膜流动性
膜
磷脂
化学
肽
生物物理学
淀粉样蛋白(真菌学)
神经毒性
脂质双层
人脑
生物化学
荧光
P3肽
阿尔茨海默病
淀粉样前体蛋白
生物
神经科学
内科学
毒性
医学
量子力学
物理
无机化学
疾病
有机化学
作者
Wernér E.G. Müller,Gunter P. Eckert,K. Scheuer,N. J. Cairns,Athanasios Maras,Wagner F. Gattaz
出处
期刊:Amyloid
[Taylor & Francis]
日期:1998-01-01
卷期号:5 (1): 10-15
被引量:65
标识
DOI:10.3109/13506129809007284
摘要
beta-amyloid peptide (A beta) and several A beta-fragments decrease the fluidity of human cortex membranes in a concentration dependent fashion. The effect of A beta on membrane fluidity increases with peptide length, is most pronounced for A beta 1-43 and can be seen at concentrations as low as 100 nmol/l. While the fragment A beta 25-35 is active, scrambled peptide (A beta 35-25) when investigated under similar conditions shows no effects on membrane fluidity. The effect of A beta peptides on fluidity of the phospholipid bilayer is more pronounced in the hydrocarbon core (labeled with the fluorescence probe 1,6-diphenylhexa-1,3,5-triene) than in the region of the hydrophilic heads (labeled with the fluorescence probe 1-[4'-(trimethylamino)phenyl]-6-phenylhexa-1,3,5-triene). It is suggested that the effect of A beta on neuronal membranes is probably a major initial mechanism in a cascade of events finally leading to neurotoxicity and cell death in Alzheimer's disease.
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