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Effects of surfactin on membrane models displaying lipid phase separation

机译:表面活性素对显示脂质相分离的膜模型的影响

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Surfactin, a bacterial amphiphilic lipopeptide is attracting more and more attention in view of its bioactive properties which are in relation with its ability to interact with lipids of biological membranes. In this work, we investigated the effect of surfactin on membrane structure using model of membranes, vesicles as well as supported bilayers, presenting coexistence of fluid-disordered (DOPC) and gel (DPPC) phases. A range of complementary methods was used including AFM, ellipsometry, dynamic light scattering, fluorescence measurements of Laurdan, DPH, calcein release, and octadecylrhodamine B dequenching. Our findings demonstrated that surfactin concentration is critical for its effect on the membrane. The results suggest that the presence of rigid domains can play an essential role in the first step of surfactin insertion and that surfactin interacts both with the membrane polar heads and the acyl chain region. A mechanism for the surfactin lipid membrane interaction, consisting of three sequential structural and morphological changes, is proposed. At concentrations below the CMC, surfactin inserted at the boundary between gel and fluid lipid domains, inhibited phase separation and stiffened the bilayer without global morphological change of liposomes. At concentrations close to CMC, surfactin solubilized the fluid phospholipid phase and increased order in the remainder of the lipid bilayer. At higher surfactin concentrations, both the fluid and the rigid bilayer structures were dissolved into mixed micelles and other structures presenting a wide size distribution.
机译:鉴于细菌的两亲性脂肽Surfactin具有生物活性,与它与生物膜的脂质相互作用的能力有关,因此越来越受到关注。在这项工作中,我们使用膜,囊泡以及支持的双层模型研究了表面活性素对膜结构的影响,提出了流体无序(DOPC)和凝胶(DPPC)相的共存。使用了一系列补充方法,包括原子力显微镜,椭圆光度法,动态光散射,Laurdan的荧光测量,DPH,钙黄绿素释放和十八烷基若丹明B淬灭。我们的发现表明,表面活性素浓度对其在膜上的作用至关重要。结果表明,刚性结构域的存在可以在表面活性素插入的第一步中起重要作用,并且表面活性素与膜极头和酰基链区域都相互作用。提出了一种表面活性素脂膜相互作用的机制,该机制由三个连续的结构和形态变化组成。在低于CMC的浓度下,表面活性素插入到凝胶和流体脂质结构域之间的边界处,抑制了相分离并使双层变硬,而没有脂质体的整体形态变化。在接近CMC的浓度下,表面活性素可溶解流体磷脂相,并在剩余的脂质双层中增加顺序。在较高的表面活性素浓度下,流体和刚性双层结构均溶解在混合的胶束中,并呈现出较宽的尺寸分布。

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