Shnyrova Anna V, Zimmerberg Joshua
Laboratory of Cellular and Molecular Biology, Program in Physical Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, USA.
Methods Enzymol. 2009;464:55-75. doi: 10.1016/S0076-6879(09)64004-0.
Enveloped virus particles select their lipid-protein components and egress by budding from the host cell membranes. The matrix protein of many enveloped viruses has been proposed as a crucial element for viral budding; however, molecular mechanisms behind membrane remodeling by the matrix protein are yet to be unraveled. Here, we describe a set of in vitro functional reconstitution assays that allow quantitative evaluation of both, membrane binding and creation of membrane curvature by the matrix protein isolated from Newcastle Disease Virus. Individual budding events orchestrated by the matrix protein can be resolved in real time. The assays may be applied for direct reconstitution of the on-membrane action of cellular proteins involved in membrane curvature induction upon binding in vivo.
包膜病毒粒子通过从宿主细胞膜出芽来选择其脂质 - 蛋白质成分并释放。许多包膜病毒的基质蛋白被认为是病毒出芽的关键因素;然而,基质蛋白介导膜重塑的分子机制尚未阐明。在此,我们描述了一组体外功能重建实验,可对从新城疫病毒分离的基质蛋白的膜结合和膜曲率形成进行定量评估。由基质蛋白精心编排的单个出芽事件可实时解析。这些实验可用于直接重建体内结合时参与诱导膜曲率的细胞蛋白的膜上作用。