Department of Physics, University of Helsinki, Helsinki, Finland.
Biophys J. 2013 May 21;104(10):2264-72. doi: 10.1016/j.bpj.2013.03.061.
The translocation of genetic material from the viral capsid to the cell is an essential part of the viral infection process. Whether the energetics of this process is driven by the energy stored within the confined nucleic acid or cellular processes pull the genome into the cell has been the subject of discussion. However, in vitro studies of genome ejection have been limited to a few head-tailed bacteriophages with a double-stranded DNA genome. Here we describe a DNA release system that operates in an archaeal virus. This virus infects an archaeon Haloarcula hispanica that was isolated from a hypersaline environment. The DNA-ejection velocity of His1, determined by single-molecule experiments, is comparable to that of bacterial viruses. We found that the ejection process is modulated by the external osmotic pressure (polyethylene glycol (PEG)) and by increased ion (Mg(2+) and Na(+)) concentration. The observed ejection was unidirectional, randomly paused, and incomplete, which suggests that cellular processes are required to complete the DNA transfer.
病毒衣壳内遗传物质向细胞内的转移是病毒感染过程中的一个重要环节。该过程的能量是由受限核酸内储存的能量驱动,还是由细胞过程将基因组拉入细胞内驱动,这一直是讨论的主题。然而,基因组弹射的体外研究仅限于少数具有双链 DNA 基因组的有尾噬菌体。在这里,我们描述了一种在古菌病毒中起作用的 DNA 释放系统。这种病毒感染了一种从高盐环境中分离出来的古菌嗜盐菌。通过单分子实验测定的 His1 的 DNA 喷射速度与细菌病毒相当。我们发现,喷射过程受到外部渗透压(聚乙二醇(PEG))和离子(Mg(2+) 和 Na(+))浓度增加的调节。观察到的喷射是单向的、随机暂停的且不完全,这表明需要细胞过程来完成 DNA 转移。