Molecular landscape of the fungal plasma membrane and implications for antifungal action

Fungal plasma membrane proteins represent key therapeutic targets for antifungal agents, yet their native structure and spatial distribution remain poorly characterized. Herein, we employ an integrative approach to investigate the organization of plasma membrane protein complexes in Candida glabrata, focusing on two abundant and essential membrane proteins, the β-(1,3)-glucan synthase (GS) and the proton pump Pma1. We show that treatment with caspofungin, an echinocandin antifungal that targets GS, disrupts the native distribution of membrane protein complexes and alters membrane biophysical properties. Perturbation of the sphingolipid biosynthesis further modulates drug susceptibility, revealing that the lipid environment plays an integral role in membrane protein organization and GS-echinocandin interactions. Our work highlights the importance of characterizing membrane proteins in their native context to understand their functions and inform the development of novel antifungal therapies.

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Publication Details

Journal
Nature Communications
Published
2025-10-14
DOI
https://doi.org/10.1038/s41467-025-64171-x
Primary Topic
Bacterial biofilms and quorum sensing
Type
article
Field-Weighted Citation Impact
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Molecular landscape of the fungal plasma membrane and implications for antifungal action

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Molecular landscape of the fungal plasma membrane and implications for antifungal action

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article en

Abstract

Fungal plasma membrane proteins represent key therapeutic targets for antifungal agents, yet their native structure and spatial distribution remain poorly characterized. Herein, we employ an integrative approach to investigate the organization of plasma membrane protein complexes in Candida glabrata, focusing on two abundant and essential membrane proteins, the β-(1,3)-glucan synthase (GS) and the proton pump Pma1. We show that treatment with caspofungin, an echinocandin antifungal that targets GS, disrupts the native distribution of membrane protein complexes and alters membrane biophysical properties. Perturbation of the sphingolipid biosynthesis further modulates drug susceptibility, revealing that the lipid environment plays an integral role in membrane protein organization and GS-echinocandin interactions. Our work highlights the importance of characterizing membrane proteins in their native context to understand their functions and inform the development of novel antifungal therapies.

Nature CommunicationsVol. 16(1)
Rutgers, The State University of New Jersey (US), City University of New York (US), Hunter College (US), Center for Discovery (US), Carnegie Mellon University (US)
Openalex Percentile: Top 74%
Bacterial biofilms and quorum sensing
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