Journal article
Guanidine hydrochloride denaturation of dopamine-induced α-synuclein oligomers: A small-angle X-ray scattering study
CLL Pham, N Kirby, K Wood, T Ryan, B Roberts, A Sokolova, KJ Barnham, CL Masters, RB Knott, R Cappai, CC Curtain, A Rekas
Proteins Structure Function and Bioinformatics | WILEY | Published : 2014
DOI: 10.1002/prot.24332
Abstract
Alpha-synuclein (α-syn) forms the amyloid-containing Lewy bodies found in the brain in Parkinson's disease. The neurotransmitter dopamine (DA) reacts with α-syn to form SDS-resistant soluble, non-amyloid, and melanin-containing oligomers. Their toxicity is debated, as is the nature of their structure and their relation to amyloid-forming conformers of α-syn. The small-angle X-ray scattering technique in combination with modeling by the ensemble optimization method showed that the un-reacted native protein populated three broad classes of conformer, while reaction with DA gave a restricted ensemble range suggesting that the rigid melanin molecule played an important part in their structure. W..
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Grants
Awarded by AINSE
Funding Acknowledgements
Grant sponsor: SAXS/WAXS beam line of the Australian Synchrotron, Victoria, Australia; Grant sponsor: Support at ANSTO was provided by AINSE; grant number: AINGRA09043; Grant sponsor: University of Melbourne-ANSTO Collaborative Research grant (to CCC); Grant sponsor: National Health and Medical Research Council of Australia (NHMRC); Grant sponsor: NHMRC Senior Research Fellows (to RC and KJB).