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Abstract
Autophagy impairment increased translational errors, particularly during oxidative stress.
- Proteomic analysis identified ribosomal proteins and RNA-binding factors as potential autophagy cargo.
- Translational machinery components were found to localize to autophagic structures in human brain tissue affected by neurodegeneration.
- The findings suggest that autophagy may play a role in maintaining the quality of protein synthesis.
- The proposed mechanism, termed translophagy, could connect autophagy dysfunction with oxidative stress and protein abnormalities in neurodegenerative diseases.
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