PRO-FitS: a novel phenotypic assay to identify enhancers of proteostasis in C. elegans
Vilasboas-Campos, D.; Fernandes, J. H.; Costa, M. D.; Pereira-Sousa, J.; Lopes, J.; Costa-Meireles, L.; Ferreira-Lomba, B.; Da Silva, J. D.; Maciel, P.; Teixeira-Castro, A.
Show abstract
The prevalence of neurodegenerative diseases (NDs) continues to rise with the aging of populations worldwide, representing a pressing need for the establishment of therapeutic strategies. Maintaining proteostasis is crucial for healthy aging, as the accumulation of misfolded and aggregated proteins is a key contributor to age-related cellular dysfunction and disease. This study introduces a novel phenotypic assay using Caenorhabditis elegans to screen for small molecule enhancers of proteostasis, aiming at mitigating the proteotoxic stress associated with NDs. This new methodology- PRO-FitS- uses C. elegans motor activity as a proxy for the PROteome Fitness State upon a noxious protein-denaturating stimulus, while allowing a fast and experimenter-free readout. We demonstrate the efficacy of the assay by validating the role of pharmacological mTOR inhibition and serotonergic signaling activation in reducing heat shock-induced proteotoxic damage at the whole-organism level. PRO-FitS will allow the identification of novel compounds that alleviate protein aggregation disorders, potentially revealing new pathways and cellular targets not previously implicated in proteotoxicity. Significance StatementNeurodegenerative diseases remain without effective cures, in part due to the lack of scalable methods to identify compounds that improve proteostasis. We developed PRO-FitS, a whole-organism, automated phenotypic assay in C. elegans that uses motor activity recovery as a proxy for proteome fitness after proteotoxic stress. This platform enables rapid, unbiased screening of small molecules and genetic modifiers, bridging the gap between cellular assays and complex animal models. By demonstrating the assays robustness in both wild-type and disease-relevant contexts, we establish PRO-FitS as a versatile tool for discovering therapeutic candidates and uncovering novel pathways relevant to protein aggregation disorders.
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
Similar papers in this journal
- Lysosomal control of proteostasis and reproductive capacity by conserved LMD-3 protein in C. elegans 94%
- C9orf72-derived arginine-containing dipeptide repeats associate with axonal transport machinery and impede microtubule-based motility 94%
- Persistent DNA damage rewires lipid metabolism and promotes histone hyperacetylation via MYS-1/Tip60. 94%
Similar papers in this journal
- Metabolic stress is a primary pathogenic event in transgenic Caenorhabditis elegans expressing neuronal human amyloid-β 95%
- Dithiothreitol causes toxicity in C. elegans by modulating the methionine-homocysteine cycle 95%
- fmo-4 promotes longevity and stress resistance via ER to mitochondria calcium regulation in C. elegans 94%
Similar papers in this journal
- Metabolic defects cause hyperactive mitochondria and Parkinson disease-like traits 94%
- A dicer-related helicase opposes the age-related pathology from SKN-1 activation in ASI neurons 93%
- Resistance to host antimicrobial peptides mediates resilience of gut commensals during infection and aging in Drosophila 93%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.