Atkinson A E, Earley F G, Beadle D J, King L A
School of Biological and Molecular Sciences, Oxford Polytechnic, Headington, England.
Eur J Biochem. 1990 Sep 11;192(2):451-8. doi: 10.1111/j.1432-1033.1990.tb19247.x.
A baculovirus transfer vector was constructed containing an entire cDNA copy of the chick nicotinic acetylcholine receptor (nAChR) alpha-subunit under control of the Autographa californica nuclear polyhedrosis virus (AcNPV) polyhedrin gene promoter. Recombinant baculovirus was obtained by co-transfection of Spodoptera frugiperda cells with infectious, wild-type AcNPV DNA and the transfer vector. Polyhedrin-negative, recombinant viruses were identified which expressed the nAChR alpha-subunit. The insect cell-expressed alpha-subunit protein had a molecular mass of 42 kDa and was shown to be targeted to the plasma membrane by fluorescence microscopy and toxin-binding assays. The levels of expression were low, approximately 1-2% of cell proteins, when compared with the levels of natural polyhedrin protein. The expressed receptor alpha-subunit was recognised by polyclonal antisera raised against purified Torpedo nAChR alpha-subunit and carried the binding site for the snake venom toxin, alpha-bungarotoxin. Bound alpha-bungarotoxin was displaced in competition binding assays by alpha-cobra toxin, carbamylcholine and d-tubocurarine, and thus had a similar pharmacological profile to that obtained with authentic receptors in muscle cells and receptors expressed in other systems i.e. Xenopus oocytes and mammalian cells. We have also shown that when the chick nAChR alpha-subunit is expressed in the absence of other receptor subunits, unexpectedly high concentrations of nicotine (10 mM) were required to displace bound alpha-bungarotoxin.
构建了一种杆状病毒转移载体,其包含在苜蓿银纹夜蛾核型多角体病毒(AcNPV)多角体蛋白基因启动子控制下的鸡烟碱型乙酰胆碱受体(nAChR)α亚基的完整cDNA拷贝。通过将草地贪夜蛾细胞与感染性野生型AcNPV DNA和转移载体共转染获得重组杆状病毒。鉴定出表达nAChRα亚基的多角体蛋白阴性重组病毒。昆虫细胞表达的α亚基蛋白分子量为42 kDa,通过荧光显微镜和毒素结合试验表明其定位于质膜。与天然多角体蛋白的水平相比,表达水平较低,约为细胞蛋白的1-2%。表达的受体α亚基被针对纯化的电鳗nAChRα亚基产生的多克隆抗血清识别,并携带蛇毒毒素α-银环蛇毒素的结合位点。在竞争结合试验中,结合的α-银环蛇毒素被α-眼镜蛇毒素、氨甲酰胆碱和d-筒箭毒碱取代,因此其药理学特征与肌肉细胞中的真实受体以及在其他系统(即非洲爪蟾卵母细胞和哺乳动物细胞)中表达的受体相似。我们还表明,当鸡nAChRα亚基在没有其他受体亚基的情况下表达时,需要出乎意料的高浓度尼古丁(10 mM)才能取代结合的α-银环蛇毒素。