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Protein relaxation in the photodissociation of myoglobin-CO complex

机译:肌红蛋白-CO复合物光解离中的蛋白质松弛

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摘要

Laser-induced optoacoustic spectroscopy has been applied to the study of the photodissociation of myoglobin-CO complexes. Time-resolved optoacoustic signals have been measured from aqueous solutions of horse myoglobin-CO complex (hMbCO) at pH 3.5 and 8, and of sperm whale myoglobin-CO complex (swMbCO) at pH 8, in the temperature range 273-300 K. The signal of hMbCO at pH 8 exhibits three components. The first, which is faster than 20 ns and is associated with a reaction enthalpy of 61 kJ mol~(-1), corresponds to Fe-CO bond breakage. The second component has a decay time of 80 ns at 293 K and is associated with an exothermic protein relaxation (-13 kJ mol~(-1)) and a volume change of -3 ml mol~(-1). The relaxation, which involves a state where the photodissociated CO is still in a protein docking site, is thermally activated, with an activation enthalpy of 51 kJ mol~(-1). The third component has a decay time of 800 ns at 293 K and an activation enthalpy of 39 kJ mol~(-1), and is associated with an endothermic process (26 kJ mol~(-1)) and an expansion of 19 ml mol~(-1). This process is ascribed to the migration of the photodissociated CO to the bulk solvent. At acidic pH, the latter process becomes faster (230 ns) and the volume change decreases. These features are correlated with the presence of an open form of the protein. swMbCO exhibits two components only, due to the overlap of the two fastest processes. The first involves a reaction enthalpy of 49 kJ mol~(-1) and a volume contraction of -4.9 ml mol~(-1). The second component (900 ns at 293K, activation enthalpy 45 kJ mol~(-1)) is associated with a reaction enthalpy of 38 kJ mol~(-1) and a volume expansion of 15.3 ml mol~(-1). These experimental findings have been interpreted by means of a new model, which also takes into account both laser flash photolysis results and structural information. The model is based on a two-dimensional scheme which describes both protein relaxation and the CO pathway following photodissociation.
机译:激光诱导的光声光谱已被用于研究肌红蛋白-CO复合物的光解离。已在温度范围273-300 K下,从pH 3.5和8的马肌红蛋白-CO复合物(hMbCO)和pH 8的抹香鲸肌红蛋白-CO复合物(swMbCO)的水溶液中测量了时间分辨的光声信号。 pH为8的hMbCO信号表现出三个成分。第一个速度快于20 ns,并与61 kJ mol〜(-1)的反应焓相关,对应于Fe-CO键断裂。第二种成分在293 K处的衰减时间为80 ns,并且与放热的蛋白质弛豫(-13 kJ mol〜(-1))和-3 ml mol〜(-1)的体积变化有关。弛豫涉及光解离的CO仍处于蛋白质对接位点的状态,并以51 kJ mol〜(-1)的活化焓进行热活化。第三组分在293 K时的衰减时间为800 ns,活化焓为39 kJ mol〜(-1),与吸热过程(26 kJ mol〜(-1))和19 ml的膨胀有关。摩尔〜(-1)。该过程归因于光解离的CO向本体溶剂的迁移。在酸性pH下,后一个过程变得更快(230 ns),体积变化减小。这些特征与蛋白质开放形式的存在有关。由于两个最快的过程的重叠,swMbCO仅显示两个组件。首先涉及49 kJ mol〜(-1)的反应焓和-4.9 ml mol〜(-1)的体积收缩。第二组分(在293K为900 ns,活化焓为45 kJ mol〜(-1))与38 kJ mol〜(-1)的反应焓和15.3 ml mol〜(-1)的体积膨胀有关。这些实验结果已通过新模型进行了解释,该模型还考虑了激光闪光光解结果和结构信息。该模型基于二维方案,该方案描述了光解离后的蛋白质松弛和CO途径。

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