Artificial water channels enable fast and selective water permeation through water-wire networks
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. F...
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Published in | Nature nanotechnology Vol. 15; no. 1; pp. 73 - 79 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.01.2020
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | 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 >10
9
water 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 ~10
4
, 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.
Cooperative water wires formed by clustering of artificial water channels enhance membrane permselectivity. |
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Bibliography: | W.S., H.J., A.A. and M.K. conceived and designed the research. W.S. and Y.-x.S. performed the experiments with the assistance of J.S.N., C.L., C.B.H., Y.-M.T., M.F., M.E.P. and J.-l.H. in specialized analytic tools. H.J. and R.C. performed computer simulations. W.S., H.J., R.C., C.D.M., P.S.C., R.J.H., S.A.S., J.-l.H., A.A. and M.K. analyzed the data. W.C., H.J., R.C., A.A., and M.K. co-wrote the paper. Department of Chemical Engineering, The University of Texas at Austin, Austin, TX 78712 USA Department of Civil, Architectural and Environmental Engineering, The University of Texas at Austin, Austin, TX 78712 USA Author contributions |
ISSN: | 1748-3387 1748-3395 |
DOI: | 10.1038/s41565-019-0586-8 |