Leopold Philip L, Pfister K Kevin
Department of Genetic Medicine, Weill Medical College of Cornell University, New York, NY, USA.
Traffic. 2006 May;7(5):516-23. doi: 10.1111/j.1600-0854.2006.00408.x.
To overcome barriers to diffusion, many viruses utilize the microtubule-associated molecular motor cytoplasmic dynein 1 to drive transport towards the nucleus of a target cell. Cytoplasmic dynein 1 generates movement towards the minus end of microtubules located at the microtubule organizing centre (MTOC), a structure that is typically in close proximity to the nucleus. Physiological cargoes for cytoplasmic dynein include membranous organelles, protein complexes and aggregates of misfolded protein. In this review, we discuss the study of microtubule-based translocation of viruses and raise questions about the mechanisms for association with and then dissociation from cytoplasmic dynein with a goal of understanding whether viruses are seen by the intracellular trafficking machinery as functional protein complexes or misfolded protein aggregates.
为了克服扩散障碍,许多病毒利用与微管相关的分子马达细胞质动力蛋白1来驱动向靶细胞核的运输。细胞质动力蛋白1产生向位于微管组织中心(MTOC)的微管负端的运动,微管组织中心通常是一个与细胞核紧密相邻的结构。细胞质动力蛋白的生理性货物包括膜性细胞器、蛋白质复合物和错误折叠蛋白质的聚集体。在本综述中,我们讨论了基于微管的病毒易位研究,并提出了关于与细胞质动力蛋白结合及随后解离机制的问题,目的是了解病毒是否被细胞内运输机制视为功能性蛋白质复合物或错误折叠蛋白质聚集体。