Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut.
Physics Department, University of Rhode Island, Kingston, Rhode Island.
Biophys J. 2018 May 8;114(9):2107-2115. doi: 10.1016/j.bpj.2018.03.036.
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.
脂质双层的物理性质,如曲率和流动性,可以影响多肽与膜的相互作用,从而影响生物事件。此外,鉴于人们对基于肽的治疗方法越来越感兴趣,了解膜性质对膜相关肽的影响具有潜在的用途。pH 低插入肽(pHLIP)是一类水溶性肽,能够以 pH 依赖性的方式插入细胞膜,从而可以利用 pH 来跟踪肽-脂相互作用。在这里,我们研究了 pHLIP 与不同大小和组成的脂质体的相互作用,以确定几个关键的膜物理性质的影响。我们发现,pHLIP 在中性 pH 下与双层表面的结合受进入膜疏水核心难易程度的控制,而膜曲率、厚度和膜中的胆固醇含量可以促进这种结合。在表面结合后,如果 pH 降低,pHLIP 折叠形成螺旋并随后插入膜的动力学取决于膜的流动性和能量动力学。我们表明,pHLIP 能够在低 pH 下形成穿过不同厚度脂质双层的螺旋。然而,对应于肽的 C 末端穿过脂质双层易位的慢相插入的动力学大约变化两倍,并且与双层厚度和流动性相关。尽管这些影响不大,但不同流动性的膜中的局部曲率变化可能会选择性地影响混合细胞群体中的表面结合。