首页> 美国卫生研究院文献>The Journal of General Physiology >Selective Open-Channel Block of Shaker (Kv1) Potassium Channels by S-Nitrosodithiothreitol (Sndtt)
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Selective Open-Channel Block of Shaker (Kv1) Potassium Channels by S-Nitrosodithiothreitol (Sndtt)

机译:S-亚硝基二硫苏糖醇(Sndtt)的摇床(Kv1)钾通道的选择性开放通道阻滞

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摘要

Large quaternary ammonium (QA) ions block voltage-gated K+ (Kv) channels by binding with a 1:1 stoichiometry in an aqueous cavity that is exposed to the cytoplasm only when channels are open. S-nitrosodithiothreitol (SNDTT; ONSCH2CH(OH)CH(OH)CH2SNO) produces qualitatively similar “open-channel block” in Kv channels despite a radically different structure. SNDTT is small, electrically neutral, and not very hydrophobic. In whole-cell voltage-clamped squid giant fiber lobe neurons, bath-applied SNDTT causes reversible time-dependent block of Kv channels, but not Na+ or Ca2+ channels. Inactivation-removed ShakerB (ShBΔ) Kv1 channels expressed in HEK 293 cells are similarly blocked and were used to study further the action of SNDTT. Dose–response data are consistent with a scheme in which two SNDTT molecules bind sequentially to a single channel, with binding of the first being sufficient to produce block. The dissociation constant for the binding of the second SNDTT molecule (K d2 = 0.14 mM) is lower than that of the first molecule (K d1 = 0.67 mM), indicating cooperativity. The half-blocking concentration (K 1/2) is ∼0.2 mM. Steady-state block by this electrically neutral compound has a voltage dependence (about −0.3 e0) similar in magnitude but opposite in directionality to that reported for QA ions. Both nitrosyl groups on SNDTT (one on each sulfur atom) are required for block, but transfer of these reactive groups to channel cysteine residues is not involved. SNDTT undergoes a slow intramolecular reaction (τ ≈ 770 s) in which these NO groups are liberated, leading to spontaneous reversal of the SNDTT effect. Competition with internal tetraethylammonium indicates that bath-applied SNDTT crosses the cell membrane to act at an internal site, most likely within the channel cavity. Finally, SNDTT is remarkably selective for Kv1 channels. When individually expressed in HEK 293 cells, rat Kv1.1–1.6 display profound time-dependent block by SNDTT, an effect not seen for Kv2.1, 3.1b, or 4.2.
机译:大的季铵(QA)离子通过在只有打开通道时才暴露于细胞质的水腔中以1:1的化学计量比结合来阻断电压门控的K + (Kv)通道。尽管结构存在根本不同,但S-亚硝基二硫苏糖醇(SNDTT; ONSCH2CH(OH)CH(OH)CH2SNO)在Kv通道中产生定性相似的“开放通道阻滞”。 SNDTT体积小,电中性且不很疏水。在全细胞电压钳制的鱿鱼巨纤维叶神经元中,浸浴的SNDTT导致可逆的时间依赖性Kv通道阻滞,但不是Na + 或Ca 2 +通道。 HEK 293细胞中表达的灭活去除的ShakerB(ShBΔ)Kv1通道也被类似地阻断,并用于进一步研究SNDTT的作用。剂量反应数据与以下方案一致:两个SNDTT分子顺序结合到单个通道,第一个结合足以产生阻断。第二个SNDTT分子的结合解离常数(K d2 = 0.14 mM)低于第一个SNDTT分子的结合解离常数(K d1 = 0.67 mM),表明具有协同作用。半封闭浓度(K 1/2)为〜0.2 mM。这种电中性化合物的稳态阻滞具有与电压相关的电压依赖性(约-0.3 e0),其大小与QA离子报道的大小相似,但方向性相反。 SNDTT上的两个亚硝酰基基团(每个硫原子上一个基团)都需要封闭,但是这些反应基团向通道半胱氨酸残基的转移并不涉及。 SNDTT经历了缓慢的分子内反应(τ≈770 s),其中这些NO基团被释放,导致SNDTT效应自发逆转。与内部四乙基铵的竞争表明,浸浴的SNDTT穿过细胞膜以在内部部位起作用,最有可能在通道腔内。最后,SNDTT对于Kv1频道具有显着的选择性。当在HEK 293细胞中单独表达时,SNDTT对大鼠Kv1.1–1.6表现出深远的时间依赖性阻滞作用,对于Kv2.1、3.1b或4.2则没有这种作用。

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