Vogel Sven K
Department of Cellular and Molecular Biophysics, Max Planck Institute of Biochemistry, Am Klopferspitz 18, Martinsried, D-82152, Germany.
Methods Mol Biol. 2016;1365:213-23. doi: 10.1007/978-1-4939-3124-8_11.
A thin layer of actin filaments in many eukaryotic cell types drives pivotal aspects of cell morphogenesis and is generally cited as the actin cortex. Myosin driven contractility and actin cytoskeleton membrane interactions form the basis of fundamental cellular processes such as cytokinesis, cell migration, and cortical flows. How the interplay between the actin cytoskeleton, the membrane, and actin binding proteins drives these processes is far from being understood. The complexity of the actin cortex in living cells and the hardly feasible manipulation of the omnipotent cellular key players, namely actin, myosin, and the membrane, are challenging in order to gain detailed insights about the underlying mechanisms. Recent progress in developing bottom-up in vitro systems where the actin cytoskeleton is combined with reconstituted membranes may provide a complementary route to reveal general principles underlying actin cortex properties. In this chapter the reconstitution of a minimal actin cortex by coupling actin filaments to a supported membrane is described. This minimal system may be very well suited to study for example protein interactions on membrane bound actin filaments in a very controlled and quantitative manner as it may be difficult to perform in living systems.
在许多真核细胞类型中,一层薄薄的肌动蛋白丝驱动着细胞形态发生的关键方面,通常被称为肌动蛋白皮层。肌球蛋白驱动的收缩性以及肌动蛋白细胞骨架与膜的相互作用构成了诸如胞质分裂、细胞迁移和皮层流动等基本细胞过程的基础。肌动蛋白细胞骨架、膜和肌动蛋白结合蛋白之间的相互作用如何驱动这些过程,目前还远未被理解。活细胞中肌动蛋白皮层的复杂性以及对全能细胞关键参与者(即肌动蛋白、肌球蛋白和膜)几乎难以实现的操作,对于深入了解其潜在机制具有挑战性。在开发自下而上的体外系统方面的最新进展,即将肌动蛋白细胞骨架与重构膜相结合,可能为揭示肌动蛋白皮层特性的一般原理提供一条补充途径。在本章中,将描述通过将肌动蛋白丝与支撑膜偶联来重构最小肌动蛋白皮层的方法。这个最小系统可能非常适合以非常可控和定量的方式研究例如膜结合肌动蛋白丝上的蛋白质相互作用,因为在活细胞系统中可能难以进行此类研究。