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基于[6]轮芳烃主体-客体体系构建的仿生手性驱动离子门。

A biomimetic chiral-driven ionic gate constructed by pillar[6]arene-based host-guest systems.

机构信息

Key Laboratory of Pesticide and Chemical Biology (CCNU), Ministry of Education, College of Chemistry, Central China Normal University, 430079, Wuhan, People's Republic of China.

出版信息

Nat Commun. 2018 Jul 5;9(1):2617. doi: 10.1038/s41467-018-05103-w.

Abstract

Inspired by glucose-sensitive ion channels, herein we describe a biomimetic glucose-enantiomer-driven ion gate via the introduction of the chiral pillar[6]arene-based host-guest systems into the artificial nanochannels. The chiral nanochannels show a high chiral-driven ionic gate for glucose enantiomers and can be switched "off" by D-glucose and be switched "on" by L-glucose. Remarkably, the chiral nanochannel also exhibited a good reversibility toward glucose enantiomers. Further research indicates that the switching behaviors differed due to the differences in binding strength between chiral pillar[6]arene and glucose enantiomers, which can lead to the different surface charge within nanochannel. Given these promising results, the studies of chiral-driven ion gates may not only give interesting insight for the research of biological and pathological processes caused by glucose-sensitive ion channels, but also help to understand the origin of the high stereoselectivity in life systems.

摘要

受葡萄糖敏感离子通道的启发,本文通过在手性杯[6]芳烃主体-客体体系引入人工纳米通道,描述了一种仿生葡萄糖对映异构体驱动的离子门。手性纳米通道对葡萄糖对映异构体表现出高的手性驱动离子门,并可以通过 D-葡萄糖关闭,通过 L-葡萄糖打开。值得注意的是,手性纳米通道对葡萄糖对映异构体也表现出良好的可逆性。进一步的研究表明,由于手性杯[6]芳烃与葡萄糖对映异构体之间的结合强度的差异,导致纳米通道内的表面电荷不同,从而导致了不同的开关行为。鉴于这些有前景的结果,手性驱动离子门的研究不仅可以为研究由葡萄糖敏感离子通道引起的生物和病理过程提供有趣的见解,而且有助于理解生命系统中高立体选择性的起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f67/6033921/ab5b9faf3b4c/41467_2018_5103_Fig1_HTML.jpg

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