedly accelerated the M-decay. These findings suggest the existence of a protonated amino acid residue (X-H) that may serve as a proton relay to reprotonate the Schiff base. Above pH 6.5, the M-decay showed two phases. The fast M-decay was pH-independent and originated from the molecule having a protonated X-H, and the slow M-decay originated from the molecule having a deprotonated X, in which the proton came directly from the outside. The analysis yielded a value of 7.5 for the pKa of X-H. The proton uptake and release occurred during M-decay and O-decay, respectively.
感觉视紫红质 II(HsSRII,也称为光视紫红质)是盐沼盐杆菌的一种负趋光性受体,盐杆菌是一种避免蓝绿光的细菌。在这项研究中,我们在大肠杆菌细胞中表达了这种蛋白质,并使用磷脂酰胆碱重新构建了纯化的蛋白质。重新构建的 HsSRII 是稳定的。我们通过毫秒到秒的时间范围的闪光光解光谱研究了光循环,并使用透明铟锡氧化物电极测量了质子的摄取/释放。Schiff 碱的抗衡离子(天冬氨酸(Asp)73)的 pKa 为 3.0。在 pH 值低于 3 时,在闪光照射下观察到耗尽带,但在差谱中未发现正带。在 pH 值高于 3 时,基本光循环为 HsSRII(490)-->M(350)-->O(520)-->Y(490)-->HsSRII,括号中的数字是最大波长。O 中间体和 Y 中间体的衰减速率与 pH 值无关,而 M 中间体的衰减速率与 pH 值有关。对于 3<pH<4.5,M 衰减是一个相,随着 pH 值的增加,速率降低。对于 4.5<pH<6.5,衰减是一个相,具有与 pH 值无关的速率,且叠氮化物明显加速了 M 衰减。这些发现表明存在一个质子化的氨基酸残基(X-H),它可能作为质子供体重新质子化 Schiff 碱。在 pH 值高于 6.5 时,M 衰减呈现两个相。快速 M 衰减与 pH 值无关,源于具有质子化 X-H 的分子,而缓慢 M 衰减源于具有去质子化 X 的分子,其中质子直接来自外部。分析得出 X-H 的 pKa 值为 7.5。质子的摄取和释放分别发生在 M 衰减和 O 衰减过程中。