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An increased throughput workflow to identify ion transport and membrane lysis agents for antimicrobial discovery

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)

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.
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)

University of Kent Author Information

Popoola, Precious I. A..

Creator's ORCID: https://orcid.org/0000-0002-3961-3782
CReDIT Contributor Roles: Investigation, Resources

Rice, Matthew.

Creator's ORCID:
CReDIT Contributor Roles: Data curation, Investigation

Hilton, Kira L. F..

Creator's ORCID: https://orcid.org/0000-0001-6425-0947
CReDIT Contributor Roles: Resources, Investigation

Ortega-Roldan, Jose L..

Creator's ORCID: https://orcid.org/0000-0002-6316-4390
CReDIT Contributor Roles: Supervision, Writing - original draft, Writing - review and editing, Funding acquisition, Visualisation

Hiscock, Jennifer R..

Creator's ORCID: https://orcid.org/0000-0002-1406-8802
CReDIT Contributor Roles: Project administration, Writing - original draft, Resources, Writing - review and editing, Funding acquisition, Supervision, Conceptualisation, Methodology, Investigation
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