Artificial water channels enable fast and selective water permeation through water-wire networks
Artificial water channels enable fast and selective water permeation through water-wire networks
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DOI:
10.1038/s41565-019-0586-8
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发表时间:
2019-12
影响因子:
38.3
通讯作者:
Woochul Song;Himanshu Joshi;Ratul Chowdhury;Joseph S. Najem;Yue-xiao Shen;Chao Lang;Codey B. Henderson;Yu-Ming Tu;Megan Farell;Megan E. Pitz;C. Maranas;P. Cremer;R. Hickey;Stephen A. Sarles;Jun‐Li Hou;A. Aksimentiev;Manish Kumar
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文献类型:
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作者:
Woochul Song;Himanshu Joshi;Ratul Chowdhury;Joseph S. Najem;Yue-xiao Shen;Chao Lang;Codey B. Henderson;Yu-Ming Tu;Megan Farell;Megan E. Pitz;C. Maranas;P. Cremer;R. Hickey;Stephen A. Sarles;Jun‐Li Hou;A. Aksimentiev;Manish Kumar
Artificial water channels are synthetic molecules that aim to mimic the structural and functional features of biological water channels (aquaporins). Here we report on a cluster-forming organic nanoarchitecture, peptide-appended hybrid[4]arene (PAH[4]), as a new class of artificial water channels. Fluorescence experiments and simulations demonstrated that PAH[4]s can form, through lateral diffusion, clusters in lipid membranes that provide synergistic membrane-spanning paths for a rapid and selective water permeation through water-wire networks. Quantitative transport studies revealed that PAH[4]s can transport >109water molecules per second per molecule, which is comparable to aquaporin water channels. The performance of these channels exceeds the upper bound limit of current desalination membranes by a factor of ~104, as illustrated by the water/NaCl permeability–selectivity trade-off curve. PAH[4]’s unique properties of a high water/solute permselectivity via cooperative water-wire formation could usher in an alternative design paradigm for permeable membrane materials in separations, energy production and barrier applications.