Journal of Bioenergetics and Biomembranes

, Volume 42, Issue 1, pp 85–95

Accelerated formation of α-synuclein oligomers by concerted action of the 20S proteasome and familial Parkinson mutations

  • Karen A. Lewis
  • Arynn Yaeger
  • George N. DeMartino
  • Philip J. Thomas
Article

DOI: 10.1007/s10863-009-9258-y

Cite this article as:
Lewis, K.A., Yaeger, A., DeMartino, G.N. et al. J Bioenerg Biomembr (2010) 42: 85. doi:10.1007/s10863-009-9258-y

Abstract

A hallmark of Parkinson disease (PD) is the formation of intracellular protein inclusions called Lewy bodies that also contain mitochondria. α-Synuclein (αSyn) is a major protein component of Lewy bodies, where it is in an amyloid conformation and a significant fraction is truncated by poorly understood proteolytic events. Previously, we demonstrated that the 20S proteasome cleaves αSyn in vitro to produce fragments like those observed in Lewy bodies and that the fragments accelerate the formation of amyloid fibrils from full-length αSyn. Three point mutations in αSyn are associated with early-onset familial PD: A30P, E46K, and A53T. However, these mutations have very different effects on the amyloidogenicity and vesicle-binding activity of αSyn, suggesting neither of these processes directly correlate with neurodegeneration. Here, we evaluate the effect of the disease-associated mutations on the fragmentation, conformation, and association reactions of αSyn in the presence of the 20S proteasome and liposomes. The 20S proteasome produced the C-terminal fragments from both the mutant and wildtype αSyn. These truncations accelerated fibrillization of all α-synucleins, but again there was no clear correlation between the PD-associated mutations and amyloid formation in the presence of liposomes. Recent data suggests that cellular toxicity is caused by a soluble oligomeric species, which is a precursor to the amyloid form and is immunologically distinguishable from both soluble monomeric and amyloid forms of αSyn. Notably, the rate of formation of the soluble, presumptively cytotoxic oligomers correlated with the disease-associated mutations when both 20S proteasome and liposomes were present. Under these conditions, the wildtype protein was also cleaved and formed the oligomeric structures, albeit at a slower rate, suggesting that 20S-mediated truncation of αSyn may play a role in sporadic PD as well. Evaluation of the biochemical reactions of the PD-associated α-synuclein mutants in our in vitro system provides insight into the possible pathogenetic mechanism of both familial and sporadic PD.

Keywords

20S proteasome Endoproteolysis Parkinson disease αSynuclein Amyloid Soluble oligomers Cytotoxicity Liposomes 

Copyright information

© Springer Science+Business Media, LLC 2010

Authors and Affiliations

  • Karen A. Lewis
    • 1
    • 2
  • Arynn Yaeger
    • 1
  • George N. DeMartino
    • 1
  • Philip J. Thomas
    • 1
  1. 1.Department of PhysiologyUniversity of Texas Southwestern Medical Center at DallasDallasUSA
  2. 2.Department of Chemistry and BiochemistryUniversity of Colorado at BoulderBoulderUSA

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