Evidence map›Paper›PMID 41809554›Full record

ArticleChemical science2026

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

Kylie Yang, Caleb Marsh, Lisa J White, Fergus W Molyneux, Thomas L Allam, Precious I A Popoola, Olivia B Keers, Matthew Rice, Kira L F Hilton, Hiral A Kotak and 5 more

Abstract read
In one paragraph

Article in Chemical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Kylie YangDepartment of Chemistry, University College London 20 Gordon Street London WC1H 0AJ UK cally.haynes@ucl.ac.uk.ORCID https://orcid.org/0000-0002-4455-3681
Caleb MarshResearch and Evaluation, UKHSA Porton Down Salisbury SP4 0JG UK Charlotte.Hind@UKHSA.gov.uk.
Lisa J WhiteSchool of Natural Sciences, University of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk.
Fergus W MolyneuxDepartment of Chemistry, University College London 20 Gordon Street London WC1H 0AJ UK cally.haynes@ucl.ac.uk.
Thomas L AllamSchool of Chemistry, University of Southampton Highfield Southampton SO17 1BJ UK.ORCID https://orcid.org/0009-0009-9897-333X
Precious I A PopoolaSchool of Natural Sciences, University of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk.ORCID https://orcid.org/0000-0002-3961-3782
Olivia B KeersSchool of Natural Sciences, University of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk.
Matthew RiceSchool of Natural Sciences, University of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk.
Kira L F HiltonSchool of Natural Sciences, University of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk.
Hiral A KotakDepartment of Chemistry, University College London 20 Gordon Street London WC1H 0AJ UK cally.haynes@ucl.ac.uk.
J Mark SuttonResearch and Evaluation, UKHSA Porton Down Salisbury SP4 0JG UK Charlotte.Hind@UKHSA.gov.uk.
Jose L Ortega-RoldanSchool of Natural Sciences, University of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk.ORCID https://orcid.org/0000-0002-6316-4390
Charlotte K HindResearch and Evaluation, UKHSA Porton Down Salisbury SP4 0JG UK Charlotte.Hind@UKHSA.gov.uk.
Jennifer R HiscockSchool of Natural Sciences, University of Kent Canterbury CT2 7NH UK J.R.Hiscock@Kent.ac.uk.ORCID https://orcid.org/0000-0002-1406-8802
Cally J E HaynesDepartment of Chemistry, University College London 20 Gordon Street London WC1H 0AJ UK cally.haynes@ucl.ac.uk.ORCID https://orcid.org/0000-0003-4262-8560

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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

Identifiers

PMID41809554
PMCPMC12970626

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.