Chloride Selective, Non-protonophoric Ion Transport with Macrocyclic Halogen Bonding Anionophores

13 March 2025, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Synthetic ion transporters hold promise as both chemical probes and potential therapeutics for diseases linked to malfunctioning protein ion transporters. However, their application in biological systems is limited, partly due to the cytotoxicity arising from unselective ion transport. Here, we demonstrate that by combining halogen bonding anion recognition with macrocyclic anion encapsulation, one can access highly active and selective anionophores. Anion transport experiments in large unilamellar vesicles revealed record chloride selectivity over proton/hydroxide ions, which is key for potential future therapeutic applications, where the dissipation of cellular pH gradients must be avoided. The mechanism underpinning selectivity is studied through Density Functional Theory (DFT) calculations and MD simulations at the membrane interface, demonstrating that the cyclic structure imposes an energetic preference for chloride binding over hydroxide, as well as a greater desolvation of hydroxide, which further disfavours its transport. We anticipate that these results will accelerate the transition towards the use of artificial chloride transport in biology.

Keywords

Anion transport
Membranes
Halogen bonding

Supplementary materials

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Description
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Supporting Information
Description
Synthesis, anion binding and transport experiments, computational methods
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