Yang, Kylie, Marsh, Caleb, White, Lisa J., Molyneux, Fergus W., Allam, Thomas L., Popoola, Precious I. A., Keers, Olivia B., Rice, Matthew, Hilton, Kira L. F., Kotak, Hiral A., and others. (2026) An increased throughput workflow to identify ion transport and membrane lysis agents for antimicrobial discovery. Chemical Science, . ISSN 2041-6539. (doi:10.1039/d5sc09781a) (KAR id:113364)
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Language: English
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| Official URL: https://doi.org/10.1039/d5sc09781a |
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Abstract
Small molecule ion transporters have shown promise as potential therapeutics for microbial infections, cancer and channelopathies. However, there are still gaps in our understanding of how ion transport function in model vesicle membranes translates to cell membranes of interest. The lipid composition of the membranes of bacterial and cancer cells differs markedly from normal human cells, yet the influence of the lipid composition on membrane function is rarely investigated – in part because of the low throughput and high cost of ion transport experiments. Here, we report an increased throughput Workflow to identify biologically relevant, pH-driven ion transport and membrane lysis pathways in vesicle membranes. We developed a set of four assays designed to report on different transport and lysis processes. We validated our assays against a panel of known transporters and produced a stepwise Workflow for the evaluation of libraries of compounds. We applied our Workflow to screen a library (Library 1) of 31 supramolecular, self-associating amphiphiles (SSAs) for transport and lysis activity in a range of vesicles with different lipid compositions, designed to mimic different types of cells, and consequently identified seven promising transporters. Antimicrobial experiments found that six of these promising transporters showed good antimicrobial activity against clinically relevant Staphylococcus aureus strains, highlighting the promise of our Workflow in identifying potential antimicrobial agents. We then applied our Workflow to investigate the ion transport and lysis properties of a second library (Library 2) of SSAs with established antimicrobial and anticancer properties, aiming to provide insight into the biological modes of action.
| Item Type: | Article |
|---|---|
| DOI/Identification number: | 10.1039/d5sc09781a |
| Projects: | 113361 |
| Subjects: | Q Science |
| Institutional Unit: | Schools > School of Natural Sciences > Chemistry and Forensic Science |
| Former Institutional Unit: |
There are no former institutional units.
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| Funders: |
Engineering and Physical Sciences Research Council (https://ror.org/0439y7842)
Biotechnology and Biological Sciences Research Council (https://ror.org/00cwqg982) UK Research and Innovation (https://ror.org/001aqnf71) University of Kent (https://ror.org/00xkeyj56) |
| SWORD Depositor: | JISC Publications Router |
| Depositing User: | JISC Publications Router |
| Date Deposited: | 10 Mar 2026 11:02 UTC |
| Last Modified: | 11 Mar 2026 03:48 UTC |
| Resource URI: | https://kar.kent.ac.uk/id/eprint/113364 (The current URI for this page, for reference purposes) |
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https://orcid.org/0000-0002-3961-3782
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