Zahradníková A, Zahradník I
Institute of Molecular Physiology and Genetics, Slovak Academy of Sciences, Bratislava, Slovak Republic.
Biophys J. 1995 Nov;69(5):1780-8. doi: 10.1016/S0006-3495(95)80048-2.
Single channel activity of the cardiac ryanodine-sensitive calcium-release channel in planar lipid membranes was studied in order to elucidate the calcium-dependent mechanism of its steady-state behavior. The single channel kinetics, observed with Cs+ as the charge carrier at different activating (cis) Ca2+ concentrations in the absence of ATP and Mg2+, were similar to earlier reports and were extended by analysis of channel modal behavior. The channel displayed three episodic levels of open probability defining three gating modes: H (high activity), L (low activity), and I (no activity). The large difference in open probabilities between the two active modes resulted from different bursting patterns and different proportions of two distinct channel open states. I-mode was without openings and can be regarded as the inactivated mode of the channel; L-mode was composed of short and sparse openings; and H-mode openings were longer and grouped into bursts. Modal gating may explain calcium-release channel adaptation (as transient prevalence of H-mode after Ca2+ binding) and the inhibitory effects of drugs (as stabilization of mode I), and it provides a basis for understanding the regulation of calcium release.
为阐明心脏兰尼碱敏感钙释放通道稳态行为的钙依赖机制,研究了其在平面脂膜中的单通道活性。在无ATP和Mg2+的情况下,以Cs+作为电荷载体,在不同激活(顺式)Ca2+浓度下观察到的单通道动力学与早期报道相似,并通过对通道模式行为的分析进行了扩展。该通道表现出三种间歇性的开放概率水平,定义了三种门控模式:H(高活性)、L(低活性)和I(无活性)。两种活性模式之间开放概率的巨大差异源于不同的爆发模式以及两种不同通道开放状态的不同比例。I模式无开放,可视为通道的失活模式;L模式由短而稀疏的开放组成;H模式的开放更长且成簇出现。模式门控可以解释钙释放通道的适应性(如Ca2+结合后H模式的短暂占优势)和药物的抑制作用(如I模式的稳定),并为理解钙释放的调节提供了基础。