We employed a BONCAT-iTRAQ labelling approach to investigate newly synthesised proteins (NSPs) in subjected to varying concentrations of the antifolate drug pyrimethamine. Our results reveal that numerous NSPs exhibited altered expression levels in response to the drug, with significant upregulation observed at higher concentrations. Key proteins involved in protein synthesis, stress responses, energy metabolism, and cytoskeletal dynamics were identified, indicating that undergoes complex adaptive responses to pyrimethamine treatment. While some of the identified pathways reflect a generic stress response, this study provides important molecular markers and mechanistic insights specific to the parasite's adaptation strategies. These findings contribute to understanding how modulates its proteome in response to drug-induced stress and lay the groundwork for further investigations into potential therapeutic targets.
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http://dx.doi.org/10.3390/pathogens13100879 | DOI Listing |
Pathogens
October 2024
School of Health and Life Sciences, Teesside University, Middlesbrough TS1 3BX, UK.
We employed a BONCAT-iTRAQ labelling approach to investigate newly synthesised proteins (NSPs) in subjected to varying concentrations of the antifolate drug pyrimethamine. Our results reveal that numerous NSPs exhibited altered expression levels in response to the drug, with significant upregulation observed at higher concentrations. Key proteins involved in protein synthesis, stress responses, energy metabolism, and cytoskeletal dynamics were identified, indicating that undergoes complex adaptive responses to pyrimethamine treatment.
View Article and Find Full Text PDFAutophagy
October 2016
a Department of Physiology , Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Autophagy is an intracellular degradation mechanism in response to nutrient starvation. Via autophagy, some nonessential cellular constituents are degraded in a lysosome-dependent manner to generate biomolecules that can be utilized for maintaining the metabolic homeostasis. Although it is known that under starvation the global protein synthesis is significantly reduced mainly due to suppression of MTOR (mechanistic target of rapamycin serine/threonine kinase), emerging evidence demonstrates that de novo protein synthesis is involved in the autophagic process.
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