| Literature DB >> 28763125 |
Luis Fonseca-Ornelas1, Carla Schmidt2, Aldo R Camacho-Zarco3, Claudio O Fernandez4, Stefan Becker1, Markus Zweckstetter1,3,5.
Abstract
Accumulation of α-synuclein (αSyn) aggregates constitutes the hallmark of synucleinopathies including Parkinson's disease. However, many steps from the innocuous, monomeric αSyn toward misfolded oligomers and fibrillar species remain unclear. Here, we show that αSyn can form in solution α-helical oligomers, which are off-pathway to fibrillization, through interaction with the tetrapyrrole phthalocyanine tetrasulfonate. Chemical cross-linking combined with mass spectrometry reveals a large number of intermolecular cross-links along the entire αSyn sequence in the phthalocyanine tetrasulfonate-stabilized αSyn oligomers. Our study suggests that stabilization of structured oligomers by small molecules provides a viable strategy to interfere with αSyn fibrillization.Entities:
Keywords: alpha-synuclein; mass spectrometry; oligomers; polymerization; proteins
Mesh:
Substances:
Year: 2017 PMID: 28763125 DOI: 10.1002/chem.201703001
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236