Bates M D, Gingrich J A, Bunzow J R, Falardeau P, Dearry A, Senogles S E, Civelli O, Caron M G
Department of Cell Biology, Howard Hughes Medical Institute, Duke University Medical Center, Durham, North Carolina 27710.
Am J Hypertens. 1990 Jun;3(6 Pt 2):29S-33S. doi: 10.1093/ajh/3.6.29s.
The D1 and D2 dopamine receptors have been biochemically characterized using specific probes based on the subtype selective antagonists SCH 23390 and spiperone, respectively. The D2 dopamine receptor was identified from several tissues by photoaffinity labeling and was purified from bovine anterior pituitary to homogeneity using a combination of affinity, lectin and hydroxylapatite chromatography. A complementary DNA (cDNA) encoding a rat brain D2 dopamine receptor has been cloned via low stringency hybridization using a portion of the beta 2-adrenergic receptor gene as a probe. Photoaffinity crosslinking and affinity chromatography have also been used to identify and purify the rat brain D1 dopamine receptor.
分别使用基于亚型选择性拮抗剂SCH 23390和螺哌隆的特异性探针,对D1和D2多巴胺受体进行了生化特性鉴定。通过光亲和标记从多个组织中鉴定出D2多巴胺受体,并使用亲和、凝集素和羟基磷灰石色谱法相结合的方法从牛垂体前叶中将其纯化至同质。利用β2-肾上腺素能受体基因的一部分作为探针,通过低严谨度杂交克隆了编码大鼠脑D2多巴胺受体的互补DNA(cDNA)。光亲和交联和亲和色谱法也已用于鉴定和纯化大鼠脑D1多巴胺受体。