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Xiangfeng Guo

Publications and source records attributed to Xiangfeng Guo.

3 recordsLinked to original sources

Visible study of mercuric ion and its conjugate in living cells of mammals and plants.

The investigation of mercuric ion and mercuric conjugate inside live specimens has drawn intense attention because of their cytotoxicity. The translocation, transportation, and distribution of Hg2+ inside either mammals or plants, however, are still invisible due to the lack of favorable fluorescent molecular sensors for Hg2+. Here, two sensors, 2,6-bis(4'-peperazino-N'-hydroxylethoxylethylene-1',8'-naphthalimide)dimethylpyridine and 2,6-bis(4'-peperazino-N'-butyl-1',8'-naphthalimide)dimethylpyridine, which were composed of nitrogen atoms of 2,6-bis(aminomethyl)pyridine as the ion receptor and the donor of photoinduced electron transfer, were applied to the cultured mammalian cells and plant cells. Their membrane permeability, low toxicity, slow bleaching/fading, and high selectivity and sensitivity to Hg2+ in a live cell rendered them attractive to become real-time and real-space sensors. For the first time, the transportation of Hg2+ cation and Hg2+ conjugate of cysteine was observed with the help of a fluorescence microscope. The chloroplast location of Hg2+ in transgenic tobacco was also visible.

Animals↗

A highly selective and sensitive fluorescent chemosensor for Hg2+ in neutral buffer aqueous solution.

A selective and sensitive fluorescent chemosensor for Hg2+, which was composed of two aminonaphthalimide fluorophores and a receptor of 2,6-bis(aminomethyl)pyridine, was synthesized through the reaction of 2,6-bis(chloromethyl)pyridine and N-[2-(2-hydroxyethoxy)ethyl]-4-piperazino-1,8-naphthalimide. The chemosensor showed an about 17-fold increase in fluorescence quantum yield upon addition of 1 equiv of Hg2+ in neutral buffer aqueous solution, and the other common metal ions did not notably disturb the detection of Hg2+.

Buffers↗

Fluorescent imaging of acute mercuric chloride exposure on cultured human kidney tubular epithelial cells.

BACKGROUND: Imaging of intracellular mercuric ion is necessary for mechanism of renal toxicity of exposure to HgCl2. The distribution of Hg2+ inside a living cell, however, is still invisible due to the lack of high selective and sensitive fluorescent molecular probe for Hg2+. METHODS: A new fluorescent probe, EPNP, was applied to the cultured cells of human kidney proximal tubular epithelial cell line (HKC) in the presence of HgCl2 and some other bivalent ions. The relative fluorescence intensity of EPNP was measured and fluorescence images were taken by laser scanning confocal microscope. RESULTS: Results showed it led to an Hg2+ concentration- and time-dependent increase in fluorescence intensity, and responded weakly for some other heavy and transition metal ions. It could be seen during acute exposure on HKC cells, Hg2+ locate perinuclear, and on nuclear membrane, which was beyond what one knew before. CONCLUSION: EPNP is a real-time and on-line probe for imaging Hg2+ in a living cell due to its high selectivity and sensitivity for Hg2+ and slow bleaching/fading. Both the probe and the new results about the distribution of intracellular Hg2+ may be helpful for relevant biologic research.

Cells, Cultured↗