Obejero-Paz C A, Jones S W, Scarpa A
Department of Physiology and Biophysics, Case Western Reserve University, Cleveland, Ohio 44106.
J Gen Physiol. 1991 Dec;98(6):1127-40. doi: 10.1085/jgp.98.6.1127.
We studied the effects of trypsin on L-type calcium current in the A7r5 smooth muscle cell line. Intracellular dialysis with trypsin increased the whole-cell current up to fivefold. The effect was concentration dependent, and was prevented by soybean trypsin inhibitor. Ensemble analysis indicated an increase in the number of functional channels, and possibly a smaller increase in the open probability, with no change in the single channel current. The shape of the current-voltage curve was unaffected. Trypsin also nearly eliminated inactivation of currents carried by Ba2+, but had little or no effect on the rapid inactivation process in Ca2+, This indicates that trypsin removes voltage-dependent but not Ca(2+)-dependent inactivation, suggesting the existence of distinct protein domains for these two mechanisms of calcium channel inactivation.
我们研究了胰蛋白酶对A7r5平滑肌细胞系中L型钙电流的影响。用胰蛋白酶进行细胞内透析可使全细胞电流增加至五倍。该效应呈浓度依赖性,并可被大豆胰蛋白酶抑制剂阻断。整体分析表明功能性通道数量增加,开放概率可能也有较小增加,而单通道电流无变化。电流 - 电压曲线的形状未受影响。胰蛋白酶还几乎消除了Ba2 + 携带电流的失活,但对Ca2 + 中的快速失活过程影响很小或没有影响。这表明胰蛋白酶去除了电压依赖性失活,但未去除Ca(2 +)依赖性失活,提示这两种钙通道失活机制存在不同的蛋白质结构域。