Author/Authors :
Yoshino، نويسنده , , Tomoyuki and Sugiyama، نويسنده , , Shigeru and Hagiwara، نويسنده , , Shoji and Fukushi، نويسنده , , Daisuke and Shichiri، نويسنده , , Motoharu and Nakao، نويسنده , , Hidenobu and Kim، نويسنده , , Jong-Min and Hirose، نويسنده , , Tamaki and Muramatsu، نويسنده , , Hiroshi and Ohtani، نويسنده , , Toshio، نويسنده ,
Abstract :
Nano-scale structures of the YOYO-1-stained barley chromosomes and lambda-phage DNA were investigated by scanning near-field optical/atomic force microscopy (SNOM/AFM). This technique enabled precise analysis of fluorescence structural images in relation to the morphology of the biomaterials. The results suggested that the fluorescence intensity does not always correspond to topographic height of the chromosomes, but roughly reflects the local amount and/or density of DNA. Various sizes of the bright fluorescence spots were clearly observed in fluorescence banding-treated chromosomes. Furthermore, fluorescence-stained lambda-phage DNA analysis by SNOM/AFM demonstrated the possibility of nanometer-scale imaging for a novel technique termed nano-fluorescence in situ hybridization (nano-FISH). Thus, SNOM/AFM is a powerful tool for analyzing the structure and the function of biomaterials with higher resolution than conventional optical microscopes.
Keywords :
Scanning near-field optical/atomic force microscopy (SNOM/AFM) , Lambda-phage DNA , Barley chromosome , Fluorescence image