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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Native and dry-heated lysozyme interactions with membrane lipid monolayers: Lipid packing modifications of a phospholipid mixture, model of the Escherichia coli cytoplasmic membrane
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Native and dry-heated lysozyme interactions with membrane lipid monolayers: Lipid packing modifications of a phospholipid mixture, model of the Escherichia coli cytoplasmic membrane

机译:天然和干热溶菌酶与膜脂质单层的相互作用:磷脂混合物的脂质堆积修饰,大肠杆菌细胞质膜模型

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Antimicrobial resistance is currently an important public health issue. The need for innovative antimicrobials is therefore growing. The ideal antimicrobial compound should limit antimicrobial resistance. Antimicrobial peptides or proteins such as hen egg white lysozyme are promising molecules that act on bacterial membranes. Hen egg white lysozyme has recently been identified as active on Gram-negative bacteria due to disruption of the outer and cytoplasmic membrane integrity. Furthermore, dry-heating (7 days and 80 degrees C) improves the membrane activity of lysozyme, resulting in higher antimicrobial activity. These in vivo findings suggest interactions between lysozyme and membrane lipids. This is consistent with the findings of several other authors who have shown lysozyme interaction with bacterial phospholipids such as phosphatidylglycerol and cardiolipin. However, until now, the interaction between lysozyme and bacterial cytoplasmic phospholipids has been in need of clarification. This study proposes the use of monolayer models with a realistic bacterial phospholipid composition in physiological conditions. The lysozyme/phospholipid interactions have been studied by surface pressure measurements, ellipsometry and atomic force microscopy. Native lysozyme has proved able to absorb and insert into a bacterial phospholipid monolayer, resulting in lipid packing reorganization, which in turn has lead to lateral cohesion modifications between phospholipids. Dry-heating of lysozyme has increased insertion capacity and ability to induce lipid packing modifications. These in vitro findings are then consistent with the increased membrane disruption potential of dry heated lysozyme in vivo compared to native lysozyme. Moreover, an eggPC monolayer study suggested that lysozyme/phospholipid interactions are specific to bacterial cytoplasmic membranes. (C) 2015 Elsevier B.V. All rights reserved.
机译:抗菌素耐药性目前是重要的公共卫生问题。因此,对创新抗菌剂的需求正在增长。理想的抗微生物化合物应限制抗微生物性。抗菌肽或蛋白质(如鸡蛋清溶菌酶)是作用于细菌膜的有前途的分子。最近,由于外部和细胞质膜完整性的破坏,鸡蛋清溶菌酶对革兰氏阴性细菌具有活性。此外,干热(7天和80摄氏度)可改善溶菌酶的膜活性,从而具有更高的抗菌活性。这些体内发现提示溶菌酶和膜脂质之间的相互作用。这与其他几位作者的发现一致,他们已经证明溶菌酶与细菌磷脂(如磷脂酰甘油和心磷脂)发生相互作用。然而,直到现在,仍需要澄清溶菌酶和细菌细胞质磷脂之间的相互作用。这项研究建议在生理条件下使用具有实际细菌磷脂成分的单层模型。溶菌酶/磷脂的相互作用已通过表面压力测量,椭偏和原子力显微镜研究。事实证明,天然溶菌酶能够吸收并插入细菌磷脂单分子层,从而导致脂质堆积重组,进而导致磷脂之间的侧向内聚修饰。溶菌酶的干式加热具有增加的插入能力和诱导脂质堆积修饰的能力。这些体外发现随后与干溶菌酶在体内相比天然溶菌酶增加的膜破坏潜力相一致。此外,eggPC单层研究表明溶菌酶/磷脂相互作用是细菌细胞质膜特有的。 (C)2015 Elsevier B.V.保留所有权利。

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