Blaustein R O, Finkelstein A
Department of Physiology & Biophysics, Albert Einstein College of Medicine, Bronx, New York 10461.
J Gen Physiol. 1990 Nov;96(5):905-19. doi: 10.1085/jgp.96.5.905.
In a recent paper (Blaustein, R. O., T. M. Koehler, R. J. Collier, and A. Finkelstein, 1989. Proc. Natl. Acad. Sci. USA. 86:2209-2213) we described the general channel-forming properties of the PA65 fragment of anthrax toxin in planar phospholipid bilayer membranes. In the present paper we extend our previous studies of the permeability properties of this channel, using a series of symmetric tetraalkylammonium (TAA) ions. Our main finding is that at micromolar concentrations on either the cis (toxin-containing) or trans side of a membrane containing many (greater than 1,000) channels, these ions, ranging in size from tetramethylammonium to tetrahexylammonium, induce a voltage-dependent reduction of membrane conductance. (We attribute a similar voltage-dependent reduction of membrane conductance by millimolar concentrations of HEPES to a cationic form of this buffer present at micromolar concentrations.) In going from large negative to large positive voltages (on the TAA side) one sees that the conductance first decreases from its value in the absence of TAA, reaches a minimum, and then rises back at larger positive voltages toward the level in the absence of TAA. Our interpretation of this behavior is that these symmetric TAA ions block the cation-selective PA65 channel in a voltage-dependent manner. We postulate that there is a single site within the channel to which TAA ions can bind and thereby block the passage of the major current-carrying ion (potassium). A blocking ion is driven into the site by modest positive voltages, but is driven off the site and through the channel by larger positive voltages, thus explaining the relief of block. (In the accompanying paper [Blaustein, R. O., E. J. A. Lea, and A. Finkelstein. 1990. J. Gen. Physiol. 96:921-942] we confirm this interpretation of the data by analysis at the single-channel level.) This means that these blocking ions can pass through the channel; the permeability to tetrahexylammonium, the largest ion studied, implies that the narrowest part of the channel has a diameter of at least 11 A.
在最近一篇论文中(布劳斯坦,R. O.,T. M. 克勒,R. J. 科利尔,以及A. 芬克尔斯坦,1989年。《美国国家科学院院刊》。86:2209 - 2213),我们描述了炭疽毒素PA65片段在平面磷脂双层膜中的一般通道形成特性。在本文中,我们使用一系列对称四烷基铵(TAA)离子扩展了对该通道通透性特性的先前研究。我们的主要发现是,在含有许多(大于1000个)通道的膜的顺式(含毒素)或反式侧,微摩尔浓度的这些离子,其大小从四甲基铵到四己基铵,会引起膜电导的电压依赖性降低。(我们将毫摩尔浓度的HEPES引起的类似膜电导电压依赖性降低归因于微摩尔浓度存在的该缓冲剂的阳离子形式。)从大的负电压到正电压(在TAA侧)变化时,可以看到电导首先从无TAA时的值降低,达到最小值,然后在更大的正电压下回升至无TAA时的水平。我们对这种行为的解释是,这些对称TAA离子以电压依赖性方式阻断阳离子选择性PA65通道。我们推测通道内有一个单一的位点,TAA离子可以结合到该位点,从而阻断主要载流离子(钾)的通过。一个阻断离子在适度正电压的作用下被驱入该位点,但在更大正电压的作用下被驱离该位点并通过通道,从而解释了阻断的解除。(在随附的论文[布劳斯坦,R. O.,E. J. A. 利,以及A. 芬克尔斯坦。1990年。《普通生理学杂志》。96:921 - 942]中,我们通过单通道水平的分析证实了对数据的这种解释。)这意味着这些阻断离子可以通过通道;对所研究的最大离子四己基铵的通透性表明通道最窄部分的直径至少为11埃。