Prinsze C, Dubbelman T M, Van Steveninck J
Sylvius Laboratories, Department of Medical Biochemistry, Leiden, The Netherlands.
Biochem J. 1991 Jun 1;276 ( Pt 2)(Pt 2):357-62. doi: 10.1042/bj2760357.
Thermal inactivation of glyceraldehyde-3-phosphate dehydrogenase appeared to be caused by a conformational mechanism, without involvement of covalent reactions. On the other hand, photodynamic inactivation of the enzyme (induced by illumination in the presence of Photofrin II) was caused by photo-oxidation of the essential thiol group in the active centre. A short photodynamic treatment of the enzyme, leading to only a limited inactivation, caused a pronounced potentiation of subsequent thermal inactivation, as measured over the temperature range 40-50 degrees C. Analysis of the experimental results according to the Arrhenius equation revealed that both the activation energy of thermal inactivation and the frequency factor (the proportionality constant) were significantly decreased by the preceding photodynamic treatment. The experimental results indicate a mechanism in which limited photodynamic treatment induced a conformational change of the protein molecule. This conformational change did not contribute to photodynamic enzyme inhibition, but was responsible for the decreased frequency factor and activation energy of subsequent thermal inactivation of the enzyme. The opposing effects of decreased activation energy and decreased frequency factor resulted in potentiation of thermal inactivation of the enzyme over the temperature range 40-50 degrees C. With other proteins, different results were obtained. With amylase the combined photodynamic and thermal effects were not synergistic, but additive, and photodynamic treatment had no effect on the frequency factor and the activation energy of thermal inactivation. With respect to myoglobin denaturation, the photodynamic and thermal effects were antagonistic over the whole practically applicable temperature range. Limited photodynamic treatment protected the protein against heat-induced precipitation, concomitantly increasing both the frequency factor and the activation energy of the process. These results offer a model for one of the possible mechanisms of synergistic interaction between photodynamic therapy and hyperthermia in cancer treatment.
3-磷酸甘油醛脱氢酶的热失活似乎是由一种构象机制引起的,不涉及共价反应。另一方面,该酶的光动力失活(在光敏剂II存在下光照诱导)是由活性中心必需巯基的光氧化引起的。对该酶进行短时光动力处理,仅导致有限的失活,在40-50摄氏度的温度范围内测量发现,这会显著增强随后的热失活。根据阿伦尼乌斯方程对实验结果进行分析表明,先前的光动力处理显著降低了热失活的活化能和频率因子(比例常数)。实验结果表明存在一种机制,即有限的光动力处理诱导了蛋白质分子的构象变化。这种构象变化对光动力酶抑制没有贡献,但导致了随后酶热失活的频率因子和活化能降低。活化能降低和频率因子降低的相反作用导致在40-50摄氏度温度范围内酶热失活增强。对于其他蛋白质,得到了不同的结果。对于淀粉酶,光动力和热效应不是协同的,而是相加的,光动力处理对热失活的频率因子和活化能没有影响。关于肌红蛋白变性,在整个实际适用的温度范围内,光动力和热效应是拮抗的。有限的光动力处理保护蛋白质免受热诱导沉淀的影响,同时增加了该过程的频率因子和活化能。这些结果为癌症治疗中光动力疗法和热疗协同相互作用的一种可能机制提供了模型。