Slepak Vladlen Z, Hurley James B
Department of Molecular and Cellular Pharmacology and Neuroscience Program, University of Miami Miller School of Medicine, Miami, FL, USA.
IUBMB Life. 2008 Jan;60(1):2-9. doi: 10.1002/iub.7.
Many signaling proteins change their location within cells in response to external stimuli. In photoreceptors, this phenomenon is remarkably robust. The G protein of rod photoreceptors and rod transducin concentrates in the outer segments (OS) of these neurons in darkness. Within approximately 30 minutes after illumination, rod transducin redistributes throughout all of the outer and inner compartments of the cell. Visual arrestin concurrently relocalises from the inner compartments to become sequestered primarily within the OS. In the past several years, the question of whether these proteins are actively moved by molecular motors or whether they are redistributed by simple diffusion has been extensively debated. This review focuses on the most essential works in the area and concludes that the basic principle driving this protein movement is diffusion. The directionality and light dependence of this movement is achieved by the interactions of arrestin and transducin with their spatially restricted binding partners.
许多信号蛋白会根据外部刺激改变其在细胞内的位置。在光感受器中,这种现象非常明显。视杆光感受器的G蛋白和视杆转导素在黑暗中集中在这些神经元的外段(OS)。光照后约30分钟内,视杆转导素重新分布到细胞的所有外段和内段。视觉抑制蛋白同时从内段重新定位,主要被隔离在OS内。在过去几年中,关于这些蛋白质是由分子马达主动移动还是通过简单扩散重新分布的问题一直存在广泛争论。这篇综述聚焦于该领域最重要的研究成果,并得出结论:驱动这种蛋白质移动的基本原理是扩散。这种移动的方向性和光依赖性是通过抑制蛋白和转导素与其空间受限的结合伴侣之间的相互作用实现的。