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首页> 外文期刊>Anti-infective agents in medicinal chemistry >Interaction of Melittin with Phospholipid- and Lipopolysaccharide-Containing Model Membranes
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Interaction of Melittin with Phospholipid- and Lipopolysaccharide-Containing Model Membranes

机译:蜂毒肽与磷脂和脂多糖模型膜的相互作用。

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Up to now the details of the mechanisms of melittin action on biological bilayer model systems in dependence on lipid composition, in particular on the kind of head groups, temperature, and ionic strength are not well understood. In particular, the influence of cholesterol present in most eu-caryotic cells and the influence of glycolipids present in bacterial membranes are far from being clear. Here, data are presented from investigations by small-angle X-ray scattering (SAXS), Fourier-transform infrared spectroscopy (FTIR), circular dichroism (CD) spectroscopy, Forster resonance electron transfer (FRET) spectroscopy, and calorimetric techniques (DSC: differential scanning calorimetry and ITC: isothermal titration calorimetry) on the interaction of melittin with different (glyco)lipids, in order to elucidate 1) the peptide secondary structure during the melittin-lipid interaction, 2) to monitor the intercalation of the peptide into membranes, 3) to characterize the aggregate structure of the lipids, 4) to characterize the influence of lipid melittin ratio with regard to the acyl chain melting behaviour as well as 5) to determine the peptide-lipid binding stoichiometry. These experiments are correlated with results from biological test systems, in which the inhibition of the lipopolysaccharide-induced cytokine expression in human immune cells by melittin was monitored.Furthermore, the findings are related to data found in literature with various membrane systems and different techniques. In this way, it is now possible to better understand the details of the melittin-membrane interactions, which is important with respect to the understanding of its anti-inflammatory and antimicrobial properties.
机译:迄今为止,尚未充分了解蜂毒肽对生物双层模型系统的作用机理的细节,该机理取决于脂质组成,特别是取决于头基的种类,温度和离子强度。特别是,大多数真核细胞中存在的胆固醇的影响以及细菌膜中存在的糖脂的影响远未弄清。这里的数据来自小角度X射线散射(SAXS),傅立叶变换红外光谱(FTIR),圆二色性(CD)光谱,福斯特共振电子转移(FRET)光谱和量热技术(DSC:差示扫描量热法和ITC:等温滴定量热法)研究蜂毒素与不同(糖)脂质的相互作用,以阐明1)在蜂毒素-脂质相互作用过程中的肽二级结构,2)监测肽嵌入膜中; 3)表征脂质的聚集结构,4)表征脂质蜂毒素比例对酰基链解链行为的影响,以及5)确定肽-脂质结合化学计量。这些实验与生物学测试系统的结果相关联,其中监测了蜂毒素对人免疫细胞中脂多糖诱导的细胞因子表达的抑制作用。此外,这些发现与文献中使用各种膜系统和不同技术的数据有关。以此方式,现在可以更好地理解蜂毒肽-膜相互作用的细节,这对于理解其抗炎和抗微生物特性是重要的。

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