Plenge P, Mellerup E T
Biochim Biophys Acta. 1984 Feb 29;770(1):22-8. doi: 10.1016/0005-2736(84)90068-3.
The characteristics of 3H-labeled imipramine and 3H-labeled paroxetine binding to human platelet membranes were determined at various temperatures between 0 and 37 degrees C. Both paroxetine and imipramine probably bind to the same molecular complex in the platelet membrane, but the binding characteristics are different for the two molecules. The dissociation constant (Kd) for imipramine increases from 0.3 nM to 7.0 nM with increasing incubation temperature in a continuous way, whereas Kd for paroxetine is almost constant, about 0.05 nM, between 0 and 19 degrees C, and first begins to increase from 0.06 nM to 0.16 nM between 20 and 37 degrees C. This suggests that the binding of paroxetine to the binding site induces a conformational change in the molecular complex of the binding site, whereas the binding of imipramine takes place without conformational changes in the binding site.
在0至37摄氏度的不同温度下,测定了3H标记的丙咪嗪和3H标记的帕罗西汀与人血小板膜结合的特性。帕罗西汀和丙咪嗪可能都与血小板膜中的同一分子复合物结合,但这两种分子的结合特性不同。随着孵育温度的持续升高,丙咪嗪的解离常数(Kd)从0.3 nM增加到7.0 nM,而帕罗西汀的Kd在0至19摄氏度之间几乎恒定,约为0.05 nM,在20至37摄氏度之间才开始从0.06 nM增加到0.16 nM。这表明帕罗西汀与结合位点的结合会诱导结合位点分子复合物的构象变化,而丙咪嗪的结合则不会导致结合位点的构象变化。