Rousseau E, Proteau S
Department of Physiology and Biophysics, Faculty of Medicine, Unversit é de Sherbrooke, QC, Canada.
Can J Physiol Pharmacol. 2001 Apr;79(4):310-9.
mRNA and protein analyses have previously shown that the diaphragm expresses two ryanodine receptor isoforms: RyR1 and RyR3. RyR1 is the main Ca2+-releasing pathway in this muscle type. We now report the conducting, gating, and immunological properties of the native and purified forms of the less abundant RyR3 channel. The conductance of this native Ca2+-release channel was 330 pS in 50 mM/250 mM trans/cis CsCH3SO3. It was activated by Ca2+ concentrations of 1-1000 microM, and did not inactivate at mM concentrations of Ca2+. Both isoforms were purified by either a sucrose density gradient or immunoprecipitation as > 450 kDa proteins on SDS-PAGE. Western blot analysis confirmed the presence of RyR1 and RyR3, which displayed conductances of 740 +/- 30 and 800 +/- 25 pS, respectively, in 250 mM KCl. We thus provide evidence that one form of the diaphragm SR Ca2+-release channels may be classified as RyR3, with gating properties different from those of the well-characterized RyR1 and RyR2 isoforms.
mRNA和蛋白质分析先前已表明,膈肌表达两种兰尼碱受体亚型:RyR1和RyR3。RyR1是这种肌肉类型中的主要Ca2+释放途径。我们现在报告了含量较少的RyR3通道的天然形式和纯化形式的传导、门控和免疫学特性。在50 mM/250 mM反式/顺式CsCH3SO3中,这种天然Ca2+释放通道的电导为330 pS。它在1 - 1000 microM的Ca2+浓度下被激活,在毫摩尔浓度的Ca2+下不会失活。两种亚型通过蔗糖密度梯度或免疫沉淀纯化,在SDS - PAGE上表现为大于450 kDa的蛋白质。蛋白质印迹分析证实了RyR1和RyR3的存在,它们在250 mM KCl中的电导分别为740 +/- 30和800 +/- 25 pS。因此,我们提供的证据表明,膈肌肌浆网Ca2+释放通道的一种形式可能被归类为RyR3,其门控特性与特征明确的RyR1和RyR2亚型不同。