| Literature DB >> 27177831 |
Zhengjian Lv1, Alexey V Krasnoslobodtsev1,2, Yuliang Zhang1, Daniel Ysselstein3, Jean Christophe Rochet3, Scott C Blanchard4, Yuri L Lyubchenko1.
Abstract
Environmental factors, such as acidic pH, facilitate the assembly of α-synuclein (α-Syn) in aggregates, but the impact of pH on the very first step of α-Syn aggregation remains elusive. Recently, we developed a single-molecule approach that enabled us to measure directly the stability of α-Syn dimers. Unlabeled α-Syn monomers were immobilized on a substrate, and fluorophore-labeled monomers were added to the solution to allow them to form dimers with immobilized α-Syn monomers. The dimer lifetimes were measured directly from the fluorescence bursts on the time trajectories. Herein, we applied the single-molecule tethered approach for probing of intermolecular interaction to characterize the effect of acidic pH on the lifetimes of α-Syn dimers. The experiments were performed at pH 5 and 7 for wild-type α-Syn and for two mutants containing familial type mutations E46K and A53T. We demonstrate that a decrease of pH resulted in more than threefold increase in the α-Syn dimers lifetimes with some variability between the α-Syn species. We hypothesize that the stabilization effect is explained by neutralization of residues 96-140 of α-Syn and this electrostatic effect facilitates the association of the two monomers. Given that dimerization is the first step of α-Syn aggregation, we posit that the electrostatic effect thereby contributes to accelerating α-Syn aggregation at acidic pH.Entities:
Keywords: alpha-synuclein protein; amyloid aggregation; interprotein interactions; protein self-assembly; single molecule fluorescence
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Year: 2016 PMID: 27177831 PMCID: PMC4958566 DOI: 10.1002/bip.22874
Source DB: PubMed Journal: Biopolymers ISSN: 0006-3525 Impact factor: 2.505