Kienberger Ferry, Zhu Rong, Moser Rosita, Rankl Christian, Blaas Dieter, Hinterdorfer Peter
Institute for Biophysics, J. Kepler University, Altenbergerstr. 69, A-4040 Linz. Austria.
Biol Proced Online. 2004;6:120-128. doi: 10.1251/bpo80. Epub 2004 Jun 29.
Dynamic force microscopy (DFM) allows imaging of the structure and the assessment of the function of biological specimens in their physiological environment. In DFM, the cantilever is oscillated at a given frequency and touches the sample only at the end of its downward movement. Accordingly, the problem of lateral forces displacing or even destroying bio-molecules is virtually inexistent as the contact time and friction forces are reduced. Here, we describe the use of DFM in studies of human rhinovirus serotype 2 (HRV2) weakly adhering to mica surfaces. The capsid of HRV2 was reproducibly imaged without any displacement of the virus. Release of the genomic RNA from the virions was initiated by exposure to low pH buffer and snapshots of the extrusion process were obtained. In the following, the technical details of previous DFM investigations of HRV2 are summarized.
动态力显微镜(DFM)能够在生物样本的生理环境中对其结构进行成像并评估其功能。在DFM中,悬臂以给定频率振荡,仅在其向下运动的末端接触样品。因此,由于接触时间和摩擦力减少,横向力使生物分子移位甚至破坏的问题几乎不存在。在此,我们描述了DFM在研究弱粘附于云母表面的人鼻病毒2型(HRV2)中的应用。HRV2的衣壳能够被重复成像,且病毒没有任何移位。通过暴露于低pH缓冲液引发病毒粒子中基因组RNA的释放,并获得了挤出过程的快照。接下来,总结了先前对HRV2进行DFM研究的技术细节。