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Measurement of Protein 53 Diffusion Coefficient in Live HeLa Cells Using Raster Image Correlation Spectroscopy (RICS)
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作者 Sungmin Hong Ying-Nai Wang +5 位作者 Hirohito Yamaguchi Harinibytaraya Sreenivasappa Chao-Kai Chou Pei-Hsiang Tsou Mien-Chie Hung jun kameoka 《Journal of Biomaterials and Nanobiotechnology》 2010年第1期31-36,共6页
We have applied Raster Image Correlation Spectroscopy (RICS) technique to characterize the dynamics of protein 53 (p53) in living cells before and after the treatment with DNA damaging agents. HeLa cells expressing Gr... We have applied Raster Image Correlation Spectroscopy (RICS) technique to characterize the dynamics of protein 53 (p53) in living cells before and after the treatment with DNA damaging agents. HeLa cells expressing Green Fluores-cent Protein (GFP) tagged p53 were incubated with and without DNA damaging agents, cisplatin or eptoposide, which are widely used as chemotherapeutic drugs. Then, the diffusion coefficient of GFP-p53 was determined by RICS and it was significantly reduced after the drug treatment while that of the one without drug treatment was not. It is suggested that the drugs induced the interaction of p53 with either other proteins or DNA. Together, our results demonstrated that RICS is able to detect the protein dynamics which may be associated with protein-protein or protein-DNA interactions in living cells and it may be useful for the drug screening. 展开更多
关键词 RASTER Image Correlation SPECTROSCOPY DIFFUSION COEFFICIENT p53 DNA DAMAGE
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A Low Cost and Versatile STED Superresolution Fluorescent Microscope
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作者 Daniel McBride Chin Su +1 位作者 jun kameoka Stanislav Vitha 《Modern Instrumentation》 2013年第3期41-48,共8页
A versatile and inexpensive super-resolution fluorescent microscope that functions as easily as a conventional confocal microscope is described. Components of the microscope were designed on a platform which was place... A versatile and inexpensive super-resolution fluorescent microscope that functions as easily as a conventional confocal microscope is described. Components of the microscope were designed on a platform which was placed atop a surplus microscope frame. All optical components and equipments used are given. The excitation and depletion beams are extracted from a compact low-cost supercontinuum light source. The focal spot of the depletion beam at the focal plane is studied and imaged by a 100 nm aperture near-field fiber tip. The collinear excitation and depletion beam focused by a 0.9 numerical aperture microscope objective produce a 90 nm lateral super-resolution as verified by imaging 100 nm diameter fluorescent beads. 展开更多
关键词 Stimulated Emission-Depletion MICROSCOPY STED
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