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Specific reaction rate of acetylcholine receptor-controlled ion translocation: a comparison of measurements with membrane vesicles and with muscle cells.

机译:乙酰胆碱受体控制的离子易位的特定反应速率:与膜囊泡和肌肉细胞的测量值比较。

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摘要

The specific reaction rate (J) of the acetylcholine receptor-controlled ion translocation has been determined. In eel Ringer's solution (pH 7.0) at 1 degrees C, J = 3 X 10(7) M-1 sec-1. J is an intrinsic constant that is characteristic of the receptor and independent of other properties of a receptor-containing cell that also determine the rates of ion translocation. Membrane vesicles (prepared from the electric organ of Electrophorus electricus) and a flow-quench technique that has a millisecond time resolution were used to measure the receptor-controlled ion translocation. Using the value of J and the molar concentrations of receptor sites and inorganic ions, we calculated that 6 X 10(3) ions are translocated per msec per receptor. Analysis of electrical noise in frog muscle cells at temperatures above 8 degrees C [Nether, E. & Stevens, C. F. (1977) Annu. Rev. Biophys. Bioeng. 6, 345-381] gave a value of about 1 X 10(4) ions msec-1 per channel. Thus, each technique gives essentially the same result. It is now possible, therefore, to correlate the results obtained when receptor function is measured in two different ways in membrane vesicles and in muscle cells: (i) chemical kinetic measurements, using membrane vesicles, which relate the ligand binding and ion translocation processes and (ii) analysis of acetylcholine noise in muscle cells [Katz, B. & Miledi, R. (1972) J. Physiol. (London) 224, 665-699], which allows one to measure elementary steps in the formation of ion channels through the cell membrane.
机译:已确定了乙酰胆碱受体控制的离子易位的特定反应速率(J)。在1摄氏度的鳗鱼林格氏溶液(pH 7.0)中,J = 3 X 10(7)M-1 sec-1。 J是固有常数,它是受体的特征,并且独立于含受体细胞的其他特性,而后者也决定了离子转运的速率。膜囊泡(由Electrophorus electricus的电器官制备)和具有毫秒级时间分辨率的流淬火技术用于测量受体控制的离子转运。使用J的值以及受体位点和无机离子的摩尔浓度,我们计算出每毫秒每个受体6个X 10(3)离子易位。温度高于8摄氏度时青蛙肌肉细胞中的电噪声分析[Nether,E.&Stevens,C. F.(1977)。生物物理学报。生恩6,6,345-381]给出了每个通道约1 X 10(4)个离子msec-1的值。因此,每种技术给出的结果基本相同。因此,现在可以关联以两种不同方式在膜囊泡和肌肉细胞中测量受体功能时获得的结果:(i)使用膜囊泡的化学动力学测量,它涉及配体结合和离子易位过程,以及(ii)分析肌肉细胞中的乙酰胆碱噪声[Katz,B。&Miledi,R。(1972)J.Physiol.Acad.Sci.USA,87:2587-5644。 (伦敦)224,665-699],它允许人们测量通过细胞膜形成离子通道的基本步骤。

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