Integrative Phosphoproteomic and Proteomic Analysis of <i>Candida albicans</i> Exposed to Oxidative Stress

<i>Candida albicans</i> is an opportunistic pathogen, which has recently been included in the high-priority list of pathogenic fungi by the World Health Organization (WHO). The scarce arsenal available to treat such invasive fungal infections makes the discovery of new antifungal targets an important task. This study utilizes DDA-MS technology to investigate both the phosphoproteomics and proteomics of <i>C. albicans</i> during its late-stage response to oxidative stress induced by H<sub>2</sub>O<sub>2</sub>, aiming to identify key proteins involved. Phosphorylation, as an important post-translational modification, plays a crucial role in the ability of <i>C. albicans</i> to survive oxidative stress. Our study enabled the identification and quantification of important changes in both protein abundance and phosphorylation events across multiple proteins following a 200 min 10 mM H<sub>2</sub>O<sub>2</sub> treatment. The use of the DDA-MS approach allowed for the identification of new actors in the response to oxidative stress. Novel phosphorylation sites were identified in kinases and transcription factors. Regarding protein kinases, Cdc5-reduced phosphorylation may mediate a transient G2 cell cycle arrest, while Kis1─the regulatory β-subunit of Snf1 kinase─might play a role in ROS scavenging following oxidative stress. In terms of transcription factors, Gzf3-decreased phosphorylation was essential for cell survival and ROS detoxification after oxidative stress.

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Publication Details

Journal
Journal of Proteome Research
Published
2025-06-02
DOI
https://doi.org/10.1021/acs.jproteome.5c00137
Citations
2
Primary Topic
Antifungal resistance and susceptibility
Type
article
Field-Weighted Citation Impact
2.79

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article

Integrative Phosphoproteomic and Proteomic Analysis of Candida albicans Exposed to Oxidative Stress

Gloria Molero, Raquel Chacon Ruiz Martinez, Concha Gil, Lucía Monteoliva et al.
2 citations
Journal of Proteome Research
Antifungal resistance and susceptibility
2.79
article

Integrative Phosphoproteomic and Proteomic Analysis of Candida albicans Exposed to Oxidative Stress

Gloria Molero, Raquel Chacon Ruiz Martinez, Concha Gil, Lucía Monteoliva, Ana Borrajo, Víctor Arribas, María Luisa Hernáez
article en
2 citations

Abstract

<i>Candida albicans</i> is an opportunistic pathogen, which has recently been included in the high-priority list of pathogenic fungi by the World Health Organization (WHO). The scarce arsenal available to treat such invasive fungal infections makes the discovery of new antifungal targets an important task. This study utilizes DDA-MS technology to investigate both the phosphoproteomics and proteomics of <i>C. albicans</i> during its late-stage response to oxidative stress induced by H<sub>2</sub>O<sub>2</sub>, aiming to identify key proteins involved. Phosphorylation, as an important post-translational modification, plays a crucial role in the ability of <i>C. albicans</i> to survive oxidative stress. Our study enabled the identification and quantification of important changes in both protein abundance and phosphorylation events across multiple proteins following a 200 min 10 mM H<sub>2</sub>O<sub>2</sub> treatment. The use of the DDA-MS approach allowed for the identification of new actors in the response to oxidative stress. Novel phosphorylation sites were identified in kinases and transcription factors. Regarding protein kinases, Cdc5-reduced phosphorylation may mediate a transient G2 cell cycle arrest, while Kis1─the regulatory β-subunit of Snf1 kinase─might play a role in ROS scavenging following oxidative stress. In terms of transcription factors, Gzf3-decreased phosphorylation was essential for cell survival and ROS detoxification after oxidative stress.

Journal of Proteome ResearchVol. 24(7)
Universidad Complutense de Madrid (ES), Abterra Biosciences (United States) (US)
Ministerio de Ciencia y Tecnología
Good health and well-being
Openalex Percentile: Top 10%
Antifungal resistance and susceptibility
2.79
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