Suppr超能文献

膜特性对胆固醇-脂质混合物中相分离和结构域形成的影响。

Effect of membrane characteristics on phase separation and domain formation in cholesterol-lipid mixtures.

作者信息

Pata Veena, Dan Nily

机构信息

Department of Chemical Engineering, Drexel University, Philadelphia, Pennsylvania 19104, USA.

出版信息

Biophys J. 2005 Feb;88(2):916-24. doi: 10.1529/biophysj.104.052241. Epub 2004 Nov 12.

Abstract

We examine, using an analytical mean-field model, the distribution of cholesterol in a lipid bilayer. The model accounts for the perturbation of lipid packing induced by the embedded cholesterol, in a manner similar to that of transmembrane proteins. We find that the membrane-induced interactions between embedded cholesterol molecules vary as a function of the cholesterol content. Thus, the effective lipid-cholesterol interaction is concentration-dependent. Moreover, it transitions from repulsive to attractive to repulsive as the cholesterol content increases. As the concentration of cholesterol in the bilayer exceeds a critical value, phase separation occurs. The coexistence between cholesterol-rich and cholesterol-poor domains is universal for any bilayer parameters, although the composition of the cholesterol-rich phase varies as a function of the lipid properties. Although we do not assume specific cholesterol-lipid interactions or the formation of a lipid-cholesterol cluster, we find that the composition of the cholesterol-rich domains is constant, independent of the cholesterol content in the bilayer.

摘要

我们使用一个解析平均场模型来研究脂质双层中胆固醇的分布。该模型以类似于跨膜蛋白的方式,考虑了嵌入胆固醇引起的脂质堆积扰动。我们发现,嵌入的胆固醇分子之间的膜诱导相互作用随胆固醇含量而变化。因此,有效的脂质 - 胆固醇相互作用是浓度依赖性的。此外,随着胆固醇含量的增加,它从排斥转变为吸引再转变为排斥。当双层中胆固醇的浓度超过临界值时,就会发生相分离。富含胆固醇和贫胆固醇区域之间的共存对于任何双层参数都是普遍存在的,尽管富含胆固醇相的组成随脂质性质而变化。虽然我们没有假设特定的胆固醇 - 脂质相互作用或脂质 - 胆固醇簇的形成,但我们发现富含胆固醇区域的组成是恒定的,与双层中的胆固醇含量无关。

相似文献

1
Effect of membrane characteristics on phase separation and domain formation in cholesterol-lipid mixtures.
Biophys J. 2005 Feb;88(2):916-24. doi: 10.1529/biophysj.104.052241. Epub 2004 Nov 12.
2
Phenomenological model and phase behavior of saturated and unsaturated lipids and cholesterol.
Biophys J. 2008 Nov 15;95(10):4756-62. doi: 10.1529/biophysj.108.136317. Epub 2008 Aug 15.
3
Lateral organization in lipid-cholesterol mixed bilayers.
Biophys J. 2007 Jan 15;92(2):440-7. doi: 10.1529/biophysj.106.093864. Epub 2006 Oct 27.
4
Sphingomyelin/phosphatidylcholine/cholesterol phase diagram: boundaries and composition of lipid rafts.
Biophys J. 2003 Oct;85(4):2406-16. doi: 10.1016/S0006-3495(03)74664-5.
5
Fluctuation-induced interactions between domains in membranes.
Phys Rev E Stat Nonlin Soft Matter Phys. 2006 Aug;74(2 Pt 1):021916. doi: 10.1103/PhysRevE.74.021916. Epub 2006 Aug 18.
6
Sphingomyelin-cholesterol domains in phospholipid membranes: atomistic simulation.
Biophys J. 2004 Aug;87(2):1092-100. doi: 10.1529/biophysj.104.041939.
7
8
Toward a mathematical model of the assembly and disassembly of membrane microdomains: comparison with experimental models.
Biophys J. 2007 Jun 15;92(12):4145-56. doi: 10.1529/biophysj.106.090233. Epub 2007 Mar 23.
9
Non-raft forming sphingomyelin-cholesterol mixtures.
Chem Phys Lipids. 2004 Nov;132(1):37-46. doi: 10.1016/j.chemphyslip.2004.09.012.

引用本文的文献

3
Limited perturbation of a DPPC bilayer by fluorescent lipid probes: a molecular dynamics study.
J Phys Chem B. 2013 May 2;117(17):4844-52. doi: 10.1021/jp400289d. Epub 2013 Apr 19.
4
Saturation with cholesterol increases vertical order and smoothes the surface of the phosphatidylcholine bilayer: a molecular simulation study.
Biochim Biophys Acta. 2012 Mar;1818(3):520-9. doi: 10.1016/j.bbamem.2011.10.023. Epub 2011 Oct 29.
5
Using spin-label electron paramagnetic resonance (EPR) to discriminate and characterize the cholesterol bilayer domain.
Chem Phys Lipids. 2011 Nov;164(8):819-29. doi: 10.1016/j.chemphyslip.2011.08.001. Epub 2011 Aug 9.
6
Instability of cholesterol clusters in lipid bilayers and the cholesterol's Umbrella effect.
J Phys Chem B. 2010 Jan 21;114(2):840-8. doi: 10.1021/jp909061h.
7
Phase behavior of lipid monolayers containing DPPC and cholesterol analogs.
Biophys J. 2006 May 1;90(9):3176-83. doi: 10.1529/biophysj.105.072959. Epub 2006 Feb 3.

本文引用的文献

1
Membrane-mediated interactions of rod-like inclusions.
Eur Phys J E Soft Matter. 2002 Apr;7(4):381-6. doi: 10.1140/epje/i2001-10103-x.
2
Domains and rafts in membranes - hidden dimensions of selforganization.
J Biol Phys. 2002 Jun;28(2):195-210. doi: 10.1023/A:1019994628793.
3
Effective interactions between inclusions in complex fluids driven out of equilibrium.
Phys Rev E Stat Nonlin Soft Matter Phys. 2003 Jun;67(6 Pt 1):061112. doi: 10.1103/PhysRevE.67.061112. Epub 2003 Jun 23.
4
Role of cholesterol in the formation and nature of lipid rafts in planar and spherical model membranes.
Biophys J. 2004 May;86(5):2965-79. doi: 10.1016/S0006-3495(04)74347-7.
5
Liquid domains in vesicles investigated by NMR and fluorescence microscopy.
Biophys J. 2004 May;86(5):2910-22. doi: 10.1016/S0006-3495(04)74342-8.
6
Analytic models for mechanotransduction: gating a mechanosensitive channel.
Proc Natl Acad Sci U S A. 2004 Mar 23;101(12):4071-6. doi: 10.1073/pnas.0307804101. Epub 2004 Mar 15.
7
Elastic interaction between "hard" or "soft" pointwise inclusions on biological membranes.
Eur Phys J E Soft Matter. 2003 Jun;11(2):141-6. doi: 10.1140/epje/i2002-10154-5.
8
Complexation of phosphatidylcholine lipids with cholesterol.
Biophys J. 2004 Mar;86(3):1345-56. doi: 10.1016/S0006-3495(04)74206-X.
9
Novel properties of cholesterol-dioleoylphosphatidylcholine mixtures.
Biochim Biophys Acta. 2003 Oct 13;1616(2):196-208. doi: 10.1016/j.bbamem.2003.08.006.
10
The effect of chain length on protein solubilization in polymer-based vesicles (polymersomes).
Biophys J. 2003 Oct;85(4):2111-8. doi: 10.1016/S0006-3495(03)74639-6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验