Dávila María J, Mayer Christian
Institute of Physical Chemistry, CENIDE, University of Duisburg-Essen, 45141 Essen, Germany.
Life (Basel). 2022 Jan 20;12(2):145. doi: 10.3390/life12020145.
Recently, an evolution experiment was carried out in a cyclic process, which involved periodic vesicle formation in combination with peptide and vesicle selection. As an outcome, an octapeptide (KSPFPFAA) was identified which rapidly integrated into the vesicle membrane and, according to its significant accumulation, is obviously connected to a particular advantage of the corresponding functionalized vesicle. Here we report a molecular dynamics study of the structural details of the functionalized vesicle membrane, which was a product of this evolution process and is connected to several survival mechanisms. In order to elucidate the particular advantage of this structure, we performed all-atom molecular dynamics simulations to examine structural changes and interactions of the peptide (KSPFPFAA) with the given octadecanoic acid/octadecylamine (1:1) bilayer under acidic conditions. The calculations clearly demonstrate the specific interactions between the peptide and the membrane and reveal the mechanisms leading to the improved vesicle survival.
最近,在一个循环过程中进行了一项进化实验,该过程涉及周期性的囊泡形成以及肽和囊泡的筛选。结果,鉴定出一种八肽(KSPFPFAA),它能迅速整合到囊泡膜中,并且根据其显著的积累情况,显然与相应功能化囊泡的特定优势相关。在此,我们报告了对功能化囊泡膜结构细节的分子动力学研究,该膜是这一进化过程的产物,并且与多种存活机制相关。为了阐明这种结构的特定优势,我们进行了全原子分子动力学模拟,以研究在酸性条件下该肽(KSPFPFAA)与给定的十八烷酸/十八烷基胺(1:1)双层膜的结构变化和相互作用。计算结果清楚地证明了肽与膜之间的特定相互作用,并揭示了导致囊泡存活率提高的机制。