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Article type: Research Article
Authors: Goux, Warren J.; * | Liu, Bingcam | Shumburo, Abdurahman M. | Parikh, Samir | Sparkman, Dennis R.
Affiliations: Department of Chemistry, University of Texas at Dallas, P.O. Box 830688, Richardson, TX 75083-0688, USA
Correspondence: [*] Corresponding author. Tel.: +1 972 883 2660; Fax: +1 972 883 2925; E-mail: wgoux@utdallas.edu.
Abstract: Protease resistant paired helical filaments (prcPHF) can be isolated from the brains of Alzheimer's diseased patients. A second type of PHF, A68 PHF, may be extracted in soluble form from brain homogenate and induced to form filaments in vitro. Here we use a variety of analytical techniques to assess the protein, carbohydrate and fatty acid composition of prcPHF and A68 PHF. High-field 1H NMR of both PHF preparations display similar fatty acid and carbohydrate proton resonances, consistent with the presence of a structurally similar glycolipid. Carbohydrate analysis showed that both preparations contained greater than 82% less than 12% C16:1 was significantly lower in A68 PHF than in prcPHF, both preparations contained otherwise similar fatty acid profiles with the most abundant lipid component being oleic acid (C18:1, 29.3 ± 9.0%) followed by palmitic (C16:0, 28.5 ± 5.6%) 17.6 ± 7.5%) preparations revealed a profile reasonably consistent with that previously determined for PHF-tau but significantly higher in glycine and lower in lysine than would be predicted from the cDNA sequence. On a weight per cent basis, protein accounted for about 51% A68 PHF samples but only about 10% Carbohydrate and fatty acid accounted for about 39% A68 PHF samples but 74% preparations showed strong correlations between the total amount of tau protein and fatty acid. These results suggest that a glycolipid component forms an integral part of the PHF structure.
Keywords: Alzheimer's disease, paired helical filaments, tau, glycolipid, NMR, GC/MS
DOI: 10.3233/JAD-2001-3504
Journal: Journal of Alzheimer's Disease, vol. 3, no. 5, pp. 455-466, 2001
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