Characterization of Heparin-induced Glyceraldehyde-3-phosphate Dehydrogenase Early Amyloid-like Oligomers and Their Implication in alpha-Synuclein Aggregation
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
---|---|
Data(s) |
07/11/2013
07/11/2013
2012
|
Resumo |
Lewy bodies and Lewy neurites, neuropathological hallmarks of several neurological diseases, are mainly made of filamentous assemblies of alpha-synuclein. However, other macromolecules including Tau, ubiquitin, glyceraldehyde-3-phosphate dehydrogenase, and glycosaminoglycans are routinely found associated with these amyloid deposits. Glyceraldehyde-3-phosphate dehydrogenase is a glycolytic enzyme that can form fibrillar aggregates in the presence of acidic membranes, but its role in Parkinson disease is still unknown. In this work, the ability of heparin to trigger the amyloid aggregation of this protein at physiological conditions of pH and temperature is demonstrated by infrared and fluorescence spectroscopy, dynamic light scattering, small angle x-ray scattering, circular dichroism, and fluorescence microscopy. Aggregation proceeds through the formation of short rod-like oligomers, which elongates in one dimension. Heparan sulfate was also capable of inducing glyceraldehyde-3-phosphate dehydrogenase aggregation, but chondroitin sulfates A, B, and C together with dextran sulfate had a negligible effect. Aided with molecular docking simulations, a putative binding site on the protein is proposed providing a rational explanation for the structural specificity of heparin and heparan sulfate. Finally, it is demonstrated that in vitro the early oligomers present in the glyceraldehyde-3-phosphate dehydrogenase fibrillation pathway promote alpha-synuclein aggregation. Taking into account the toxicity of alpha-synuclein prefibrillar species, the heparin-induced glyceraldehyde-3-phosphate dehydrogenase early oligomers might come in useful as a novel therapeutic strategy in Parkinson disease and other synucleinopathies. Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) [PIP 2518] Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET) Consejo Investigaciones de la Universidad Nacional de Tucuman (CIUNT) [26/D439-1] Consejo Investigaciones de la Universidad Nacional de Tucuman (CIUNT) Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) |
Identificador |
JOURNAL OF BIOLOGICAL CHEMISTRY, BETHESDA, v. 287, n. 4, supl. 1, Part 1, pp. 2398-2409, 43831, 2012 0021-9258 http://www.producao.usp.br/handle/BDPI/42835 10.1074/jbc.M111.303503 |
Idioma(s) |
eng |
Publicador |
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC BETHESDA |
Relação |
JOURNAL OF BIOLOGICAL CHEMISTRY |
Direitos |
closedAccess Copyright AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC |
Palavras-Chave | #X-RAY-SCATTERING #PARKINSONS-DISEASE #FIBRIL FORMATION #FILAMENTOUS INCLUSIONS #MOONLIGHTING PROTEINS #INFRARED-SPECTROSCOPY #ALZHEIMERS-DISEASE #LEWY BODIES #BETA #GLYCOSAMINOGLYCANS #BIOCHEMISTRY & MOLECULAR BIOLOGY |
Tipo |
article original article publishedVersion |