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Bilayer Thickness and Curvature Influence Binding and Insertion of a pHLIP Peptide

机译:双层厚度和曲率影响益共线肽的结合和插入

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摘要

The physical properties of lipid bilayers, such as curvature and fluidity, can affect the interactions of polypeptides with membranes, influencing biological events. Additionally, given the growing interest in peptide-based therapeutics, understanding the influence of membrane properties on membrane-associated peptides has potential utility. pH low insertion peptides (pHLIPs) are a family of water-soluble peptides that can insert across cell membranes in a pH-dependent manner, enabling the use of pH to follow peptide-lipid interactions. Here we study pHLIP interactions with liposomes varying in size and composition, to determine the influence of several key membrane physical properties. We find that pHLIP binding to bilayer surfaces at neutral pH is governed by the ease of access to the membrane's hydrophobic core, which can be facilitated by membrane curvature, thickness, and the cholesterol content of the membrane. After surface binding, if the pH is lowered, the kinetics of pHLIP folding to form a helix and subsequent insertion across the membrane depends on the fluidity and energetic dynamics of the membrane. We showed that pHLIP is capable of forming a helix across lipid bilayers of different thicknesses at low pH. However, the kinetics of the slow phase of insertion corresponding to the translocation of C-terminal end of the peptide across lipid bilayer, vary approximately twofold, and correlate with bilayer thickness and fluidity. Although these influences are not large, local curvature variations in membranes of different fluidity could selectively influence surface binding in mixed cell populations.
机译:脂质双层的物理性质,例如曲率和流动性,可以影响多肽与膜的相互作用,影响生物事件。另外,鉴于对基于肽的治疗剂的兴趣日益增长,了解膜特性对膜相关肽的影响具有潜在的效用。 pH低插入肽(Phlips)是一种水溶性肽的家族,可以以pH依赖性方式穿过细胞膜,使得使用pH以遵循肽 - 脂质相互作用。在这里,我们研究与大小和组成不同的脂质体的phlip相互作用,以确定几个关键膜物理性质的影响。我们发现,在中性pH下与双层表面的phlip结合是通过对膜的疏水芯的易于进入的疏水芯的控制,这可以通过膜的膜曲率,厚度和膜的胆固醇含量促进。在表面结合后,如果pH降低,则PHLIP折叠的动力学以形成螺旋并随后插入膜的随后取决于膜的流动性和能量动态。我们表明,Phlip能够在低pH下穿过不同厚度的脂质双层的螺旋。然而,与脂质双层的肽的C末端的易位的插入缓慢相的动力学,变化大约两倍,与双层厚度和流动性相关。尽管这些影响不大,但不同流动性膜的局部曲率变化可以选择性地影响混合细胞群中的表面结合。

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