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Probing the Mint2 Protein-Protein Interaction Network Relevant to the Pathophysiology of Alzheimer's Disease.

Thomas M T JensenLouise S ClemmensenChristian R O BartlingLinda M Haugaard-KedströmKristian Strømgaard
Published in: Chembiochem : a European journal of chemical biology (2018)
The intracellular adaptor protein Mint2 binds amyloid precursor protein (APP) and presenilin-1, which are both central constituents of the amyloidogenic pathway associated with Alzheimer's disease (AD). Additional interaction partners have also been suggested for Mint2; several of them are also pertinent to AD pathogenesis. However, no comparative mapping of the Mint2 protein-protein interaction network is available. Here we provide a systematic characterization of seven interaction partners and address their specificities towards the different binding domains of Mint2, which reveal domain-specific and -nonspecific interaction partners. Moreover, we show that the last two C-terminal amino acids of Mint2 are both important for the intramolecular interaction with the PDZ1 domain and for the stability of Mint2.
Keyphrases
  • protein protein
  • small molecule
  • binding protein
  • genome wide
  • human immunodeficiency virus
  • hiv infected