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Probing the Mint2 Protein-Protein Interaction Network Relevant to the Pathophysiology of Alzheimer's Disease
- Source :
- ChemBioChem. 19:1119-1122
- Publication Year :
- 2018
- Publisher :
- Wiley, 2018.
-
Abstract
- 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.
- Subjects :
- 0301 basic medicine
chemistry.chemical_classification
biology
Chemistry
Organic Chemistry
Signal transducing adaptor protein
Computational biology
Biochemistry
Protein–protein interaction
Amino acid
Pathogenesis
03 medical and health sciences
030104 developmental biology
0302 clinical medicine
Interaction network
Amyloid precursor protein
biology.protein
Molecular Medicine
Phosphorylation
Molecular Biology
030217 neurology & neurosurgery
Intracellular
Subjects
Details
- ISSN :
- 14394227
- Volume :
- 19
- Database :
- OpenAIRE
- Journal :
- ChemBioChem
- Accession number :
- edsair.doi.dedup.....4b7b68468adc78dbac84652776429e63
- Full Text :
- https://doi.org/10.1002/cbic.201800004