https://scholars.lib.ntu.edu.tw/handle/123456789/406777
標題: | A kinetic analysis of the mechanism of £]-amyloid induced G protein activation | 作者: | Wang S.S.-S. Kazantzi V. Good T.A. |
公開日期: | 2003 | 卷: | 221 | 期: | 2 | 起(迄)頁: | 269-278 | 來源出版物: | Journal of Theoretical Biology | 摘要: | £]-Amyloid (A£]) is the primary protein component of senile plaques found in Alzheimer's disease. In an aggregated (amyloid fibril, protofibril, or low molecular weight oligomer) state, A£] has been consistently shown to be toxic to neurons, but the molecular mechanism of this toxicity is poorly understood. We have previously shown that A£] activates a Gi/o protein, and that inhibition of this specific G protein activation attenuated A£]-induced cell toxicity. In the present study, we use a kinetic analysis to examine the mechanism of A£]-induced G protein activation. Using synthetic A£](1-40) and phospholipid vesicles containing purified G0£\ subunits, we examined the relationship between A£] concentration, G0£\ subunit concentration, GTP concentration and rate of GTP hydrolysis experimentally. We found that at low concentrations of A£] (less than 10 £gM), A£] increased the rate of GTP hydrolysis over the rate of hydrolysis in the absence of peptide, however, at high concentrations of A£], significantly decreased rates of GTP hydrolysis were observed. We postulated several molecular level mechanisms for the observed rate behavior, from those mechanisms derived rate equations, and then tested the mechanisms against our experimental rate data. Based on our results, we identified a plausible mechanism for A£]-induced G protein activation which is consistent with available experimental data. This work demonstrates the utility of an engineering approach to examining steps in the mechanism of A£]-induced cell toxicity and could provide insight into our understanding of the mechanism of Alzheimer's disease. ? 2002 Elsevier Science B.V. All rights reserved. |
URI: | https://scholars.lib.ntu.edu.tw/handle/123456789/406777 | ISSN: | 00225193 | DOI: | 10.1006/jtbi.2003.3189 |
顯示於: | 化學工程學系 |
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