Fast kinetics of environmentally induced α-synuclein aggregation mediated by structural alteration in NAC region and result in structure dependent cytotoxicity

• Published in: Scientific reports 2020-10, Vol.10 (1), p.18412, Article 18412
• Main Authors: Srivastava, Tulika, Raj, Ritu, Dubey, Amit, Kumar, Dinesh, Chaturvedi, Rajnish K., Sharma, Sandeep K., Priya, Smriti
• Format: Article
• Language: English
• Subjects: 631/45; 631/535; 631/92; 692/499; 692/699; alpha-Synuclein - chemistry; alpha-Synuclein - metabolism; Apoptosis; Biopolymers - chemistry; Biopolymers - metabolism; Circular Dichroism; Cytotoxicity; Environmental Pollutants - pharmacology; Environmental stress; Fibrils; Humanities and Social Sciences; Humans; Kinetics; Membrane potential; Microscopy, Electron, Transmission; Molecular dynamics; Molecular Dynamics Simulation; Molecular weight; Morphology; Movement disorders; multidisciplinary; Neurodegenerative diseases; Neurotoxicity; Parkinson Disease - metabolism; Parkinson's disease; Pesticides; Protein Aggregation, Pathological; Protein interaction; Protein structure; Protein Structure, Secondary; Proteins; Risk Factors; Rotenone; Rotenone - pharmacology; Science; Science (multidisciplinary); Synuclein; Toxicology
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-75361-6

Aggregation of α-synuclein (α-syn) is associated with the manifestation of various pathogenic synucleinopathies, including Parkinson’s disease attributed to both genetic and environmental stress factors. The initial events triggering α-syn aggregation and disease initiation due to environmental stress factors are still largely unknown. Here, to understand the mechanism of misfolding and aggregation initiation, we induced α-syn aggregation with rotenone, an established chemical inducer of PD like symptoms. We found that rotenone accelerates the formation of structurally distinct oligomers and fibrils that act as templates and increase the formation of conformers capable of spreading to the neighboring neuronal cells. Molecular dynamics simulations and NMR studies revealed the involvement of NAC region and formation of helical conformations resulting in structural variations in oligomers and fibrils. These structural variations affect the cytotoxic potential of oligomers and fibrils, where, the beta sheet rich oligomers and fibrils alter the membrane potential of neuronal cells and lead to early apoptosis. Our results describe the initial mechanistic events in pathogenic protein aggregation, where initial structural alterations in response to external stress factors dictate the toxicity of resulting conformers. This information will further provide insights in the understanding of protein aggregation, disease progression and pathogenesis.