Franke C, Dudel J
Pflugers Arch. 1987 Mar;408(3):300-6. doi: 10.1007/BF02181473.
Single glutamate activated ionic channels were recorded with the patch clamp technique from untreated crayfish muscle fibres with M omega seals, and after treatment with collagenase, with G omega seals. In regions with single channel activity spontaneous synaptic currents could also be recorded, and the channels were therefore identified as synaptic. The single channel current amplitude was -7 to -8 pA at the resting potential of -70 mV, representing a conductance of 100 pS. The amplitudes decreased by a factor of two when the temperature was lowered by 10 degrees C. Openings occurred in bursts, and the mean burst length varied between 0.3 ms (50 microM glutamate in the pipette) and 0.8 ms (1 mM glutamate in the pipette). After treatment with collagenase, G omega seals could be formed. The conductance of the channel and the mean burst length was not affected by the enzyme, but after treatment active spots could be found easier and they were distributed more uniformly along the fibre. After treatment the concentrations of glutamate necessary to elicit channel openings were higher (100 microM compared to 20-50 microM) and simultaneous openings of two or more channels were observed very rarely. Synaptic currents could not be recorded from preparations cleaned by collagenase (2 mg/ml) for longer than 60 min.
使用膜片钳技术,在具有MΩ封接的未处理小龙虾肌肉纤维以及用胶原酶处理后具有GΩ封接的情况下,记录单个谷氨酸激活的离子通道。在具有单通道活性的区域,也可以记录到自发突触电流,因此这些通道被确定为突触通道。在-70mV的静息电位下,单通道电流幅度为-7至-8pA,电导为100pS。当温度降低10℃时,幅度降低两倍。通道开放呈簇状,平均簇持续时间在0.3ms(移液管中50μM谷氨酸)至0.8ms(移液管中1mM谷氨酸)之间变化。用胶原酶处理后,可以形成GΩ封接。通道的电导和平均簇持续时间不受该酶的影响,但处理后更容易找到活性位点,并且它们沿纤维分布更均匀。处理后,引发通道开放所需的谷氨酸浓度更高(100μM,而不是20 - 50μM),并且很少观察到两个或更多通道同时开放。用胶原酶(2mg/ml)处理超过60分钟的标本无法记录到突触电流。