Fischer J, Sharp G W
Biochem J. 1978 Nov 15;176(2):505-10. doi: 10.1042/bj1760505.
A comparison was made of the effects of cholera toxin and p[NH]ppG on the binding affinity of beta-adrenergic receptors in toad erythrocyte membranes. This was determined by studying the ability of isoproterenol and propranolol to compete for the receptor with (-)-[3H]dihydroalprenolol. p[NH]ppG decreased the receptor affinity for the agonist isoproterenol (i.e. a 'right' shift in the displacement-concentration curve), but was without effect on the affinity for the antagonist propranolol. Toad erythrocyte membranes after treatment with cholera toxin exhibited increased receptor affinity for isoproterenol (i.e. a 'left' shift in the displacement curve), but did not affect the affinity for propranolol. p[NH[ppG was able to exert its right shift even in cholera-toxin treated membranes. The ability of cholera toxin to alter beta-adrenergic-receptor affinity is interpreted as further evidence that the toxin affects the nucleotide-regulatory component of adenylate cyclase. The regulatory component affected may be the catecholamine-sensitive guanosine triphosphatase.
对霍乱毒素和对氨苯甲酰基-5'-磷酸鸟苷(p[NH]ppG)对蟾蜍红细胞膜中β-肾上腺素能受体结合亲和力的影响进行了比较。这是通过研究异丙肾上腺素和普萘洛尔与(-)-[3H]二氢阿普洛尔竞争受体的能力来确定的。p[NH]ppG降低了受体对激动剂异丙肾上腺素的亲和力(即位移-浓度曲线的“右”移),但对拮抗剂普萘洛尔的亲和力没有影响。用霍乱毒素处理后的蟾蜍红细胞膜对异丙肾上腺素的受体亲和力增加(即位移曲线的“左”移),但不影响对普萘洛尔的亲和力。即使在霍乱毒素处理的膜中,p[NH]ppG也能够产生其右移作用。霍乱毒素改变β-肾上腺素能受体亲和力的能力被解释为毒素影响腺苷酸环化酶的核苷酸调节成分的进一步证据。受影响的调节成分可能是儿茶酚胺敏感的鸟苷三磷酸酶。