Mills A, Allet B, Bernard A, Chabert C, Brandt E, Cavegn C, Chollet A, Kawashima E
Glaxo Institute for Molecular Biology SA, Plan-les-Ouates/Geneva, Switzerland.
FEBS Lett. 1993 Apr 5;320(2):130-4. doi: 10.1016/0014-5793(93)80077-8.
The human D4 dopamine receptor has been genetically engineered for expression in insect cells using the baculovirus system. A D4 cDNA gene fusion construct [(1991) Nature 350, 610-614] was synthetically modified to remove two introns from the coding region, and expressed in S. frugiperda (Sf9) cells as a fusion with a short sequence from the polyhedrin protein. Binding assays with [3H]spiperone indicated high levels of D4 receptor binding 90 h after infection and a pharmacological profile identical to that reported for D4 receptors expressed in COS-7 cells using the cDNA gene hybrid. We also show that the agonist binding affinity of D4 receptors expressed in Sf9 cells can be shifted by GTP-gamma-S, indicating coupling to G-proteins.
人类D4多巴胺受体已通过杆状病毒系统进行基因工程改造,以便在昆虫细胞中表达。一个D4 cDNA基因融合构建体[(1991年)《自然》350, 610 - 614]经过合成修饰,从编码区去除了两个内含子,并在草地贪夜蛾(Sf9)细胞中作为与多角体蛋白的短序列融合体进行表达。用[3H]司哌罗宁进行的结合试验表明,感染后90小时D4受体结合水平很高,并且药理学特征与使用cDNA基因杂种在COS - 7细胞中表达的D4受体所报道的特征相同。我们还表明,Sf9细胞中表达的D4受体的激动剂结合亲和力可被GTP - γ - S改变,表明其与G蛋白偶联。