Perrais David, Merrifield Christien J
Laboratoire de Physiologie Cellulaire de la Synapse, CNRS UMR 5091, Université Bordeaux 2, Institut François Magendie, 146 rue Léo Saignat, 33077 Bordeaux Cedex, France.
Dev Cell. 2005 Nov;9(5):581-92. doi: 10.1016/j.devcel.2005.10.002.
Clathrin-mediated endocytosis is the main path for receptor internalization in metazoans and is essential for controlling cell integrity and signaling. It is driven by a large array of protein and lipid interactions that have been deciphered mainly by biochemical and genetic means. To place these interactions into context, and ultimately build a fully operative model of endocytosis at the molecular level, it is necessary to know the kinetic details of the role of each protein in this process. In this review, we describe the recent efforts made, by using live cell imaging, to define clear steps in the formation of endocytic vesicles and to observe the recruitment of key proteins during membrane invagination, the scission of a newly formed vesicle, and its movement away from the plasma membrane.
网格蛋白介导的内吞作用是后生动物中受体内化的主要途径,对于控制细胞完整性和信号传导至关重要。它由大量蛋白质和脂质相互作用驱动,这些相互作用主要通过生化和遗传手段得以阐明。为了将这些相互作用置于相应背景中,并最终构建一个分子水平上完全可运作的内吞作用模型,有必要了解每种蛋白质在这一过程中作用的动力学细节。在本综述中,我们描述了近期通过活细胞成像所做的努力,以明确内吞小泡形成过程中的清晰步骤,并观察关键蛋白质在膜内陷、新形成小泡的分裂以及其从质膜脱离过程中的募集情况。