Laver D R
School of Biological Sciences, University of Sydney, Australia.
J Membr Biol. 1990 Oct;118(1):55-67. doi: 10.1007/BF01872204.
The patch-clamp technique is used here to investigate the kinetics of Ca2+ block in single high-conductance Ca2(+)-activated K+ channels. These channels are detected in the membrane surrounding cytoplasmic drops from Chara australis, a membrane which originates from the tonoplast of the parent cell. The amplitudes and durations of single channel events are measured over a wide range of membrane potential (-300 to 200 mV). Ca2+ on either side of the channel reduces its K+ conductance and alters its ion-gating characteristics in a voltage-dependent manner. This Ca2(+)-induced attenuation of conductance is analyzed using the theory of diffusion-limited ion flow through pores. Interaction of external Ca2+ with the channel's ion-gating mechanism is examined in terms of a kinetic model for ion-gating that includes two voltage-dependent gating mechanisms. The kinetics of channel block by external Ca2+ indicates that (i) external Ca2+ binds at two sites, a superficial site and a deep site, located at 8 and 40% along the trans-pore potential difference, (ii) the external vestibule cannot be occupied by more than one Ca2+ or K+, and (iii) the kinetics of Ca2+ binding at the deep site is coupled with that of a voltage-dependent gate on the external side of the channel. Kinetics of channel block by internal Ca2+ indicates that more than one Ca2+ is involved.
本文采用膜片钳技术研究单个高电导Ca2+激活K+通道中Ca2+阻断的动力学。这些通道存在于澳大利亚无隔藻细胞质滴周围的膜中,该膜源自母细胞的液泡膜。在很宽的膜电位范围(-300至200 mV)内测量单通道事件的幅度和持续时间。通道两侧的Ca2+会降低其K+电导,并以电压依赖的方式改变其离子门控特性。利用扩散限制离子通过孔道流动的理论分析这种Ca2+诱导的电导衰减。根据一个包含两个电压依赖门控机制的离子门控动力学模型,研究外部Ca2+与通道离子门控机制的相互作用。外部Ca2+对通道的阻断动力学表明:(i)外部Ca2+在两个位点结合,一个浅表位点和一个深部位点,分别位于跨孔电位差的8%和40%处;(ii)外部前庭不能被一个以上的Ca2+或K+占据;(iii)深部位点Ca2+结合的动力学与通道外侧电压依赖门控的动力学相关联。内部Ca2+对通道的阻断动力学表明涉及不止一个Ca2+。