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Pembery, A.

Publications and source records attributed to Pembery, A..

2 recordsLinked to original sources

HaloUMI: Physics-informed analysis of inhibition halo assays

Quantification of microbial growth inhibition is central to assays from antibiotic susceptibility to antifungal sensitivity, yet existing approaches struggle with irregular inhibition zones and variation in microbial lawn density. Here, we present Halo Unbiased Measurement of growth Inhibition (HaloUMI), an open-source Python graphical interface for automated, high-throughput analysis of lawn-based microbial assays. HaloUMI integrates robust image processing with physics-informed modelling to quantify inhibition zones without assuming circular geometry, enabling analysis of uniform and irregular halo phenotypes. Using diffusion- and growth-based physical modelling, HaloUMI experimentally validates a correction for variation in microbial lawn density, a major source of assay variability that can confound quantitative comparison of inhibition phenotypes. Validation using simulations and yeast killer-toxin assays demonstrates precise, reproducible measurement across diverse conditions. HaloUMI is applicable to multiple assay formats, including microbial interaction, mating, and conventional disc-diffusion assays, providing an accessible and generalisable framework for quantitative analysis of microbial growth inhibition.

biophysics↗

Ktd1 is a phospho-regulated member of the Dup240 family that mediates defence against killer toxin K28

The DUP240 gene family in Saccharomyces cerevisiae encodes ten proteins containing two transmembrane domains (TMDs). Despite decades of interest driven by their high sequence similarity, little functional information exists regarding whether Dup240 family members share redundant or distinct roles. In this study, we combined computational modelling, subcellular localisation, and functional assays across the family to identify shared and unique features. Computational modelling revealed that Ktd1 possesses a unique structural element adjacent to its TMD region. Out of six successfully localised family members, Ktd1 was the only protein predominantly targeted to the vacuolar membrane and the sole Dup240 required for defence against the K28 killer toxin. Computational predictions further indicated that Ktd1 undergoes extensive post-translational regulation, containing multiple validated phosphorylation sites. Screening potential regulatory kinases and phosphatases identified several enzymes required for K28 defence, which were independently validated using liquid-based toxin sensitivity assays. A multicopy suppressor screen demonstrated that KTD1 overexpression rescued K28 sensitivity across most enzyme mutant backgrounds, confirming Ktd1 acts downstream or in parallel to many factors. However, the phosphatase Sit4 and the kinase Hog1 scored as most likely co-factors in Ktd1 mediated defence. Live-cell fluorescence imaging of these two enzymes revealed no dramatic spatial re-localisation during K28 exposure, suggesting that phospho-dependent regulation of Ktd1-mediated defence may occur through transient signalling events. Together, these findings identify Ktd1 as the central effector of the Dup240 family in toxin defence and provide a mechanistic framework for understanding Dup240 regulation.

cell biology↗