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Fluorescence anisotropy measurement of green fluorescent protein for nano-environment probing

机译:纳米环境探测绿色荧光蛋白的荧光各向异性测量

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Fluorescence anisotropy of GFP molecules, suspended in solution and immobilized on a glass substrate, was measured to investigate the application for nano-environment probe. Nano-environment around living cell is of interest in relation with wide range of fields, such as cell interaction in cancer tissue, nerve signal transmission and so on. However, nano-environment is so sensitive to the interference of probe or measurement itself. For example, measurement of neuron potential is performed by inserting electrode to the tissue, or staining with toxic dye. For measurement of nano-environment GFP has some superior characteristics. GFP molecule itself is soluble protein and has little toxicity to the cell. It need no prosthetic group for fluorescent activity, and easily introduced by genetic method. We investigated the fluorescence anisotropy of GFP for probing molecular motion in the nano space. Anisotropy of free molecule in solution was compatible with theoretical value. Immobilized molecule, on the contrary, showed higher anisotropy than theoretically expected. This extraordinary value may come from hydrophobic interaction of GFP with glass surface, that can be utilized for nano-probing.
机译:测量悬浮在溶液中的GFP分子的荧光各向异性,并在玻璃基板上固定在玻璃基板上,以研究纳米环境探针的应用。纳米环境周围的活细胞与各种领域的关系感兴趣,例如癌组织中的细胞相互作用,神经信号传输等。然而,纳米环境对探针或测量本身的干扰非常敏感。例如,通过将电极插入组织或用毒性染料染色来进行神经元电位的测量。用于测量纳米环境GFP具有一些优异的特性。 GFP分子本身是可溶的蛋白质,对细胞略微毒性。它不需要对荧光活性的假体组,并且通过遗传方法轻松引入。我们研究了用于探测纳米空间中的分子运动的GFP的荧光各向异性。溶液中的自由分子的各向异性与理论值相容。相反,固定的分子显示比理论上更高的各向异性。这种非凡的值可以来自GFP与玻璃表面的疏水相互作用,其可用于纳米探测器。

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