Microbiology Department, Faculty of Sciences, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Proteomics Unit, Universidad Complutense de Madrid, 28040 Madrid, Spain.
Int J Mol Sci. 2024 Aug 16;25(16):8938. doi: 10.3390/ijms25168938.
Previous reports have demonstrated that the peptide derived from LfcinB, R-1-R, exhibits anti- activity, which is enhanced when combined with an extract from the plant. However, the mechanism of action remains unexplored. In this research, a proteomic study was carried out, followed by a bioinformatic analysis and biological assays in both the SC5314 strain and a fluconazole-resistant isolate of after incubation with R-1-R. The proteomic data revealed that treatment with R-1-R led to the up-regulation of most differentially expressed proteins compared to the controls in both strains. These proteins are primarily involved in membrane and cell wall biosynthesis, membrane transport, oxidative stress response, the mitochondrial respiratory chain, and DNA damage response. Additionally, proteomic analysis of the parental strain SC5314 treated with R-1-R combined with an ethanolic extract of was performed. The differentially expressed proteins following this combined treatment were involved in similar functional processes as those treated with the R-1-R peptide alone but were mostly down-regulated (data are available through ProteomeXchange with identifier PXD053558). Biological assays validated the proteomic results, evidencing cell surface damage, reactive oxygen species generation, and decreased mitochondrial membrane potential. These findings provide insights into the complex antifungal mechanisms of the R-1-R peptide and its combination with the extract, potentially informing future studies on natural product derivatives.
先前的报告已经证明,LfcinB 衍生肽 R-1-R 具有抗真菌活性,与植物提取物联合使用时活性增强。然而,其作用机制仍未得到探索。在这项研究中,我们进行了蛋白质组学研究,随后对 R-1-R 孵育后的 SC5314 菌株和氟康唑耐药的 进行了生物信息学分析和生物学检测。蛋白质组学数据显示,与对照相比,R-1-R 处理后两种菌株中大多数差异表达蛋白的表达上调。这些蛋白主要参与膜和细胞壁生物合成、膜转运、氧化应激反应、线粒体呼吸链和 DNA 损伤反应。此外,我们还对用 R-1-R 联合 乙醇提取物处理的 亲本菌株 SC5314 进行了蛋白质组学分析。与单独用 R-1-R 肽处理相比,经这种联合处理后的差异表达蛋白参与了类似的功能过程,但大多被下调(通过 ProteomeXchange 可获得标识符 PXD053558 的相关数据)。生物学检测验证了蛋白质组学的结果,证明了细胞表面损伤、活性氧生成和线粒体膜电位降低。这些发现为 R-1-R 肽及其与 提取物的复杂抗真菌机制提供了深入了解,可能为天然产物衍生物的未来研究提供信息。