Wong Y H, Demoliou-Mason C D, Barnard E A
MRC Molecular Neurobiology Unit, Medical Research Council Centre, Cambridge, England.
J Neurochem. 1988 Jul;51(1):114-21. doi: 10.1111/j.1471-4159.1988.tb04843.x.
Pertussis toxin-catalyzed ADP-ribosylation of the guanine nucleotide-binding proteins Gi and Go is shown to proceed in Mg2+-digitonin extracts from rat brain; the Mr 41,000 and Mr 39,000 peptides are labelled there as in the membranes. The ADP-ribosylation in detergent solution retains the differential sensitivity to guanine nucleotide analogues. This reaction also removes the partial inhibition by the guanine nucleotides of the binding of opioid agonists, as does the same treatment in the membranes. The partial inhibition of agonist binding by Na+, however, is left unchanged. The binding of the antagonist naloxone is little affected by Na+ or by guanine nucleotides in the treated membranes, but the treated soluble receptors show an enhanced binding in high-Na+ medium, although still guanine nucleotide insensitive. The data suggest that the toxin reaction in the absence of guanine nucleotides and agonist stabilizes the opioid receptor in a receptor-G-protein coupled state which is no longer sensitive to guanine nucleotides but retains its sensitivity to the Na+ ions.
百日咳毒素催化的鸟嘌呤核苷酸结合蛋白Gi和Go的ADP核糖基化反应,在大鼠脑的Mg2+-洋地黄皂苷提取物中进行;那里的41,000 Mr和39,000 Mr肽段与在细胞膜中一样被标记。去污剂溶液中的ADP核糖基化反应保留了对鸟嘌呤核苷酸类似物的差异敏感性。该反应也消除了鸟嘌呤核苷酸对阿片类激动剂结合的部分抑制作用,细胞膜中的相同处理也是如此。然而,Na+对激动剂结合的部分抑制作用保持不变。拮抗剂纳洛酮的结合在处理过的细胞膜中受Na+或鸟嘌呤核苷酸的影响很小,但处理过的可溶性受体在高Na+介质中显示出增强的结合,尽管仍然对鸟嘌呤核苷酸不敏感。数据表明,在不存在鸟嘌呤核苷酸和激动剂的情况下,毒素反应使阿片受体稳定在受体-G蛋白偶联状态,该状态不再对鸟嘌呤核苷酸敏感,但保留了对Na+离子的敏感性。