Amino acid substitutions in the pore affect the anomalous mole fraction effect of Cav1.2 channels

作者:Li, Zhe; Huang, He; Yang, Bo; Jiang, Hong; Gao, Guo-Feng; Peterson, Blaise Z.; Huang, Cong-Xin*
来源:Molecular Medicine Reports, 2013, 7(2): 571-576.
DOI:10.3892/mmr.2012.1210

摘要

The anomalous mole fraction effect (AMFE) is an important indicator of ion-ion interactions in the pore of voltage-gated Ca2+ channels (VGCCs). The residues at position 1144 that differ in several classes of VGCCs are important to the permeation of the pore. Phe-1144 (F, Ca(v)1) was substituted with glycine (G, Ca(v)2) and lysine (K, Ca(v)3) and the effects of mutation on the voltage and concentration dependency of AMFE were observed. Whole-cell currents were recorded in external solutions with Ca2+ and Ba2+ at the indicated ratios with a total divalent cation concentration of 2, 10 or 20 mM, at holding potentials from -80 to -20 mV. Results showed the ratio of Ba2+ to Ca2+ currents determined at 2 mM to be different from that determined under higher concentrations for wild-type channels but this ratio was not different when tail currents were evoked at different potentials. AMFE was greatest at relatively positive potentials (-20 mV) and when the total divalent cation concentrations were kept low (2 mM). AMFE was attenuated for FIG while it was accentuated for F/K compared with wild-type, respectively. The results demonstrated that glycine and lysine substitutions of Phe-1144 affect AMFE through different mechanisms. Additionally, residues at position 1144 were shown to be major determinates of channel permeation of several classes of VGCCs.

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