Patlak J, Horn R
J Gen Physiol. 1982 Mar;79(3):333-51. doi: 10.1085/jgp.79.3.333.
We have studied the effect of N-bromoacetamide (NBA) on the behavior of single sodium channel currents in excised patches of rat myotube membrane at 10 degree C. Inward sodium currents were activated by voltage steps from holding potentials of about -100 mV to test potentials of -40 mV. The cytoplasmic-face solution was isotonic CsF. Application of NBA or pronase to the cytoplasmic face of the membrane irreversibly removed sodium channel inactivation, as determined by averaged single-channel records. Teh lifetime of the open channel at -40 mV was increased about 10-fold by NBA treatment without affecting the amplitude of single-channel currents. A binomial analysis was used both before and after treatment to determine the number of channels within the excised patch. NBA was shown to have little effect on activation kinetics, as determined by an examination of both the rising phase of averaged currents and measurements f the delay between the start of the pulse and the first channel opening. Our data support a kinetic model of sodium channel activation in which the rate constant leading back from the open state to the last closed state is slower than expected from a strict Hodgkin-Huxley model. The data also suggest that the normal open-channel lifetime is primarily determined by the inactivation process in the voltage range we have examined.
我们研究了N-溴乙酰胺(NBA)对10℃下大鼠肌管膜游离膜片上单钠通道电流行为的影响。内向钠电流通过从约-100mV的保持电位到-40mV的测试电位的电压阶跃来激活。胞质面溶液为等渗CsF。通过平均单通道记录确定,将NBA或链霉蛋白酶应用于膜的胞质面可不可逆地消除钠通道失活。经NBA处理后,-40mV下开放通道的寿命增加了约10倍,而不影响单通道电流的幅度。在处理前后均使用二项式分析来确定游离膜片中通道的数量。通过检查平均电流的上升相以及测量脉冲开始与第一个通道开放之间的延迟来确定,NBA对激活动力学几乎没有影响。我们的数据支持钠通道激活的动力学模型,其中从开放状态回到最后一个关闭状态的速率常数比严格的霍奇金-赫胥黎模型预期的要慢。数据还表明,在我们研究的电压范围内,正常的开放通道寿命主要由失活过程决定。