Fluorescence imaging and spectroscopy of biomaterials in air and liquid by scanning near-field optical/atomic force microscopy.

Scanning microscopy Pub Date : 1996-01-01
H Muramatsu, N Chiba, K Nakajima, T Ataka, M Fujihira, J Hitomi, T Ushiki
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Abstract

We have developed scanning near-field optical/atomic force microscopy (SNOM/AFM). The SNOM/AFM uses a bent optical fiber simultaneously as a dynamic force AFM cantilever and a SNOM probe. Resonant frequency of the optical fiber cantilever is 15-40 kHz. Optical resolution of the SNOM/AFM images shows less than 50 nm. The SNOM/AFM system contains photon counting system and polychrometer/intensified coupled charge devise (ICCD) system to observe fluorescence image and spectrograph of micro areas, respectively. Cultured cells were stained with fluorescein isothiocyanate (FITC)-labeled anti-keratin antibody or FITC-labeled phalloidin after treatment with Triton X-100. Fluorescence and topographic images were obtained in air and water. The fluorescence images showed clear images of keratin and actin filaments. The SNOM/AFM is perfect to observe biomaterials in liquid with a liquid chamber while the topographic Images showed subcellular structures which correspond to keratin and actin filaments.

用扫描近场光学/原子力显微镜研究空气和液体中生物材料的荧光成像和光谱。
我们开发了扫描近场光学/原子力显微镜(SNOM/AFM)。SNOM/AFM使用弯曲光纤同时作为动力AFM悬臂和SNOM探针。光纤悬臂梁的谐振频率为15 ~ 40khz。SNOM/AFM图像的光学分辨率小于50 nm。SNOM/AFM系统包括光子计数系统和多色计/强化耦合电荷装置(ICCD)系统,分别用于观察微区荧光图像和摄谱仪。Triton X-100处理后,用异硫氰酸荧光素(FITC)标记的抗角蛋白抗体或FITC标记的phalloidin对培养细胞进行染色。在空气和水中获得荧光和地形图像。荧光图像显示清晰的角蛋白和肌动蛋白纤维。SNOM/AFM在液体腔中完美地观察了生物材料,其形貌图像显示了与角蛋白和肌动蛋白丝相对应的亚细胞结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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