Tian W D, Sage J T, Champion P M
Department of Physics, Northeastern University, Boston, MA 02115.
J Mol Biol. 1993 Sep 5;233(1):155-66. doi: 10.1006/jmbi.1993.1491.
Kinetic and Raman spectroscopic studies are combined to analyze ligand association and dissociation rates as a function of pH in aqueous solutions of myoglobin. A double-pulse flash photolysis protocol is used to kinetically select a rapidly rebinding (open pocket) fraction of the myoglobin ensemble and determine the timescale for averaging (approximately 1 to 10 microseconds) between the "open" and "closed" distal pocket protein conformations. Since this timescale is fast compared to the rate of ligand migration from the solution to the heme pocket (approximately 10(-4)s), a time-averaged population analysis, rather than a superposition of states, can be used to describe the ligand association and dissociation kinetics. Raman spectroscopy provides the relative populations of the open and closed distal pocket states as a function of pH which, in parallel with kinetics measurements, are used to determine the rates for ligand association and dissociation specific to these states. In aqueous solution at 293 K (1 mM CO) we find kon0 = 5.6 x 10(3) s-1, koff0 = 8.5 x 10(-2) s-1 for the open state and kon1 = 5.0 x 10(2) s-1, koff1 = 1.3 x 10(-2) s-1 for the closed state. The order of magnitude increase in the dissociation and association rates of the open form suggests that it may play a significant role in the ligand binding process, even though it comprises only approximately 5% of the time-averaged population at pH 7. For oxygen binding at 293 K (1.36 mM O2) we find kon0 = 4.6 x 10(4) s-1, koff0 approximately 10(4 +/- 2) s-1 for the open state and kon1 = 2.0 x 10(4) s-1, koff1 = 13 s-1 for the closed state. The dramatic increase in the dissociation rate of the open form is probably due to the loss of the hydrogen bond with the distal histidine, which stabilizes the bound O2 in the closed state. Overall, these results demonstrate that the open conformation plays a significant role in determining the ligand association and dissociation rates and suggest that environmentally induced modulations of the open population could be used as a biomolecular control mechanism for the uptake and delivery of oxygen in muscle cells.
结合动力学和拉曼光谱研究,以分析肌红蛋白水溶液中配体结合和解离速率与pH值的函数关系。采用双脉冲闪光光解方案从肌红蛋白集合中动力学选择快速重新结合(开放口袋)部分,并确定“开放”和“封闭”远端口袋蛋白构象之间平均化的时间尺度(约1至10微秒)。由于该时间尺度比配体从溶液迁移到血红素口袋的速率(约10^(-4)秒)快,因此可以使用时间平均群体分析而非状态叠加来描述配体结合和解离动力学。拉曼光谱提供开放和封闭远端口袋状态的相对群体作为pH值的函数,与动力学测量并行,用于确定特定于这些状态的配体结合和解离速率。在293 K的水溶液中(1 mM CO),我们发现开放状态下的kon0 = 5.6 x 10^3 s^(-1),koff0 = 8.5 x 10^(-2) s^(-1),封闭状态下的kon1 = 5.0 x 10^2 s^(-1),koff1 = 1.3 x 10^(-2) s^(-1)。开放形式的解离和结合速率数量级增加表明它可能在配体结合过程中起重要作用,尽管在pH 7时它仅占时间平均群体的约5%。对于293 K下的氧结合(1.36 mM O2),我们发现开放状态下的kon0 = 4.6 x 10^4 s^(-1),koff0约为10^(4±2) s^(-1),封闭状态下的kon1 = 2.0 x 10^4 s^(-1),koff1 = 13 s^(-1)。开放形式解离速率的显著增加可能是由于与远端组氨酸的氢键丢失,该氢键在封闭状态下稳定结合的O2。总体而言,这些结果表明开放构象在确定配体结合和解离速率方面起重要作用,并表明环境诱导的开放群体调制可作为肌肉细胞中氧摄取和输送的生物分子控制机制。