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Ion selectivity predictions from a two-site permeation model for the cyclic nucleotide-gated channel of retinal rod cells.

机译:从两点渗透模型对视网膜杆细胞的环状核苷酸门控通道的离子选择性预测。

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摘要

We developed a two-site, Eyring rate theory model of ionic permeation for cyclic nucleotide-gated channels (CNGCs). The parameters of the model were optimized by simultaneously fitting current-voltage (IV) data sets from excised photoreceptor patches in electrolyte solutions containing one or more of the following ions: Na+, Ca2+, Mg2+, and K+. The model accounted well for 1) the shape of the IV relations; 2) the binding affinity for Na+; 3) reversal potential values with single-sided additions of Ca2+ or Mg2+ and biionic KCl; and 4) the K1 and voltage dependence for divalent block from the cytoplasmic side of the channel. The differences between the predicted K1's for extracellular block by Ca2+ and Mg2+ and the values obtained from heterologous expression of only the alpha-subunit of the channel suggest that the beta-subunit or a cell-specific factor affects the interaction of divalent cations at the external but not the internal face of the channel. The model predicts concentration-dependent permeability ratios with single-sided addition of Ca2+ and Mg2+ and anomalous mole fraction effects under a limited set of conditions for both monovalent and divalent cations. Ca2+ and Mg2+ are predicted to carry 21% and 10%, respectively, of the total current in the retinal rod cell at -60 mV.
机译:我们针对环核苷酸门控通道(CNGCs)开发了离子渗透的两点艾氏速率理论模型。该模型的参数是通过同时从包含以下一种或多种以下离子的电解质溶液中,从切下的感光体贴片中拟合电流-电压(IV)数据集来优化的:Na +,Ca2 +,Mg2 +和K +。该模型很好地解释了1)IV关系的形状; 2)对Na +的结合亲和力; 3)单面添加Ca2 +或Mg2 +和双离子KCl的反转电位值;和4)K1和电压依赖性从通道的细胞质侧的二价阻断。 Ca2 +和Mg2 +对细胞外阻滞的预测K1与仅通过通道的α-亚基异源表达获得的值之间的差异表明,β-亚基或细胞特异性因子会影响外部的二价阳离子的相互作用但不是渠道的内部面孔。该模型预测了单价添加Ca2 +和Mg2 +时浓度依赖性的渗透率以及单价和二价阳离子在一组有限条件下的异常摩尔分数效应。预计在-60 mV的视网膜视杆细胞中,Ca2 +和Mg2 +分别占总电流的21%和10%。

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