Department of Physics, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Biophys J. 2011 Jun 22;100(12):2875-82. doi: 10.1016/j.bpj.2011.05.014.
Viral infection begins with the binding of a virus to a specific target on the surface of the host cell, followed by viral genome delivery into the host and a continuation of the infection process. Before binding occurs, the virus must first find its receptor by a process whose details are largely unknown. We applied high-resolution fluorescence microscopy and single-particle tracking to elucidate the target-finding process in bacteriophage λ as it infects an Escherichia coli cell. By monitoring the motion of individual viruses through the early stages of infection, we identified a unique spatial focusing process that allows a virus to arrive from its initial random landing site to its destination at the cell pole. The search process is governed by the interaction between the virus and the LamB receptors, and by the spatial organization of the receptor network on the cell surface. Our findings allowed us to develop a theoretical model for the target-finding process that reproduces the key features observed in experiment. We discuss the possible implications of our findings for the process of viral receptor-finding in higher systems.
病毒感染始于病毒与宿主细胞表面特定靶标的结合,随后是病毒基因组进入宿主并继续感染过程。在结合发生之前,病毒必须首先通过一个其细节在很大程度上未知的过程找到其受体。我们应用高分辨率荧光显微镜和单粒子跟踪技术来阐明噬菌体 λ在感染大肠杆菌细胞时的靶标寻找过程。通过监测单个病毒在感染早期的运动,我们确定了一种独特的空间聚焦过程,使病毒能够从初始随机着陆点到达细胞极的目的地。搜索过程受病毒与 LamB 受体之间的相互作用以及受体在细胞表面的空间组织的控制。我们的研究结果使我们能够开发出一种用于目标寻找过程的理论模型,该模型再现了实验中观察到的关键特征。我们讨论了我们的发现对高等系统中病毒受体寻找过程的可能影响。