首页> 美国卫生研究院文献>Biochemical Journal >Potentiation of thermal inactivation of glyceraldehyde-3-phosphate dehydrogenase by photodynamic treatment. A possible model for the synergistic interaction between photodynamic therapy and hyperthermia.
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Potentiation of thermal inactivation of glyceraldehyde-3-phosphate dehydrogenase by photodynamic treatment. A possible model for the synergistic interaction between photodynamic therapy and hyperthermia.

机译:通过光动力处理增强3-磷酸甘油醛脱氢酶的热失活。光动力疗法与热疗之间协同相互作用的可能模型。

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摘要

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.
机译:甘油醛-3-磷酸脱氢酶的热失活似乎是由构象机制引起的,没有发生共价反应。另一方面,该酶的光动力学失活(在光敏蛋白II存在下通过光照诱导)是由活性中心中基本硫醇基的光氧化引起的。在40-50摄氏度的温度范围内,对酶进行短暂的光动力学处理(仅导致有限的失活)引起随后热失活的显着增强。根据Arrhenius方程对实验结果的分析表明,两者通过前面的光动力学处理,热失活的活化能和频率因子(比例常数)显着降低。实验结果表明了一种机制,其中有限的光动力处理诱导了蛋白质分子的构象变化。这种构象变化无助于光动力酶的抑制,但是造成频率因子降低和随后的酶热失活的活化能的原因。降低的活化能和降低的频率因数的相反作用导致在40-50摄氏度的温度范围内酶的热失活增强。对于其他蛋白质,获得了不同的结果。淀粉酶的光动力和热效应不是协同的,而是加和的,光动力处理对频率因子和热失活的活化能没有影响。关于肌红蛋白变性,在整个实际适用温度范围内,光动力和热效应是拮抗的。有限的光动力处理可保护蛋白质免受热诱导的沉淀,从而同时增加频率因子和过程的活化能。这些结果为光动力疗法与癌症治疗中的高温之间的协同相互作用的可能机制之一提供了模型。

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