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中国物理学会期刊

蜂毒肽与单组分脂膜相互作用的单分子研究

Single-molecule study of interaction between melittin and one-component lipid membrane

CSTR: 32037.14.aps.70.20210477
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  • 近年来, 单分子追踪技术的出现和发展为研究细胞膜界面生物学过程提供了一条新的途径, 然而细胞膜内生物分子运动的异质性特征使得从大量分子轨迹中区分和分离不同的分子运动模式变得非常困难, 迫切需要发展简单易行的分析方法. 本文以蜂毒肽和单组分平板支撑脂膜的相互作用体系为例, 发展了一种利用单分子运动位移标准差的频数分布来区分和分离不同运动模式脂分子的数据分析方法, 提供了比传统基于位移或回旋半径频数分布的分析方法更高的准确度和更多的定量信息. 利用该方法成功分离得到了脂分子在平板膜内的快慢两种运动状态, 并发现其分布情况部分相符于脂分子在上下叶的位置分布; 在不同浓度蜂毒肽的表面吸附或跨膜成孔作用的影响下, 这两部分脂分子的运动受到了不同的干扰. 本文针对生物膜体系内分子运动的复杂异质性特征发展了一种实现分子运动模式分离的数据分析方法, 并利用此方法获得了蜂毒肽破膜成孔的不同阶段对脂膜上下叶的不同影响. 该方法的开发将对利用单分子追踪技术研究生物体系动力学过程有重要帮助.

     

    In recent years, the emergence and development of single-molecule tracking technology has provided a new way to study the biological process in a cell membrane. However, the heterogeneity of biomolecular motions in cell membranes makes it difficult to distinguish and separate different molecular motion patterns from a large number of molecular trajectories. In this work, taking the system of interaction between melittin and a single-component supported phospholipid bilayer (SLB) membrane as an example, a type of data analysis method is developed through using the frequency distribution of standard deviations of single molecular motion displacements to distinguish and separate lipid molecules in different motion modes. It provides higher accuracy and more quantitative information than traditional analysis methods based on the frequency distribution of displacement or radius of gyration. By using this method, we successfully separate the two moving states of lipids in the SLB, and find that such a distribution is partly consistent with the location distribution of lipids in the upper leaflet and lower leaflet. Under the influence of surface adsorption or transmembrane poration of melittin at different concentrations, the movements of these two types of lipids are disturbed in different ways. In this work, a data analysis method for the separation of molecular motion patterns is developed according to the complex heterogeneity of molecular motions in a phospholipid membrane system. The different effects on the upper leaflet and lower leaflet of a lipid membrane due to melittin actions at different stages are obtained. The method developed in this work will be of great help in studying the dynamic processes of biological systems by using single-molecule tracking technology.

     

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