Taussig R, Iñiguez-Lluhi J A, Gilman A G
Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas 75235-9041.
Science. 1993 Jul 9;261(5118):218-21. doi: 10.1126/science.8327893.
Evidence suggests that both alpha and beta gamma subunits of heterotrimeric guanine nucleotide-binding regulatory proteins (G proteins) inhibit adenylyl cyclase. Although type I adenylyl cyclase is inhibited directly by exogenous beta gamma, inhibition of adenylyl cyclase by Gi alpha has not been convincingly demonstrated in vitro. Concentration-dependent inhibition of adenylyl cyclases by purified Gi alpha subunits is described. Activated Gi alpha but not G(o) alpha was effective, and myristoylation of Gi alpha was required. The characteristics of the inhibitory effect were dependent on the type of adenylyl cyclase and the nature of the activator of the enzyme. The concentrations of Gi alpha required to inhibit adenylyl cyclase were substantially higher than those normally thought to be relevant physiologically. However, analysis indicates that these concentrations may be relevant and reasonable.
有证据表明,异三聚体鸟嘌呤核苷酸结合调节蛋白(G蛋白)的α亚基和βγ亚基均能抑制腺苷酸环化酶。虽然I型腺苷酸环化酶可被外源性βγ直接抑制,但在体外尚未令人信服地证明Giα对腺苷酸环化酶的抑制作用。本文描述了纯化的Giα亚基对腺苷酸环化酶的浓度依赖性抑制作用。活化的Giα而非G(o)α具有抑制作用,且Giα需要肉豆蔻酰化。抑制作用的特征取决于腺苷酸环化酶的类型和该酶激活剂的性质。抑制腺苷酸环化酶所需的Giα浓度显著高于通常认为的生理相关浓度。然而,分析表明这些浓度可能是相关且合理的。