Stein P, Palade P
Department of Physiology and Biophysics, University of Texas Medical Branch, Galveston 77550.
Biophys J. 1988 Aug;54(2):357-63. doi: 10.1016/S0006-3495(88)82967-9.
In skeletal muscle, twitch contraction is caused by the rapid release of Ca2+ from the sarcoplasmic reticulum (SR) (Endo, M. 1977. Physiol. Rev. 57:71-108) via Ca2+ conducting channels in the SR membrane (Smith, J. S., R. Coronado, and G. Meissner, 1985. Nature (Lond.). 316:446-449; Suarez-Isla, B. A., G. Orozco, P. F. Heller, and J. P. Froehlich. 1986. Proc. Natl. Acad. Sci. USA. 83:7741-7745). To facilitate study of these and other intracellular channels, we have developed a method which allows direct patch-clamp recording of currents through SR channels in native membrane. The Ca2+-release channel studied using this method exhibits two predominant conductance levels (80-100 pS and 120-160 pS), conducts Ca2+ preferentially over K+ (PCa/Pk = 6.5), is highly voltage sensitive, blocked on one side by ruthenium red (1 microM), and displays enhanced activity in the presence of caffeine (5 mM). Studied in skinned fibers, this channel appears fundamentally similar to homologous channels from isolated rabbit SR incorporated into bilayers, with some distinct differences.
在骨骼肌中,单收缩是由肌浆网(SR)(远藤,M. 1977年。《生理学评论》57:71 - 108)通过SR膜中的钙离子传导通道快速释放Ca2+引起的(史密斯,J. S.,R. 科罗纳多,和G. 迈斯纳,1985年。《自然》(伦敦)。316:446 - 449;苏亚雷斯 - 伊斯拉,B. A.,G. 奥罗斯科,P. F. 赫勒,和J. P. 弗勒利希。1986年。《美国国家科学院院刊》。83:7741 - 7745)。为便于研究这些及其他细胞内通道,我们开发了一种方法,可直接对通过天然膜中SR通道的电流进行膜片钳记录。用该方法研究的Ca2+释放通道表现出两个主要的电导水平(80 - 100皮安和120 - 160皮安),对Ca2+的传导优先于K+(PCa/Pk = 6.5),对电压高度敏感,一侧被钌红(1微摩尔)阻断,并且在咖啡因(5毫摩尔)存在时显示出增强的活性。在皮肤纤维中研究时,该通道与整合到双层膜中的分离兔SR的同源通道基本相似,但也存在一些明显差异。