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四氢嘧啶、羟乙基四氢嘧啶和 β-羟基丁酸对不同复杂性的磷脂双层膜的温度和压力稳定性的影响。

Effect of ectoine, hydroxyectoine and β-hydroxybutyrate on the temperature and pressure stability of phospholipid bilayer membranes of different complexity.

机构信息

Physical Chemistry I - Biophysical Chemistry, Faculty of Chemistry and Chemical Biology, TU Dortmund University, Otto-Hahn Street 4a, 44227 Dortmund, Germany.

Physical Chemistry I - Biophysical Chemistry, Faculty of Chemistry and Chemical Biology, TU Dortmund University, Otto-Hahn Street 4a, 44227 Dortmund, Germany; Institute for Biochemistry, Westfälische Wilhelms Universität Münster, Wilhelm Klemm Str. 2, 48149 Münster, Germany.

出版信息

Colloids Surf B Biointerfaces. 2019 Jun 1;178:404-411. doi: 10.1016/j.colsurfb.2019.03.026. Epub 2019 Mar 16.

Abstract

Previous research has shown that ectoines fluidize lipid monolayers by increasing the liquid expanded region in DPPC monolayers and also decreasing the line tension responsible for the phase morphology. Here, we explored possible effects of the compatible osmolytes ectoine, hydroxyectoine and β-hydroxybutyrate on lipid bilayer membranes, including effects of temperature and pressure. The effect of the protective osmolytes on the phase transition of DPPC bilayers was investigated by fluorescence spectroscopy, differential scanning calorimetry and pressure perturbation calorimetry. A slight change of the phase behavior was observed, which resulted in a stabilization of the gel phase, which may be caused by an alteration of the hydration properties at the lipid interface and H-bond and electrostatic interactions in the headgroup region. We then explored the cosolvents' effects on giant unilamellar vesicles (GUVs) formed by lipid mixtures exhibiting phase separation into liquid-ordered (l) and liquid-disordered (l) domains using BODIPY-PC and the DiI dye as labels. The presence of both, ectoine and hydroxyectoine showed significant effects on the lateral organization increasing the fluid domains. Moreover, we observed a considerable increase in the adhesion behavior of small vesicles onto GUV surfaces. Diffusion studies by fluorescence recovery after photobleaching experiments on POPC giant vesicles quantitatively showed a hydroxyectoine-induced increase of the diffusion coefficient values, clearly demonstrating an increase in the lateral mobility of lipid within the bilayer membrane. This study provides clear evidence for the fluidizing effect of the compatible solutes on bilayer lipid membranes. A marked effect, however, was only detected if phase separated domains exist.

摘要

先前的研究表明,通过增加 DPPC 单层膜中的液体膨胀区域并降低对相形态起作用的线张力,胞外多糖使脂质单层膜流动化。在这里,我们探讨了相容的渗透剂如 4-羟乙基哌嗪乙磺酸、羟乙基脲和 β-羟基丁酸对脂质双层膜的可能影响,包括温度和压力的影响。通过荧光光谱法、差示扫描量热法和压力微扰量热法研究了保护渗透剂对 DPPC 双层膜相变的影响。观察到相行为的轻微变化,导致凝胶相的稳定化,这可能是由于脂质界面的水合性质以及头基区域的氢键和静电相互作用的改变所致。然后,我们研究了共溶剂对由脂质混合物形成的具有相分离成有序液体(l)和无序液体(l)域的巨大单层囊泡(GUV)的影响,使用 BODIPY-PC 和 DiI 染料作为标记。同时存在 4-羟乙基哌嗪乙磺酸和羟乙基脲对增加流体域的侧向组织具有显著影响。此外,我们观察到小囊泡在 GUV 表面上的粘附行为有相当大的增加。通过荧光恢复后光漂白实验对 POPC 巨囊泡进行扩散研究,定量地显示了羟乙基脲诱导的扩散系数值增加,这清楚地表明了双层膜中脂质的侧向流动性增加。这项研究为相容的渗透剂对双层脂质膜的流动化作用提供了明确的证据。然而,只有在存在相分离域的情况下才检测到明显的效果。

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