Zuchero J Bradley
Department of Cellular and Molecular Pharmacology, University of California, San Francisco, CA, USA.
Methods Mol Biol. 2007;370:213-26. doi: 10.1007/978-1-59745-353-0_15.
The actin cytoskeleton is essential to all eukaryotic cells. In addition to playing important structural roles, assembly of actin into filaments powers diverse cellular processes, including cell motility and endocytosis. Actin polymerization is tightly regulated by various cofactors, which control spatial and temporal assembly of actin as well as the physical properties of these filaments. Development of an in vitro model of actin polymerization from purified components has allowed for great advances in determining the effects of these proteins on the actin cytoskeleton. The pyrene actin assembly assay is a powerful tool for determining the effect of a protein on the kinetics of actin assembly, either directly or as mediated by proteins such as nucleators or capping factors. In addition, fluorescently labeled phalloidin can be used to visualize the filaments that are created in vitro to give insight into how these proteins influence actin filament superstructure.
肌动蛋白细胞骨架对所有真核细胞都至关重要。除了发挥重要的结构作用外,肌动蛋白组装成细丝还驱动多种细胞过程,包括细胞运动和内吞作用。肌动蛋白聚合受到各种辅助因子的严格调控,这些因子控制着肌动蛋白的时空组装以及这些细丝的物理特性。利用纯化成分建立肌动蛋白聚合的体外模型,在确定这些蛋白质对肌动蛋白细胞骨架的影响方面取得了巨大进展。芘肌动蛋白组装测定法是一种强大的工具,可直接或通过成核剂或封端因子等蛋白质介导,确定蛋白质对肌动蛋白组装动力学的影响。此外,荧光标记的鬼笔环肽可用于可视化体外形成的细丝,以深入了解这些蛋白质如何影响肌动蛋白细丝的超结构。