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Optimizing DNA Visualization with a Solver P47H Atomic-Force Microscope

机译:使用Solver P47H原子力显微镜优化DNA可视化

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摘要

The conditions for visualizing DNA molecules with a Solver P47H atomic-force microscope (NT-MTD, Moscow, Russia) were optimized. The DNA samples had different sizes, types, and conformations (pBR-322 plasmid DNA and chicken erythrocyte DNA) and were immobilized on mica. The microscope was equipped with a Smena-B detecting head and was operated in a tapping mode. The dependence of the amplitude of tip oscillations on the spacing between the tip and the test sample's surface was used to determine the optimum parameters of scanning. The highest quality and reproducibility of the DNA images were attained by scanning with a small initial amplitude (9-23 nm) of cantilever oscillations and an optimum gain (0.08-0.3). Images with the highest contrast were obtained in the amplitude curve's region corresponding to a repulsive interaction regime. The operating amplitude was set at one-half (or slightly less than) the initial amplitude of tip oscillations.
机译:优化了使用Solver P47H原子力显微镜(NT-MTD,俄罗斯莫斯科)观察DNA分子的条件。 DNA样品具有不同的大小,类型和构象(pBR-322质粒DNA和鸡红细胞DNA),并固定在云母上。显微镜配备有Smena-B检测头,并在敲击模式下操作。尖端振荡幅度对尖端与试样表面之间间距的依赖性被用来确定最佳的扫描参数。通过以较小的悬臂振荡的初始振幅(9-23 nm)和最佳增益(0.08-0.3)进行扫描,可以获得最高质量和可重复性的DNA图像。在幅度曲线的区域中获得了具有最高对比度的图像,该区域对应于排斥相互作用机制。将操作幅度设置为尖端振荡的初始幅度的一半(或略小于)。

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