Targeting Protein Aggregation in ALS
- PMID: 39456257
- PMCID: PMC11506292
- DOI: 10.3390/biom14101324
Targeting Protein Aggregation in ALS
Abstract
Proteinopathies involve the abnormal accumulation of specific proteins. Maintaining the balance of the proteome is a finely regulated process managed by a complex network of cellular machinery responsible for protein synthesis, folding, and degradation. However, stress and ageing can disrupt this balance, leading to widespread protein aggregation. Currently, several therapies targeting protein aggregation are in clinical trials for ALS. These approaches mainly focus on two strategies: addressing proteins that are prone to aggregation due to mutations and targeting the cellular mechanisms that maintain protein homeostasis to prevent aggregation. This review will cover these emerging drugs. Advances in ALS research not only offer hope for better outcomes for ALS patients but also provide valuable insights and methodologies that can benefit the broader field of neurodegenerative disease drug discovery.
Keywords: amyotrophic lateral sclerosis; clinical trials; drug discovery; inflammation; neurodegeneration; protein aggregation; protein homeostasis; therapeutics.
Conflict of interest statement
Author Michele Perni was employed by the company Baz-Therapeutics Inc. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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