Hsia J A, Moss J, Hewlett E L, Vaughan M
Biochem Biophys Res Commun. 1984 Mar 30;119(3):1068-74. doi: 10.1016/0006-291x(84)90883-0.
NG108-15 cells contain both the inhibitory and stimulatory guanyl nucleotide-binding regulatory proteins of the cyclase system. Choleragen activates cyclase directly by ADP-ribosylating the stimulatory guanyl nucleotide-binding protein; prostaglandin E1 does not further increase activity of cells treated with maximally effective concentrations of choleragen. Including pertussis toxin during incubation with this concentration of choleragen, however, further augments both cyclase activity and cAMP accumulation by intact cells. These observations suggest that the inhibitory guanyl nucleotide-binding protein exerts basal inhibition on catalytic activity which cannot be overcome by maximally effective concentrations of choleragen, stimulatory hormones, or both.
NG108 - 15细胞含有环化酶系统的抑制性和刺激性鸟苷酸结合调节蛋白。霍乱毒素通过对刺激性鸟苷酸结合蛋白进行ADP核糖基化作用直接激活环化酶;前列腺素E1不会进一步增加用最大有效浓度霍乱毒素处理过的细胞的活性。然而,在用该浓度霍乱毒素孵育期间加入百日咳毒素,会进一步增强完整细胞的环化酶活性和环磷酸腺苷(cAMP)积累。这些观察结果表明,抑制性鸟苷酸结合蛋白对催化活性发挥基础抑制作用,这种抑制作用无法被最大有效浓度的霍乱毒素、刺激性激素或两者共同作用所克服。