Takeuchi T, Tanaka S, Rechnitz G A
Department of Chemistry, University of Hawaii, Manoa, Honolulu 96822.
Anal Biochem. 1992 May 15;203(1):158-62. doi: 10.1016/0003-2697(92)90057-e.
A nonisotopic receptor assay using the biotin-1012-S conjugate was developed and the usefulness of this conjugate as a probe ligand for the benzodiazepine receptor was evaluated. The conjugate was incubated in a receptor suspension, and then the concentration of free conjugate in the supernatant was determined nonisotopically with a solid-phase avidin-biotin binding assay. Studies on the ligand saturation with the conjugate demonstrated that the conjugate has very high affinity and specificity for the receptors and the biotin labeling does not decrease the affinity of 1012-S. This assay method was applied to the characterization of binding sites of benzodiazepine receptors in cow brain. Competition interactions between the conjugate and benzodiazepine drugs gave well-defined dose-response curves. These results confirm the possibility that this conjugate could serve as a probe for the study of receptor-ligand interactions and provide the basis of a new nonisotopic receptor assay for benzodiazepine drugs.
开发了一种使用生物素 - 1012 - S共轭物的非同位素受体测定法,并评估了该共轭物作为苯二氮䓬受体探针配体的效用。将共轭物在受体悬浮液中孵育,然后通过固相抗生物素蛋白 - 生物素结合测定法非同位素地测定上清液中游离共轭物的浓度。用共轭物进行的配体饱和研究表明,该共轭物对受体具有非常高的亲和力和特异性,并且生物素标记不会降低1012 - S的亲和力。该测定方法应用于牛脑苯二氮䓬受体结合位点的表征。共轭物与苯二氮䓬药物之间的竞争相互作用给出了明确的剂量反应曲线。这些结果证实了该共轭物可作为研究受体 - 配体相互作用探针的可能性,并为苯二氮䓬药物新的非同位素受体测定提供了基础。