Levey G S, Klein I
J Clin Invest. 1972 Jun;51(6):1578-82. doi: 10.1172/JCI106955.
We have recently described the preparation of a solubilized cat myocardial adenylate cyclase which is unresponsive to histamine, norepinephrine, glucagon, and thyroxine, the hormones which activate the particulate enzyme. Since hormone receptors may consist of proteins and phospholipids, we determined the effect of several phospholipids on restoring the responsiveness of the solubilized adenylate cyclase to histamine. The addition of phosphatidylserine completely restored the histamine-mediated activation of the solubilized enzyme in contrast to phosphatidylethanolamine and phosphatidylinositol which were without effect. The concentration of histamine producing half-maximal activation of adenylate cyclase, 2 x 10(-5) M, was virtually identical with that observed in the particulate preparation. The antihistamine, diphenhydramine, 8 x 10(-5) M, abolished activation of adenylate cyclase by histamine in both the solubilized and particulate preparations. Phosphatidylserine also restored glucagon responsiveness, but did not restore norepinephrine responsiveness. It would appear that phosphatidylserine produced the necessary molecular configuration of the adenylate cyclase for histamine binding and activation of the enzyme.
我们最近描述了一种溶解的猫心肌腺苷酸环化酶的制备方法,该酶对组胺、去甲肾上腺素、胰高血糖素和甲状腺素无反应,而这些激素可激活颗粒状酶。由于激素受体可能由蛋白质和磷脂组成,我们测定了几种磷脂对恢复溶解的腺苷酸环化酶对组胺反应性的影响。与无作用的磷脂酰乙醇胺和磷脂酰肌醇相比,添加磷脂酰丝氨酸可完全恢复组胺介导的溶解酶的激活。产生腺苷酸环化酶半数最大激活的组胺浓度,即2×10⁻⁵M,与在颗粒制剂中观察到的浓度几乎相同。抗组胺药苯海拉明(8×10⁻⁵M)在溶解制剂和颗粒制剂中均消除了组胺对腺苷酸环化酶的激活作用。磷脂酰丝氨酸也恢复了胰高血糖素反应性,但未恢复去甲肾上腺素反应性。看来磷脂酰丝氨酸产生了腺苷酸环化酶与组胺结合及激活该酶所需的分子构型。