选择性
钾
离子通道
冠醚
化学
钾通道
膜
跨膜通道
超分子化学
纳米技术
材料科学
聚合物
离子
电压门控钾通道
纳米颗粒
离子运输机
钠
化学工程
弹性(物理)
仿生学
细胞通透性
膜电位
生物物理学
作者
Chao Li,Chongpeng Chen,Jingyan Shi,Wang Han,Qingfei Fu,Lijun Yang
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-01-01
卷期号:12 (1): eaea6329-eaea6329
被引量:2
标识
DOI:10.1126/sciadv.aea6329
摘要
Biological potassium channels exemplify nature's precision in ion discrimination, governing critical processes such as osmotic regulation and neuronal signaling. Developing artificial potassium channels with biological-level and dynamic selectivity is of fundamental importance for intelligent nanofluidic devices. Here, we present a biomimetic mechanoresponsive potassium channel using telechelic polymers with 18-crown-6 and 2-ureido-4-pyrimidinone terminals, achieving a record potassium/sodium selectivity of 104.7. Quadruple hydrogen-bonded supramolecular networks enable both membrane elasticity and pressure-responsive crown ether aggregation state modulation. Mechanical deformation induces a structural reconfiguration that decelerates potassium conduction while accelerating sodium transport, effectively mimicking action potential generation through the reversible inversion of sodium/potassium flux. This mechanoregulatable iontronic mechanism establishes foundational principles for dynamic single-ion selectivity membranes surpassing static biological analogs, highlighting its potential in ion separation, desalination, and renewable energy conversion.
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