bioRxiv Science⌕ Search

bioRxiv · 10.64898/2026.04.27.721028

The lipid raft marker flotillin FloA drives relocalization of the plasma membrane H+-ATPase PmaA as a protective response to calcium stress

Abstract

Biological membranes are laterally heterogeneous and contain specialized microdomains called lipid rafts. Lipid rafts serve as organizational platforms that cluster signaling molecules or modulate membrane protein conformation through their unique lipid environment. There are specific lipid raft marker proteins whose functions remain obscure. One of these proteins is flotillin which has been linked to endocytosis. Here, we investigated the regulation and function of FloA, the sole flotillin homolog in the model fungus Aspergillus nidulans. FloA expression is specifically upregulated in response to calcium stress, which is a regulatory pattern also conserved in Aspergillus fumigatus. Whereas in A. fumigatus floA is regulated by the calcium regulatory protein CrzA, this is not the case in A. nidulans. BioID proximity labeling revealed that A. nidulans FloA physically interacts with proteins in the endocytic pathway as well as another lipid raft marker, the plasma membrane H+-ATPase PmaA. Under calcium stress, PmaA undergoes internalization from the cytoplasmic membrane. However, when floA is deleted, PmaA internalization is prevented, resulting in cell death. Together, we demonstrate that FloA is essential for the internalization of PmaA during calcium stress, a process that prevents intracellular calcium overload and promotes cell viability. Our results also provide further evidence for flotillin-assisted endocytosis. Author abstractLipids and proteins in a cell membrane can cluster together in small regions often called "lipid rafts", which help the cell interact with its surroundings. Lipid rafts can bring receptors together or influence how membrane proteins behave. Flotillin is a protein which is often found within lipid rafts, but its exact role is not well understood. Instead of using complex mammalian systems, we studied flotillins in the fungus Aspergillus nidulans, which is a simpler model organism that allows for a better understanding of cellular processes. We found that more flotillins are produced when the fungus is exposed to calcium stress. When flotillins were missing, the cells were unable to remove the protein PmaA from the cell membrane during calcium stress. As a result, the fungus could not cope with the calcium stress and eventually died. Therefore, we propose that flotillins are important for the fungus to reorganize its membranes and coping with calcium stress.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Kawashima, M., Krüger, T., Rosin, M., Tröger-Görler, S., Heinekamp, T., Brakhage, A. A.. 2026-04-29. The lipid raft marker flotillin FloA drives relocalization of the plasma membrane H+-ATPase PmaA as a protective response to calcium stress. https://doi.org/10.64898/2026.04.27.721028

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

A population-scale landscape of the subgingival microbiome reveals divergent routes to periodontal dysbiosis

Periodontitis is an archetypical mucosal inflammatory disease in which microbiome dysbiosis at the tooth-epithelial interface interacts with host genetic and behavioral risk factors to drive immune-mediated tissue destruction. Although subgingival microbiome compositional shifts are thought to parallel disease severity, microbiome variation at the population-level and its relationship to periodontal clinical phenotypes and disease-modifying factors remain poorly defined. Here, we use unsupervised manifold learning to map the compositional landscape of the subgingival microbiome in 1,355 adults spanning periodontal health to severe periodontitis. We identified eight latent microbiome states organized along a branching continuum from eubiosis to dysbiosis. An intermediate microbial configuration marked ecological destabilization and bifurcation into two distinct periodontitis-associated dysbiotic trajectories, distinguished by links to gingival inflammation and smoking. Although the microbiome trajectories broadly tracked periodontal destruction, a minority of individuals showed discordant microbiome-clinical phenotypes, with some individuals with periodontitis retaining otherwise eubiotic microbiomes enriched for low-abundance pathobionts, while some cases of health or mild disease had highly dysbiotic communities, suggesting distinct host susceptibility. Together, these findings define a population-scale ecological landscape of the subgingival microbiome, reveal divergent trajectories to periodontal dysbiosis, and highlight heterogeneity in the relationship between microbial community structure and clinical disease expression.

microbiology↗

Beta-lactam enhancement against methicillin-resistant Staphylococcus aureus by cell wall blockade is autolysis-dependent: a butyrolactone derivative as case in point

Methicillin-resistant Staphylococcus aureus (MRSA) is non-susceptible to beta-lactams. Blockade of cell wall biosynthesis is a potential target for beta-lactam enhancement but requires further investigation. A butyrolactone derivative enhanced beta-lactams against MRSA strains by reducing the availability of D-Ala-D-Ala. Unlike D-cycloserine, it did not inhibit D-Ala-D-Ala ligase (Ddl). Nor did it show an additive or synergistic effect when combined with cycloserine, indicating a unique mechanism for blocking cell wall precursor production that does not involve the traditional Lipid II pathway. Notably, beta-lactam potentiation by our chemical or D-cycloserine was highly dependent on the intrinsic autolytic ability of the tested MRSA strains. Strains that resisted lysis upon Triton X-100 exposure showed a minimal increase in beta-lactam susceptibility, whereas highly autolytic strains showed significant changes in their beta-lactam MICs. We have thus identified autolytic ability as the Achilles Heel in the strategy of targeting cell wall biosynthesis for beta-lactam potentiation.

microbiology↗

Rapid and largely reversible shifts in the canine fecal metabolome during dietary change

Diet can rapidly change the fecal metabolome, but less is known about recovery after the original diet is restored. We used untargeted UPLC-MS metabolomics to analyze 72 fecal samples from nine Pumi dogs during an owner-managed switch from dry food to raw food and back to dry food. Diet phase accounted for a large proportion of variation in both ionization modes. More than 13,000 LC-MS features changed at the first sampling point after the switch to raw food, with a similarly large response after return to dry food. Among features significant in both comparisons, more than 99% changed in opposite directions. At the final sampling point, no positive-mode (ESI+) features and only 13 negative-mode (ESI-) features differed from the second dry-food baseline under the same threshold. BARF-associated patterns persisted in analyses excluding individual dogs and in pedigree-adjusted candidate models, although individual feature effects depended on normalization. Putative metabolites from several biochemical classes differed in their response and recovery. The fecal metabolome therefore changed rapidly and returned largely toward baseline, with differences among dogs.

microbiology↗