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Synthesis and Characterization of SAMs and Tethered Bilayer Membranes from Unsymmetrically Substituted 1,2-Dithianes

机译:非对称取代的1,2-二乙胺的SAMs和束缚的双层膜的合成与表征

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摘要

The synthesis of a series of new membrane-forming compounds,based on previously established components used in an ion-channel switch(ICS) biosensor(Nature 1997,387,580) is described.All new compounds are derived from 4,5-dihydroxy-l,2-dithiane,and contain a hydrophilic reservoir section(based on ethylene glycol units) and a lypophilic section(based on the natural lipid phytanol).Ellipsometry and contact angle measurements indicate that self-assembled monolayers(SAMs) formed from the new materials possess thicknesses and membrane packing comparable to previously reported biosensor components.Tethered bilayer lipid membranes(t-BLMs) incorporating the novel materials were studied using impedance spectroscopy with the ion-carrier valinomycin.The electrical behavior and calculated membrane thickness of the t-BLMs are comparable to those derived from the standard ICS components and this demonstrates that the novel membrane-forming compounds form stable membranes that are sufficiently fluid to transport potassium ions in the presence of valinomycin.
机译:基于先前在离子通道开关(ICS)生物传感器中使用的已建立的组分(Nature 1997,387,580),描述了一系列新的成膜化合物的合成。所有新化合物均衍生自4,5-二羟基-1 ,2-二噻吩,并包含一个亲水的储层部分(基于乙二醇单元)和一个亲脂的部分(基于天然脂质植醇)。椭偏和接触角测量表明,由新材料形成的自组装单分子层(SAMs)具有与以前报道的生物传感器组件相当的厚度和膜堆积。使用阻抗光谱技术,结合离子载体缬氨霉素,研究了结合了这种新型材料的束缚双层脂质膜(t-BLM)。与标准ICS成分衍生的产品相比具有可比性,这表明新型成膜化合物可形成稳定的膜,并具有足够的流动性。 o在缬氨霉素存在下转运钾离子。

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