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利用扫描近场光学/原子力显微镜对单个DNA分子进行形貌和荧光同步成像以进行DNA分析。

Simultaneous topographic and fluorescence imaging of single DNA molecules for DNA analysis with a scanning near-field optical/atomic force microscope.

作者信息

Kim J M, Ohtani T, Sugiyama S, Hirose T, Muramatsu H

机构信息

Department of Food Engineering, National Food Research Institute, Tsukuba, Ibaraki, Japan.

出版信息

Anal Chem. 2001 Dec 15;73(24):5984-91. doi: 10.1021/ac010536i.

Abstract

High-resolution fluorescence imaging of lambda-phage DNA molecules, intercalated with the dye YOYO-1, has been performed by a SNOM/AFM based on a bent-type optical fiber probe. A modified design of the optical probe has been made, and successful near-field optical resolution has been obtained for the strongly stretched lambda-phage DNA molecules. The best optical resolution was estimated at 45 nm for the dye-intercalated single lambda-DNA molecules by a mean width evaluation. In our comparison between the far-field fluorescence and high-resolution near-field fluorescence images for the DNA, it has been found that the near-field images much better defined the intercalation state of the dye. Finally, the relation between the DNA shapes and the dye distribution states, and the discrimination between the double-stranded and single-stranded DNA molecules, are discussed by comparing the topography and fluorescence images of the SNOM/AFM.

摘要

基于弯曲型光纤探针的扫描近场光学显微镜/原子力显微镜(SNOM/AFM)对嵌入染料YOYO-1的λ噬菌体DNA分子进行了高分辨率荧光成像。对光学探针进行了改进设计,并对强烈拉伸的λ噬菌体DNA分子成功获得了近场光学分辨率。通过平均宽度评估,估计染料嵌入的单个λ-DNA分子的最佳光学分辨率为45纳米。在我们对DNA的远场荧光和高分辨率近场荧光图像的比较中,发现近场图像能更好地确定染料的嵌入状态。最后,通过比较SNOM/AFM的形貌和荧光图像,讨论了DNA形状与染料分布状态之间的关系以及双链和单链DNA分子之间的区分。

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