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Formation of cholesterol bilayer domains precedes formation of cholesterol crystals in cholesterol/dimyristoylphosphatidylcholine membranes: EPR and DSC studies.胆固醇/二肉豆蔻酰磷脂酰胆碱膜中胆固醇双层域的形成先于胆固醇晶体的形成:EPR 和 DSC 研究。
J Phys Chem B. 2013 Aug 1;117(30):8994-9003. doi: 10.1021/jp402394m. Epub 2013 Jul 18.
2
Formation of cholesterol Bilayer Domains Precedes Formation of Cholesterol Crystals in Membranes Made of the Major Phospholipids of Human Eye Lens Fiber Cell Plasma Membranes.胆固醇双层域的形成先于人眼晶状体纤维细胞膜主要磷脂形成的膜中胆固醇晶体的形成。
Curr Eye Res. 2020 Feb;45(2):162-172. doi: 10.1080/02713683.2019.1662058. Epub 2019 Sep 3.
3
Detection of cholesterol bilayer domains in intact biological membranes: Methodology development and its application to studies of eye lens fiber cell plasma membranes.检测完整生物膜中的胆固醇双层结构域:方法学的发展及其在眼晶状体纤维细胞质膜研究中的应用。
Exp Eye Res. 2019 Jan;178:72-81. doi: 10.1016/j.exer.2018.09.020. Epub 2018 Sep 29.
4
Using spin-label electron paramagnetic resonance (EPR) to discriminate and characterize the cholesterol bilayer domain.使用自旋标记电子顺磁共振(EPR)来区分和表征胆固醇双层域。
Chem Phys Lipids. 2011 Nov;164(8):819-29. doi: 10.1016/j.chemphyslip.2011.08.001. Epub 2011 Aug 9.
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Glycophorin-induced cholesterol-phospholipid domains in dimyristoylphosphatidylcholine bilayer vesicles.血型糖蛋白在二肉豆蔻酰磷脂酰胆碱双层囊泡中诱导形成胆固醇 - 磷脂结构域。
Biochemistry. 1991 May 21;30(20):4909-16. doi: 10.1021/bi00234a011.
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Cholesterol and cholesterol bilayer domains inhibit binding of alpha-crystallin to the membranes made of the major phospholipids of eye lens fiber cell plasma membranes.胆固醇和胆固醇双层结构域抑制 alpha-晶体蛋白与眼晶状体纤维细胞膜主要磷脂组成的膜的结合。
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Confocal Microscopy Confirmed that in Phosphatidylcholine Giant Unilamellar Vesicles with very High Cholesterol Content Pure Cholesterol Bilayer Domains Form.共焦显微镜证实,在具有非常高胆固醇含量的磷脂酰胆碱巨大单层囊泡中,纯胆固醇双层域形成。
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X-ray structure, thermodynamics, elastic properties and MD simulations of cardiolipin/dimyristoylphosphatidylcholine mixed membranes.心磷脂/二肉豆蔻酰磷脂酰胆碱混合膜的 X 射线结构、热力学、弹性性质和 MD 模拟。
Chem Phys Lipids. 2014 Feb;178:1-10. doi: 10.1016/j.chemphyslip.2013.12.010. Epub 2013 Dec 28.
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Phase-separation and domain-formation in cholesterol-sphingomyelin mixture: pulse-EPR oxygen probing.胆固醇-神经鞘磷脂混合物中的相分离和域形成:脉冲 EPR 氧探测。
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Lipid chain dynamics and molecular location of diacylglycerol in hydrated binary mixtures with phosphatidylcholine: spin label ESR studies.在与磷脂酰胆碱形成的水合二元混合物中,二酰基甘油的脂链动力学和分子定位:自旋标记电子顺磁共振研究
Biochemistry. 1996 Mar 26;35(12):3831-6. doi: 10.1021/bi952688b.

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Cholesterol Content Regulates the Interaction of αA-, αB-, and α-Crystallin with the Model of Human Lens-Lipid Membranes.胆固醇含量调节 αA-、αB-和 α-晶状体蛋白与人类晶状体脂膜模型的相互作用。
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Electrostatic switch mechanisms of membrane protein trafficking and regulation.膜蛋白运输与调控的静电开关机制
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Electroformation of Giant Unilamellar Vesicles from Damp Lipid Films Formed by Vesicle Fusion.通过囊泡融合形成的潮湿脂质膜电形成巨型单层囊泡。
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Membrane Models and Experiments Suitable for Studies of the Cholesterol Bilayer Domains.适用于胆固醇双层结构域研究的膜模型与实验
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本文引用的文献

1
Comparative computer simulation study of cholesterol in hydrated unary and binary lipid bilayers and in an anhydrous crystal.胆固醇在水合单相和双相比脂质双层以及无水晶体中的比较计算机模拟研究。
J Phys Chem B. 2013 Jul 25;117(29):8758-69. doi: 10.1021/jp402839r. Epub 2013 Jul 12.
2
Properties of membranes derived from the total lipids extracted from the human lens cortex and nucleus.从人晶状体皮质和核中提取的总脂质所衍生的膜的特性。
Biochim Biophys Acta. 2013 Jun;1828(6):1432-40. doi: 10.1016/j.bbamem.2013.02.006. Epub 2013 Feb 21.
3
Spontaneous formation of two-dimensional and three-dimensional cholesterol crystals in single hydrated lipid bilayers.在单层水合脂质双层中胆固醇晶体的二维和三维自发形成。
Biophys J. 2012 Jul 18;103(2):255-64. doi: 10.1016/j.bpj.2012.05.025. Epub 2012 Jul 17.
4
Properties of fiber cell plasma membranes isolated from the cortex and nucleus of the porcine eye lens.从猪眼晶状体皮质和核中分离的纤维细胞质膜的特性。
Exp Eye Res. 2012 Apr;97(1):117-29. doi: 10.1016/j.exer.2012.01.012. Epub 2012 Feb 2.
5
Functions of cholesterol and the cholesterol bilayer domain specific to the fiber-cell plasma membrane of the eye lens.眼晶状体纤维细胞膜中胆固醇和胆固醇双层域的功能。
J Membr Biol. 2012 Jan;245(1):51-68. doi: 10.1007/s00232-011-9412-4. Epub 2011 Dec 30.
6
Saturation with cholesterol increases vertical order and smoothes the surface of the phosphatidylcholine bilayer: a molecular simulation study.胆固醇饱和增加了垂直有序性并使磷脂酰胆碱双层表面变得平滑:一项分子模拟研究。
Biochim Biophys Acta. 2012 Mar;1818(3):520-9. doi: 10.1016/j.bbamem.2011.10.023. Epub 2011 Oct 29.
7
Phases and domains in sphingomyelin-cholesterol membranes: structure and properties using EPR spin-labeling methods.鞘磷脂-胆固醇膜的相和域:使用 EPR 自旋标记方法的结构和性质。
Eur Biophys J. 2012 Feb;41(2):147-59. doi: 10.1007/s00249-011-0766-4. Epub 2011 Oct 28.
8
Using spin-label electron paramagnetic resonance (EPR) to discriminate and characterize the cholesterol bilayer domain.使用自旋标记电子顺磁共振(EPR)来区分和表征胆固醇双层域。
Chem Phys Lipids. 2011 Nov;164(8):819-29. doi: 10.1016/j.chemphyslip.2011.08.001. Epub 2011 Aug 9.
9
Phase-separation and domain-formation in cholesterol-sphingomyelin mixture: pulse-EPR oxygen probing.胆固醇-神经鞘磷脂混合物中的相分离和域形成:脉冲 EPR 氧探测。
Biophys J. 2011 Aug 17;101(4):837-46. doi: 10.1016/j.bpj.2011.07.014.
10
Crystalline lipid domains: characterization by X-ray diffraction and their relation to biology.结晶脂质域:X 射线衍射的特征及其与生物学的关系。
Angew Chem Int Ed Engl. 2011 Apr 11;50(16):3620-9. doi: 10.1002/anie.201004470. Epub 2011 Feb 25.

胆固醇/二肉豆蔻酰磷脂酰胆碱膜中胆固醇双层域的形成先于胆固醇晶体的形成:EPR 和 DSC 研究。

Formation of cholesterol bilayer domains precedes formation of cholesterol crystals in cholesterol/dimyristoylphosphatidylcholine membranes: EPR and DSC studies.

机构信息

Department of Biophysics, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA.

出版信息

J Phys Chem B. 2013 Aug 1;117(30):8994-9003. doi: 10.1021/jp402394m. Epub 2013 Jul 18.

DOI:10.1021/jp402394m
PMID:23834375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3762674/
Abstract

Saturation-recovery EPR along with DSC were used to determine the cholesterol content at which pure cholesterol bilayer domains (CBDs) and cholesterol crystals begin to form in dimyristoylphosphatidylcholine (DMPC) membranes. To preserve compositional homogeneity throughout the membrane suspension, lipid multilamellar dispersions were prepared using a rapid solvent exchange method. The cholesterol content increased from 0 to 75 mol %. With spin-labeled cholesterol analogues, it was shown that the CBDs begin to form at ~50 mol % cholesterol. It was confirmed by DSC that the cholesterol solubility threshold for DMPC membranes is detected at ~66 mol % cholesterol. At levels above this cholesterol content, monohydrate cholesterol crystals start to form. The major finding is that the formation of CBDs precedes formation of cholesterol crystals. The region of the phase diagram for cholesterol contents between 50 and 66 mol % is described as a structured one-phase region in which CBDs have to be supported by the surrounding DMPC bilayer saturated with cholesterol. Thus, the phase boundary located at 66 mol % cholesterol separates the structured one-phase region (liquid-ordered phase of DMPC with CBDs) from the two-phase region where the structured liquid-ordered phase of DMPC coexists with cholesterol crystals. It is likely that CBDs are precursors of monohydrate cholesterol crystals.

摘要

利用饱和恢复电子顺磁共振(EPR)和差示扫描量热法(DSC)来确定在二肉豆蔻酰磷脂酰胆碱(DMPC)膜中纯胆固醇双层域(CBD)和胆固醇晶体开始形成的胆固醇含量。为了在整个膜悬浮液中保持组成均一性,使用快速溶剂交换方法制备了脂质多层分散体。胆固醇含量从 0 增加到 75mol%。使用带有自旋标记的胆固醇类似物,表明 CBD 开始在约 50mol%胆固醇时形成。DSC 证实 DMPC 膜的胆固醇溶解度阈值在约 66mol%胆固醇时被检测到。在高于此胆固醇含量的水平下,一水合胆固醇晶体开始形成。主要发现是 CBD 的形成先于胆固醇晶体的形成。胆固醇含量在 50 至 66mol%之间的相图区域被描述为具有结构的单相区域,其中 CBD 必须由周围充满胆固醇的 DMPC 双层支持。因此,位于 66mol%胆固醇处的相边界将具有 CBD 的结构化有序相(DMPC 的有序相)与具有胆固醇晶体的两相区域分开。CBD 很可能是一水合胆固醇晶体的前体。