Xu L, Jones R V, Meissner G
Department of Biochemistry, University of North Carolina, Chapel Hill 27599-7260.
Arch Biochem Biophys. 1989 Nov 1;274(2):609-16. doi: 10.1016/0003-9861(89)90476-1.
Vesicle-45Ca2+ ion flux and planar lipid bilayer single-channel measurements have shown that the Ca2+ release channel of skeletal muscle sarcoplasmic reticulum (SR) is activated by micromolar concentrations of Cibacron Blue F3A-G (Reactive Blue 2) and Reactive Red 120. Cibacron Blue increased the 45Ca2+ efflux rate from heavy SR vesicles by apparently interacting with both the adenine nucleotide and caffeine activating sites of the channel. Dye-induced 45Ca2+ release was inhibited by Mg2+ and ruthenium red. In single channel recordings with the purified channel protein complex, Cibacron Blue increased the open time of the Ca2+ release channel without an apparent change in the conductance of the main and subconductance states of the channel.
囊泡 - 45Ca2+离子通量和平面脂质双分子层单通道测量表明,骨骼肌肌浆网(SR)的Ca2+释放通道可被微摩尔浓度的汽巴克隆蓝F3A - G(活性蓝2)和活性红120激活。汽巴克隆蓝通过与通道的腺嘌呤核苷酸和咖啡因激活位点相互作用,明显增加了重肌浆网囊泡中45Ca2+的流出速率。染料诱导的45Ca2+释放受到Mg2+和钌红的抑制。在用纯化的通道蛋白复合物进行的单通道记录中,汽巴克隆蓝增加了Ca2+释放通道的开放时间,而通道主要和亚电导状态的电导没有明显变化。