Ryanodine receptor/calcium release channel conformations as reflected in the different effects of propranolol on its ryanodine binding and channel activity.
作者信息
Zchut S, Feng W, Shoshan-Barmatz V
机构信息
Department of Life Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Propranolol, a beta-blocker, inhibited or stimulated ryanodine binding to both the membrane-bound and purified ryanodine receptor (RyR) depending on the assay conditions. At high NaCl concentrations, propranolol increased the number of ryanodine-binding sites (Bmax) with no effect on the binding affinity. In the presence of 0.2 M NaCl, ryanodine binding was inhibited by propranolol. Half-maximal inhibition was obtained at 1.2 mM and complete inhibition at 2 mM propranolol. The inhibitory effect of propranolol obtained at low NaCl concentration was not restored by increasing the NaCl concentration to 1 M. 2. Modulators of the RyR that are known to alter its conformational states, such as adenine nucleotides, Ca2+ concentration and pH, modified the effect of propranolol on ryanodine binding. In the presence of propranolol and at low NaCl concentrations, ryanodine binding was inhibited and showed no Ca(2+)-, pH-, or time-dependence. 3. Propranolol immediately and completely blocked the channel opening of RyR reconstituted into a planar lipid bilayer. Propranolol-modified non-active channel was reactivated to a subconductive state (about 40% of the control conductance) by ATP. 4. Competition experiments between lidocaine (a stimulatory drug) or tetracaine (an inhibitory drug) and propranolol at 0.2 or 1.0 M NaCl, respectively, suggest the existence of different interaction sites for local anaesthetics and propranolol. 5. These results suggest that propranolol interacts directly with the RyR and modifies its ryanodine binding and single-channel activities. Propranolol effects are altered by the RyR conformational state, suggesting its possible use as a conformational probe for RyR.
摘要
普萘洛尔是一种β受体阻滞剂,根据实验条件,它能抑制或刺激ryanodine与膜结合型和纯化的ryanodine受体(RyR)的结合。在高NaCl浓度下,普萘洛尔增加了ryanodine结合位点的数量(Bmax),而对结合亲和力没有影响。在0.2 M NaCl存在的情况下,普萘洛尔抑制了ryanodine的结合。在1.2 mM时获得半数最大抑制,在2 mM普萘洛尔时完全抑制。将NaCl浓度提高到1 M并不能恢复在低NaCl浓度下获得的普萘洛尔的抑制作用。2. 已知能改变RyR构象状态的调节剂,如腺嘌呤核苷酸、Ca2+浓度和pH,改变了普萘洛尔对ryanodine结合的影响。在普萘洛尔存在且NaCl浓度较低的情况下,ryanodine结合受到抑制,且不表现出Ca(2+)、pH或时间依赖性。3. 普萘洛尔能立即并完全阻断重构到平面脂质双分子层中的RyR的通道开放。普萘洛尔修饰的非活性通道被ATP重新激活到亚传导状态(约为对照电导的40%)。4. 利多卡因(一种刺激性药物)或丁卡因(一种抑制性药物)与普萘洛尔分别在0.2或1.0 M NaCl条件下的竞争实验表明,局部麻醉药和普萘洛尔存在不同的相互作用位点。5. 这些结果表明,普萘洛尔直接与RyR相互作用,改变其ryanodine结合和单通道活性。普萘洛尔的作用因RyR构象状态而改变,表明它可能用作RyR的构象探针。