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