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[膜中转运蛋白的人工模型]

[Artificial models of transport proteins in membrane].

作者信息

Kobuke Y

机构信息

Department of Materials Science, Faculty of Engineering, Shizuoka University, Japan.

出版信息

Nihon Rinsho. 1996 Mar;54(3):737-43.

PMID:8904231
Abstract

Artificial molecules were designed to mimic membrane transport proteins which produce large and selective ion fluxes across biological membrane with functions of flux-control. Several amphiphilic lipid molecules were assembled in bilayer lipids to make supramolecular ion channels which gave single ion channel currents across planar lipid bilayers. Stable and constant conductance levels were observed with transitions between open and closed states. Unimolecular channels were also designed by using macrocyclic resorcinol tetramer, calix [6] arene or cyclodextrin. These unimolecular channels gave a single conductance and a sharp ion selectivity. All these channels were cation selective over anion. Ionic currents was successfully modulated by the application of membrane potential or photochemical isomerization.

摘要

人工分子被设计用来模拟膜转运蛋白,这些膜转运蛋白能在生物膜上产生大量且具有选择性的离子通量,并具有通量控制功能。几种两亲性脂质分子组装在双层脂质中形成超分子离子通道,这些通道能在平面脂质双层上产生单离子通道电流。在开放和关闭状态之间转换时观察到稳定且恒定的电导水平。还利用大环间苯二酚四聚体、杯[6]芳烃或环糊精设计了单分子通道。这些单分子通道具有单一的电导和敏锐的离子选择性。所有这些通道对阳离子的选择性高于阴离子。通过施加膜电位或光化学异构化成功地调节了离子电流。

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