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Updated: Dec 11, 2025

Mapping Dysfunctional Protein-Protein Interactions in Disease
Published on: October 24, 2025
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein
Christian Haenig1, Nir Atias2, Alexander K Taylor3
1Neuroproteomics, Max Delbrück Center for Molecular Medicine, 13125 Berlin, Germany.
Abstract:
Interactome maps are valuable resources to elucidate protein function and disease mechanisms. Here, we report on an interactome map that focuses on neurodegenerative disease (ND), connects ∼5,000 human proteins via ∼30,000 candidate interactions and is generated by systematic yeast two-hybrid interaction screening of ∼500 ND-related proteins and integration of literature interactions. This network reveals interconnectivity across diseases and links many known ND-causing proteins, such as α-synuclein, TDP-43, and ATXN1, to a host of proteins previously unrelated to NDs. It facilitates the identification of interacting proteins that significantly influence mutant TDP-43 and HTT toxicity in transgenic flies, as well as of ARF-GEP100 that controls misfolding and aggregation of multiple ND-causing proteins in experimental model systems. Furthermore, it enables the prediction of ND-specific subnetworks and the identification of proteins, such as ATXN1 and MKL1, that are abnormally aggregated in postmortem brains of Alzheimer's disease patients, suggesting widespread protein aggregation in NDs.
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