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Fluorescence Interference Contrast Based Approach to Study Real Time Interaction of Melittin with Plasma Membranes

机译:基于荧光干涉对比的方法研究蜂毒肽与血浆膜的实时相互作用

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Melittin is an anti-bacterial and hemolytic toxic peptide found in bee venom. Cell lysis behavior of peptides has been widely investigated, but the exact interaction mechanism of lytic peptides with lipid membranes and its constituents has not been understood completely. In this paper we study the melittin interaction with lipid plasma membranes in real time using non-invasive and non-contact fluorescence interference contrast microscopy (FLIC). Particularly the interaction of melittin with plasma membranes was studied in a controlled molecular environment, where these plasma membrane were composed of saturated lipid, 1,2-diphytanoyl-sn-glycero-3-phosphocholine (DPhPC) and unsaturated lipid, 1,2-dioleoyl-sn-glycero-3-phosphocholine(DOPC) with and without cholesterol. We found out that melittin starts to form nanometer size pores in the plasma membranes shortly after interacting with membranes. But the addition of cholesterol in plasma membrane slows down the pore formation process. Our results show that inclusion of cholesterol to the plasma membranes make them more resilient towards pore formation and lysis of membrane.
机译:蜂毒肽是一种在蜜蜂毒液中发现的抗菌和溶血毒性肽。肽的细胞裂解行为已被广泛研究,但是裂解肽与脂质膜及其成分的确切相互作用机理尚未完全了解。在本文中,我们使用非侵入性和非接触式荧光干涉对比显微镜(FLIC)实时研究蜂毒肽与脂质质膜的相互作用。特别是在受控分子环境中研究了蜂毒肽与质膜的相互作用,其中这些质膜由饱和脂质1,2-二植烷酰基-sn-甘油-3-磷酸胆碱(DPhPC)和不饱和脂质1,2-2-组成。含和不含胆固醇的二油酰基-sn-甘油-3-磷酸胆碱(DOPC)。我们发现蜂毒肽与细胞膜相互作用后不久就开始在质膜上形成纳米尺寸的孔。但是在质膜中添加胆固醇会减慢孔的形成过程。我们的结果表明,质膜中包含胆固醇使它们对孔的形成和膜的溶解更具弹性。

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