Audus K L, Gordon M A
J Immunopharmacol. 1982;4(1-2):1-12. doi: 10.3109/08923978209031071.
A single population of high affinity, saturable, tricyclic antidepressant (3-H-desipramine) binding sites has been identified on the membranes of murine lymphocytes. There are approximately 300 binding sites per cell and the apparent dissociation constant (Kd) for these binding sites is about 0.4 nM. Competition studies between the radiolabeled ligand in concentrations near the Kd and other members of the class of tricyclic antidepressants indicate that binding is competitive, reversible, and does not display interactions characteristic of cooperativity.
在小鼠淋巴细胞的细胞膜上已鉴定出一类高亲和力、可饱和的三环类抗抑郁药(3-H-去甲丙咪嗪)结合位点。每个细胞大约有300个结合位点,这些结合位点的表观解离常数(Kd)约为0.4 nM。在接近Kd浓度的放射性标记配体与其他三环类抗抑郁药之间的竞争研究表明,结合是竞争性的、可逆的,并且不表现出协同作用的特征性相互作用。