Accelerated α‐synuclein fibrillation in crowded milieu

FEBS Letters

Li, Jie¹  M. Cooper, Elisa¹  Fink, Anthony L¹  Bower, Kiowa S¹  Uversky, Vladimir N¹ 

[1] Department of Chemistry and Biochemistry, University of California, Santa Cruz, CA 95064, USA

关键词: α-Synuclein;    Fibril;    Natively unfolded;    Molecular crowding;    Parkinson's disease;   

DOI  :  10.1016/S0014-5793(02)02446-8

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

Parkinson's disease is the second most common age-related neurodegenerative disease, resulting from loss of dopaminergic neurons in the substantia nigra. The aggregation and fibrillation of α-synuclein has been implicated as a causative factor in the disease, and the process of fibril formation has been intensively studied in vitro with dilute protein solutions. However, the intracellular environment of proteins is crowded with other macromolecules, whose concentration can reach 400 g/l. To address this discrepancy, the effect of molecular crowding on α-synuclein fibrillation has being studied. The addition of high concentrations of different polymers (proteins, polysaccharides and polyethylene glycols) dramatically accelerated α-synuclein fibrillation in vitro. The magnitude of the accelerating effect depended on the nature of the polymer, its length and concentration. Our results suggest that the major factor responsible for the accelerated fibrillation under crowded conditions is the excluded volume.

【 授权许可】

Unknown