Kienberger Ferry, Zhu Rong, Moser Rosita, Blaas Dieter, Hinterdorfer Peter
Institute for Biophysics, J. Kepler University, A-4040 Linz, Austria.
J Virol. 2004 Apr;78(7):3203-9. doi: 10.1128/jvi.78.7.3203-3209.2004.
Human rhinoviruses were imaged under physiological conditions by dynamic force microscopy. Topographical images revealed various polygonal areas on the surfaces of the 30-nm viral particles. RNA release was initiated by exposure to a low-pH buffer. The lengths of the RNAs that were released but still connected to the virus capsid varied between 40 and 330 nm, whereas RNA molecules that were completely released from the virus were observed with lengths up to 1 micro m. Fork-like structure elements with 30-nm extensions were sometimes resolved at one end of the RNA molecules. They possibly correspond to the characteristic multi-stem-loop conformation, the internal ribosomal entry site, located at the 5' region of the genome. This study demonstrates that dynamic force microscopy can be used to study viral RNA release in situ under physiological conditions.
通过动态力显微镜在生理条件下对人鼻病毒进行成像。形貌图像显示30纳米病毒颗粒表面存在各种多边形区域。通过暴露于低pH缓冲液引发RNA释放。释放但仍与病毒衣壳相连的RNA长度在40至330纳米之间变化,而从病毒中完全释放的RNA分子长度可达1微米。在RNA分子的一端有时能分辨出具有30纳米延伸的叉状结构元件。它们可能对应于位于基因组5'区域的特征性多茎环构象,即内部核糖体进入位点。这项研究表明,动态力显微镜可用于在生理条件下原位研究病毒RNA释放。