Grahn A Marika, Daugelavicius Rimantas, Bamford Dennis H
Department of Biosciences and Institute of Biotechnology, University of Helsinki, Finland.
Mol Microbiol. 2002 Dec;46(5):1199-209. doi: 10.1046/j.1365-2958.2002.03250.x.
DNA translocation across the barriers of recipient cells is not well understood. Viral DNA delivery mechanisms offer an opportunity to obtain useful information in systems in which the process can be arrested to a number of stages. PRD1 is an icosahedral double-stranded (ds)DNA bacterial virus with an internal membrane. It is an atypical dsDNA phage, as any of the vertex spikes can be used for receptor recognition. In this report, we dissect the PRD1 DNA entry into a number of steps: (i) outer membrane (OM) penetration; (ii) peptidoglycan digestion; (iii) cytoplasmic membrane (CM) penetration; and (iv) DNA translocation. We present a model for PRD1 DNA entry proposing that the initial stage of entry is powered by the pressure build-up during DNA packaging. The viral protein P11 is shown to function as the first DNA delivery protein needed to penetrate the OM. We also report a DNA translocation machinery composed of at least three viral integral membrane proteins, P14, P18 and P32.
目前人们对DNA穿过受体细胞屏障的过程还了解甚少。病毒DNA传递机制为在该过程可在多个阶段被阻断的系统中获取有用信息提供了一个契机。PRD1是一种具有内膜的二十面体双链(ds)DNA细菌病毒。它是一种非典型的dsDNA噬菌体,因为任何一个顶点刺突都可用于受体识别。在本报告中,我们将PRD1的DNA进入过程剖析为多个步骤:(i)外膜(OM)穿透;(ii)肽聚糖消化;(iii)细胞质膜(CM)穿透;以及(iv)DNA转位。我们提出了一个PRD进入DNA的模型,认为进入的初始阶段是由DNA包装过程中积累的压力驱动的。病毒蛋白P11被证明是穿透外膜所需的第一种DNA传递蛋白。我们还报告了一种由至少三种病毒整合膜蛋白P14、P18和P32组成的DNA转位机制。