Thomas J W, Tallman J F
J Biol Chem. 1981 Oct 10;256(19):9838-42.
The specific photoaffinity labeling of membrane-bound and detergent-solubilized benzodiazepine binding sites has been investigated using UV irradiated [3H] flunitrazepam as a photochemical probe. The time course and the regional and pharmacological specificity of the photolabeling reaction has been determined for "brain-specific" benzodiazepine binding sites; "peripheral-type" binding sites treated in an identical manner were not specifically labeled. Comparison of the number of sites labeled and blocked by [3H]flunitrazepam photolabeling of detergent-solubilized preparations indicated that about one site was blocked and unavailable for reversible binding for each site photolabeled. In contrast, when membrane-bound sites were photolabeled, about four sites were inactivated for each site photolabeled. Examination of photolabeled binding sites from various brain regions including cortex, striatum, and hippocampus using sodium dodecyl sulfate-polyacrylamide gel electrophoresis gave only a single labeled band of apparent Mr = 48,000.
利用紫外线照射的[³H]氟硝西泮作为光化学探针,对膜结合型和去污剂增溶型苯二氮䓬结合位点进行了特异性光亲和标记研究。已确定了“脑特异性”苯二氮䓬结合位点光标记反应的时间进程、区域和药理学特异性;以相同方式处理的“外周型”结合位点未被特异性标记。对去污剂增溶制剂进行[³H]氟硝西泮光标记后,比较标记位点和被阻断位点的数量表明,每个被光标记的位点约有一个位点被阻断且无法进行可逆结合。相比之下,当对膜结合位点进行光标记时,每个被光标记的位点约有四个位点失活。使用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳对包括皮质、纹状体和海马体在内的不同脑区的光标记结合位点进行检测,仅得到一条表观分子量为48,000的单一标记带。