Target Fluorescent Probes for Detecting Hydrogen Peroxide in Macrophage Cell
碩士 === 國立臺灣大學 === 生化科學研究所 === 98 === One major contributor to oxidative damage is hydrogen peroxide (H2O2), which has been considered mostly as reactive oxidative species (ROS), and mediate pathogenic processes. In addition, H2O2 is emerging as a newly recognized as a secondary messenger in cellular...
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ndltd-TW-098NTU051031152015-11-02T04:04:02Z http://ndltd.ncl.edu.tw/handle/77722282994735171162 Target Fluorescent Probes for Detecting Hydrogen Peroxide in Macrophage Cell 以標的螢光探針研究巨噬細胞內之過氧化氫 Ching-Min Chang 張靖敏 碩士 國立臺灣大學 生化科學研究所 98 One major contributor to oxidative damage is hydrogen peroxide (H2O2), which has been considered mostly as reactive oxidative species (ROS), and mediate pathogenic processes. In addition, H2O2 is emerging as a newly recognized as a secondary messenger in cellular signal transduction. However, a substantial challenge in elucidating its diverse roles in complex biological environments is the lack of methods for probing this reactive oxygen metabolite in living systems specifically. Here, we reported the synthesis and application of Probe 1 (1a and 1b), two new fluorescent probes that showed high selectivity for H2O2 and were capable of visualizing the addition of exogenous H2O2 to living cells. These probes were able to serve as a tool for evaluating the H2O2 production in complex physiological and pathological processes. The main purpose of this study was to create an easy, time-saving, and a straightforward platform for measurement the exact H2O2 concentration in living RAW 264.7 cell. Through quantitating the relative fluorescence intensity in vivo by spectrofluoromerty, we might discover new small molecules for potential antioxidants in the future. Shih-Hsiung Wu 吳世雄 2010 學位論文 ; thesis 85 en_US |
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碩士 === 國立臺灣大學 === 生化科學研究所 === 98 === One major contributor to oxidative damage is hydrogen peroxide (H2O2), which has been considered mostly as reactive oxidative species (ROS), and mediate pathogenic processes. In addition, H2O2 is emerging as a newly recognized as a secondary messenger in cellular signal transduction. However, a substantial challenge in elucidating its diverse roles in complex biological environments is the lack of methods for probing this reactive oxygen metabolite in living systems specifically. Here, we reported the synthesis and application of Probe 1 (1a and 1b), two new fluorescent probes that showed high selectivity for H2O2 and were capable of visualizing the addition of exogenous H2O2 to living cells. These probes were able to serve as a tool for evaluating the H2O2 production in complex physiological and pathological processes. The main purpose of this study was to create an easy, time-saving, and a straightforward platform for measurement the exact H2O2 concentration in living RAW 264.7 cell. Through quantitating the relative fluorescence intensity in vivo by spectrofluoromerty, we might discover new small molecules for potential antioxidants in the future.
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author2 |
Shih-Hsiung Wu |
author_facet |
Shih-Hsiung Wu Ching-Min Chang 張靖敏 |
author |
Ching-Min Chang 張靖敏 |
spellingShingle |
Ching-Min Chang 張靖敏 Target Fluorescent Probes for Detecting Hydrogen Peroxide in Macrophage Cell |
author_sort |
Ching-Min Chang |
title |
Target Fluorescent Probes for Detecting Hydrogen Peroxide in Macrophage Cell |
title_short |
Target Fluorescent Probes for Detecting Hydrogen Peroxide in Macrophage Cell |
title_full |
Target Fluorescent Probes for Detecting Hydrogen Peroxide in Macrophage Cell |
title_fullStr |
Target Fluorescent Probes for Detecting Hydrogen Peroxide in Macrophage Cell |
title_full_unstemmed |
Target Fluorescent Probes for Detecting Hydrogen Peroxide in Macrophage Cell |
title_sort |
target fluorescent probes for detecting hydrogen peroxide in macrophage cell |
publishDate |
2010 |
url |
http://ndltd.ncl.edu.tw/handle/77722282994735171162 |
work_keys_str_mv |
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