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Multi-protein complex involved in ALS interactome

Molecular classification
Protein complex
01

Overview

The "multi-protein complex involved in the ALS interactome" refers to a dynamic assembly of proteins that are functionally and physically interconnected, playing key roles in the pathogenesis of Amyotrophic Lateral Sclerosis (ALS). Key components include TDP-43, FUS, Ataxin-2, OPTN, UBQLN2, and C9orf72. These proteins participate in transient complexes that regulate RNA metabolism, protein homeostasis, stress granule dynamics, cytoskeletal organization, and cell survival. Targeting these multi-protein assemblies offers new therapeutic avenues for ALS.

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Mechanism of action

Modulation of protein-protein interactions within the complex; modulation of chaperone activity; disruption of pathological aggregation.

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Biological functions

RNA processing and regulationProtein quality control via ubiquitin-proteasome systemStress granule formation under cellular stress conditionsCytoskeleton reorganization
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Disease associations

Neurodegenerative diseaseAmyotrophic Lateral Sclerosis (ALS)
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Safety considerations

Potential for off-target effects due to the involvement of core complex components in multiple cellular processes.Complexity of targeting protein-protein interactions.

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