Dynamics and heterogeneity of bovine hippocampal membranes: Role of cholesterol and proteins

被引:36
作者
Mukherjee, Soumi
Kombrabail, Mamata
Krishnamoorthy, G.
Chattopadhyay, Amitabha
机构
[1] Tata Inst Fundamental Res, Dept Chem Sci, Bombay 400005, Maharashtra, India
[2] Ctr Cellular & Mol Biol, Hyderabad 500007, Andhra Pradesh, India
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2007年 / 1768卷 / 09期
关键词
hippocampal membrane; cholesterol; fluorescence lifetime distribution; maximum entropy method; time-resolved fluorescence anisotropy;
D O I
10.1016/j.bbamem.2007.05.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The structural and dynamic consequence of alterations in membrane lipid composition (specifically cholesterol) in neuronal membranes is poorly understood. Previous work from our laboratory has established bovine hippocampal membranes as a convenient natural source for studying neuronal receptors. In this paper, we have explored the role of cholesterol and proteins in the dynamics and heterogeneity of bovine hippocampal membranes using fluorescence lifetime distribution analysis of the environment-sensitive fluorescent probe Nile Red incorporated into such membranes by the maximum entropy method (MEM), and time-resolved fluorescence anisotropy measurements. The peak position and the width of the lifetime distribution of Nile Red show a progressive reduction with increasing cholesterol depletion from native hippocampal membranes indicating that the extent of heterogeneity decreases with decrease in membrane cholesterol content. This is accompanied by a concomitant decrease of the fluorescence anisotropy and rotational correlation time. Our results point out that the microenvironment experienced by Nile Red is relatively insensitive to the presence of proteins in hippocampal membranes. Interestingly, Nile Red lifetime distribution in liposomes of lipid extracts is similar to that of native membranes indicating that proteins do not contribute significantly to the high level of heterogeneity observed in native membranes. These results could be relevant in understanding the neuronal diseases characterized by defective membrane lipid metabolism. (C) 2007 Elsevier B.V All rights reserved.
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页码:2130 / 2144
页数:15
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