Shpakov A O, Gur'ianov I A, Avdeeva E V, Vorob'ev V I, Vlasov G P
Tsitologiia. 2004;46(11):1011-22.
For the aims of studying molecular mechanisms of functioning of adenylyl cyclase signaling systems (ACS), we investigated the influence of synthetic polycationic peptides of the star-like structure (dendrons), containing 48-60 sequence of HIV-1 TAT-protein, on the functional activity of ACS components in smooth muscles of the mollusc Anodonta cygnea and in rat skeletal muscles. It has been shown that the following peptides (Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Pro-Pro-Gln)2-Lys-epsilonAhx(= epsilon-aminohexanoic acid)-Cys(Acm), referred to as peptide I, (Gly-Arg-Gly-Asp-Ser-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Pro-Pro-Gln)2-Lys-epsilonAhx-Cys(Acm) (peptide II), [(Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Pro-Pro-Gln)2-Lys-epsilonAhx-Cys]2 (peptide III), and [(Gly-Arg-Gly-Asp-Ser-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Pro-Pro-Gln)2-Lys-epsilonAhx-Cys]2 (peptide IV) inhibit in a dose-dependent manner the adenylyl cyclase (AC) activity stimulated by both nonhormanal agents (GppNHp and forskolin) and hormones, such as serotonin (mollusc) and isoproterenol (rat). Peptides III and IV (tetrameric dendrons) were most effective in comparison with peptides I and II (dimeric dendrons). The AC activity stimulated by hormones and forskolin was most sensitive to the action of dendrons. All dendrons stimulated GTP-binding activity of G-proteins: dimeric dendrons were most effective at 10(-5) M concentration, whereas tetrameric dendrons at 10(-6) M. In the presence of dendrons, the affinity of beta-antagonist [3H]-dihydroalprenolol to P-adrenergic receptor in rat muscle mem- branes was unchanged. At the same time, the affinity of beta-agonist isoproterenol to the receptor decreased, and no shift to the right was observed on the curve of isoproterenol-induced [3H]-dihydroalprenolol displacement in the presence of GTP. The obtained data show the disturbance of the coupling between the receptor and G-protein, which is the main reason of dendron inhibitory action on AC stimulation by hormones. Besides, these data demonstrated that hormones could disturb the functional activity of AC, i.e. a catalytic component of ACS.
为了研究腺苷酸环化酶信号系统(ACS)的分子作用机制,我们研究了具有星状结构的合成聚阳离子肽(树枝状分子)对天鹅绒蛞蝓平滑肌和大鼠骨骼肌中ACS组分功能活性的影响,该肽包含HIV-1 TAT蛋白的48 - 60序列。结果表明,以下肽(Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Pro-Pro-Gln)2-Lys-εAhx(=ε-氨基己酸)-Cys(Acm),称为肽I,(Gly-Arg-Gly-Asp-Ser-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Pro-Pro-Gln)2-Lys-εAhx-Cys(Acm)(肽II),[(Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Pro-Pro-Gln)2-Lys-εAhx-Cys]2(肽III)和[(Gly-Arg-Gly-Asp-Ser-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Pro-Pro-Gln)2-Lys-εAhx-Cys]2(肽IV)以剂量依赖性方式抑制由非激素剂(GppNHp和福斯可林)以及激素(如5-羟色胺(蛞蝓)和异丙肾上腺素(大鼠))刺激的腺苷酸环化酶(AC)活性。与肽I和II(二聚体树枝状分子)相比,肽III和IV(四聚体树枝状分子)最有效。由激素和福斯可林刺激的AC活性对树枝状分子的作用最敏感。所有树枝状分子均刺激G蛋白的GTP结合活性:二聚体树枝状分子在10^(-5) M浓度下最有效,而四聚体树枝状分子在10^(-6) M浓度下最有效。在存在树枝状分子的情况下,β拮抗剂[3H]-二氢阿普洛尔与大鼠肌肉膜中β-肾上腺素能受体的亲和力未改变。同时,β激动剂异丙肾上腺素与受体的亲和力降低,并且在存在GTP的情况下,异丙肾上腺素诱导的[3H]-二氢阿普洛尔置换曲线未观察到向右移动。获得的数据表明受体与G蛋白之间的偶联受到干扰,这是树枝状分子对激素刺激AC产生抑制作用的主要原因。此外,这些数据表明激素可能会干扰AC的功能活性,即ACS的催化组分。