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首页> 外文期刊>Journal of Biochemistry >Identification of Radicals Formed in the Reaction Mixtures of Rat Liver Microsomes with ADP, Fe3+ and NADPH Using HPLC–EPR and HPLC–EPR–MS
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Identification of Radicals Formed in the Reaction Mixtures of Rat Liver Microsomes with ADP, Fe3+ and NADPH Using HPLC–EPR and HPLC–EPR–MS

机译:用HPLC-EPR和HPLC-EPR-MS鉴定大鼠肝微粒体与ADP,Fe 3 + 和NADPH的反应混合物中形成的自由基

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The reaction of rat liver microsomes with Fe3+, ADP and NADPH was examined using EPR, HPLC–EPR and HPLC–EPR–MS combined use of spin trapping technique. A prominent EPR spectrum (αN = 1.58 mT and αHβ = 0.26 mT) was observed in the complete reaction mixture. The EPR spectrum was hardly observed for the complete reaction mixture without rat liver microsomes. The radicals appear to be derived from microsomal components. The EPR spectrum was also hardly observed in the absence of Fe3+. Addition of some iron chelators such as EDTA, citrate and ADP resulted in the dramatic change in the EPR intensity. Iron ions seem to be essential for this reaction. For the complete reaction mixture with boiled microsomes, a weak EPR spectrum was observed, suggesting that enzymes participate in the reaction. Five peaks were separated on the HPLC–EPR elution profile of the complete reaction mixture of rat liver microsomes with ADP, Fe3+ and NADPH. The retention times of the peaks 1 to 5 were 19.4, 22.5, 27.3, 29.8 and 31.4 min, respectively. To identify the radical adducts, HPLC–EPR–MS analyses were performed for the three prominent peaks. The HPLC–EPR–MS analyses showed that a new radical adduct, 4-POBN/1-hydroxypentyl radical, in addition to 4-POBN/ethyl radical adducts, forms in a reaction mixture of rat liver microsomes with ADP, Fe3+ and NADPH.
机译:采用EPR,HPLC-EPR和HPLC-EPR-MS结合自旋阱技术,研究了大鼠肝微粒体与Fe 3 + ,ADP和NADPH的反应。在整个反应混合物中观察到了显着的EPR光谱(α N = 1.58 mT,α H β= 0.26 mT)。没有大鼠肝微粒体,几乎没有观察到完整反应混合物的EPR光谱。自由基似乎源自微粒体组分。在没有Fe 3 + 的情况下,也几乎没有观察到EPR谱。加入一些铁螯合剂,例如EDTA,柠檬酸盐和ADP,导致EPR强度发生了巨大变化。铁离子似乎对该反应至关重要。对于带有煮沸微粒体的完整反应混合物,观察到弱的EPR光谱,表明酶参与了反应。大鼠肝微粒体与ADP,Fe 3 + 和NADPH的完整反应混合物的HPLC-EPR洗脱谱上有五个峰分离。峰1至5的保留时间分别为19.4、22.5、27.3、29.8和31.4分钟。为了鉴定自由基加合物,对三个突出峰进行了HPLC-EPR-MS分析。 HPLC-EPR-MS分析表明,在大鼠肝微粒体与ADP的反应混合物中,除了4-POBN /乙基自由基加合物外,还形成了一个新的自由基加合物4-POBN / 1-羟基戊基。 3 + 和NADPH。

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