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2
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3
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Calorimetric and spectroscopic studies of the effects of cholesterol on the thermotropic phase behavior and organization of a homologous series of linear saturated phosphatidylglycerol bilayer membranes.胆固醇对一系列线性饱和磷脂酰甘油双层膜的热致相行为和组织结构影响的量热法和光谱学研究。
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本文引用的文献

1
Curvature effect on the structure of phospholipid bilayers.曲率对磷脂双层膜结构的影响。
Langmuir. 2007 Jan 30;23(3):1292-9. doi: 10.1021/la062455t.
2
Composition dependence of vesicle morphology and mixing properties in a bacterial model membrane system.细菌模型膜系统中囊泡形态和混合特性的组成依赖性
Biochim Biophys Acta. 2005 Oct 1;1716(1):40-8. doi: 10.1016/j.bbamem.2005.08.003.
3
Structure of phospholipid-cholesterol membranes: an x-ray diffraction study.磷脂 - 胆固醇膜的结构:一项X射线衍射研究。
Phys Rev E Stat Nonlin Soft Matter Phys. 2005 Jun;71(6 Pt 1):061924. doi: 10.1103/PhysRevE.71.061924. Epub 2005 Jun 29.
4
Molecular mechanisms of membrane perturbation by antimicrobial peptides and the use of biophysical studies in the design of novel peptide antibiotics.抗菌肽引起膜扰动的分子机制以及生物物理研究在新型肽类抗生素设计中的应用。
Comb Chem High Throughput Screen. 2005 May;8(3):241-56. doi: 10.2174/1386207053764576.
5
Molecular structure of the lecithin ripple phase.卵磷脂波纹相的分子结构。
Proc Natl Acad Sci U S A. 2005 Apr 12;102(15):5392-6. doi: 10.1073/pnas.0408249102. Epub 2005 Apr 4.
6
Thermodynamic and structural characterization of amino acid-linked dialkyl lipids.氨基酸连接的二烷基脂质的热力学和结构表征。
Chem Phys Lipids. 2005 Mar;134(1):29-39. doi: 10.1016/j.chemphyslip.2004.11.001. Epub 2004 Dec 9.
7
Simulating induced interdigitation in membranes.模拟膜中的诱导交叉指化现象。
Biophys J. 2004 Sep;87(3):1596-605. doi: 10.1529/biophysj.104.045005.
8
Changes in phosphatidylcholine headgroup tilt and water order induced by monovalent salts: molecular dynamics simulations.单价盐诱导的磷脂酰胆碱头部基团倾斜和水序变化:分子动力学模拟
Biophys J. 2004 Jun;86(6):3772-82. doi: 10.1529/biophysj.103.035816.
9
Mesoscopic structure in the chain-melting regime of anionic phospholipid vesicles: DMPG.阴离子磷脂囊泡链熔化状态下的介观结构:二肉豆蔻酰磷脂酰甘油(DMPG)
Biophys J. 2004 Jun;86(6):3722-33. doi: 10.1529/biophysj.103.033803.
10
Structure and fluctuations of charged phosphatidylserine bilayers in the absence of salt.无盐条件下带电磷脂酰丝氨酸双层膜的结构与涨落
Biophys J. 2004 Mar;86(3):1574-86. doi: 10.1016/S0006-3495(04)74225-3.

关于磷脂酰甘油形成交错相的倾向。

On the propensity of phosphatidylglycerols to form interdigitated phases.

作者信息

Pabst Georg, Danner Sabine, Karmakar Sanat, Deutsch Günter, Raghunathan Velayudhan A

机构信息

Institute of Biophysics and Nanosystems Research, Austrian Academy of Sciences, 8042 Graz, Austria.

出版信息

Biophys J. 2007 Jul 15;93(2):513-25. doi: 10.1529/biophysj.106.101592. Epub 2007 Apr 20.

DOI:10.1529/biophysj.106.101592
PMID:17449673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1896241/
Abstract

We have determined the phase behavior of disaturated phosphatidylglycerols (PGs) of chain lengths n(CH2) = 14-18 at high pH and ionic strength using calorimetry, dilatometry, as well as x-ray diffraction. PGs with n(CH2) = 14 and 16 show thermotropic behavior similar to that of phosphatidylcholines (PCs). The area/lipid obtained in the gel phase is smaller than that reported for PCs despite the expected larger effective headgroup size. This can be explained by the tilting of the PG headgroup out of the bilayer plane, and we provide experimental evidence for a headgroup tilt transition. For distearoyl PG, we further find that the "usual" gel phase coexists with an interdigitated phase, which exhibits a transition from an orthorhombic into a hexagonal chain packing. The total amount of the interdigitated phase depends significantly on the temperature but is found to be largely independent of temperature equilibration time and different sample preparation protocols. Thus, the development of the interdigitated phase appears to be kinetically trapped. The formation of interdigitated phases in PGs at much smaller chain lengths than in PCs is of high relevance to interaction studies with antimicrobial peptides, as it provides a mechanism for the discrimination of membranes composed of different lipid species.

摘要

我们使用量热法、膨胀法以及X射线衍射法,测定了链长为n(CH2)=14 - 18的二饱和磷脂酰甘油(PGs)在高pH值和离子强度下的相行为。链长为n(CH2)=14和16的PGs表现出与磷脂酰胆碱(PCs)相似的热致行为。尽管预期PG的有效头基尺寸更大,但在凝胶相中测得的每个脂质的面积却比PCs报道的要小。这可以通过PG头基倾斜出双层平面来解释,并且我们提供了头基倾斜转变的实验证据。对于二硬脂酰PG,我们进一步发现“通常”的凝胶相与一种叉指相共存,叉指相表现出从正交晶系到六方链堆积的转变。叉指相的总量显著依赖于温度,但发现其在很大程度上与温度平衡时间和不同的样品制备方案无关。因此,叉指相的形成似乎在动力学上被捕获。与PCs相比,PGs在更短链长时形成叉指相对抗菌肽相互作用研究具有高度相关性,因为它为区分由不同脂质种类组成的膜提供了一种机制。