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Synthetic cation transporters incorporating crown ethers and calixarenes as headgroups and central relays: a comparison of sodium and chloride selectivity

机译:以冠醚和杯芳烃为头基和中央继电器的合成阳离子转运蛋白:钠和氯选择性的比较

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摘要

An earlier study showed that a calix[4]arene could function as a central relay unit to form an ion conductance pathway through a phospholipid bilayer membrane. The present study expands the range of compounds from calix[4]arene to calix[6]arene and incorporates them either as central units or as headgroups, substituting one or more diaza-18-crown-6 residues in functioning hydraphiles. Ion release was assayed by detecting either Na+ or Cl release from phospholipid vesicles. The ion transport activity for calix[4]arenes in either position is modest, but is almost non-existent when calix[6] residues were incorporated either as head groups or central relay units. The poor activity of the calix[6]arenes may result from an inability to penetrate to the midplane of the bilayer or pass entirely through it to form a conductance pathway. The transmembrane “flip-flop” may result from high polarity or steric bulk, or both. A hydraphile incorporating a single –NHCOC6H4OCH2CONH– as a central relay proved to be an excellent Na+ conductor, but less selective for Cl. The fact that this new hydraphile molecule shows selectivity for Na + over Cl transport and possesses two secondary amide residues in the central relay suggests a means to control ion selectivity in synthetic ion transporters.
机译:一项较早的研究表明,杯[4]芳烃可以充当中央中继单元,形成通过磷脂双层膜的离子电导途径。本研究将化合物的范围从杯[4]芳烃扩大到杯[6]芳烃,并以中心单元或头基形式结合它们,在功能性亲水物中取代一个或多个diaza-18-crown-6残基。通过检测Na + 或Cl -从磷脂囊泡中释放来测定离子释放。杯[4]芳烃在任何位置的离子迁移活性都中等,但是当杯[6]残基作为头基或中央中继单元引入时,几乎不存在。杯[6]芳烃的活性差可能是由于无法穿透双层的中平面或不能完全穿过双层的中层以形成电导途径。跨膜“触发器”可能是由于高极性或位阻体或两者兼而有之。含有单个–NHCOC6H4OCH2CONH–作为中心继电器的亲水基被证明是一种出色的Na + 导体,但对Cl -的选择性较低。这种新的亲水分子在Cl -转运中显示出对Na + 的选择性,并且在中央继电器中具有两个仲酰胺残基,这一事实表明了一种控制合成离子中离子选择性的方法运输者。

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