https://scholars.lib.ntu.edu.tw/handle/123456789/61238
標題: | The influence of phospholipid membranes on bovine calcitonin peptide's secondary structure and induced neurotoxic effects | 作者: | Wang, Steven S.-S. Good, Theresa A. Rymer, Dawn L. |
關鍵字: | Calcitonin;Amyloid;Cholesterol;Gangliosides;Secondary structure;Neurotoxicity | 公開日期: | 2005 | 起(迄)頁: | - | 來源出版物: | The International Journal of Biochemistry & Cell Biology 37(2005), 1656–1669 | 摘要: | The peptide hormone, calcitonin, which is associated with medullary carcinoma of the thyroid, has a marked tendency to form amyloid fibrils and may be a useful model in probing the role of peptide–membrane interactions in -sheet and amyloid formation and amyloid neurotoxicity. Using bovine calcitonin, we found that, like other amyloids, the peptide was toxic only when in a - sheet-rich, amyloid form, butwas non-toxic, when it lacked an amyloid structure.We found that the peptide bound with significant affinity to membranes that contained either cholesterol and gangliosides. In addition, incubation of calcitonin with cholesterol-rich and ganglioside-containing membranes resulted in significant changes in peptide structure yielding a peptide enriched in -sheet and amyloid content. Because the cholesterol- and ganglioside-rich phospholipid systems enhanced the calcitonin -sheet and amyloid contents, and peptide amyloid contentwas associated with neurotoxicity,we then investigated whether depleting cellular cholesterol and gangliosides affected calcitonin neurotoxicity. We found that cholesterol and ganglioside removal significantly reduced the calcitonin-induced PC12 cell neurotoxicity. Similar results have been observed with other amyloid-forming peptides such as -amyloid (A) of Alzheimer’s disease and suggest that modulation of membrane composition and peptide–membrane interactions may prove useful in the control of amyloid formation and amyloid neurotoxicity. |
URI: | http://ntur.lib.ntu.edu.tw//handle/246246/2006111501232845 | 其他識別: | 246246/2006111501232845 | DOI: | 10.1016/j.biocel.2005.02.006 |
顯示於: | 化學工程學系 |
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