| Literature DB >> 26323479 |
Amulya Nidhi Shrivastava1, Virginie Redeker2, Nicolas Fritz3, Laura Pieri2, Leandro G Almeida1, Maria Spolidoro1, Thomas Liebmann3, Luc Bousset2, Marianne Renner1, Clément Léna1, Anita Aperia3, Ronald Melki4, Antoine Triller5.
Abstract
Extracellular α-synuclein (α-syn) assemblies can be up-taken by neurons; however, their interaction with the plasma membrane and proteins has not been studied specifically. Here we demonstrate that α-syn assemblies form clusters within the plasma membrane of neurons. Using a proteomic-based approach, we identify the α3-subunit of Na+/K+-ATPase (NKA) as a cell surface partner of α-syn assemblies. The interaction strength depended on the state of α-syn, fibrils being the strongest, oligomers weak, and monomers none. Mutations within the neuron-specific α3-subunit are linked to rapid-onset dystonia Parkinsonism (RDP) and alternating hemiplegia of childhood (AHC). We show that freely diffusing α3-NKA are trapped within α-syn clusters resulting in α3-NKA redistribution and formation of larger nanoclusters. This creates regions within the plasma membrane with reduced local densities of α3-NKA, thereby decreasing the efficiency of Na+ extrusion following stimulus. Thus, interactions of α3-NKA with extracellular α-syn assemblies reduce its pumping activity as its mutations in RDP/AHC.Entities:
Keywords: Parkinson's disease; misfolding disease; protein aggregation and clustering; single particle tracking; super‐resolution imaging
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Year: 2015 PMID: 26323479 PMCID: PMC4601662 DOI: 10.15252/embj.201591397
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598