Rochette-Egly C, Boschetti E, Basset P, Egly J M
J Chromatogr. 1982 Jun 4;241(2):333-44. doi: 10.1016/s0021-9673(00)81758-6.
The ability of a number of antipsychotic drugs such as phenothiazines to bind to calmodulin with high affinity in a calcium-dependent manner was applied to the study of the nature of their interactions with calmodulin. Thus, a series of phenothiazine derivatives and analogues were immobilized on agarose and examined for their binding characteristics to calmodulin. The binding of calmodulin to fluphenazine, perphenazine and 7-aminotriflupromazine involved on the one hand non-specific electrostatic interactions which are abolished by increasing the eluent salt concentration, and on the other hand, Ca2+-dependent interactions which are reversed by EGTA addition. However, the Ca2+-dependent binding of calmodulin was less specific with phenothiazine structural analogues (neutral Red, diphenylamine) and was suppressed with other phenothiazine derivatives (thionine, Azure C, Toluidine Blue) or analogues (Brilliant Cresyl Blue). It is suggested that the calcium-dependent interactions between calmodulin and drugs involve a charge transfer pi-pi interaction which may be modulated by the electron donor-acceptor properties of the substituents of the aromatic ring. Affinity chromatography using immobilized fluphenazine was also used as the basis for the purification of calmodulin from a number of tissues in a rapid one-step procedure.
许多抗精神病药物如吩噻嗪类能够以钙依赖的方式与钙调蛋白高亲和力结合,这一特性被应用于研究它们与钙调蛋白相互作用的本质。因此,一系列吩噻嗪衍生物和类似物被固定在琼脂糖上,并检测它们与钙调蛋白的结合特性。钙调蛋白与氟奋乃静、奋乃静和7-氨基三氟丙嗪的结合一方面涉及非特异性静电相互作用,这种相互作用会因洗脱液盐浓度的增加而消失,另一方面涉及Ca2+依赖的相互作用,这种相互作用会因加入EGTA而逆转。然而,钙调蛋白与吩噻嗪结构类似物(中性红、二苯胺)的Ca2+依赖结合特异性较低,而与其他吩噻嗪衍生物(硫堇、天青C、甲苯胺蓝)或类似物(灿烂甲酚蓝)的结合则受到抑制。有人提出,钙调蛋白与药物之间的钙依赖相互作用涉及电荷转移π-π相互作用,这种相互作用可能受芳香环取代基的电子供体-受体性质的调节。使用固定化氟奋乃静的亲和色谱法也被用作在快速一步法中从多种组织中纯化钙调蛋白的基础。