Herrmann A, Clague M J, Blumenthal R
Humboldt-Universität zu Berlin, Fachbereich Biologie, Germany.
Biophys J. 1993 Jul;65(1):528-34. doi: 10.1016/S0006-3495(93)81054-3.
Nonadsorbing polymers such as dextran and poly(ethylene glycol) enhance binding as well as extents of fusion of influenza virus with erythrocytes. Kinetics and extent of viral membrane fusion were measured using an assay based on lipid mixing of a fluorescent dye. The effects of nonadsorbing polymers were in the concentration range from 0 to 10 wt%, far below the concentration required to overcome hydration repulsion forces. The enhancing effects were dependent on the molecular weight of nonadsorbing polymer, and only occurred at molecular weight > 1500; this links the phenomena we observe to the so-called "excluded volume effect" of nonadsorbing polymers. The time delay between triggering and the onset of influenza virus fusion was significantly reduced in the presence of nonadsorbing polymers. High molecular weight poly(ethylene glycol) also induced fusion of vesicular stomatitis virus with intact erythrocytes, which do not serve as target of vesicular stomatitis virus fusion in the absence of the polymer. The forces between membranes which determine rate-limiting processes in viral fusion and how they are affected by nonadsorbing polymers are discussed.
诸如右旋糖酐和聚乙二醇之类的非吸附性聚合物既能增强流感病毒与红细胞的结合,也能提高融合程度。利用基于荧光染料脂质混合的检测方法来测定病毒膜融合的动力学和程度。非吸附性聚合物的作用浓度范围为0至10重量%,远低于克服水化排斥力所需的浓度。增强作用取决于非吸附性聚合物的分子量,且仅在分子量大于1500时才会出现;这将我们观察到的现象与非吸附性聚合物的所谓“排除体积效应”联系起来。在存在非吸附性聚合物的情况下,流感病毒触发与融合开始之间的时间延迟显著缩短。高分子量聚乙二醇还能诱导水泡性口炎病毒与完整红细胞发生融合,而在没有该聚合物的情况下,完整红细胞并非水泡性口炎病毒的融合靶标。本文讨论了决定病毒融合限速过程的膜间作用力以及它们如何受到非吸附性聚合物的影响。